geneid | 5188 |
---|---|
ensemblid | ENSG00000059691.12 |
hgncid | 8849 |
symbol | GATB |
name | glutamyl-tRNA amidotransferase subunit B |
refseq_nuc | NM_004564.3 |
refseq_prot | NP_004555.1 |
ensembl_nuc | ENST00000263985.11 |
ensembl_prot | ENSP00000263985.6 |
mane_status | MANE Select |
chr | chr4 |
start | 151670504 |
end | 151761007 |
strand | - |
ver | v1.2 |
region | chr4:151670504-151761007 |
region5000 | chr4:151665504-151766007 |
regionname0 | GATB_chr4_151670504_151761007 |
regionname5000 | GATB_chr4_151665504_151766007 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 557 | 260 | 60 | 48 | 114 | 8 | 28 | 92 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0002 | 0/0 | 557 | 47 | 22 | 3 | 20 | 2 | 0 | 11 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0003 | 0/0 | 557 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0004 | 0/0 | 557 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0005 | 0/0 | 557 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0006 | 0/0 | 557 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0007 | 0/0 | 557 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0008 | 0/0 | 557 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0009 | 0/0 | 557 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1674 | 244 | 58 | 45 | 106 | 7 | 27 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
c0002 | 0/0 | 1674 | 47 | 22 | 3 | 20 | 2 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
c0003 | 0/0 | 1674 | 9 | 0 | 2 | 6 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
c0004 | 0/0 | 1674 | 4 | 4 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
c0005 | 0/1 | 1674 | 3 | 0 | 1 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
c0006 | 0/0 | 1674 | 2 | 2 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
c0007 | 0/0 | 1674 | 2 | 2 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
c0008 | 0/0 | 1674 | 2 | 2 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
c0009 | 0/0 | 1674 | 2 | 1 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
c0010 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
c0011 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
c0012 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
c0013 | 0/0 | 1674 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
c0014 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0200 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0280 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1674 | 244 | 58 | 45 | 106 | 7 | 27 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0001c0003 | 0/0 | 1674 | 9 | 0 | 2 | 6 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0001c0005 | 0/1 | 1674 | 3 | 0 | 1 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0001c0009 | 0/0 | 1674 | 2 | 1 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0001c0011 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0001c0012 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0002c0002 | 0/0 | 1674 | 47 | 22 | 3 | 20 | 2 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0003c0004 | 0/0 | 1674 | 4 | 4 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0004c0008 | 0/0 | 1674 | 2 | 2 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0005c0006 | 0/0 | 1674 | 2 | 2 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0006c0007 | 0/0 | 1674 | 2 | 2 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0007c0014 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0008c0013 | 0/0 | 1674 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0009c0010 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2369 | 153 | 52 | 22 | 57 | 6 | 16 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0001c0001t0002 | 1/0 | 2369 | 91 | 6 | 23 | 49 | 1 | 11 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0001c0003t0001 | 0/0 | 2369 | 3 | 0 | 0 | 3 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0001c0003t0002 | 0/0 | 2369 | 6 | 0 | 2 | 3 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0001c0005t0002 | 0/1 | 2369 | 3 | 0 | 1 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0001c0009t0001 | 0/0 | 2369 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0001c0009t0002 | 0/0 | 2369 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0001c0011t0002 | 0/0 | 2369 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0001c0012t0001 | 0/0 | 2369 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0002c0002t0001 | 0/0 | 2369 | 47 | 22 | 3 | 20 | 2 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0003c0004t0001 | 0/0 | 2369 | 4 | 4 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0004c0008t0001 | 0/0 | 2369 | 2 | 2 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0005c0006t0001 | 0/0 | 2369 | 2 | 2 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0006c0007t0002 | 0/0 | 2369 | 2 | 2 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0007c0014t0002 | 0/0 | 2369 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0008c0013t0001 | 0/0 | 2369 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
a0009c0010t0001 | 0/0 | 2369 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | copy fasta | chr4 | 151665504 | 151766007 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0200 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0003t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0003t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0003t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0003t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0003t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0005t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0005t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0005t0002g0280 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0009t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0009t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0011t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0001c0012t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0003c0004t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0003c0004t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0003c0004t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0003c0004t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0004c0008t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0004c0008t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0005c0006t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0005c0006t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0006c0007t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0006c0007t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0007c0014t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0008c0013t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
a0009c0010t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | GBR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | GBR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | FIN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | FIN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG00323 | hp1 | a0001 | c0005 | t0002 | g0279 | EUR | FIN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0033 | EUR | FIN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | CHS | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | CHS | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0291 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0299 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0301 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0015 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0273 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0281 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01255 | hp2 | a0001 | c0005 | t0002 | g0204 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01258 | hp2 | a0008 | c0013 | t0001 | g0092 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0290 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0240 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01361 | hp1 | a0001 | c0003 | t0002 | g0209 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0027 | EUR | IBS | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | IBS | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01884 | hp1 | a0003 | c0004 | t0001 | g0312 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0303 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01978 | hp1 | a0001 | c0003 | t0002 | g0249 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0026 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0045 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | CDX | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | CDX | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CDX | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | CDX | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02451 | hp2 | a0001 | c0012 | t0001 | g0293 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02523 | hp2 | a0009 | c0010 | t0001 | g0052 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02572 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0260 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02622 | hp2 | a0005 | c0006 | t0001 | g0044 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02717 | hp2 | a0002 | c0002 | t0001 | g0047 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02809 | hp1 | a0005 | c0006 | t0001 | g0030 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0046 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02897 | hp1 | a0006 | c0007 | t0002 | g0014 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02970 | hp2 | a0003 | c0004 | t0001 | g0314 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02976 | hp2 | a0003 | c0004 | t0001 | g0311 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0048 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03209 | hp2 | a0004 | c0008 | t0001 | g0190 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03453 | hp1 | a0003 | c0004 | t0001 | g0313 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03453 | hp2 | a0001 | c0009 | t0001 | g0182 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03540 | hp1 | a0006 | c0007 | t0002 | g0013 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0228 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0284 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0224 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0242 | SAS | STU | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | BEB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | BEB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | STU | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0225 | SAS | BEB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | STU | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | CHB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | CHB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18747 | hp2 | a0001 | c0003 | t0002 | g0245 | EAS | CHB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | YRI | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0020 | AFR | YRI | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18939 | hp2 | a0001 | c0009 | t0002 | g0232 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18945 | hp2 | a0001 | c0003 | t0001 | g0145 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18948 | hp1 | a0001 | c0003 | t0001 | g0161 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18949 | hp2 | a0007 | c0014 | t0002 | g0302 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | LWK | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | LWK | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19043 | hp1 | a0004 | c0008 | t0001 | g0191 | AFR | LWK | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | LWK | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19057 | hp1 | a0001 | c0003 | t0001 | g0162 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19060 | hp2 | a0001 | c0003 | t0002 | g0255 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19068 | hp2 | a0001 | c0011 | t0002 | g0244 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19082 | hp1 | a0001 | c0003 | t0002 | g0216 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | YRI | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0049 | AFR | YRI | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ASW | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ASW | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | TSI | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0223 | EUR | TSI | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA20905 | hp1 | a0001 | c0003 | t0002 | g0254 | SAS | GIH | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | GIH | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | USA | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | USA | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0278 | AFR | USA | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | USA | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | LWK | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
homoSapiens_chm13v2 | hp1 | a0001 | c0005 | t0002 | g0280 | REF | REF | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0200 | REF | REF | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:151688651
|
T | C | 1 | a0008 | 1 | HG01258.hp2 | missense_variant | MODERATE | c.1310A>G | p.Gln437Arg | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/13 | 1335/2369 | 1310/1674 | 437/557 | chr4 | 151688651 | ||
chr4:151701381
|
T | C | 1 | a0004 | 2 | HG03209.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.1145A>G | p.Glu382Gly | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/13 | 1170/2369 | 1145/1674 | 382/557 | chr4 | 151701381 | ||
chr4:151705266
|
T | C | 1 | a0005 | 2 | HG02622.hp2 HG02809.hp1 |
missense_variant | MODERATE | c.881A>G | p.Tyr294Cys | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/13 | 906/2369 | 881/1674 | 294/557 | chr4 | 151705266 | ||
chr4:151717074
|
C | A | 1 | a0006 | 2 | HG02897.hp1 HG03540.hp1 |
missense_variant&splice_region_variant | MODERATE | c.442G>T | p.Ala148Ser | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 4/13 | 467/2369 | 442/1674 | 148/557 | chr4 | 151717074 | ||
chr4:151758837
|
G | A | 1 | a0007 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.262C>T | p.Arg88Cys | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/13 | 287/2369 | 262/1674 | 88/557 | chr4 | 151758837 | ||
chr4:151760834
|
A | G | 1 | a0009 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.149T>C | p.Leu50Pro | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/13 | 174/2369 | 149/1674 | 50/557 | chr4 | 151760834 | ||
chr4:151760846
|
G | A | 1 | a0003 | 4 | HG01884.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
missense_variant | MODERATE | c.137C>T | p.Ala46Val | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/13 | 162/2369 | 137/1674 | 46/557 | chr4 | 151760846 | ||
chr4:151760894
|
G | T | 3 | a0002a0005a0006 | 51 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(48): Show |
missense_variant | MODERATE | c.89C>A | p.Ala30Asp | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/13 | 114/2369 | 89/1674 | 30/557 | chr4 | 151760894 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:151671237
|
C | T | 1 | a0001c0012 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.1611G>A | p.Ala537Ala | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 13/13 | 1636/2369 | 1611/1674 | 537/557 | chr4 | 151671237 | ||
chr4:151688632
|
C | T | 1 | a0001c0003 | 9 | HG01361.hp1 HG01978.hp1 NA18747.hp2 others(6): Show |
splice_region_variant&synonymous_variant | LOW | c.1329G>A | p.Glu443Glu | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/13 | 1354/2369 | 1329/1674 | 443/557 | chr4 | 151688632 | ||
chr4:151688674
|
A | C | 1 | a0001c0005 | 3 | HG00323.hp1 HG01255.hp2 homoSapiens_chm13v2.hp1 |
synonymous_variant | LOW | c.1287T>G | p.Thr429Thr | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/13 | 1312/2369 | 1287/1674 | 429/557 | chr4 | 151688674 | ||
chr4:151701476
|
G | A | 1 | a0001c0009 | 2 | HG03453.hp2 NA18939.hp2 |
synonymous_variant | LOW | c.1050C>T | p.Asp350Asp | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/13 | 1075/2369 | 1050/1674 | 350/557 | chr4 | 151701476 | ||
chr4:151708048
|
A | G | 1 | a0001c0011 | 1 | NA19068.hp2 | synonymous_variant | LOW | c.817T>C | p.Leu273Leu | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/13 | 842/2369 | 817/1674 | 273/557 | chr4 | 151708048 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:151671039
|
T | C | 10 | a0001c0001t0001a0001c0003t0001a0001c0009t0001others(7): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*135A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 13/13 | 135 | chr4 | 151671039 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:151671317
|
A | ATTAC | 211 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(208): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1546-19_1546-16dup others(4): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151671317 | ||||||
chr4:151671563
|
G | T | 4 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(1): Show | 4 | HG02965.hp1 HG03195.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1546-261C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151671563 | ||||||
chr4:151671781
|
A | G | 211 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(208): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1546-479T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151671781 | ||||||
chr4:151671794
|
G | A | 1 | a0002c0002t0001g0028 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1546-492C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151671794 | ||||||
chr4:151671801
|
C | T | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1546-499G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151671801 | ||||||
chr4:151671803
|
G | C | 5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(2): Show | 5 | HG01891.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546-501C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151671803 | ||||||
chr4:151671979
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1546-677G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151671979 | ||||||
chr4:151672054
|
G | C | 2 | a0006c0007t0002g0013a0006c0007t0002g0014 | 2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1545+708C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151672054 | ||||||
chr4:151672127
|
C | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0212 | 2 | HG00140.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1545+635G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151672127 | ||||||
chr4:151672198
|
C | T | 4 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0001g0120others(1): Show | 4 | HG02083.hp1 HG02132.hp1 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.1545+564G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151672198 | ||||||
chr4:151672230
|
A | G | 32 | a0001c0001t0001g0141a0002c0002t0001g0003a0002c0002t0001g0015others(29): Show | 33 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1545+532T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151672230 | ||||||
chr4:151672257
|
T | C | 211 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(208): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1545+505A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151672257 | ||||||
chr4:151672258
|
C | T | 3 | a0003c0004t0001g0311a0003c0004t0001g0312a0003c0004t0001g0314 | 3 | HG01884.hp1 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1545+504G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151672258 | ||||||
chr4:151672318
|
C | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0185 | 2 | HG00639.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1545+444G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151672318 | ||||||
chr4:151672383
|
G | GTTC | 3 | a0001c0001t0002g0275a0001c0001t0002g0276a0001c0001t0002g0277 | 3 | NA19057.hp2 NA19064.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1545+376_1545+378d others(5): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151672383 | ||||||
chr4:151672397
|
G | A | 1 | a0001c0001t0002g0303 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1545+365C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151672397 | ||||||
chr4:151672424
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1545+338T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151672424 | ||||||
chr4:151673046
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1411-150G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673046 | ||||||
chr4:151673068
|
G | T | 1 | a0002c0002t0001g0043 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1411-172C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673068 | ||||||
chr4:151673252
|
T | TG | 58 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(55): Show | 59 | HG00280.hp1 HG00558.hp1 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.1411-357dupC | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673252 | ||||||
chr4:151673252
|
T | TGG | 83 | a0001c0001t0001g0053a0001c0001t0001g0057a0001c0001t0001g0059others(80): Show | 83 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.1411-358_1411-357d others(4): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673252 | ||||||
chr4:151673252
|
T | TGGG | 7 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0143others(4): Show | 7 | HG00140.hp2 HG00280.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1411-357_1411-356i others(5): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673252 | ||||||
chr4:151673253
|
G | T | 2 | a0005c0006t0001g0030a0005c0006t0001g0044 | 2 | HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1411-357C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673253 | ||||||
chr4:151673254
|
G | GT | 5 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0201others(2): Show | 5 | HG02040.hp2 NA18948.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.1411-359_1411-358i others(3): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673254 | ||||||
chr4:151673254
|
GC | G | 26 | a0001c0001t0001g0141a0001c0009t0001g0182a0002c0002t0001g0002others(23): Show | 27 | HG00323.hp2 HG01515.hp1 HG02132.hp2 others(24): Show |
intron_variant | MODIFIER | c.1411-359delG | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673254 | ||||||
chr4:151673255
|
C | CG | 29 | a0001c0001t0001g0238a0001c0001t0002g0195a0001c0001t0002g0196others(26): Show | 29 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1411-360dupC | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673255 | ||||||
chr4:151673255
|
C | G | 185 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(182): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1411-359G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673255 | ||||||
chr4:151673572
|
G | A | 31 | a0001c0001t0001g0141a0002c0002t0001g0003a0002c0002t0001g0015others(28): Show | 32 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1411-676C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673572 | ||||||
chr4:151673573
|
A | G | 31 | a0001c0001t0001g0141a0002c0002t0001g0003a0002c0002t0001g0015others(28): Show | 32 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1411-677T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673573 | ||||||
chr4:151673662
|
T | C | 212 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(209): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1411-766A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673662 | ||||||
chr4:151674145
|
C | T | 6 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(3): Show | 6 | HG02486.hp2 HG03139.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.1411-1249G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151674145 | ||||||
chr4:151674147
|
C | T | 2 | a0001c0001t0002g0202a0001c0001t0002g0203 | 2 | NA19005.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1411-1251G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151674147 | ||||||
chr4:151674221
|
A | G | 212 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(209): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1411-1325T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151674221 | ||||||
chr4:151674386
|
A | T | 68 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(65): Show | 68 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.1411-1490T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151674386 | ||||||
chr4:151674645
|
C | T | 8 | a0001c0009t0001g0182a0002c0002t0001g0002a0002c0002t0001g0012others(5): Show | 9 | HG02630.hp1 HG03041.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1411-1749G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151674645 | ||||||
chr4:151674676
|
A | G | 1 | a0001c0001t0002g0230 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1411-1780T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151674676 | ||||||
chr4:151674684
|
C | G | 211 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(208): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1411-1788G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151674684 | ||||||
chr4:151674994
|
G | A | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137 | 3 | HG01243.hp1 HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1411-2098C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151674994 | ||||||
chr4:151674996
|
A | G | 1 | a0002c0002t0001g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1411-2100T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151674996 | ||||||
chr4:151675150
|
G | A | 2 | a0006c0007t0002g0013a0006c0007t0002g0014 | 2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1411-2254C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151675150 | ||||||
chr4:151675218
|
C | T | 2 | a0006c0007t0002g0013a0006c0007t0002g0014 | 2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1411-2322G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151675218 | ||||||
chr4:151675356
|
T | C | 212 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(209): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1411-2460A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151675356 | ||||||
chr4:151675374
|
C | T | 31 | a0001c0001t0001g0141a0002c0002t0001g0003a0002c0002t0001g0015others(28): Show | 32 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1411-2478G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151675374 | ||||||
chr4:151675388
|
T | C | 214 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(211): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1411-2492A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151675388 | ||||||
chr4:151675516
|
G | A | 211 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(208): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1411-2620C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151675516 | ||||||
chr4:151675673
|
G | A | 1 | a0002c0002t0001g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1411-2777C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151675673 | ||||||
chr4:151675676
|
C | T | 1 | a0001c0001t0002g0202 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1411-2780G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151675676 | ||||||
chr4:151675918
|
A | G | 1 | a0002c0002t0001g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1411-3022T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151675918 | ||||||
chr4:151675995
|
A | G | 32 | a0001c0001t0001g0141a0002c0002t0001g0003a0002c0002t0001g0015others(29): Show | 33 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1411-3099T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151675995 | ||||||
chr4:151676050
|
C | G | 212 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(209): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1411-3154G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151676050 | ||||||
chr4:151676153
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1411-3257C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151676153 | ||||||
chr4:151676225
|
C | T | 1 | a0001c0001t0002g0250 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1411-3329G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151676225 | ||||||
chr4:151676388
|
A | G | 212 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(209): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1410+3425T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151676388 | ||||||
chr4:151676389
|
A | G | 2 | a0006c0007t0002g0013a0006c0007t0002g0014 | 2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1410+3424T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151676389 | ||||||
chr4:151676530
|
AGGCTTGG others(7): Show |
A | 31 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(28): Show | 31 | HG00558.hp1 HG00597.hp1 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.1410+3269_1410+328 others(18): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151676530 | ||||||
chr4:151676873
|
G | C | 1 | a0001c0001t0001g0070 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1410+2940C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151676873 | ||||||
chr4:151677353
|
C | T | 2 | a0001c0001t0001g0236a0002c0002t0001g0045 | 2 | HG02145.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.1410+2460G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151677353 | ||||||
chr4:151677451
|
C | T | 211 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(208): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1410+2362G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151677451 | ||||||
chr4:151677465
|
TAC | T | 31 | a0001c0001t0001g0141a0002c0002t0001g0003a0002c0002t0001g0015others(28): Show | 32 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1410+2346_1410+234 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151677465 | ||||||
chr4:151677515
|
G | A | 4 | a0001c0001t0001g0067a0001c0001t0001g0074a0001c0001t0001g0075others(1): Show | 4 | NA18969.hp1 NA19009.hp1 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.1410+2298C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151677515 | ||||||
chr4:151677546
|
T | C | 211 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(208): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1410+2267A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151677546 | ||||||
chr4:151677670
|
G | A | 3 | a0001c0001t0002g0004a0001c0001t0002g0214a0001c0001t0002g0215 | 4 | HG00639.hp2 HG00741.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1410+2143C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151677670 | ||||||
chr4:151677724
|
C | G | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1410+2089G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151677724 | ||||||
chr4:151677840
|
C | T | 211 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(208): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1410+1973G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151677840 | ||||||
chr4:151677874
|
T | TA | 8 | a0001c0009t0001g0182a0002c0002t0001g0002a0002c0002t0001g0012others(5): Show | 9 | HG02630.hp1 HG03041.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1410+1938dupT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151677874 | ||||||
chr4:151678094
|
G | C | 1 | a0001c0001t0001g0082 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1410+1719C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678094 | ||||||
chr4:151678153
|
C | G | 1 | a0001c0001t0001g0123 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1410+1660G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678153 | ||||||
chr4:151678222
|
C | A | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1410+1591G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678222 | ||||||
chr4:151678316
|
C | G | 1 | a0001c0001t0001g0152 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1410+1497G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678316 | ||||||
chr4:151678356
|
T | C | 1 | a0001c0001t0001g0310 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1410+1457A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678356 | ||||||
chr4:151678437
|
TTC | T | 203 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(200): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1410+1374_1410+137 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678437 | ||||||
chr4:151678437
|
TTCTC | T | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078 | 3 | NA18612.hp2 NA18977.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1410+1372_1410+137 others(8): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678437 | ||||||
chr4:151678500
|
A | T | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1410+1313T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678500 | ||||||
chr4:151678620
|
A | AAACAGAG others(304): Show |
1 | a0001c0001t0001g0156 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1410+1192_1410+119 others(315): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678620 | ||||||
chr4:151678620
|
A | AAACAGAG others(308): Show |
2 | a0001c0003t0001g0161a0001c0003t0001g0162 | 2 | NA18948.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1410+1192_1410+119 others(319): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678620 | ||||||
chr4:151678620
|
A | AAACAGAG others(316): Show |
1 | a0001c0001t0001g0155 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1410+1192_1410+119 others(327): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678620 | ||||||
chr4:151678620
|
A | AAACAGAG others(317): Show |
1 | a0001c0001t0001g0153 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1410+1192_1410+119 others(328): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678620 | ||||||
chr4:151678620
|
A | AAACAGAG others(318): Show |
1 | a0001c0001t0001g0154 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1410+1192_1410+119 others(329): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678620 | ||||||
chr4:151678620
|
A | AAACAGAG others(328): Show |
1 | a0001c0001t0001g0151 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1410+1192_1410+119 others(339): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678620 | ||||||
chr4:151678620
|
A | AAACAGAG others(329): Show |
1 | a0001c0001t0001g0158 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1410+1192_1410+119 others(340): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678620 | ||||||
chr4:151678620
|
A | AAACAGAG others(348): Show |
2 | a0001c0001t0001g0138a0001c0003t0001g0145 | 2 | NA18945.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1410+1192_1410+119 others(359): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678620 | ||||||
chr4:151678620
|
A | AAACAGAG others(351): Show |
1 | a0001c0001t0001g0139 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1410+1192_1410+119 others(362): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678620 | ||||||
chr4:151678750
|
G | A | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1410+1063C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678750 | ||||||
chr4:151678841
|
A | C | 2 | a0001c0001t0001g0134a0001c0001t0001g0164 | 2 | HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1410+972T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678841 | ||||||
chr4:151678883
|
G | GT | 202 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(199): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1410+929dupA | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678883 | ||||||
chr4:151678883
|
G | GTTT | 11 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0151others(8): Show | 11 | HG00597.hp1 NA18941.hp2 NA18945.hp2 others(8): Show |
intron_variant | MODIFIER | c.1410+927_1410+929d others(5): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678883 | ||||||
chr4:151678935
|
C | T | 2 | a0006c0007t0002g0013a0006c0007t0002g0014 | 2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1410+878G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678935 | ||||||
chr4:151679063
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1410+750A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151679063 | ||||||
chr4:151679218
|
C | T | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1410+595G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151679218 | ||||||
chr4:151679299
|
A | G | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1410+514T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151679299 | ||||||
chr4:151679445
|
C | A | 1 | a0005c0006t0001g0030 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1410+368G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151679445 | ||||||
chr4:151679456
|
C | T | 1 | a0001c0001t0002g0198 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1410+357G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151679456 | ||||||
chr4:151679547
|
T | C | 205 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(202): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1410+266A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151679547 | ||||||
chr4:151679994
|
T | G | 205 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(202): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1332-103A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151679994 | ||||||
chr4:151680171
|
A | G | 7 | a0002c0002t0001g0002a0002c0002t0001g0012a0002c0002t0001g0016others(4): Show | 8 | HG02630.hp1 HG03041.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1332-280T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680171 | ||||||
chr4:151680201
|
A | G | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-310T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680201 | ||||||
chr4:151680202
|
T | C | 1 | a0001c0001t0002g0284 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1332-311A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680202 | ||||||
chr4:151680253
|
C | T | 2 | a0006c0007t0002g0013a0006c0007t0002g0014 | 2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1332-362G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680253 | ||||||
chr4:151680278
|
T | TA | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-388dupT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680278 | ||||||
chr4:151680278
|
T | TAA | 8 | a0001c0001t0001g0057a0001c0001t0001g0088a0001c0001t0001g0120others(5): Show | 8 | HG00280.hp2 HG00735.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1332-389_1332-388d others(4): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680278 | ||||||
chr4:151680314
|
C | T | 4 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(1): Show | 4 | HG02965.hp1 HG03195.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1332-423G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680314 | ||||||
chr4:151680423
|
T | TA | 7 | a0002c0002t0001g0002a0002c0002t0001g0012a0002c0002t0001g0016others(4): Show | 8 | HG02630.hp1 HG03041.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1332-533dupT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680423 | ||||||
chr4:151680515
|
A | G | 1 | a0001c0001t0002g0287 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1332-624T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680515 | ||||||
chr4:151680612
|
C | T | 1 | a0002c0002t0001g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1332-721G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680612 | ||||||
chr4:151680689
|
G | A | 172 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(169): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1332-798C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680689 | ||||||
chr4:151680750
|
G | A | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-859C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680750 | ||||||
chr4:151680799
|
G | A | 5 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0148others(2): Show | 5 | HG02055.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1332-908C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680799 | ||||||
chr4:151680814
|
G | A | 5 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1332-923C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680814 | ||||||
chr4:151680890
|
T | C | 2 | a0001c0001t0002g0241a0001c0001t0002g0281 | 2 | HG01255.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1332-999A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680890 | ||||||
chr4:151681095
|
A | C | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-1204T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151681095 | ||||||
chr4:151681178
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1332-1287T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151681178 | ||||||
chr4:151681197
|
A | G | 1 | a0001c0009t0002g0232 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1332-1306T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151681197 | ||||||
chr4:151681433
|
G | A | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-1542C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151681433 | ||||||
chr4:151681447
|
TA | T | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-1557delT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151681447 | ||||||
chr4:151681511
|
C | G | 1 | a0001c0001t0001g0151 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1332-1620G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151681511 | ||||||
chr4:151681646
|
A | G | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-1755T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151681646 | ||||||
chr4:151681834
|
A | G | 8 | a0001c0009t0001g0182a0002c0002t0001g0002a0002c0002t0001g0012others(5): Show | 9 | HG02630.hp1 HG03041.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1332-1943T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151681834 | ||||||
chr4:151681953
|
A | G | 32 | a0001c0001t0001g0141a0002c0002t0001g0003a0002c0002t0001g0015others(29): Show | 33 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1332-2062T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151681953 | ||||||
chr4:151681979
|
A | T | 8 | a0001c0009t0001g0182a0002c0002t0001g0002a0002c0002t0001g0012others(5): Show | 9 | HG02630.hp1 HG03041.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1332-2088T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151681979 | ||||||
chr4:151682012
|
T | C | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-2121A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682012 | ||||||
chr4:151682025
|
A | G | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-2134T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682025 | ||||||
chr4:151682126
|
G | A | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-2235C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682126 | ||||||
chr4:151682205
|
G | A | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-2314C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682205 | ||||||
chr4:151682263
|
G | A | 31 | a0001c0001t0001g0141a0002c0002t0001g0003a0002c0002t0001g0015others(28): Show | 32 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1332-2372C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682263 | ||||||
chr4:151682323
|
C | T | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-2432G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682323 | ||||||
chr4:151682376
|
C | G | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-2485G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682376 | ||||||
chr4:151682463
|
T | C | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-2572A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682463 | ||||||
chr4:151682503
|
C | T | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-2612G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682503 | ||||||
chr4:151682553
|
C | T | 1 | a0002c0002t0001g0033 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1332-2662G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682553 | ||||||
chr4:151682597
|
A | G | 1 | a0003c0004t0001g0311 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1332-2706T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682597 | ||||||
chr4:151682691
|
C | T | 39 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(36): Show | 41 | HG00323.hp2 HG00597.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1332-2800G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682691 | ||||||
chr4:151682713
|
T | C | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-2822A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682713 | ||||||
chr4:151682784
|
G | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0184 | 2 | HG02129.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1332-2893C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682784 | ||||||
chr4:151682831
|
G | A | 8 | a0001c0009t0001g0182a0002c0002t0001g0002a0002c0002t0001g0012others(5): Show | 9 | HG02630.hp1 HG03041.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1332-2940C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682831 | ||||||
chr4:151682879
|
G | A | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-2988C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682879 | ||||||
chr4:151683065
|
C | T | 4 | a0002c0002t0001g0043a0003c0004t0001g0311a0003c0004t0001g0312others(1): Show | 4 | HG00597.hp2 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1332-3174G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683065 | ||||||
chr4:151683150
|
C | T | 1 | a0002c0002t0001g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1332-3259G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683150 | ||||||
chr4:151683169
|
T | C | 1 | a0001c0001t0002g0228 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1332-3278A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683169 | ||||||
chr4:151683179
|
C | G | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-3288G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683179 | ||||||
chr4:151683194
|
C | CTTTAT | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-3304_1332-330 others(9): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683194 | ||||||
chr4:151683315
|
T | G | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-3424A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683315 | ||||||
chr4:151683368
|
C | T | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-3477G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683368 | ||||||
chr4:151683391
|
T | C | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-3500A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683391 | ||||||
chr4:151683406
|
C | T | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-3515G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683406 | ||||||
chr4:151683472
|
G | A | 2 | a0001c0001t0002g0206a0001c0001t0002g0240 | 2 | HG01346.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.1332-3581C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683472 | ||||||
chr4:151683567
|
T | C | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-3676A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683567 | ||||||
chr4:151683571
|
T | C | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-3680A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683571 | ||||||
chr4:151683711
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1332-3820G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683711 | ||||||
chr4:151683774
|
A | C | 1 | a0001c0001t0001g0087 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1332-3883T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683774 | ||||||
chr4:151683842
|
A | C | 1 | a0001c0001t0001g0095 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1332-3951T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683842 | ||||||
chr4:151683860
|
A | G | 33 | a0001c0001t0001g0141a0002c0002t0001g0003a0002c0002t0001g0015others(30): Show | 34 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1332-3969T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683860 | ||||||
chr4:151683875
|
C | T | 205 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(202): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1332-3984G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683875 | ||||||
chr4:151684018
|
A | G | 205 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(202): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1332-4127T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151684018 | ||||||
chr4:151684128
|
T | C | 8 | a0001c0009t0001g0182a0002c0002t0001g0002a0002c0002t0001g0012others(5): Show | 9 | HG02630.hp1 HG03041.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1332-4237A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151684128 | ||||||
chr4:151684147
|
C | A | 2 | a0006c0007t0002g0013a0006c0007t0002g0014 | 2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1332-4256G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151684147 | ||||||
chr4:151684160
|
C | A | 213 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-4269G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151684160 | ||||||
chr4:151684297
|
A | G | 208 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(205): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1331+4333T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151684297 | ||||||
chr4:151684442
|
G | C | 1 | a0001c0001t0002g0198 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1331+4188C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151684442 | ||||||
chr4:151684469
|
G | A | 212 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(209): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1331+4161C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151684469 | ||||||
chr4:151684568
|
G | C | 35 | a0001c0001t0001g0141a0001c0001t0001g0297a0001c0001t0001g0310others(32): Show | 36 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1331+4062C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151684568 | ||||||
chr4:151684684
|
G | A | 1 | a0001c0001t0002g0228 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1331+3946C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151684684 | ||||||
chr4:151684991
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1331+3639A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151684991 | ||||||
chr4:151685046
|
G | A | 2 | a0002c0002t0001g0026a0002c0002t0001g0033 | 2 | HG00323.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1331+3584C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685046 | ||||||
chr4:151685109
|
C | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1331+3521G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685109 | ||||||
chr4:151685395
|
G | A | 142 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(139): Show | 142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.1331+3235C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685395 | ||||||
chr4:151685421
|
T | C | 209 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(206): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.1331+3209A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685421 | ||||||
chr4:151685430
|
C | T | 1 | a0001c0001t0002g0273 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1331+3200G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685430 | ||||||
chr4:151685529
|
G | T | 2 | a0002c0002t0001g0018a0002c0002t0001g0046 | 2 | HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1331+3101C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685529 | ||||||
chr4:151685550
|
T | G | 209 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(206): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.1331+3080A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685550 | ||||||
chr4:151685571
|
C | T | 150 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(147): Show | 150 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1331+3059G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685571 | ||||||
chr4:151685587
|
A | T | 1 | a0001c0001t0002g0299 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1331+3043T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685587 | ||||||
chr4:151685666
|
A | G | 148 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(145): Show | 148 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1331+2964T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685666 | ||||||
chr4:151685671
|
G | A | 148 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(145): Show | 148 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1331+2959C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685671 | ||||||
chr4:151685823
|
T | G | 148 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(145): Show | 148 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1331+2807A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685823 | ||||||
chr4:151685890
|
AG | A | 147 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(144): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1331+2739delC | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685890 | ||||||
chr4:151685891
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1331+2739C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685891 | ||||||
chr4:151685896
|
T | C | 1 | a0001c0001t0002g0284 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1331+2734A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685896 | ||||||
chr4:151686039
|
C | T | 147 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(144): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1331+2591G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686039 | ||||||
chr4:151686064
|
A | C | 1 | a0001c0001t0002g0222 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1331+2566T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686064 | ||||||
chr4:151686068
|
C | CA | 147 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(144): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1331+2561dupT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686068 | ||||||
chr4:151686126
|
C | T | 147 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(144): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1331+2504G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686126 | ||||||
chr4:151686166
|
C | A | 143 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(140): Show | 143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1331+2464G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686166 | ||||||
chr4:151686192
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0106 | 2 | NA19010.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1331+2438G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686192 | ||||||
chr4:151686200
|
C | A | 1 | a0001c0001t0001g0310 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1331+2430G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686200 | ||||||
chr4:151686290
|
T | C | 147 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(144): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1331+2340A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686290 | ||||||
chr4:151686304
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1331+2326C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686304 | ||||||
chr4:151686396
|
A | C | 144 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(141): Show | 144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1331+2234T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686396 | ||||||
chr4:151686416
|
G | C | 147 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(144): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1331+2214C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686416 | ||||||
chr4:151686434
|
A | G | 147 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(144): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1331+2196T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686434 | ||||||
chr4:151686471
|
A | G | 147 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(144): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1331+2159T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686471 | ||||||
chr4:151686510
|
G | A | 147 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(144): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1331+2120C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686510 | ||||||
chr4:151686535
|
T | G | 1 | a0001c0001t0002g0211 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1331+2095A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686535 | ||||||
chr4:151686652
|
G | GC | 73 | a0001c0001t0001g0091a0001c0001t0001g0141a0001c0001t0001g0236others(70): Show | 75 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.1331+1977dupG | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686652 | ||||||
chr4:151686652
|
G | GCC | 28 | a0001c0001t0001g0102a0001c0001t0001g0186a0001c0001t0001g0212others(25): Show | 29 | HG00140.hp2 HG00323.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1331+1976_1331+197 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686652 | ||||||
chr4:151686652
|
G | GCCC | 15 | a0001c0001t0001g0117a0001c0012t0001g0293a0002c0002t0001g0003others(12): Show | 16 | HG01515.hp1 HG02074.hp2 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.1331+1975_1331+197 others(7): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686652 | ||||||
chr4:151686652
|
G | GCCCCGCC | 33 | a0001c0001t0001g0055a0001c0001t0001g0059a0001c0001t0001g0064others(30): Show | 33 | HG00140.hp1 HG01070.hp1 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.1331+1977_1331+197 others(11): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686652 | ||||||
chr4:151686652
|
G | GCCCCGCC others(1): Show |
51 | a0001c0001t0001g0053a0001c0001t0001g0057a0001c0001t0001g0058others(48): Show | 51 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1331+1977_1331+197 others(12): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686652 | ||||||
chr4:151686652
|
G | GCCCCGCC others(2): Show |
23 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0061others(20): Show | 23 | HG00597.hp1 HG00639.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.1331+1977_1331+197 others(13): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686652 | ||||||
chr4:151686652
|
G | GCCCCGCC others(3): Show |
8 | a0001c0001t0001g0071a0001c0001t0001g0084a0001c0001t0001g0089others(5): Show | 8 | HG01109.hp2 HG02257.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1331+1977_1331+197 others(14): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686652 | ||||||
chr4:151686652
|
G | GCCCCGCC others(4): Show |
3 | a0001c0001t0001g0129a0001c0001t0001g0172a0001c0003t0001g0162 | 3 | HG02572.hp1 NA18939.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1331+1977_1331+197 others(15): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686652 | ||||||
chr4:151686652
|
G | GCCCCGCC others(5): Show |
3 | a0001c0001t0001g0100a0001c0001t0001g0158a0001c0003t0001g0161 | 3 | NA18948.hp1 NA18961.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1331+1977_1331+197 others(16): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686652 | ||||||
chr4:151686652
|
G | GCCCCGCC others(6): Show |
2 | a0001c0001t0001g0093a0001c0001t0001g0179 | 2 | HG01978.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1331+1977_1331+197 others(17): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686652 | ||||||
chr4:151686652
|
GCCCCCC | G | 14 | a0001c0001t0001g0067a0001c0001t0001g0070a0001c0001t0001g0072others(11): Show | 14 | HG01934.hp1 HG01981.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.1331+1972_1331+197 others(10): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686652 | ||||||
chr4:151686654
|
C | A | 1 | a0001c0001t0002g0284 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1331+1976G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686654 | ||||||
chr4:151686657
|
C | G | 1 | a0001c0001t0001g0118 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1331+1973G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686657 | ||||||
chr4:151686662
|
C | G | 1 | a0001c0001t0001g0062 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1331+1968G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686662 | ||||||
chr4:151686663
|
A | C | 2 | a0001c0001t0001g0062a0001c0001t0001g0138 | 2 | NA18963.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1331+1967T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686663 | ||||||
chr4:151686663
|
A | G | 145 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1331+1967T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686663 | ||||||
chr4:151686700
|
C | A | 1 | a0001c0001t0001g0186 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1331+1930G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686700 | ||||||
chr4:151686705
|
C | T | 3 | a0001c0001t0002g0261a0001c0001t0002g0262a0001c0001t0002g0263 | 3 | HG02155.hp2 NA18612.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.1331+1925G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686705 | ||||||
chr4:151686721
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1331+1909A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686721 | ||||||
chr4:151686729
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1331+1901G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686729 | ||||||
chr4:151686779
|
T | C | 149 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(146): Show | 149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1331+1851A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686779 | ||||||
chr4:151686828
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1331+1802C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686828 | ||||||
chr4:151687069
|
C | T | 41 | a0001c0001t0001g0141a0002c0002t0001g0002a0002c0002t0001g0003others(38): Show | 43 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1331+1561G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151687069 | ||||||
chr4:151687183
|
G | A | 3 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271 | 3 | HG01934.hp1 HG01981.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1331+1447C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151687183 | ||||||
chr4:151687187
|
T | G | 147 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(144): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1331+1443A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151687187 | ||||||
chr4:151687319
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1331+1311C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151687319 | ||||||
chr4:151687436
|
C | T | 1 | a0006c0007t0002g0014 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1331+1194G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151687436 | ||||||
chr4:151687721
|
T | A | 1 | a0001c0001t0001g0148 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1331+909A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151687721 | ||||||
chr4:151687738
|
C | T | 9 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(6): Show | 9 | HG01891.hp1 HG02280.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1331+892G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151687738 | ||||||
chr4:151688003
|
G | C | 1 | a0002c0002t0001g0019 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1331+627C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151688003 | ||||||
chr4:151688137
|
C | T | 147 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(144): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1331+493G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151688137 | ||||||
chr4:151688152
|
G | A | 147 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(144): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1331+478C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151688152 | ||||||
chr4:151688178
|
G | A | 2 | a0001c0001t0001g0086a0009c0010t0001g0052 | 2 | HG02523.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1331+452C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151688178 | ||||||
chr4:151688404
|
C | A | 5 | a0001c0009t0001g0182a0003c0004t0001g0311a0003c0004t0001g0312others(2): Show | 5 | HG01884.hp1 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1331+226G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151688404 | ||||||
chr4:151688542
|
A | G | 189 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(186): Show | 191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1331+88T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151688542 | ||||||
chr4:151688548
|
A | C | 189 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(186): Show | 191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1331+82T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151688548 | ||||||
chr4:151688768
|
TA | T | 201 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(198): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
splice_region_variant&intron_variant | LOW | c.1198-6delT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151688768 | ||||||
chr4:151688777
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1198-14T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151688777 | ||||||
chr4:151688846
|
C | CA | 138 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(135): Show | 138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.1198-84_1198-83ins others(1): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151688846 | ||||||
chr4:151688876
|
T | G | 1 | a0002c0002t0001g0002 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1198-113A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151688876 | ||||||
chr4:151688965
|
T | C | 192 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(189): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1198-202A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151688965 | ||||||
chr4:151689028
|
G | C | 1 | a0001c0001t0001g0158 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1198-265C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151689028 | ||||||
chr4:151689150
|
T | C | 5 | a0001c0001t0001g0084a0001c0001t0001g0104a0001c0001t0001g0105others(2): Show | 5 | HG02040.hp2 HG02071.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.1198-387A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151689150 | ||||||
chr4:151689166
|
C | T | 43 | a0001c0001t0001g0141a0002c0002t0001g0002a0002c0002t0001g0003others(40): Show | 45 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1198-403G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151689166 | ||||||
chr4:151689391
|
A | G | 144 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(141): Show | 144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1198-628T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151689391 | ||||||
chr4:151689435
|
T | G | 150 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(147): Show | 150 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1198-672A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151689435 | ||||||
chr4:151689496
|
G | A | 1 | a0001c0001t0002g0272 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1198-733C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151689496 | ||||||
chr4:151689517
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1198-754T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151689517 | ||||||
chr4:151689698
|
A | G | 5 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1198-935T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151689698 | ||||||
chr4:151689742
|
T | C | 65 | a0001c0001t0001g0141a0001c0001t0001g0294a0001c0001t0001g0295others(62): Show | 68 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.1198-979A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151689742 | ||||||
chr4:151689797
|
A | G | 45 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(42): Show | 47 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1198-1034T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151689797 | ||||||
chr4:151689807
|
C | T | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1198-1044G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151689807 | ||||||
chr4:151689980
|
G | A | 3 | a0001c0001t0002g0223a0001c0001t0002g0224a0001c0001t0002g0225 | 3 | HG03669.hp2 HG04184.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1198-1217C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151689980 | ||||||
chr4:151690162
|
C | T | 13 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(10): Show | 14 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1198-1399G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151690162 | ||||||
chr4:151690314
|
T | G | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1198-1551A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151690314 | ||||||
chr4:151690375
|
C | T | 2 | a0001c0001t0002g0194a0001c0001t0002g0299 | 2 | HG00741.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1198-1612G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151690375 | ||||||
chr4:151690388
|
T | G | 43 | a0001c0001t0001g0141a0002c0002t0001g0002a0002c0002t0001g0003others(40): Show | 45 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1198-1625A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151690388 | ||||||
chr4:151690465
|
T | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1198-1702A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151690465 | ||||||
chr4:151690522
|
C | T | 29 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(26): Show | 29 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.1198-1759G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151690522 | ||||||
chr4:151690924
|
A | G | 9 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(6): Show | 9 | HG01891.hp1 HG02280.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1198-2161T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151690924 | ||||||
chr4:151690986
|
G | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1198-2223C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151690986 | ||||||
chr4:151691297
|
T | C | 65 | a0001c0001t0001g0141a0001c0001t0001g0294a0001c0001t0001g0295others(62): Show | 68 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.1198-2534A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151691297 | ||||||
chr4:151691536
|
C | T | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1198-2773G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151691536 | ||||||
chr4:151691635
|
C | T | 1 | a0001c0001t0002g0301 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1198-2872G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151691635 | ||||||
chr4:151691842
|
G | A | 45 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(42): Show | 47 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1198-3079C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151691842 | ||||||
chr4:151691997
|
CAG | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1198-3236_1198-323 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151691997 | ||||||
chr4:151692083
|
G | A | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1198-3320C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151692083 | ||||||
chr4:151692102
|
T | C | 45 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(42): Show | 47 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1198-3339A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151692102 | ||||||
chr4:151692145
|
C | G | 4 | a0001c0001t0001g0294a0001c0012t0001g0293a0002c0002t0001g0001others(1): Show | 5 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1198-3382G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151692145 | ||||||
chr4:151692328
|
C | T | 45 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(42): Show | 47 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1198-3565G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151692328 | ||||||
chr4:151692390
|
A | G | 45 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(42): Show | 47 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1198-3627T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151692390 | ||||||
chr4:151692434
|
T | A | 5 | a0001c0009t0001g0182a0003c0004t0001g0311a0003c0004t0001g0312others(2): Show | 5 | HG01884.hp1 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1198-3671A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151692434 | ||||||
chr4:151692687
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1198-3924G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151692687 | ||||||
chr4:151692800
|
G | A | 205 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(202): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.1198-4037C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151692800 | ||||||
chr4:151692951
|
G | C | 1 | a0001c0001t0001g0294 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1198-4188C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151692951 | ||||||
chr4:151693084
|
C | T | 2 | a0004c0008t0001g0190a0004c0008t0001g0191 | 2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1198-4321G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693084 | ||||||
chr4:151693092
|
C | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1198-4329G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693092 | ||||||
chr4:151693100
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1198-4337G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693100 | ||||||
chr4:151693112
|
T | C | 139 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(136): Show | 139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1198-4349A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693112 | ||||||
chr4:151693176
|
TAA | T | 45 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(42): Show | 47 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1198-4415_1198-441 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693176 | ||||||
chr4:151693187
|
A | T | 1 | a0001c0001t0001g0310 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1198-4424T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693187 | ||||||
chr4:151693281
|
T | C | 45 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(42): Show | 47 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1198-4518A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693281 | ||||||
chr4:151693337
|
C | G | 45 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(42): Show | 47 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1198-4574G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693337 | ||||||
chr4:151693337
|
C | T | 5 | a0001c0009t0001g0182a0003c0004t0001g0311a0003c0004t0001g0312others(2): Show | 5 | HG01884.hp1 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1198-4574G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693337 | ||||||
chr4:151693387
|
T | A | 45 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(42): Show | 47 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1198-4624A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693387 | ||||||
chr4:151693502
|
AC | A | 60 | a0001c0001t0001g0141a0001c0001t0001g0294a0001c0001t0001g0295others(57): Show | 63 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1198-4740delG | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693502 | ||||||
chr4:151693576
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1198-4813T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693576 | ||||||
chr4:151693668
|
C | G | 6 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(3): Show | 6 | HG02486.hp2 HG03139.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.1198-4905G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693668 | ||||||
chr4:151693712
|
G | A | 4 | a0001c0001t0001g0102a0001c0001t0001g0116a0001c0001t0001g0117others(1): Show | 4 | HG00140.hp2 HG01361.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1198-4949C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693712 | ||||||
chr4:151693805
|
T | G | 1 | a0001c0001t0001g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1198-5042A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693805 | ||||||
chr4:151693828
|
G | C | 41 | a0001c0001t0001g0141a0002c0002t0001g0002a0002c0002t0001g0003others(38): Show | 43 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1198-5065C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693828 | ||||||
chr4:151694044
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1198-5281A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151694044 | ||||||
chr4:151694641
|
A | C | 13 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(10): Show | 14 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1198-5878T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151694641 | ||||||
chr4:151694865
|
A | C | 2 | a0004c0008t0001g0190a0004c0008t0001g0191 | 2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1198-6102T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151694865 | ||||||
chr4:151695084
|
G | A | 45 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(42): Show | 47 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1197+6245C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151695084 | ||||||
chr4:151695092
|
G | A | 1 | a0001c0009t0002g0232 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1197+6237C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151695092 | ||||||
chr4:151695403
|
C | G | 1 | a0001c0001t0001g0236 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1197+5926G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151695403 | ||||||
chr4:151695543
|
G | A | 3 | a0001c0001t0001g0130a0001c0001t0001g0177a0002c0002t0001g0045 | 3 | HG02145.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1197+5786C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151695543 | ||||||
chr4:151695608
|
G | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1197+5721C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151695608 | ||||||
chr4:151695732
|
C | T | 1 | a0001c0001t0002g0208 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1197+5597G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151695732 | ||||||
chr4:151695930
|
A | AT | 16 | a0001c0001t0001g0055a0001c0001t0001g0091a0001c0001t0001g0118others(13): Show | 16 | HG01106.hp2 HG01361.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1197+5398dupA | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151695930 | ||||||
chr4:151695930
|
A | ATTTTTTT | 35 | a0001c0001t0001g0141a0001c0009t0001g0182a0002c0002t0001g0002others(32): Show | 37 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1197+5392_1197+539 others(11): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151695930 | ||||||
chr4:151695930
|
A | ATTTTTTT others(3): Show |
1 | a0002c0002t0001g0015 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1197+5389_1197+539 others(14): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151695930 | ||||||
chr4:151695930
|
AT | A | 12 | a0001c0001t0001g0112a0001c0001t0001g0295a0001c0001t0001g0296others(9): Show | 12 | HG00639.hp1 HG01891.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1197+5398delA | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151695930 | ||||||
chr4:151696164
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1197+5165T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151696164 | ||||||
chr4:151696167
|
T | G | 43 | a0001c0001t0001g0141a0002c0002t0001g0002a0002c0002t0001g0003others(40): Show | 45 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1197+5162A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151696167 | ||||||
chr4:151696293
|
C | A | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1197+5036G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151696293 | ||||||
chr4:151696350
|
T | A | 7 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0146others(4): Show | 7 | HG02055.hp1 HG02451.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1197+4979A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151696350 | ||||||
chr4:151696357
|
T | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1197+4972A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151696357 | ||||||
chr4:151696427
|
G | A | 1 | a0001c0001t0002g0287 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1197+4902C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151696427 | ||||||
chr4:151696430
|
T | C | 65 | a0001c0001t0001g0141a0001c0001t0001g0294a0001c0001t0001g0295others(62): Show | 68 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.1197+4899A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151696430 | ||||||
chr4:151697016
|
T | C | 3 | a0002c0002t0001g0012a0002c0002t0001g0020a0002c0002t0001g0022 | 3 | HG03471.hp1 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1197+4313A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697016 | ||||||
chr4:151697229
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1197+4100C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697229 | ||||||
chr4:151697512
|
G | A | 2 | a0004c0008t0001g0190a0004c0008t0001g0191 | 2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1197+3817C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697512 | ||||||
chr4:151697536
|
C | T | 13 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(10): Show | 14 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1197+3793G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697536 | ||||||
chr4:151697671
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1197+3658T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697671 | ||||||
chr4:151697832
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1197+3497C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697832 | ||||||
chr4:151697917
|
C | A | 205 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(202): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.1197+3412G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697917 | ||||||
chr4:151697937
|
A | ATG | 5 | a0001c0001t0002g0192a0001c0001t0002g0268a0001c0001t0002g0288others(2): Show | 5 | HG00741.hp1 HG01975.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.1197+3390_1197+339 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697937 | ||||||
chr4:151697937
|
A | ATGTG | 4 | a0003c0004t0001g0311a0003c0004t0001g0312a0003c0004t0001g0313others(1): Show | 4 | HG01884.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1197+3388_1197+339 others(8): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697937 | ||||||
chr4:151697937
|
A | G | 45 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(42): Show | 47 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1197+3392T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697937 | ||||||
chr4:151697943
|
G | GTGTGTGT others(97): Show |
1 | a0001c0001t0001g0144 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1197+3385_1197+338 others(108): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697943 | ||||||
chr4:151697943
|
GTGTGTGT others(7): Show |
G | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1197+3372_1197+338 others(18): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697943 | ||||||
chr4:151697947
|
G | GTGTATAT others(11): Show |
1 | a0001c0001t0001g0124 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1197+3381_1197+338 others(22): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697947 | ||||||
chr4:151697949
|
G | GTATATAT others(7): Show |
2 | a0001c0001t0001g0123a0001c0001t0001g0188 | 2 | NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1197+3379_1197+338 others(18): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697949 | ||||||
chr4:151697949
|
G | GTATATAT others(9): Show |
3 | a0001c0001t0001g0125a0001c0001t0001g0126a0002c0002t0001g0049 | 3 | HG03139.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1197+3379_1197+338 others(20): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697949 | ||||||
chr4:151697949
|
G | GTATATAT others(35): Show |
1 | a0001c0001t0001g0147 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1197+3379_1197+338 others(46): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697949 | ||||||
chr4:151697949
|
G | GTATATAT others(39): Show |
4 | a0001c0001t0001g0091a0001c0001t0001g0130a0001c0001t0001g0177others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1197+3379_1197+338 others(50): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697949 | ||||||
chr4:151697949
|
G | GTATATAT others(41): Show |
1 | a0001c0001t0001g0187 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1197+3379_1197+338 others(52): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697949 | ||||||
chr4:151697949
|
G | GTATATAT others(43): Show |
1 | a0001c0001t0001g0090 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1197+3379_1197+338 others(54): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697949 | ||||||
chr4:151697949
|
G | GTATATAT others(45): Show |
1 | a0001c0001t0001g0146 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1197+3379_1197+338 others(56): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697949 | ||||||
chr4:151697949
|
G | GTATATAT others(71): Show |
1 | a0001c0001t0001g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1197+3379_1197+338 others(82): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697949 | ||||||
chr4:151697949
|
GTGTGTAT others(3): Show |
G | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1197+3370_1197+337 others(14): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697949 | ||||||
chr4:151697949
|
GTGTGTAT others(5): Show |
G | 48 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(45): Show | 48 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.1197+3368_1197+337 others(16): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697949 | ||||||
chr4:151697949
|
GTGTGTAT others(7): Show |
G | 1 | a0001c0001t0001g0081 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1197+3366_1197+337 others(18): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697949 | ||||||
chr4:151697951
|
G | A | 76 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(73): Show | 76 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.1197+3378C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697951 | ||||||
chr4:151697951
|
G | GTATATAT others(3): Show |
2 | a0002c0002t0001g0025a0002c0002t0001g0027 | 2 | HG01515.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1197+3377_1197+337 others(14): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697951 | ||||||
chr4:151697951
|
G | GTATATAT others(45): Show |
1 | a0001c0001t0001g0152 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1197+3377_1197+337 others(56): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697951 | ||||||
chr4:151697951
|
GTGTA | G | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305 | 3 | HG02970.hp1 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1197+3374_1197+337 others(8): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697951 | ||||||
chr4:151697953
|
G | A | 82 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(79): Show | 82 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1197+3376C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | ||||||
chr4:151697953
|
G | GTA | 32 | a0001c0001t0001g0201a0001c0001t0001g0246a0001c0001t0001g0269others(29): Show | 33 | HG00438.hp2 HG00639.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.1197+3374_1197+337 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | ||||||
chr4:151697953
|
G | GTATA | 22 | a0001c0001t0001g0270a0001c0001t0001g0300a0001c0001t0002g0005others(19): Show | 23 | HG01361.hp1 HG01934.hp1 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.1197+3372_1197+337 others(8): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | ||||||
chr4:151697953
|
G | GTATATA | 17 | a0001c0001t0001g0271a0001c0001t0002g0194a0001c0001t0002g0208others(14): Show | 17 | HG01109.hp1 HG01192.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.1197+3370_1197+337 others(10): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | ||||||
chr4:151697953
|
G | GTATATAT others(1): Show |
10 | a0001c0001t0001g0141a0001c0001t0001g0267a0001c0001t0002g0199others(7): Show | 11 | HG00597.hp2 HG02074.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.1197+3368_1197+337 others(12): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | ||||||
chr4:151697953
|
G | GTATATAT others(3): Show |
9 | a0001c0001t0002g0193a0001c0001t0002g0224a0001c0001t0002g0225others(6): Show | 9 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1197+3366_1197+337 others(14): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | ||||||
chr4:151697953
|
G | GTATATAT others(5): Show |
1 | a0002c0002t0001g0012 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1197+3364_1197+337 others(16): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | ||||||
chr4:151697953
|
G | GTATATAT others(7): Show |
3 | a0001c0001t0002g0198a0001c0001t0002g0304a0002c0002t0001g0041 | 3 | NA18747.hp1 NA19011.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1197+3362_1197+337 others(18): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | ||||||
chr4:151697953
|
G | GTATATAT others(9): Show |
2 | a0001c0001t0002g0218a0001c0001t0002g0242 | 2 | HG03688.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1197+3360_1197+337 others(20): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | ||||||
chr4:151697953
|
G | GTATATAT others(13): Show |
1 | a0001c0001t0002g0260 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1197+3356_1197+337 others(24): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | ||||||
chr4:151697953
|
G | GTGTA | 5 | a0001c0001t0002g0229a0001c0001t0002g0263a0001c0009t0002g0232others(2): Show | 5 | HG02135.hp1 HG02717.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.1197+3375_1197+337 others(8): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | ||||||
chr4:151697953
|
G | GTGTATA | 12 | a0001c0001t0002g0195a0001c0001t0002g0205a0001c0001t0002g0261others(9): Show | 12 | HG01106.hp1 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1197+3375_1197+337 others(10): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | ||||||
chr4:151697953
|
G | GTGTATAT others(1): Show |
8 | a0001c0001t0001g0294a0001c0001t0002g0256a0001c0001t0002g0275others(5): Show | 10 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1197+3375_1197+337 others(12): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | ||||||
chr4:151697953
|
G | GTGTATAT others(7): Show |
1 | a0002c0002t0001g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1197+3375_1197+337 others(18): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | ||||||
chr4:151697953
|
GTATATAT others(9): Show |
G | 1 | a0001c0001t0002g0197 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1197+3360_1197+337 others(20): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | ||||||
chr4:151697953
|
GTATATAT others(17): Show |
G | 2 | a0001c0001t0002g0006a0001c0001t0002g0266 | 3 | HG02055.hp2 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1197+3352_1197+337 others(28): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | ||||||
chr4:151697955
|
A | G | 9 | a0001c0001t0001g0090a0001c0001t0001g0123a0001c0001t0001g0146others(6): Show | 9 | HG00323.hp1 HG01255.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1197+3374T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697955 | ||||||
chr4:151697957
|
A | ATATATAT others(37): Show |
1 | a0001c0001t0001g0148 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1197+3371_1197+337 others(48): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697957 | ||||||
chr4:151697957
|
A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0150 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1197+3371_1197+337 others(44): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697957 | ||||||
chr4:151697965
|
A | ATGTGTGT others(37): Show |
1 | a0001c0001t0001g0059 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1197+3363_1197+336 others(48): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | ||||||
chr4:151697965
|
A | ATGTGTGT others(35): Show |
3 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0160 | 3 | HG01981.hp1 NA18957.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1197+3363_1197+336 others(46): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | ||||||
chr4:151697965
|
A | ATGTGTGT others(33): Show |
25 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0056others(22): Show | 25 | HG00558.hp1 HG00597.hp1 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.1197+3363_1197+336 others(44): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | ||||||
chr4:151697965
|
A | ATGTGTGT others(31): Show |
6 | a0001c0001t0001g0062a0001c0001t0001g0127a0001c0001t0001g0134others(3): Show | 6 | HG00438.hp1 HG01975.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1197+3363_1197+336 others(42): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | ||||||
chr4:151697965
|
A | ATGTGTGT others(33): Show |
1 | a0001c0001t0001g0065 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1197+3363_1197+336 others(44): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | ||||||
chr4:151697965
|
A | ATGTGTGT others(29): Show |
14 | a0001c0001t0001g0054a0001c0001t0001g0079a0001c0001t0001g0080others(11): Show | 14 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1197+3363_1197+336 others(40): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | ||||||
chr4:151697965
|
A | ATGTGTGT others(31): Show |
3 | a0001c0001t0001g0099a0001c0001t0001g0142a0001c0001t0001g0184 | 3 | HG02129.hp2 HG02165.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1197+3363_1197+336 others(42): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | ||||||
chr4:151697965
|
A | ATGTGTGT others(27): Show |
4 | a0001c0001t0001g0087a0001c0001t0001g0129a0001c0001t0001g0171others(1): Show | 4 | HG02572.hp1 HG03492.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.1197+3363_1197+336 others(38): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | ||||||
chr4:151697965
|
A | ATGTGTGT others(29): Show |
1 | a0001c0001t0001g0097 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1197+3363_1197+336 others(40): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | ||||||
chr4:151697965
|
A | ATGTGTGT others(25): Show |
4 | a0001c0001t0001g0098a0001c0001t0001g0128a0001c0001t0001g0170others(1): Show | 4 | HG02922.hp1 NA18939.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.1197+3363_1197+336 others(36): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | ||||||
chr4:151697965
|
A | ATGTGTGT others(57): Show |
1 | a0001c0001t0001g0165 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1197+3363_1197+336 others(68): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | ||||||
chr4:151697965
|
A | ATGTGTGT others(55): Show |
1 | a0001c0001t0001g0166 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1197+3363_1197+336 others(66): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | ||||||
chr4:151697965
|
A | ATGTGTGT others(33): Show |
2 | a0001c0001t0001g0095a0001c0001t0001g0168 | 2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1197+3363_1197+336 others(44): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | ||||||
chr4:151697965
|
A | ATGTGTGT others(31): Show |
1 | a0001c0001t0001g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1197+3363_1197+336 others(42): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | ||||||
chr4:151697965
|
A | ATGTGTGT others(27): Show |
2 | a0001c0001t0001g0122a0001c0001t0001g0175 | 2 | HG00280.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1197+3363_1197+336 others(38): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | ||||||
chr4:151697967
|
A | G | 64 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(61): Show | 64 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1197+3362T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697967 | ||||||
chr4:151697977
|
A | ATATGTG | 3 | a0001c0001t0001g0130a0001c0001t0001g0177a0002c0002t0001g0045 | 3 | HG02145.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1197+3351_1197+335 others(10): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697977 | ||||||
chr4:151697979
|
A | G | 51 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1197+3350T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697979 | ||||||
chr4:151697981
|
A | G | 51 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1197+3348T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697981 | ||||||
chr4:151697983
|
A | G | 5 | a0001c0001t0001g0090a0001c0001t0001g0146a0001c0001t0001g0148others(2): Show | 5 | HG03130.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1197+3346T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697983 | ||||||
chr4:151697985
|
A | G | 7 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0146others(4): Show | 7 | HG02055.hp1 HG02451.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1197+3344T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697985 | ||||||
chr4:151698256
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1197+3073G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151698256 | ||||||
chr4:151698265
|
A | G | 9 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(6): Show | 9 | HG01891.hp1 HG02280.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1197+3064T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151698265 | ||||||
chr4:151698298
|
T | A | 1 | a0001c0001t0002g0241 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1197+3031A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151698298 | ||||||
chr4:151698408
|
A | C | 3 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0187 | 3 | HG03209.hp1 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1197+2921T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151698408 | ||||||
chr4:151698810
|
C | T | 1 | a0001c0001t0002g0233 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1197+2519G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151698810 | ||||||
chr4:151698811
|
C | T | 1 | a0001c0001t0002g0278 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1197+2518G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151698811 | ||||||
chr4:151698849
|
C | T | 1 | a0001c0001t0002g0103 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1197+2480G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151698849 | ||||||
chr4:151698878
|
T | G | 1 | a0001c0001t0001g0054 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1197+2451A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151698878 | ||||||
chr4:151698966
|
G | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1197+2363C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151698966 | ||||||
chr4:151698987
|
T | G | 1 | a0002c0002t0001g0050 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1197+2342A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151698987 | ||||||
chr4:151699071
|
G | A | 1 | a0001c0001t0002g0197 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1197+2258C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151699071 | ||||||
chr4:151699344
|
G | A | 9 | a0001c0001t0001g0067a0001c0001t0001g0070a0001c0001t0001g0072others(6): Show | 9 | NA18612.hp2 NA18977.hp2 NA18998.hp2 others(6): Show |
intron_variant | MODIFIER | c.1197+1985C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151699344 | ||||||
chr4:151699387
|
C | CA | 53 | a0001c0001t0001g0084a0001c0001t0001g0091a0001c0001t0001g0104others(50): Show | 55 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1197+1941dupT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151699387 | ||||||
chr4:151699387
|
CA | C | 12 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0078others(9): Show | 12 | HG01891.hp1 HG02486.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1197+1941delT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151699387 | ||||||
chr4:151699452
|
A | G | 13 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(10): Show | 14 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1197+1877T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151699452 | ||||||
chr4:151699636
|
C | T | 2 | a0004c0008t0001g0190a0004c0008t0001g0191 | 2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1197+1693G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151699636 | ||||||
chr4:151699737
|
A | G | 43 | a0001c0001t0001g0141a0002c0002t0001g0002a0002c0002t0001g0003others(40): Show | 45 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1197+1592T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151699737 | ||||||
chr4:151699777
|
T | TAC | 58 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0111others(55): Show | 60 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.1197+1550_1197+155 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151699777 | ||||||
chr4:151699777
|
T | TACAC | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1197+1548_1197+155 others(8): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151699777 | ||||||
chr4:151699998
|
A | C | 51 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1197+1331T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151699998 | ||||||
chr4:151700085
|
C | T | 51 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1197+1244G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151700085 | ||||||
chr4:151700546
|
A | T | 1 | a0001c0001t0001g0099 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1197+783T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151700546 | ||||||
chr4:151700617
|
A | G | 1 | a0001c0009t0001g0182 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1197+712T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151700617 | ||||||
chr4:151700710
|
C | T | 1 | a0001c0001t0002g0227 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1197+619G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151700710 | ||||||
chr4:151700983
|
T | C | 2 | a0001c0001t0001g0178a0001c0001t0001g0181 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1197+346A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151700983 | ||||||
chr4:151701070
|
T | C | 4 | a0003c0004t0001g0311a0003c0004t0001g0312a0003c0004t0001g0313others(1): Show | 4 | HG01884.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1197+259A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151701070 | ||||||
chr4:151701288
|
C | T | 6 | a0001c0001t0001g0201a0001c0001t0002g0285a0001c0001t0002g0286others(3): Show | 6 | HG01928.hp1 NA18949.hp1 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.1197+41G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151701288 | ||||||
chr4:151701647
|
C | G | 1 | a0001c0001t0001g0310 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1008-129G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151701647 | ||||||
chr4:151701651
|
T | G | 2 | a0001c0001t0002g0227a0001c0001t0002g0242 | 2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1008-133A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151701651 | ||||||
chr4:151702133
|
T | C | 310 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(307): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.1008-615A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151702133 | ||||||
chr4:151702151
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1008-633G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151702151 | ||||||
chr4:151702185
|
T | C | 4 | a0001c0001t0002g0228a0001c0009t0001g0182a0004c0008t0001g0190others(1): Show | 4 | HG03209.hp2 HG03453.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1008-667A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151702185 | ||||||
chr4:151702245
|
AT | A | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1008-728delA | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151702245 | ||||||
chr4:151702333
|
A | C | 1 | a0001c0001t0001g0112 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1008-815T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151702333 | ||||||
chr4:151702343
|
A | G | 41 | a0001c0001t0001g0141a0002c0002t0001g0002a0002c0002t0001g0003others(38): Show | 43 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1008-825T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151702343 | ||||||
chr4:151702702
|
C | T | 1 | a0002c0002t0001g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1007+1149G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151702702 | ||||||
chr4:151703269
|
C | G | 1 | a0003c0004t0001g0314 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1007+582G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151703269 | ||||||
chr4:151703399
|
T | C | 1 | a0001c0001t0001g0308 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1007+452A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151703399 | ||||||
chr4:151703815
|
G | A | 10 | a0001c0001t0001g0138a0001c0001t0001g0153a0001c0001t0001g0154others(7): Show | 11 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1007+36C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151703815 | ||||||
chr4:151703820
|
A | G | 46 | a0001c0001t0001g0141a0001c0001t0001g0295a0001c0001t0001g0296others(43): Show | 48 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1007+31T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151703820 | ||||||
chr4:151704063
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.963-168C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704063 | ||||||
chr4:151704080
|
C | CT | 6 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0295others(3): Show | 6 | HG01243.hp2 HG02145.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.963-186dupA | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704080 | ||||||
chr4:151704080
|
CT | C | 20 | a0001c0001t0001g0172a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 21 | HG00597.hp2 HG01515.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.963-186delA | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704080 | ||||||
chr4:151704193
|
T | C | 6 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0008others(3): Show | 7 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.963-298A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704193 | ||||||
chr4:151704208
|
T | C | 1 | a0001c0001t0002g0207 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.963-313A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704208 | ||||||
chr4:151704225
|
T | C | 41 | a0001c0001t0001g0141a0002c0002t0001g0002a0002c0002t0001g0003others(38): Show | 43 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.963-330A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704225 | ||||||
chr4:151704265
|
T | C | 4 | a0001c0001t0002g0189a0001c0001t0002g0210a0001c0001t0002g0250others(1): Show | 4 | HG00438.hp2 NA19010.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.963-370A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704265 | ||||||
chr4:151704294
|
A | G | 53 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(50): Show | 56 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.963-399T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704294 | ||||||
chr4:151704297
|
T | C | 3 | a0001c0001t0002g0223a0001c0001t0002g0224a0001c0001t0002g0225 | 3 | HG03669.hp2 HG04184.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.963-402A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704297 | ||||||
chr4:151704310
|
A | C | 1 | a0001c0001t0001g0159 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.963-415T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704310 | ||||||
chr4:151704493
|
G | A | 1 | a0002c0002t0001g0011 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.963-598C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704493 | ||||||
chr4:151704539
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.963-644G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704539 | ||||||
chr4:151704542
|
C | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0085a0001c0001t0001g0108 | 3 | HG01070.hp1 HG01192.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.962+643G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704542 | ||||||
chr4:151704552
|
T | C | 12 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(9): Show | 13 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.962+633A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704552 | ||||||
chr4:151704643
|
C | T | 6 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0008others(3): Show | 7 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.962+542G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704643 | ||||||
chr4:151704738
|
C | A | 1 | a0001c0001t0001g0294 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.962+447G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704738 | ||||||
chr4:151704742
|
G | C | 49 | a0001c0001t0001g0141a0002c0002t0001g0001a0002c0002t0001g0002others(46): Show | 52 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.962+443C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704742 | ||||||
chr4:151704868
|
C | T | 5 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.962+317G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704868 | ||||||
chr4:151705142
|
C | T | 5 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.962+43G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151705142 | ||||||
chr4:151705164
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.962+21G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151705164 | ||||||
chr4:151705325
|
A | G | 7 | a0002c0002t0001g0002a0002c0002t0001g0012a0002c0002t0001g0016others(4): Show | 8 | HG02630.hp1 HG03041.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.878-56T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151705325 | ||||||
chr4:151705363
|
TA | T | 26 | a0001c0001t0001g0057a0001c0001t0001g0088a0001c0001t0001g0111others(23): Show | 27 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.878-95delT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151705363 | ||||||
chr4:151705486
|
G | A | 1 | a0001c0012t0001g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.878-217C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151705486 | ||||||
chr4:151705732
|
C | A | 1 | a0001c0001t0001g0156 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.878-463G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151705732 | ||||||
chr4:151705766
|
A | G | 3 | a0001c0001t0002g0223a0001c0001t0002g0224a0001c0001t0002g0225 | 3 | HG03669.hp2 HG04184.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.878-497T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151705766 | ||||||
chr4:151706078
|
G | C | 51 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.878-809C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706078 | ||||||
chr4:151706116
|
A | G | 1 | a0001c0001t0001g0156 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.878-847T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706116 | ||||||
chr4:151706132
|
A | G | 3 | a0001c0001t0001g0087a0001c0001t0001g0174a0001c0001t0001g0183 | 3 | NA18953.hp2 NA19006.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.878-863T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706132 | ||||||
chr4:151706194
|
G | A | 41 | a0001c0001t0001g0141a0002c0002t0001g0002a0002c0002t0001g0003others(38): Show | 43 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.878-925C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706194 | ||||||
chr4:151706216
|
A | T | 1 | a0001c0001t0001g0152 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.878-947T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706216 | ||||||
chr4:151706287
|
G | A | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG01934.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.878-1018C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706287 | ||||||
chr4:151706368
|
GGCT | G | 51 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.878-1102_878-1100d others(5): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706368 | ||||||
chr4:151706409
|
C | T | 5 | a0001c0001t0002g0256a0001c0001t0002g0257a0001c0001t0002g0261others(2): Show | 5 | HG02155.hp2 NA18612.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.878-1140G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706409 | ||||||
chr4:151706421
|
C | CACT | 53 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(50): Show | 56 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.878-1155_878-1153d others(5): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706421 | ||||||
chr4:151706647
|
C | G | 2 | a0001c0001t0001g0306a0001c0001t0001g0309 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.877+1341G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706647 | ||||||
chr4:151706675
|
G | GGC | 199 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(196): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.877+1312_877+1313i others(4): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706675 | ||||||
chr4:151706751
|
T | C | 2 | a0001c0001t0001g0294a0001c0012t0001g0293 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.877+1237A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706751 | ||||||
chr4:151706793
|
T | C | 49 | a0001c0001t0001g0141a0002c0002t0001g0001a0002c0002t0001g0002others(46): Show | 52 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.877+1195A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706793 | ||||||
chr4:151706807
|
G | A | 49 | a0001c0001t0001g0141a0002c0002t0001g0001a0002c0002t0001g0002others(46): Show | 52 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.877+1181C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706807 | ||||||
chr4:151706964
|
G | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.877+1024C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706964 | ||||||
chr4:151707307
|
T | C | 1 | a0002c0002t0001g0026 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.877+681A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151707307 | ||||||
chr4:151707519
|
G | C | 41 | a0001c0001t0001g0141a0002c0002t0001g0002a0002c0002t0001g0003others(38): Show | 43 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.877+469C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151707519 | ||||||
chr4:151707676
|
G | A | 5 | a0001c0001t0002g0193a0001c0001t0002g0229a0001c0001t0002g0230others(2): Show | 5 | HG02135.hp1 HG02523.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+312C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151707676 | ||||||
chr4:151707680
|
T | A | 1 | a0001c0001t0002g0103 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.877+308A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151707680 | ||||||
chr4:151708234
|
G | T | 1 | a0001c0001t0002g0301 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.764-133C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151708234 | ||||||
chr4:151708468
|
G | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.764-367C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151708468 | ||||||
chr4:151708471
|
GT | G | 5 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.764-371delA | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151708471 | ||||||
chr4:151709234
|
C | T | 1 | a0001c0001t0002g0290 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.764-1133G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151709234 | ||||||
chr4:151709266
|
C | T | 2 | a0004c0008t0001g0190a0004c0008t0001g0191 | 2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.764-1165G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151709266 | ||||||
chr4:151709775
|
CTATA | C | 197 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(194): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.764-1678_764-1675d others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151709775 | ||||||
chr4:151709798
|
T | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.764-1697A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151709798 | ||||||
chr4:151709835
|
C | T | 2 | a0001c0001t0001g0086a0009c0010t0001g0052 | 2 | HG02523.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.764-1734G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151709835 | ||||||
chr4:151710032
|
A | C | 41 | a0001c0001t0001g0141a0002c0002t0001g0002a0002c0002t0001g0003others(38): Show | 43 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.764-1931T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151710032 | ||||||
chr4:151710049
|
C | T | 5 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.764-1948G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151710049 | ||||||
chr4:151710159
|
T | A | 41 | a0001c0001t0001g0141a0002c0002t0001g0002a0002c0002t0001g0003others(38): Show | 43 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.764-2058A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151710159 | ||||||
chr4:151710248
|
A | G | 2 | a0001c0001t0001g0077a0001c0009t0002g0232 | 2 | NA18939.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.764-2147T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151710248 | ||||||
chr4:151710320
|
A | G | 141 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(138): Show | 141 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.764-2219T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151710320 | ||||||
chr4:151710439
|
C | A | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133 | 3 | HG02145.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.764-2338G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151710439 | ||||||
chr4:151710485
|
G | A | 201 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(198): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.764-2384C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151710485 | ||||||
chr4:151710668
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.764-2567C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151710668 | ||||||
chr4:151710745
|
A | T | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0171others(1): Show | 4 | HG03492.hp2 HG03654.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.764-2644T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151710745 | ||||||
chr4:151710775
|
C | T | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137 | 3 | HG01243.hp1 HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.764-2674G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151710775 | ||||||
chr4:151710992
|
C | T | 4 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.764-2891G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151710992 | ||||||
chr4:151711077
|
C | T | 6 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(3): Show | 6 | HG02486.hp2 HG03139.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.764-2976G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151711077 | ||||||
chr4:151711225
|
T | A | 1 | a0001c0001t0001g0110 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.764-3124A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151711225 | ||||||
chr4:151711249
|
T | C | 5 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.764-3148A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151711249 | ||||||
chr4:151711305
|
C | A | 2 | a0001c0001t0002g0290a0001c0001t0002g0291 | 2 | HG00642.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.764-3204G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151711305 | ||||||
chr4:151711817
|
C | T | 40 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0012others(37): Show | 42 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.764-3716G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151711817 | ||||||
chr4:151711821
|
G | A | 1 | a0001c0001t0002g0303 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.764-3720C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151711821 | ||||||
chr4:151711853
|
T | C | 1 | a0005c0006t0001g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.764-3752A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151711853 | ||||||
chr4:151711949
|
G | T | 1 | a0001c0001t0001g0292 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.764-3848C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151711949 | ||||||
chr4:151712515
|
C | T | 201 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(198): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.763+3494G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151712515 | ||||||
chr4:151712693
|
C | G | 1 | a0001c0001t0001g0144 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.763+3316G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151712693 | ||||||
chr4:151712780
|
A | C | 2 | a0001c0001t0002g0275a0001c0001t0002g0276 | 2 | NA19057.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.763+3229T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151712780 | ||||||
chr4:151712902
|
G | A | 5 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.763+3107C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151712902 | ||||||
chr4:151712969
|
C | T | 40 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0012others(37): Show | 42 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.763+3040G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151712969 | ||||||
chr4:151713085
|
A | T | 10 | a0001c0001t0001g0294a0001c0012t0001g0293a0002c0002t0001g0001others(7): Show | 11 | HG01884.hp2 HG01891.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.763+2924T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151713085 | ||||||
chr4:151713278
|
C | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.763+2731G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151713278 | ||||||
chr4:151713370
|
C | T | 2 | a0002c0002t0001g0001a0002c0002t0001g0007 | 3 | HG01884.hp2 HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.763+2639G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151713370 | ||||||
chr4:151713417
|
G | A | 4 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.763+2592C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151713417 | ||||||
chr4:151713447
|
C | T | 1 | a0001c0009t0001g0182 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.763+2562G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151713447 | ||||||
chr4:151713656
|
A | G | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.763+2353T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151713656 | ||||||
chr4:151714126
|
G | A | 3 | a0001c0001t0002g0004a0001c0001t0002g0214a0001c0001t0002g0215 | 4 | HG00639.hp2 HG00741.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.763+1883C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151714126 | ||||||
chr4:151714435
|
C | A | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.763+1574G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151714435 | ||||||
chr4:151714599
|
C | T | 4 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(1): Show | 4 | HG02965.hp1 HG03195.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.763+1410G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151714599 | ||||||
chr4:151714600
|
G | A | 5 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.763+1409C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151714600 | ||||||
chr4:151714651
|
A | G | 201 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(198): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.763+1358T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151714651 | ||||||
chr4:151715012
|
G | A | 2 | a0001c0001t0002g0288a0001c0001t0002g0289 | 2 | NA18945.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.763+997C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151715012 | ||||||
chr4:151715159
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.763+850A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151715159 | ||||||
chr4:151715499
|
A | G | 1 | a0001c0001t0002g0303 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.763+510T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151715499 | ||||||
chr4:151716236
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.641-105T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 4/12 | chr4 | 151716236 | ||||||
chr4:151716277
|
C | CT | 10 | a0001c0001t0001g0064a0001c0001t0001g0067a0001c0001t0001g0091others(7): Show | 10 | HG01169.hp1 HG01175.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.641-147dupA | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 4/12 | chr4 | 151716277 | ||||||
chr4:151716277
|
CT | C | 13 | a0001c0001t0001g0085a0001c0001t0001g0111a0001c0001t0001g0119others(10): Show | 13 | HG01070.hp1 HG01515.hp1 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.641-147delA | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 4/12 | chr4 | 151716277 | ||||||
chr4:151716370
|
A | G | 1 | a0001c0001t0001g0310 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.641-239T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 4/12 | chr4 | 151716370 | ||||||
chr4:151716473
|
G | A | 1 | a0001c0001t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.641-342C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 4/12 | chr4 | 151716473 | ||||||
chr4:151716505
|
G | A | 20 | a0002c0002t0001g0003a0002c0002t0001g0015a0002c0002t0001g0019others(17): Show | 21 | HG00597.hp2 HG01109.hp1 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.640+371C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 4/12 | chr4 | 151716505 | ||||||
chr4:151716548
|
C | T | 27 | a0002c0002t0001g0003a0002c0002t0001g0015a0002c0002t0001g0019others(24): Show | 28 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.640+328G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 4/12 | chr4 | 151716548 | ||||||
chr4:151716870
|
G | A | 1 | a0001c0001t0002g0263 | 1 | NA18612.hp1 | splice_region_variant&intron_variant | LOW | c.640+6C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 4/12 | chr4 | 151716870 | ||||||
chr4:151717163
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.442-89G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151717163 | ||||||
chr4:151717482
|
T | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-408A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151717482 | ||||||
chr4:151717653
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.442-579G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151717653 | ||||||
chr4:151717708
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.442-634G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151717708 | ||||||
chr4:151717879
|
C | G | 2 | a0001c0001t0001g0294a0001c0012t0001g0293 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.442-805G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151717879 | ||||||
chr4:151717919
|
G | A | 1 | a0001c0001t0002g0205 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.442-845C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151717919 | ||||||
chr4:151717956
|
A | C | 1 | a0001c0001t0001g0147 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.442-882T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151717956 | ||||||
chr4:151717957
|
G | C | 1 | a0001c0001t0001g0147 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.442-883C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151717957 | ||||||
chr4:151717959
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.442-885A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151717959 | ||||||
chr4:151717962
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.442-888A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151717962 | ||||||
chr4:151717963
|
G | C | 1 | a0001c0001t0001g0147 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.442-889C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151717963 | ||||||
chr4:151718095
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.442-1021G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151718095 | ||||||
chr4:151718124
|
A | T | 1 | a0001c0001t0002g0194 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.442-1050T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151718124 | ||||||
chr4:151718132
|
G | A | 29 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(26): Show | 29 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.442-1058C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151718132 | ||||||
chr4:151718137
|
T | G | 1 | a0001c0001t0001g0067 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.442-1063A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151718137 | ||||||
chr4:151718762
|
A | ATTTCAGT others(3): Show |
1 | a0001c0001t0001g0067 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.441+653_441+662dup others(10): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151718762 | ||||||
chr4:151718887
|
AGTAACTG others(10): Show |
A | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+521_441+537del others(17): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151718887 | ||||||
chr4:151719147
|
GC | G | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0071 | 3 | HG01109.hp2 HG01175.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.441+277delG | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151719147 | ||||||
chr4:151719153
|
A | G | 273 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(270): Show | 278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.441+272T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151719153 | ||||||
chr4:151719235
|
C | T | 195 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(192): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.441+190G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151719235 | ||||||
chr4:151719242
|
C | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+183G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151719242 | ||||||
chr4:151719262
|
G | A | 2 | a0001c0001t0001g0091a0001c0001t0001g0176 | 2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.441+163C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151719262 | ||||||
chr4:151719287
|
C | T | 3 | a0001c0001t0001g0130a0001c0001t0001g0177a0002c0002t0001g0045 | 3 | HG02145.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.441+138G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151719287 | ||||||
chr4:151719364
|
C | G | 2 | a0001c0001t0001g0294a0001c0012t0001g0293 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.441+61G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151719364 | ||||||
chr4:151719573
|
C | T | 1 | a0001c0001t0002g0243 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.328-35G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151719573 | ||||||
chr4:151719574
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.328-36C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151719574 | ||||||
chr4:151719614
|
G | A | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0171 | 3 | HG03492.hp2 HG03688.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.328-76C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151719614 | ||||||
chr4:151719658
|
C | T | 1 | a0001c0001t0002g0278 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.328-120G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151719658 | ||||||
chr4:151719743
|
G | A | 5 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-205C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151719743 | ||||||
chr4:151719764
|
A | T | 2 | a0002c0002t0001g0047a0002c0002t0001g0048 | 2 | HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.328-226T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151719764 | ||||||
chr4:151719827
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.328-289C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151719827 | ||||||
chr4:151719857
|
T | C | 1 | a0001c0001t0001g0310 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.328-319A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151719857 | ||||||
chr4:151719963
|
T | C | 2 | a0006c0007t0002g0013a0006c0007t0002g0014 | 2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.328-425A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151719963 | ||||||
chr4:151720050
|
G | A | 51 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.328-512C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151720050 | ||||||
chr4:151720070
|
C | T | 1 | a0001c0009t0001g0182 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.328-532G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151720070 | ||||||
chr4:151720434
|
C | A | 2 | a0004c0008t0001g0190a0004c0008t0001g0191 | 2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.328-896G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151720434 | ||||||
chr4:151720489
|
G | C | 2 | a0004c0008t0001g0190a0004c0008t0001g0191 | 2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.328-951C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151720489 | ||||||
chr4:151720504
|
T | C | 8 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0008others(5): Show | 9 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.328-966A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151720504 | ||||||
chr4:151720515
|
C | T | 6 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0008others(3): Show | 7 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-977G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151720515 | ||||||
chr4:151720789
|
G | C | 201 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(198): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.328-1251C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151720789 | ||||||
chr4:151720809
|
A | G | 10 | a0001c0001t0001g0294a0001c0012t0001g0293a0002c0002t0001g0001others(7): Show | 11 | HG01884.hp2 HG01891.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.328-1271T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151720809 | ||||||
chr4:151720844
|
TGGGATGA others(3): Show |
T | 6 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0008others(3): Show | 7 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-1316_328-1307d others(12): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151720844 | ||||||
chr4:151721023
|
G | T | 1 | a0001c0001t0001g0148 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.328-1485C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151721023 | ||||||
chr4:151721025
|
T | G | 1 | a0001c0001t0001g0073 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.328-1487A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151721025 | ||||||
chr4:151721221
|
G | A | 5 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-1683C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151721221 | ||||||
chr4:151721422
|
G | C | 1 | a0001c0001t0002g0215 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.328-1884C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151721422 | ||||||
chr4:151721446
|
A | C | 1 | a0001c0001t0001g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.328-1908T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151721446 | ||||||
chr4:151721491
|
C | T | 1 | a0002c0002t0001g0035 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.328-1953G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151721491 | ||||||
chr4:151721644
|
G | A | 1 | a0001c0001t0002g0207 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.328-2106C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151721644 | ||||||
chr4:151721872
|
C | T | 2 | a0004c0008t0001g0190a0004c0008t0001g0191 | 2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.328-2334G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151721872 | ||||||
chr4:151722032
|
G | A | 201 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(198): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.328-2494C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151722032 | ||||||
chr4:151722237
|
T | A | 5 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-2699A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151722237 | ||||||
chr4:151722408
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.328-2870G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151722408 | ||||||
chr4:151722601
|
C | T | 1 | a0001c0001t0002g0194 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.328-3063G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151722601 | ||||||
chr4:151722820
|
C | T | 190 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(187): Show | 192 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.328-3282G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151722820 | ||||||
chr4:151723099
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.328-3561T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151723099 | ||||||
chr4:151723125
|
G | A | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137 | 3 | HG01243.hp1 HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.328-3587C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151723125 | ||||||
chr4:151723519
|
G | A | 1 | a0002c0002t0001g0003 | 2 | HG02074.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.328-3981C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151723519 | ||||||
chr4:151723723
|
T | C | 1 | a0001c0001t0002g0103 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.328-4185A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151723723 | ||||||
chr4:151723939
|
G | A | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-4401C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151723939 | ||||||
chr4:151724006
|
C | T | 8 | a0001c0001t0001g0095a0001c0001t0001g0131a0001c0001t0001g0132others(5): Show | 8 | HG02145.hp2 HG02280.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.328-4468G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151724006 | ||||||
chr4:151724177
|
C | T | 1 | a0001c0001t0002g0217 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.328-4639G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151724177 | ||||||
chr4:151724318
|
C | G | 2 | a0001c0001t0001g0152a0001c0009t0001g0182 | 2 | HG01169.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.328-4780G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151724318 | ||||||
chr4:151724336
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.328-4798G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151724336 | ||||||
chr4:151724356
|
T | C | 2 | a0001c0001t0001g0130a0001c0001t0001g0177 | 2 | HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.328-4818A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151724356 | ||||||
chr4:151724518
|
A | G | 1 | a0001c0001t0002g0189 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.328-4980T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151724518 | ||||||
chr4:151724570
|
C | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-5032G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151724570 | ||||||
chr4:151724876
|
G | C | 1 | a0001c0001t0002g0242 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.328-5338C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151724876 | ||||||
chr4:151725024
|
G | C | 1 | a0001c0001t0001g0294 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.328-5486C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151725024 | ||||||
chr4:151725174
|
T | A | 2 | a0001c0001t0001g0122a0001c0001t0001g0175 | 2 | HG00280.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.328-5636A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151725174 | ||||||
chr4:151725396
|
T | A | 190 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(187): Show | 192 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.328-5858A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151725396 | ||||||
chr4:151725433
|
T | C | 2 | a0001c0001t0001g0086a0009c0010t0001g0052 | 2 | HG02523.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.328-5895A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151725433 | ||||||
chr4:151725538
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.328-6000C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151725538 | ||||||
chr4:151725745
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.328-6207G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151725745 | ||||||
chr4:151725839
|
A | G | 2 | a0001c0001t0002g0221a0001c0001t0002g0222 | 2 | HG01074.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.328-6301T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151725839 | ||||||
chr4:151726425
|
T | A | 137 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(134): Show | 137 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.328-6887A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151726425 | ||||||
chr4:151726496
|
C | A | 3 | a0001c0001t0002g0261a0001c0001t0002g0262a0001c0001t0002g0263 | 3 | HG02155.hp2 NA18612.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.328-6958G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151726496 | ||||||
chr4:151726573
|
T | C | 1 | a0002c0002t0001g0042 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.328-7035A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151726573 | ||||||
chr4:151726679
|
A | G | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-7141T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151726679 | ||||||
chr4:151726690
|
T | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-7152A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151726690 | ||||||
chr4:151727109
|
C | T | 7 | a0002c0002t0001g0002a0002c0002t0001g0012a0002c0002t0001g0016others(4): Show | 8 | HG02630.hp1 HG03041.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.328-7571G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151727109 | ||||||
chr4:151727238
|
G | A | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-7700C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151727238 | ||||||
chr4:151727884
|
T | A | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-8346A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151727884 | ||||||
chr4:151727909
|
T | C | 1 | a0001c0001t0001g0183 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.328-8371A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151727909 | ||||||
chr4:151727987
|
G | A | 2 | a0001c0001t0002g0198a0001c0001t0002g0199 | 2 | NA18960.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.328-8449C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151727987 | ||||||
chr4:151728213
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.328-8675G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151728213 | ||||||
chr4:151728274
|
A | G | 1 | a0008c0013t0001g0092 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.328-8736T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151728274 | ||||||
chr4:151728456
|
T | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0099 | 2 | HG02258.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.328-8918A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151728456 | ||||||
chr4:151728583
|
C | T | 1 | a0001c0001t0002g0217 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.328-9045G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151728583 | ||||||
chr4:151728629
|
A | G | 1 | a0002c0002t0001g0015 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.328-9091T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151728629 | ||||||
chr4:151728775
|
T | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-9237A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151728775 | ||||||
chr4:151728784
|
T | C | 1 | a0002c0002t0001g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.328-9246A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151728784 | ||||||
chr4:151728811
|
T | C | 1 | a0001c0001t0001g0061 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.328-9273A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151728811 | ||||||
chr4:151728859
|
T | C | 2 | a0001c0001t0001g0294a0001c0012t0001g0293 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.328-9321A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151728859 | ||||||
chr4:151728880
|
T | C | 44 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(41): Show | 44 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.328-9342A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151728880 | ||||||
chr4:151729280
|
A | T | 1 | a0001c0001t0001g0091 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.328-9742T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151729280 | ||||||
chr4:151729374
|
C | T | 5 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG02486.hp2 HG03139.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-9836G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151729374 | ||||||
chr4:151729405
|
G | A | 7 | a0002c0002t0001g0002a0002c0002t0001g0012a0002c0002t0001g0016others(4): Show | 8 | HG02630.hp1 HG03041.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.328-9867C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151729405 | ||||||
chr4:151729573
|
G | T | 2 | a0001c0001t0002g0275a0001c0001t0002g0276 | 2 | NA19057.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.328-10035C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151729573 | ||||||
chr4:151729730
|
T | G | 200 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(197): Show | 203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.328-10192A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151729730 | ||||||
chr4:151729927
|
T | C | 2 | a0004c0008t0001g0190a0004c0008t0001g0191 | 2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.328-10389A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151729927 | ||||||
chr4:151729959
|
G | A | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0071 | 3 | HG01109.hp2 HG01175.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.328-10421C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151729959 | ||||||
chr4:151730137
|
C | T | 2 | a0004c0008t0001g0190a0004c0008t0001g0191 | 2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.328-10599G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151730137 | ||||||
chr4:151730175
|
C | T | 5 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG02486.hp2 HG03139.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-10637G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151730175 | ||||||
chr4:151730282
|
G | A | 1 | a0001c0003t0001g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.328-10744C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151730282 | ||||||
chr4:151730351
|
A | G | 196 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(193): Show | 199 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.328-10813T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151730351 | ||||||
chr4:151730683
|
C | T | 6 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0008others(3): Show | 7 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-11145G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151730683 | ||||||
chr4:151730929
|
C | A | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137 | 3 | HG01243.hp1 HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.328-11391G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151730929 | ||||||
chr4:151730990
|
G | A | 5 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-11452C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151730990 | ||||||
chr4:151731067
|
T | C | 1 | a0001c0001t0002g0291 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.328-11529A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731067 | ||||||
chr4:151731088
|
TCCCTCCC others(11): Show |
T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-11568_328-1155 others(22): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731088 | ||||||
chr4:151731255
|
C | T | 9 | a0001c0001t0001g0067a0001c0001t0001g0070a0001c0001t0001g0072others(6): Show | 9 | NA18612.hp2 NA18977.hp2 NA18998.hp2 others(6): Show |
intron_variant | MODIFIER | c.328-11717G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731255 | ||||||
chr4:151731267
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.328-11729C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731267 | ||||||
chr4:151731325
|
C | T | 1 | a0001c0001t0002g0103 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.328-11787G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731325 | ||||||
chr4:151731349
|
A | G | 200 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(197): Show | 203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.328-11811T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731349 | ||||||
chr4:151731405
|
G | A | 1 | a0001c0001t0002g0284 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.328-11867C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731405 | ||||||
chr4:151731447
|
C | T | 1 | a0001c0001t0002g0220 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.328-11909G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731447 | ||||||
chr4:151731494
|
G | C | 1 | a0001c0001t0001g0142 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.328-11956C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731494 | ||||||
chr4:151731508
|
C | T | 6 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0008others(3): Show | 7 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-11970G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731508 | ||||||
chr4:151731531
|
T | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-11993A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731531 | ||||||
chr4:151731665
|
G | A | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12127C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731665 | ||||||
chr4:151731674
|
G | A | 1 | a0001c0001t0002g0303 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.328-12136C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731674 | ||||||
chr4:151731694
|
C | T | 6 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0008others(3): Show | 7 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-12156G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731694 | ||||||
chr4:151731713
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.328-12175C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731713 | ||||||
chr4:151731715
|
C | A | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129 | 3 | HG02257.hp1 HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.328-12177G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731715 | ||||||
chr4:151731726
|
T | C | 200 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(197): Show | 203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.328-12188A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731726 | ||||||
chr4:151731760
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.328-12222C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731760 | ||||||
chr4:151731809
|
GTCTGAGA others(33): Show |
G | 1 | a0001c0001t0001g0164 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.328-12311_328-1227 others(44): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731809 | ||||||
chr4:151731832
|
T | C | 199 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(196): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.328-12294A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731832 | ||||||
chr4:151731843
|
C | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12305G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731843 | ||||||
chr4:151731849
|
A | G | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12311T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731849 | ||||||
chr4:151731878
|
GCAGCCAC others(50): Show |
G | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12397_328-1234 others(61): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731878 | ||||||
chr4:151731900
|
A | C | 69 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(66): Show | 69 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.328-12362T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731900 | ||||||
chr4:151731932
|
GGGCCAGC others(40): Show |
G | 49 | a0001c0001t0001g0086a0001c0001t0001g0141a0001c0001t0001g0143others(46): Show | 51 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.328-12441_328-1239 others(51): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731932 | ||||||
chr4:151731940
|
C | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12402G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731940 | ||||||
chr4:151731948
|
CCGGG | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12414_328-1241 others(8): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731948 | ||||||
chr4:151731953
|
A | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12415T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731953 | ||||||
chr4:151731955
|
G | A | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12417C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731955 | ||||||
chr4:151731958
|
A | G | 147 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(144): Show | 148 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.328-12420T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731958 | ||||||
chr4:151731962
|
G | A | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12424C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731962 | ||||||
chr4:151731975
|
T | C | 145 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(142): Show | 146 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.328-12437A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731975 | ||||||
chr4:151731975
|
T | TCC | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12438_328-1243 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731975 | ||||||
chr4:151731979
|
C | T | 16 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0100others(13): Show | 16 | HG00438.hp1 HG02129.hp2 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.328-12441G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731979 | ||||||
chr4:151731982
|
C | CAGCCACC others(3): Show |
4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12445_328-1244 others(14): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731982 | ||||||
chr4:151731992
|
C | T | 69 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(66): Show | 69 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.328-12454G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731992 | ||||||
chr4:151731993
|
G | A | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12455C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731993 | ||||||
chr4:151732007
|
TGGGGGGT others(41): Show |
T | 2 | a0004c0008t0001g0190a0004c0008t0001g0191 | 2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.328-12517_328-1247 others(52): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732007 | ||||||
chr4:151732023
|
G | A | 2 | a0001c0001t0002g0213a0001c0001t0002g0264 | 2 | NA18940.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.328-12485C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732023 | ||||||
chr4:151732026
|
C | G | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12488G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732026 | ||||||
chr4:151732054
|
TG | T | 197 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(194): Show | 200 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.328-12517delC | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732054 | ||||||
chr4:151732055
|
G | A | 3 | a0001c0003t0002g0216a0001c0003t0002g0254a0001c0003t0002g0255 | 3 | NA19060.hp2 NA19082.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.328-12517C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732055 | ||||||
chr4:151732071
|
G | A | 21 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(18): Show | 21 | HG00140.hp1 HG01106.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.328-12533C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732071 | ||||||
chr4:151732092
|
G | C | 42 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0012others(39): Show | 44 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.328-12554C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732092 | ||||||
chr4:151732115
|
CGCCCGGC others(33): Show |
C | 10 | a0001c0001t0002g0202a0001c0001t0002g0203a0001c0001t0002g0256others(7): Show | 10 | HG02056.hp1 HG02155.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.328-12617_328-1257 others(44): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732115 | ||||||
chr4:151732132
|
G | A | 4 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12594C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732132 | ||||||
chr4:151732138
|
G | A | 26 | a0001c0001t0001g0246a0001c0001t0001g0274a0001c0001t0002g0005others(23): Show | 27 | HG00438.hp2 HG01361.hp1 HG01978.hp1 others(24): Show |
intron_variant | MODIFIER | c.328-12600C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732138 | ||||||
chr4:151732159
|
CGGCCACC others(30): Show |
C | 2 | a0001c0001t0001g0294a0001c0012t0001g0293 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.328-12658_328-1262 others(41): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732159 | ||||||
chr4:151732527
|
A | G | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01928.hp1 HG02818.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-12989T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732527 | ||||||
chr4:151732694
|
A | G | 1 | a0001c0001t0002g0217 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.328-13156T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732694 | ||||||
chr4:151732714
|
TA | T | 20 | a0001c0001t0001g0081a0001c0001t0001g0085a0001c0001t0001g0090others(17): Show | 20 | HG00639.hp1 HG01070.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.328-13177delT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732714 | ||||||
chr4:151732728
|
A | G | 2 | a0001c0001t0001g0174a0001c0001t0001g0183 | 2 | NA18953.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.328-13190T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732728 | ||||||
chr4:151732783
|
C | T | 1 | a0001c0003t0002g0216 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.328-13245G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732783 | ||||||
chr4:151732849
|
T | C | 2 | a0004c0008t0001g0190a0004c0008t0001g0191 | 2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.328-13311A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732849 | ||||||
chr4:151732923
|
G | A | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0071 | 3 | HG01109.hp2 HG01175.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.328-13385C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732923 | ||||||
chr4:151732977
|
G | A | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-13439C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732977 | ||||||
chr4:151733421
|
A | G | 6 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(3): Show | 6 | HG02109.hp2 HG02280.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.328-13883T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151733421 | ||||||
chr4:151733610
|
A | G | 2 | a0004c0008t0001g0190a0004c0008t0001g0191 | 2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.328-14072T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151733610 | ||||||
chr4:151733899
|
T | A | 1 | a0001c0001t0001g0060 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.328-14361A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151733899 | ||||||
chr4:151734214
|
G | T | 1 | a0001c0001t0001g0143 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.328-14676C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151734214 | ||||||
chr4:151734293
|
C | T | 1 | a0001c0001t0002g0194 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.328-14755G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151734293 | ||||||
chr4:151734350
|
CA | C | 142 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(139): Show | 142 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.328-14813delT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151734350 | ||||||
chr4:151734363
|
A | T | 3 | a0001c0001t0002g0004a0001c0001t0002g0214a0001c0001t0002g0215 | 4 | HG00639.hp2 HG00741.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-14825T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151734363 | ||||||
chr4:151734572
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.328-15034G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151734572 | ||||||
chr4:151734577
|
CAG | C | 8 | a0001c0001t0001g0095a0001c0001t0001g0131a0001c0001t0001g0132others(5): Show | 8 | HG02145.hp2 HG02280.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.328-15041_328-1504 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151734577 | ||||||
chr4:151734654
|
G | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-15116C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151734654 | ||||||
chr4:151734682
|
T | G | 1 | a0001c0003t0001g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.328-15144A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151734682 | ||||||
chr4:151734731
|
T | C | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155 | 3 | NA18941.hp2 NA18957.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.328-15193A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151734731 | ||||||
chr4:151734830
|
GA | G | 5 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG02486.hp2 HG03139.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-15293delT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151734830 | ||||||
chr4:151735053
|
A | G | 1 | a0001c0001t0001g0308 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.328-15515T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735053 | ||||||
chr4:151735235
|
G | GA | 15 | a0001c0001t0002g0264a0002c0002t0001g0001a0002c0002t0001g0002others(12): Show | 17 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-15698dupT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735235 | ||||||
chr4:151735235
|
G | GAA | 33 | a0002c0002t0001g0003a0002c0002t0001g0015a0002c0002t0001g0018others(30): Show | 34 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.328-15699_328-1569 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735235 | ||||||
chr4:151735247
|
A | C | 6 | a0001c0001t0001g0130a0001c0001t0001g0177a0001c0001t0001g0178others(3): Show | 6 | HG02965.hp1 HG03195.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.328-15709T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735247 | ||||||
chr4:151735405
|
T | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-15867A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735405 | ||||||
chr4:151735503
|
C | A | 1 | a0001c0001t0001g0121 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.328-15965G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735503 | ||||||
chr4:151735588
|
T | C | 186 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(183): Show | 189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.328-16050A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735588 | ||||||
chr4:151735734
|
G | GTATATAT others(3): Show |
2 | a0001c0001t0001g0107a0001c0001t0001g0130 | 2 | HG03516.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.328-16197_328-1619 others(14): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | ||||||
chr4:151735734
|
G | GTATATAT others(5): Show |
1 | a0001c0001t0001g0164 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.328-16197_328-1619 others(16): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | ||||||
chr4:151735734
|
G | GTATATAT others(9): Show |
4 | a0001c0001t0001g0090a0001c0001t0001g0132a0001c0001t0001g0146others(1): Show | 4 | HG02717.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-16197_328-1619 others(20): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | ||||||
chr4:151735734
|
G | GTATATAT others(11): Show |
8 | a0001c0001t0001g0067a0001c0001t0001g0070a0001c0001t0001g0072others(5): Show | 8 | HG00280.hp1 HG02735.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.328-16197_328-1619 others(22): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | ||||||
chr4:151735734
|
G | GTATATAT others(13): Show |
16 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0071others(13): Show | 16 | HG01070.hp1 HG01109.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.328-16197_328-1619 others(24): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | ||||||
chr4:151735734
|
G | GTATATAT others(15): Show |
16 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0078others(13): Show | 16 | HG01074.hp1 HG01258.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.328-16197_328-1619 others(26): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | ||||||
chr4:151735734
|
G | GTATATAT others(17): Show |
13 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0084others(10): Show | 13 | HG00639.hp1 HG01169.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.328-16197_328-1619 others(28): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | ||||||
chr4:151735734
|
G | GTATATAT others(19): Show |
20 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0080others(17): Show | 20 | HG00140.hp1 HG00558.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.328-16197_328-1619 others(30): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | ||||||
chr4:151735734
|
G | GTATATAT others(21): Show |
7 | a0001c0001t0001g0056a0001c0001t0001g0100a0001c0001t0001g0135others(4): Show | 7 | HG01243.hp1 HG01433.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-16197_328-1619 others(32): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | ||||||
chr4:151735734
|
G | GTATATAT others(23): Show |
9 | a0001c0001t0001g0057a0001c0001t0001g0061a0001c0001t0001g0089others(6): Show | 9 | HG00280.hp2 HG00597.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.328-16197_328-1619 others(34): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | ||||||
chr4:151735734
|
G | GTATATAT others(25): Show |
14 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0087others(11): Show | 14 | HG00438.hp1 HG01106.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.328-16197_328-1619 others(36): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | ||||||
chr4:151735734
|
G | GTATATAT others(27): Show |
14 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0063others(11): Show | 14 | HG00558.hp1 HG02129.hp2 HG02148.hp1 others(11): Show |
intron_variant | MODIFIER | c.328-16197_328-1619 others(38): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | ||||||
chr4:151735734
|
G | GTATATAT others(29): Show |
3 | a0001c0001t0001g0064a0001c0001t0001g0172a0001c0003t0001g0161 | 3 | NA18939.hp1 NA18948.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.328-16197_328-1619 others(40): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | ||||||
chr4:151735734
|
G | GTATATAT others(31): Show |
2 | a0001c0001t0001g0186a0001c0003t0001g0162 | 2 | HG02258.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.328-16197_328-1619 others(42): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | ||||||
chr4:151735734
|
G | GTATATAT others(33): Show |
7 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0119others(4): Show | 7 | HG02258.hp2 HG03225.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.328-16197_328-1619 others(44): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | ||||||
chr4:151735734
|
G | GTATATAT others(35): Show |
3 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0292 | 3 | HG03927.hp2 NA18973.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.328-16197_328-1619 others(46): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | ||||||
chr4:151735734
|
G | GTATATAT others(37): Show |
1 | a0001c0001t0001g0066 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.328-16197_328-1619 others(48): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | ||||||
chr4:151735736
|
G | A | 141 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(138): Show | 141 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.328-16198C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735736 | ||||||
chr4:151735736
|
G | GTA | 5 | a0001c0001t0002g0197a0001c0001t0002g0207a0001c0001t0002g0265others(2): Show | 5 | HG01261.hp1 HG02523.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-16200_328-1619 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735736 | ||||||
chr4:151735736
|
G | GTATATAT others(21): Show |
1 | a0001c0001t0001g0097 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.328-16199_328-1619 others(32): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735736 | ||||||
chr4:151735736
|
GTA | G | 47 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(44): Show | 50 | HG00323.hp2 HG00642.hp1 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.328-16200_328-1619 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735736 | ||||||
chr4:151735788
|
T | G | 1 | a0001c0001t0001g0163 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.328-16250A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735788 | ||||||
chr4:151735866
|
C | T | 2 | a0004c0008t0001g0190a0004c0008t0001g0191 | 2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.328-16328G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735866 | ||||||
chr4:151735908
|
A | C | 4 | a0001c0001t0001g0294a0001c0012t0001g0293a0004c0008t0001g0190others(1): Show | 4 | HG02451.hp2 HG02486.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-16370T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735908 | ||||||
chr4:151736198
|
T | A | 6 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(3): Show | 6 | HG02109.hp2 HG02280.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.328-16660A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151736198 | ||||||
chr4:151736289
|
A | G | 1 | a0001c0001t0002g0273 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.328-16751T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151736289 | ||||||
chr4:151736672
|
T | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-17134A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151736672 | ||||||
chr4:151736781
|
C | T | 4 | a0001c0001t0001g0294a0001c0012t0001g0293a0004c0008t0001g0190others(1): Show | 4 | HG02451.hp2 HG02486.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-17243G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151736781 | ||||||
chr4:151736794
|
G | A | 1 | a0002c0002t0001g0015 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.328-17256C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151736794 | ||||||
chr4:151736839
|
G | C | 1 | a0001c0001t0002g0208 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.328-17301C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151736839 | ||||||
chr4:151737037
|
G | A | 5 | a0001c0001t0001g0141a0001c0001t0001g0178a0001c0001t0001g0179others(2): Show | 5 | HG02896.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-17499C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151737037 | ||||||
chr4:151737076
|
G | A | 1 | a0001c0001t0002g0199 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.328-17538C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151737076 | ||||||
chr4:151737121
|
G | T | 1 | a0001c0001t0001g0144 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.328-17583C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151737121 | ||||||
chr4:151737206
|
G | A | 42 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0012others(39): Show | 44 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.328-17668C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151737206 | ||||||
chr4:151737286
|
G | A | 34 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0095others(31): Show | 34 | HG00438.hp1 HG01243.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.328-17748C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151737286 | ||||||
chr4:151737555
|
CG | C | 4 | a0001c0001t0001g0294a0001c0012t0001g0293a0004c0008t0001g0190others(1): Show | 4 | HG02451.hp2 HG02486.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-18018delC | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151737555 | ||||||
chr4:151737637
|
C | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-18099G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151737637 | ||||||
chr4:151737751
|
C | T | 4 | a0001c0001t0001g0084a0001c0001t0001g0104a0001c0001t0001g0105others(1): Show | 4 | HG02040.hp2 HG02071.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-18213G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151737751 | ||||||
chr4:151737829
|
G | A | 4 | a0001c0001t0002g0006a0001c0001t0002g0266a0006c0007t0002g0013others(1): Show | 5 | HG02055.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-18291C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151737829 | ||||||
chr4:151737909
|
A | G | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-18371T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151737909 | ||||||
chr4:151737916
|
G | A | 5 | a0001c0001t0001g0267a0001c0001t0001g0269a0001c0001t0001g0270others(2): Show | 5 | HG01934.hp1 HG01981.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-18378C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151737916 | ||||||
chr4:151737995
|
G | A | 6 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0008others(3): Show | 7 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-18457C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151737995 | ||||||
chr4:151738239
|
C | A | 1 | a0001c0001t0001g0075 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.328-18701G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151738239 | ||||||
chr4:151738446
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.328-18908G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151738446 | ||||||
chr4:151738767
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0001g0143 | 2 | HG00280.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.328-19229G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151738767 | ||||||
chr4:151738804
|
G | A | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-19266C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151738804 | ||||||
chr4:151739109
|
T | C | 4 | a0001c0001t0001g0294a0001c0012t0001g0293a0004c0008t0001g0190others(1): Show | 4 | HG02451.hp2 HG02486.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-19571A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151739109 | ||||||
chr4:151739281
|
A | T | 1 | a0001c0001t0001g0142 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.327+19491T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151739281 | ||||||
chr4:151739385
|
T | G | 2 | a0006c0007t0002g0013a0006c0007t0002g0014 | 2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.327+19387A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151739385 | ||||||
chr4:151739429
|
G | A | 6 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0008others(3): Show | 7 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.327+19343C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151739429 | ||||||
chr4:151739442
|
A | G | 1 | a0001c0001t0002g0213 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.327+19330T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151739442 | ||||||
chr4:151739480
|
G | A | 6 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(3): Show | 6 | NA18612.hp2 NA18977.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.327+19292C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151739480 | ||||||
chr4:151739534
|
T | C | 1 | a0001c0001t0001g0188 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.327+19238A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151739534 | ||||||
chr4:151739663
|
C | G | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+19109G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151739663 | ||||||
chr4:151739695
|
G | C | 1 | a0001c0001t0002g0272 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.327+19077C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151739695 | ||||||
chr4:151739909
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.327+18863C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151739909 | ||||||
chr4:151739975
|
G | A | 4 | a0001c0001t0001g0294a0001c0012t0001g0293a0004c0008t0001g0190others(1): Show | 4 | HG02451.hp2 HG02486.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+18797C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151739975 | ||||||
chr4:151740049
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.327+18723C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151740049 | ||||||
chr4:151740073
|
C | G | 1 | a0001c0001t0001g0141 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.327+18699G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151740073 | ||||||
chr4:151740238
|
C | T | 1 | a0002c0002t0001g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.327+18534G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151740238 | ||||||
chr4:151740244
|
T | C | 2 | a0001c0001t0001g0174a0001c0001t0001g0183 | 2 | NA18953.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.327+18528A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151740244 | ||||||
chr4:151740272
|
A | G | 2 | a0001c0001t0001g0212a0001c0001t0002g0301 | 2 | HG00140.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.327+18500T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151740272 | ||||||
chr4:151740751
|
TG | T | 6 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(3): Show | 6 | HG02109.hp2 HG02280.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.327+18020delC | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151740751 | ||||||
chr4:151740874
|
G | A | 1 | a0001c0001t0002g0273 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.327+17898C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151740874 | ||||||
chr4:151741042
|
A | G | 1 | a0001c0001t0002g0211 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.327+17730T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151741042 | ||||||
chr4:151741072
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.327+17700G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151741072 | ||||||
chr4:151741304
|
G | C | 1 | a0001c0001t0001g0175 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.327+17468C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151741304 | ||||||
chr4:151741388
|
C | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0087 | 2 | NA19060.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.327+17384G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151741388 | ||||||
chr4:151741795
|
G | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+16977C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151741795 | ||||||
chr4:151742090
|
G | GT | 178 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(175): Show | 181 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.327+16681dupA | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151742090 | ||||||
chr4:151742090
|
G | GTT | 13 | a0001c0001t0001g0070a0001c0001t0001g0079a0001c0001t0001g0081others(10): Show | 13 | HG00597.hp1 HG01243.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.327+16680_327+1668 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151742090 | ||||||
chr4:151742174
|
T | C | 202 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(199): Show | 205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.327+16598A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151742174 | ||||||
chr4:151742242
|
T | C | 200 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(197): Show | 203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.327+16530A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151742242 | ||||||
chr4:151742289
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG00140.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.327+16483G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151742289 | ||||||
chr4:151742310
|
G | A | 5 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+16462C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151742310 | ||||||
chr4:151742553
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.327+16219C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151742553 | ||||||
chr4:151742638
|
C | A | 1 | a0004c0008t0001g0191 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.327+16134G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151742638 | ||||||
chr4:151742722
|
C | A | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+16050G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151742722 | ||||||
chr4:151742819
|
G | A | 200 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(197): Show | 203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.327+15953C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151742819 | ||||||
chr4:151743011
|
A | T | 195 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(192): Show | 198 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.327+15761T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151743011 | ||||||
chr4:151743191
|
TCA | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+15579_327+1558 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151743191 | ||||||
chr4:151743381
|
T | C | 3 | a0001c0001t0002g0275a0001c0001t0002g0276a0001c0001t0002g0277 | 3 | NA19057.hp2 NA19064.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.327+15391A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151743381 | ||||||
chr4:151743673
|
T | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+15099A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151743673 | ||||||
chr4:151743972
|
T | C | 1 | a0001c0001t0001g0310 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.327+14800A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151743972 | ||||||
chr4:151744200
|
A | G | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137 | 3 | HG01243.hp1 HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.327+14572T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151744200 | ||||||
chr4:151744252
|
A | C | 1 | a0001c0001t0001g0134 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.327+14520T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151744252 | ||||||
chr4:151744372
|
G | A | 6 | a0001c0001t0002g0197a0001c0001t0002g0278a0001c0001t0002g0281others(3): Show | 6 | HG00323.hp1 HG01255.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.327+14400C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151744372 | ||||||
chr4:151744410
|
T | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+14362A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151744410 | ||||||
chr4:151744510
|
G | C | 4 | a0001c0001t0001g0294a0001c0012t0001g0293a0004c0008t0001g0190others(1): Show | 4 | HG02451.hp2 HG02486.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+14262C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151744510 | ||||||
chr4:151744853
|
C | T | 3 | a0002c0002t0001g0002a0002c0002t0001g0016a0002c0002t0001g0017 | 4 | HG03041.hp2 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+13919G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151744853 | ||||||
chr4:151744870
|
A | T | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133 | 3 | HG02145.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.327+13902T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151744870 | ||||||
chr4:151744991
|
C | A | 1 | a0001c0001t0002g0205 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.327+13781G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151744991 | ||||||
chr4:151745026
|
A | C | 6 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0008others(3): Show | 7 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.327+13746T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151745026 | ||||||
chr4:151745446
|
G | A | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+13326C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151745446 | ||||||
chr4:151745531
|
C | T | 1 | a0001c0001t0002g0206 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.327+13241G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151745531 | ||||||
chr4:151745616
|
A | C | 192 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(189): Show | 195 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.327+13156T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151745616 | ||||||
chr4:151745918
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.327+12854G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151745918 | ||||||
chr4:151746019
|
T | C | 200 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(197): Show | 203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.327+12753A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151746019 | ||||||
chr4:151746036
|
T | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+12736A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151746036 | ||||||
chr4:151746151
|
C | G | 2 | a0001c0001t0001g0130a0001c0001t0001g0177 | 2 | HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.327+12621G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151746151 | ||||||
chr4:151746419
|
T | A | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+12353A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151746419 | ||||||
chr4:151746622
|
C | A | 1 | a0002c0002t0001g0033 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.327+12150G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151746622 | ||||||
chr4:151746654
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.327+12118G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151746654 | ||||||
chr4:151746795
|
T | C | 1 | a0001c0001t0002g0283 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.327+11977A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151746795 | ||||||
chr4:151746894
|
T | G | 2 | a0001c0001t0002g0290a0001c0001t0002g0291 | 2 | HG00642.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.327+11878A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151746894 | ||||||
chr4:151747072
|
A | G | 196 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(193): Show | 199 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.327+11700T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151747072 | ||||||
chr4:151747291
|
A | G | 1 | a0004c0008t0001g0191 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.327+11481T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151747291 | ||||||
chr4:151747632
|
T | A | 1 | a0001c0001t0001g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.327+11140A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151747632 | ||||||
chr4:151747633
|
A | C | 200 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(197): Show | 203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.327+11139T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151747633 | ||||||
chr4:151748154
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.327+10618T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151748154 | ||||||
chr4:151748198
|
A | G | 1 | a0001c0001t0002g0205 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.327+10574T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151748198 | ||||||
chr4:151748356
|
A | G | 5 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+10416T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151748356 | ||||||
chr4:151748357
|
C | CCG | 5 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+10414_327+1041 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151748357 | ||||||
chr4:151748360
|
C | T | 5 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+10412G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151748360 | ||||||
chr4:151748453
|
A | G | 1 | a0006c0007t0002g0013 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.327+10319T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151748453 | ||||||
chr4:151749116
|
T | C | 11 | a0002c0002t0001g0003a0002c0002t0001g0034a0002c0002t0001g0035others(8): Show | 12 | HG00597.hp2 HG02056.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.327+9656A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151749116 | ||||||
chr4:151749135
|
T | G | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+9637A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151749135 | ||||||
chr4:151749146
|
A | C | 1 | a0001c0005t0002g0204 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.327+9626T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151749146 | ||||||
chr4:151749171
|
A | G | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+9601T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151749171 | ||||||
chr4:151749461
|
A | G | 200 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(197): Show | 203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.327+9311T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151749461 | ||||||
chr4:151749613
|
C | T | 138 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(135): Show | 138 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.327+9159G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151749613 | ||||||
chr4:151749628
|
C | A | 200 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(197): Show | 203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.327+9144G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151749628 | ||||||
chr4:151749632
|
T | TATA | 200 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(197): Show | 203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.327+9137_327+9139d others(5): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151749632 | ||||||
chr4:151749760
|
G | A | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+9012C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151749760 | ||||||
chr4:151749850
|
C | T | 5 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+8922G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151749850 | ||||||
chr4:151749951
|
G | A | 1 | a0001c0001t0002g0284 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.327+8821C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151749951 | ||||||
chr4:151750035
|
C | T | 2 | a0001c0001t0002g0202a0001c0001t0002g0203 | 2 | NA19005.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.327+8737G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750035 | ||||||
chr4:151750072
|
A | G | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+8700T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750072 | ||||||
chr4:151750120
|
A | G | 5 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG02486.hp2 HG03139.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+8652T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750120 | ||||||
chr4:151750125
|
C | T | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129 | 3 | HG02257.hp1 HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.327+8647G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750125 | ||||||
chr4:151750148
|
T | A | 2 | a0001c0001t0002g0285a0001c0001t0002g0286 | 2 | NA18994.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.327+8624A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750148 | ||||||
chr4:151750173
|
G | A | 144 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(141): Show | 145 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.327+8599C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750173 | ||||||
chr4:151750208
|
T | C | 4 | a0001c0001t0001g0294a0001c0012t0001g0293a0004c0008t0001g0190others(1): Show | 4 | HG02451.hp2 HG02486.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+8564A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750208 | ||||||
chr4:151750253
|
T | C | 196 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(193): Show | 199 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.327+8519A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750253 | ||||||
chr4:151750280
|
G | A | 2 | a0006c0007t0002g0013a0006c0007t0002g0014 | 2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.327+8492C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750280 | ||||||
chr4:151750318
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.327+8454G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750318 | ||||||
chr4:151750418
|
GCTATGTG others(10): Show |
G | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+8337_327+8353d others(19): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750418 | ||||||
chr4:151750488
|
C | G | 186 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(183): Show | 189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.327+8284G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750488 | ||||||
chr4:151750866
|
T | C | 1 | a0001c0001t0002g0287 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.327+7906A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750866 | ||||||
chr4:151750901
|
T | C | 1 | a0003c0004t0001g0314 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.327+7871A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750901 | ||||||
chr4:151750969
|
C | G | 186 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(183): Show | 189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.327+7803G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750969 | ||||||
chr4:151751084
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.327+7688A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151751084 | ||||||
chr4:151751569
|
A | G | 1 | a0001c0001t0001g0201 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.327+7203T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151751569 | ||||||
chr4:151751688
|
C | T | 1 | a0001c0001t0002g0103 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.327+7084G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151751688 | ||||||
chr4:151751730
|
T | G | 186 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(183): Show | 189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.327+7042A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151751730 | ||||||
chr4:151751864
|
T | C | 313 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(310): Show | 319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.327+6908A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151751864 | ||||||
chr4:151751969
|
A | T | 1 | a0001c0001t0001g0102 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.327+6803T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151751969 | ||||||
chr4:151752034
|
T | C | 8 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(5): Show | 8 | HG02109.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.327+6738A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151752034 | ||||||
chr4:151752386
|
T | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+6386A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151752386 | ||||||
chr4:151752593
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.327+6179C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151752593 | ||||||
chr4:151752753
|
T | G | 1 | a0001c0001t0001g0060 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.327+6019A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151752753 | ||||||
chr4:151752781
|
T | C | 2 | a0004c0008t0001g0190a0004c0008t0001g0191 | 2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.327+5991A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151752781 | ||||||
chr4:151753166
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.327+5606A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151753166 | ||||||
chr4:151753181
|
T | C | 2 | a0004c0008t0001g0190a0004c0008t0001g0191 | 2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.327+5591A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151753181 | ||||||
chr4:151753240
|
A | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+5532T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151753240 | ||||||
chr4:151753251
|
T | C | 2 | a0001c0001t0002g0288a0001c0001t0002g0289 | 2 | NA18945.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.327+5521A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151753251 | ||||||
chr4:151753767
|
C | G | 5 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG02486.hp2 HG03139.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+5005G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151753767 | ||||||
chr4:151754286
|
C | T | 1 | a0002c0002t0001g0046 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.327+4486G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151754286 | ||||||
chr4:151754295
|
T | C | 28 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(25): Show | 28 | HG00140.hp1 HG00558.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.327+4477A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151754295 | ||||||
chr4:151754369
|
C | T | 1 | a0002c0002t0001g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.327+4403G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151754369 | ||||||
chr4:151754406
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.327+4366G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151754406 | ||||||
chr4:151754621
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.327+4151G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151754621 | ||||||
chr4:151754810
|
G | C | 3 | a0001c0001t0001g0067a0001c0001t0001g0074a0001c0001t0001g0075 | 3 | NA19009.hp1 NA19082.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.327+3962C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151754810 | ||||||
chr4:151754873
|
T | C | 2 | a0001c0001t0002g0290a0001c0001t0002g0291 | 2 | HG00642.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.327+3899A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151754873 | ||||||
chr4:151755198
|
T | C | 198 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(195): Show | 201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.327+3574A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151755198 | ||||||
chr4:151755257
|
A | G | 1 | a0002c0002t0001g0015 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.327+3515T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151755257 | ||||||
chr4:151755269
|
T | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+3503A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151755269 | ||||||
chr4:151755310
|
A | G | 2 | a0006c0007t0002g0013a0006c0007t0002g0014 | 2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.327+3462T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151755310 | ||||||
chr4:151755339
|
G | GTATTATG others(5): Show |
1 | a0001c0001t0001g0310 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.327+3432_327+3433i others(14): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151755339 | ||||||
chr4:151755340
|
T | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+3432A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151755340 | ||||||
chr4:151755344
|
G | T | 1 | a0001c0001t0001g0310 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.327+3428C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151755344 | ||||||
chr4:151755676
|
T | G | 6 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(3): Show | 6 | NA18944.hp1 NA18964.hp1 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.327+3096A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151755676 | ||||||
chr4:151755705
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.327+3067C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151755705 | ||||||
chr4:151755775
|
T | C | 4 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(1): Show | 4 | HG02965.hp1 HG03195.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+2997A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151755775 | ||||||
chr4:151756257
|
A | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+2515T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151756257 | ||||||
chr4:151756375
|
T | C | 186 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(183): Show | 189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.327+2397A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151756375 | ||||||
chr4:151756409
|
T | C | 4 | a0003c0004t0001g0311a0003c0004t0001g0312a0003c0004t0001g0313others(1): Show | 4 | HG01884.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+2363A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151756409 | ||||||
chr4:151756428
|
C | T | 28 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(25): Show | 28 | HG00140.hp1 HG00558.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.327+2344G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151756428 | ||||||
chr4:151756465
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG03688.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.327+2307G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151756465 | ||||||
chr4:151756677
|
A | G | 2 | a0001c0001t0002g0198a0001c0001t0002g0199 | 2 | NA18960.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.327+2095T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151756677 | ||||||
chr4:151756758
|
A | G | 4 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+2014T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151756758 | ||||||
chr4:151756917
|
T | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+1855A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151756917 | ||||||
chr4:151757195
|
G | A | 11 | a0002c0002t0001g0003a0002c0002t0001g0034a0002c0002t0001g0035others(8): Show | 12 | HG00597.hp2 HG02056.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.327+1577C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151757195 | ||||||
chr4:151757467
|
A | AT | 179 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(176): Show | 182 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.327+1304dupA | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151757467 | ||||||
chr4:151757467
|
A | ATT | 24 | a0001c0001t0001g0053a0001c0001t0001g0067a0001c0001t0001g0068others(21): Show | 24 | HG00140.hp1 HG01070.hp1 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.327+1303_327+1304d others(4): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151757467 | ||||||
chr4:151757512
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.327+1260C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151757512 | ||||||
chr4:151757677
|
C | T | 2 | a0001c0001t0001g0294a0001c0012t0001g0293 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.327+1095G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151757677 | ||||||
chr4:151757756
|
C | T | 1 | a0001c0001t0001g0067 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.327+1016G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151757756 | ||||||
chr4:151757772
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.327+1000G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151757772 | ||||||
chr4:151757773
|
G | A | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078 | 3 | NA18612.hp2 NA18977.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.327+999C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151757773 | ||||||
chr4:151757822
|
T | C | 202 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(199): Show | 205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.327+950A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151757822 | ||||||
chr4:151757836
|
T | C | 1 | a0001c0001t0001g0300 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.327+936A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151757836 | ||||||
chr4:151758060
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.327+712A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151758060 | ||||||
chr4:151758258
|
T | G | 1 | a0001c0001t0001g0310 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.327+514A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151758258 | ||||||
chr4:151758260
|
T | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+512A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151758260 | ||||||
chr4:151758295
|
C | G | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+477G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151758295 | ||||||
chr4:151758373
|
C | T | 12 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(9): Show | 12 | HG01109.hp2 HG01175.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.327+399G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151758373 | ||||||
chr4:151758390
|
A | G | 14 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(11): Show | 14 | HG00558.hp1 HG00735.hp2 NA18944.hp1 others(11): Show |
intron_variant | MODIFIER | c.327+382T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151758390 | ||||||
chr4:151758498
|
T | C | 1 | a0001c0001t0002g0301 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.327+274A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151758498 | ||||||
chr4:151758537
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.327+235C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151758537 | ||||||
chr4:151758570
|
A | G | 143 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(140): Show | 143 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.327+202T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151758570 | ||||||
chr4:151758664
|
A | G | 137 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(134): Show | 137 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.327+108T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151758664 | ||||||
chr4:151758948
|
G | GATGTATT others(12): Show |
2 | a0001c0001t0002g0303a0001c0001t0002g0304 | 2 | HG01928.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.177-45_177-27dupGG others(17): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151758948 | ||||||
chr4:151759246
|
T | A | 1 | a0001c0001t0002g0189 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.177-324A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151759246 | ||||||
chr4:151759281
|
T | A | 6 | a0002c0002t0001g0045a0002c0002t0001g0046a0002c0002t0001g0047others(3): Show | 6 | HG02145.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.177-359A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151759281 | ||||||
chr4:151759385
|
A | G | 6 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0008others(3): Show | 7 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.177-463T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151759385 | ||||||
chr4:151759454
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.177-532A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151759454 | ||||||
chr4:151759469
|
A | T | 1 | a0001c0001t0002g0189 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.177-547T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151759469 | ||||||
chr4:151759549
|
T | C | 139 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(136): Show | 139 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.177-627A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151759549 | ||||||
chr4:151759741
|
T | C | 1 | a0001c0001t0001g0305 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.177-819A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151759741 | ||||||
chr4:151759791
|
C | CAT | 8 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(5): Show | 8 | HG01884.hp1 HG02818.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.177-871_177-870dup others(2): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151759791 | ||||||
chr4:151760174
|
CT | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.176+632delA | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151760174 | ||||||
chr4:151760305
|
T | C | 1 | a0001c0001t0001g0310 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.176+502A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151760305 | ||||||
chr4:151760354
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.176+453C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151760354 | ||||||
chr4:151760683
|
G | C | 1 | a0001c0001t0001g0188 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.176+124C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151760683 | ||||||
chr4:151760800
|
A | G | 137 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(134): Show | 137 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
splice_region_variant&intron_variant | LOW | c.176+7T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151760800 |