geneid | 7072 |
---|---|
ensemblid | ENSG00000116001.17 |
hgncid | 11802 |
symbol | TIA1 |
name | TIA1 cytotoxic granule associated RNA binding protein |
refseq_nuc | NM_022173.4 |
refseq_prot | NP_071505.2 |
ensembl_nuc | ENST00000433529.7 |
ensembl_prot | ENSP00000401371.2 |
mane_status | MANE Select |
chr | chr2 |
start | 70209444 |
end | 70248628 |
strand | - |
ver | v1.2 |
region | chr2:70209444-70248628 |
region5000 | chr2:70204444-70253628 |
regionname0 | TIA1_chr2_70209444_70248628 |
regionname5000 | TIA1_chr2_70204444_70253628 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 386 | 389 | 96 | 66 | 176 | 10 | 39 | 136 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0002 | 0/0 | 386 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0003 | 0/0 | 386 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0004 | 0/0 | 386 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1161 | 379 | 87 | 66 | 175 | 10 | 39 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
c0002 | 0/0 | 1161 | 4 | 4 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
c0003 | 0/0 | 1161 | 3 | 3 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
c0004 | 0/0 | 1161 | 3 | 2 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
c0005 | 0/0 | 1161 | 2 | 2 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
c0006 | 0/0 | 1161 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
c0007 | 0/0 | 1161 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
c0008 | 0/0 | 1161 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 3474 | 264 | 64 | 35 | 119 | 9 | 35 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
t0002 | 0/0 | 3474 | 41 | 1 | 7 | 30 | 1 | 2 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
t0003 | 0/0 | 3475 | 37 | 0 | 18 | 17 | 0 | 2 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
t0004 | 0/0 | 3474 | 10 | 8 | 2 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
t0005 | 0/0 | 3476 | 5 | 5 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
t0006 | 0/0 | 3475 | 4 | 1 | 1 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
t0007 | 0/0 | 3475 | 4 | 4 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
t0008 | 0/0 | 3476 | 4 | 4 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
t0009 | 0/0 | 3474 | 3 | 3 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
t0010 | 0/0 | 3474 | 3 | 0 | 3 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
t0011 | 0/0 | 3474 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
t0012 | 0/0 | 3474 | 2 | 2 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
t0013 | 0/0 | 3474 | 2 | 1 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
t0014 | 0/0 | 3474 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
t0015 | 0/0 | 3475 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
t0016 | 0/0 | 3476 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
t0017 | 0/0 | 3474 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
t0018 | 0/0 | 3475 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
t0019 | 0/0 | 3474 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
t0020 | 0/0 | 3473 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
t0021 | 0/0 | 3474 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
t0022 | 0/0 | 3474 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
t0023 | 0/0 | 3474 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
t0024 | 0/0 | 3474 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
t0025 | 0/0 | 3474 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
t0026 | 0/0 | 3474 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 1 | 2 | 3 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0006 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0210 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0266 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1161 | 379 | 87 | 66 | 175 | 10 | 39 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0002 | 0/0 | 1161 | 4 | 4 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0003 | 0/0 | 1161 | 3 | 3 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0005 | 0/0 | 1161 | 2 | 2 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0008 | 0/0 | 1161 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0002c0004 | 0/0 | 1161 | 3 | 2 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0003c0006 | 0/0 | 1161 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0004c0007 | 0/0 | 1161 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4634 | 255 | 59 | 33 | 118 | 9 | 34 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0001t0002 | 0/0 | 4634 | 41 | 1 | 7 | 30 | 1 | 2 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0001t0003 | 0/0 | 4635 | 37 | 0 | 18 | 17 | 0 | 2 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0001t0004 | 0/0 | 4634 | 10 | 8 | 2 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0001t0005 | 0/0 | 4636 | 5 | 5 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0001t0006 | 0/0 | 4635 | 4 | 1 | 1 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0001t0008 | 0/0 | 4636 | 4 | 4 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0001t0009 | 0/0 | 4634 | 3 | 3 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0001t0010 | 0/0 | 4634 | 3 | 0 | 3 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0001t0011 | 0/0 | 4634 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0001t0013 | 0/0 | 4634 | 2 | 1 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0001t0014 | 0/0 | 4634 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0001t0015 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0001t0016 | 0/0 | 4636 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0001t0017 | 0/0 | 4634 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0001t0018 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0001t0019 | 0/0 | 4634 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0001t0020 | 0/0 | 4633 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0001t0021 | 0/0 | 4634 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0001t0022 | 0/0 | 4634 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0001t0023 | 0/0 | 4634 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0001t0024 | 0/0 | 4634 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0001t0025 | 0/0 | 4634 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0001t0026 | 0/0 | 4634 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0002t0007 | 0/0 | 4635 | 4 | 4 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0003t0001 | 0/0 | 4634 | 3 | 3 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0005t0012 | 0/0 | 4634 | 2 | 2 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0001c0008t0001 | 0/0 | 4634 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0002c0004t0001 | 0/0 | 4634 | 3 | 2 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0003c0006t0001 | 0/0 | 4634 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
a0004c0007t0001 | 0/0 | 4634 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | copy fasta | chr2 | 70204444 | 70253628 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 1 | 2 | 3 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0210 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0266 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0004g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0004g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0004g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0004g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0004g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0005g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0005g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0005g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0005g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0006g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0006g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0006g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0008g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0008g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0008g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0008g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0009g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0009g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0009g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0010g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0010g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0011g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0011g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0013g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0013g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0014g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0015g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0016g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0017g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0018g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0019g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0020g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0021g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0022g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0023g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0024g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0025g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0001t0026g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0002t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0002t0007g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0002t0007g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0002t0007g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0003t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0003t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0003t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0005t0012g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0005t0012g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0001c0008t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0002c0004t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0002c0004t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0002c0004t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0003c0006t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
a0004c0007t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0214 | EUR | GBR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | GBR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0268 | EUR | FIN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | FIN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | CHS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | CHS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | CHS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG00642 | hp1 | a0001 | c0001 | t0010 | g0359 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | CHS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0299 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0313 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01099 | hp1 | a0001 | c0001 | t0023 | g0211 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0039 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01167 | hp2 | a0001 | c0001 | t0026 | g0360 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0335 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01243 | hp1 | a0002 | c0004 | t0001 | g0346 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01243 | hp2 | a0001 | c0001 | t0006 | g0079 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0065 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0073 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0043 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0064 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0045 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0270 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | IBS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0229 | EUR | IBS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | IBS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01884 | hp1 | a0001 | c0001 | t0009 | g0339 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0336 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0071 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0297 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01943 | hp1 | a0001 | c0001 | t0010 | g0021 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0322 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0060 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01952 | hp2 | a0003 | c0006 | t0001 | g0116 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0063 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0066 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0067 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG01993 | hp2 | a0001 | c0001 | t0010 | g0021 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0317 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02055 | hp1 | a0001 | c0001 | t0008 | g0367 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02055 | hp2 | a0001 | c0001 | t0006 | g0070 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02083 | hp2 | a0001 | c0008 | t0001 | g0218 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02145 | hp2 | a0001 | c0001 | t0008 | g0364 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CDX | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CDX | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CDX | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | CDX | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02258 | hp1 | a0002 | c0004 | t0001 | g0349 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0320 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02280 | hp1 | a0001 | c0005 | t0012 | g0087 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0321 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0068 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0049 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0350 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02451 | hp2 | a0001 | c0001 | t0005 | g0365 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02572 | hp2 | a0001 | c0001 | t0008 | g0363 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02622 | hp1 | a0001 | c0001 | t0019 | g0198 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02630 | hp2 | a0001 | c0001 | t0013 | g0354 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0271 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02717 | hp2 | a0001 | c0001 | t0009 | g0341 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02723 | hp2 | a0001 | c0002 | t0007 | g0284 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0356 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02738 | hp2 | a0004 | c0007 | t0001 | g0185 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02886 | hp1 | a0001 | c0001 | t0008 | g0366 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0328 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0337 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03017 | hp2 | a0001 | c0001 | t0014 | g0023 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03041 | hp1 | a0002 | c0004 | t0001 | g0353 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03098 | hp1 | a0001 | c0003 | t0001 | g0347 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03139 | hp2 | a0001 | c0003 | t0001 | g0351 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03195 | hp1 | a0001 | c0001 | t0022 | g0085 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0358 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03225 | hp1 | a0001 | c0001 | t0018 | g0286 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0269 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03453 | hp2 | a0001 | c0002 | t0007 | g0332 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03486 | hp1 | a0001 | c0003 | t0001 | g0343 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03486 | hp2 | a0001 | c0002 | t0007 | g0288 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0361 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03540 | hp2 | a0001 | c0001 | t0009 | g0338 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0333 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0040 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0038 | SAS | STU | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | STU | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0306 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | BEB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0319 | SAS | STU | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | YRI | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | CHB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | CHB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0345 | AFR | YRI | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0357 | AFR | YRI | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18940 | hp1 | a0001 | c0001 | t0006 | g0108 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18948 | hp2 | a0001 | c0001 | t0011 | g0330 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18952 | hp2 | a0001 | c0001 | t0013 | g0237 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18959 | hp2 | a0001 | c0001 | t0021 | g0106 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18975 | hp1 | a0001 | c0001 | t0025 | g0304 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18983 | hp2 | a0001 | c0001 | t0017 | g0295 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18985 | hp1 | a0001 | c0001 | t0016 | g0074 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | LWK | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19030 | hp2 | a0001 | c0005 | t0012 | g0100 | AFR | LWK | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19043 | hp1 | a0001 | c0001 | t0024 | g0340 | AFR | LWK | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19067 | hp2 | a0001 | c0001 | t0015 | g0325 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19084 | hp1 | a0001 | c0001 | t0011 | g0329 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19086 | hp2 | a0001 | c0001 | t0006 | g0219 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19240 | hp1 | a0001 | c0002 | t0007 | g0287 | AFR | YRI | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ASW | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ASW | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0303 | EUR | TSI | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | TSI | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | GIH | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | GIH | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0362 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | USA | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | USA | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0334 | AFR | USA | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | USA | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA21309 | hp1 | a0001 | c0001 | t0020 | g0202 | AFR | LWK | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | LWK | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0266 | REF | REF | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0210 | REF | REF | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:70212756
|
G | T | 1 | a0003 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.1124C>A | p.Pro375His | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 1322/4634 | 1124/1161 | 375/386 | chr2 | 70212756 | ||
chr2:70214430
|
T | C | 1 | a0004 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.953A>G | p.Gln318Arg | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/13 | 1151/4634 | 953/1161 | 318/386 | chr2 | 70214430 | ||
chr2:70214436
|
G | C | 1 | a0002 | 3 | HG01243.hp1 HG02258.hp1 HG03041.hp1 |
missense_variant | MODERATE | c.947C>G | p.Ala316Gly | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/13 | 1145/4634 | 947/1161 | 316/386 | chr2 | 70214436 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:70212758
|
C | T | 1 | a0001c0003 | 3 | HG03098.hp1 HG03139.hp2 HG03486.hp1 |
synonymous_variant | LOW | c.1122G>A | p.Gln374Gln | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 1320/4634 | 1122/1161 | 374/386 | chr2 | 70212758 | ||
chr2:70212794
|
C | T | 1 | a0001c0002 | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
synonymous_variant | LOW | c.1086G>A | p.Pro362Pro | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 1284/4634 | 1086/1161 | 362/386 | chr2 | 70212794 | ||
chr2:70214459
|
C | T | 1 | a0001c0005 | 2 | HG02280.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.924G>A | p.Gln308Gln | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/13 | 1122/4634 | 924/1161 | 308/386 | chr2 | 70214459 | ||
chr2:70236127
|
T | C | 1 | a0001c0008 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.75A>G | p.Gln25Gln | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/13 | 273/4634 | 75/1161 | 25/386 | chr2 | 70236127 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:70209672
|
A | G | 1 | a0001c0002t0007 | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3047T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 3047 | chr2 | 70209672 | |||||
chr2:70209686
|
C | T | 9 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(6): Show | 60 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*3033G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 3033 | chr2 | 70209686 | |||||
chr2:70209791
|
C | A | 1 | a0001c0005t0012 | 2 | HG02280.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2928G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 2928 | chr2 | 70209791 | |||||
chr2:70210109
|
TA | T | 6 | a0001c0001t0002a0001c0001t0011a0001c0001t0015others(3): Show | 47 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*2609delT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 2609 | chr2 | 70210109 | |||||
chr2:70210203
|
G | C | 1 | a0001c0001t0021 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2516C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 2516 | chr2 | 70210203 | |||||
chr2:70210283
|
T | C | 1 | a0001c0001t0011 | 2 | NA18948.hp2 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2436A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 2436 | chr2 | 70210283 | |||||
chr2:70210411
|
A | G | 1 | a0001c0001t0019 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2308T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 2308 | chr2 | 70210411 | |||||
chr2:70210496
|
T | A | 1 | a0001c0001t0022 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2223A>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 2223 | chr2 | 70210496 | |||||
chr2:70210910
|
A | G | 2 | a0001c0001t0009a0001c0001t0024 | 4 | HG01884.hp1 HG02717.hp2 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1809T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 1809 | chr2 | 70210910 | |||||
chr2:70211140
|
T | C | 1 | a0001c0001t0023 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1579A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 1579 | chr2 | 70211140 | |||||
chr2:70211420
|
G | GT | 9 | a0001c0001t0002a0001c0001t0003a0001c0001t0011others(6): Show | 89 | HG00544.hp2 HG00609.hp2 HG00621.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*1298dupA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 1298 | chr2 | 70211420 | |||||
chr2:70211420
|
G | GTT | 2 | a0001c0001t0005a0001c0001t0008 | 9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1297_*1298dupAA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 1298 | chr2 | 70211420 | |||||
chr2:70211421
|
T | G | 1 | a0001c0001t0013 | 2 | HG02630.hp2 NA18952.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1298A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 1298 | chr2 | 70211421 | |||||
chr2:70211474
|
G | A | 1 | a0001c0001t0024 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1245C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 1245 | chr2 | 70211474 | |||||
chr2:70211892
|
C | T | 1 | a0001c0001t0008 | 4 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*827G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 827 | chr2 | 70211892 | |||||
chr2:70211926
|
G | C | 1 | a0001c0001t0017 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*793C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 793 | chr2 | 70211926 | |||||
chr2:70212272
|
C | T | 5 | a0001c0001t0002a0001c0001t0011a0001c0001t0015others(2): Show | 46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*447G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 447 | chr2 | 70212272 | |||||
chr2:70212316
|
G | GT | 3 | a0001c0001t0006a0001c0001t0015a0001c0001t0016 | 6 | HG01243.hp2 HG02055.hp2 NA18940.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*402dupA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 402 | chr2 | 70212316 | |||||
chr2:70212327
|
T | A | 1 | a0001c0001t0004 | 10 | HG01192.hp1 HG01433.hp1 HG01884.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*392A>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 392 | chr2 | 70212327 | |||||
chr2:70212394
|
T | C | 1 | a0001c0001t0025 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*325A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 325 | chr2 | 70212394 | |||||
chr2:70248443
|
C | T | 1 | a0001c0001t0014 | 1 | HG03017.hp2 | 5_prime_UTR_variant | MODIFIER | c.-13G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/13 | 13 | chr2 | 70248443 | |||||
chr2:70248567
|
G | A | 1 | a0001c0001t0010 | 3 | HG00642.hp1 HG01943.hp1 HG01993.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-137C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/13 | chr2 | 70248567 | ||||||
chr2:70248586
|
C | A | 1 | a0001c0001t0026 | 1 | HG01167.hp2 | 5_prime_UTR_variant | MODIFIER | c.-156G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/13 | 156 | chr2 | 70248586 | |||||
chr2:70248596
|
G | A | 2 | a0001c0001t0005a0001c0001t0008 | 9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-166C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/13 | chr2 | 70248596 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:70212873
|
G | A | 1 | a0001c0001t0006g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1035-28C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70212873 | ||||||
chr2:70212978
|
T | C | 2 | a0001c0001t0003g0048a0001c0001t0003g0053 | 2 | HG02129.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1035-133A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70212978 | ||||||
chr2:70213035
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1035-190A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213035 | ||||||
chr2:70213077
|
T | G | 1 | a0001c0001t0004g0335 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1035-232A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213077 | ||||||
chr2:70213122
|
G | A | 1 | a0001c0001t0001g0344 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1035-277C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213122 | ||||||
chr2:70213212
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1035-367G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213212 | ||||||
chr2:70213230
|
T | G | 1 | a0001c0001t0001g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1035-385A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213230 | ||||||
chr2:70213257
|
T | C | 1 | a0001c0001t0002g0303 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1035-412A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213257 | ||||||
chr2:70213280
|
A | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1035-435T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213280 | ||||||
chr2:70213316
|
C | A | 45 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(42): Show | 46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.1035-471G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213316 | ||||||
chr2:70213345
|
C | CT | 10 | a0001c0001t0001g0104a0001c0001t0001g0109a0001c0001t0001g0113others(7): Show | 10 | HG02922.hp2 NA18964.hp1 NA18982.hp1 others(7): Show |
intron_variant | MODIFIER | c.1035-501dupA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213345 | ||||||
chr2:70213345
|
CT | C | 10 | a0001c0001t0001g0031a0001c0001t0001g0186a0001c0001t0001g0209others(7): Show | 10 | HG01169.hp2 HG01257.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1035-501delA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213345 | ||||||
chr2:70213350
|
T | C | 9 | a0001c0001t0001g0134a0001c0001t0001g0178a0001c0001t0001g0179others(6): Show | 9 | HG02004.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1035-505A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213350 | ||||||
chr2:70213374
|
C | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(84): Show | 99 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1035-529G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213374 | ||||||
chr2:70213485
|
T | C | 1 | a0001c0001t0018g0286 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1035-640A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213485 | ||||||
chr2:70213599
|
T | G | 1 | a0001c0001t0003g0055 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1034+750A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213599 | ||||||
chr2:70213657
|
CT | C | 45 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(42): Show | 46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.1034+691delA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213657 | ||||||
chr2:70213801
|
A | G | 1 | a0001c0001t0018g0286 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1034+548T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213801 | ||||||
chr2:70214042
|
G | A | 1 | a0001c0001t0018g0286 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1034+307C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70214042 | ||||||
chr2:70214050
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1034+299C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70214050 | ||||||
chr2:70214199
|
T | TA | 45 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(42): Show | 46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.1034+149dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70214199 | ||||||
chr2:70214218
|
G | A | 4 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0096others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1034+131C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70214218 | ||||||
chr2:70214229
|
G | A | 58 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(55): Show | 60 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.1034+120C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70214229 | ||||||
chr2:70214632
|
TAAAAAAA others(1): Show |
T | 6 | a0001c0001t0001g0025a0001c0001t0001g0103a0001c0001t0001g0124others(3): Show | 6 | HG02602.hp2 HG02698.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.889-146_889-139del others(8): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 11/12 | chr2 | 70214632 | ||||||
chr2:70214643
|
A | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(187): Show | 206 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.889-149T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 11/12 | chr2 | 70214643 | ||||||
chr2:70214651
|
A | AC | 42 | a0001c0001t0001g0075a0001c0001t0001g0192a0001c0001t0001g0201others(39): Show | 43 | HG00609.hp2 HG00735.hp2 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.889-158_889-157ins others(1): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 11/12 | chr2 | 70214651 | ||||||
chr2:70214651
|
A | C | 310 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(307): Show | 334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.889-157T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 11/12 | chr2 | 70214651 | ||||||
chr2:70214668
|
A | G | 1 | a0001c0001t0018g0286 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.889-174T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 11/12 | chr2 | 70214668 | ||||||
chr2:70214720
|
G | C | 19 | a0001c0001t0001g0014a0001c0001t0001g0186a0001c0001t0001g0189others(16): Show | 20 | HG02074.hp1 HG02083.hp2 NA18747.hp1 others(17): Show |
intron_variant | MODIFIER | c.889-226C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 11/12 | chr2 | 70214720 | ||||||
chr2:70214811
|
T | C | 1 | a0001c0001t0002g0318 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.889-317A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 11/12 | chr2 | 70214811 | ||||||
chr2:70214864
|
T | G | 38 | a0001c0001t0001g0075a0001c0001t0003g0004a0001c0001t0003g0027others(35): Show | 39 | HG00609.hp2 HG00735.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.889-370A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 11/12 | chr2 | 70214864 | ||||||
chr2:70215047
|
A | G | 4 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(1): Show | 5 | HG02109.hp1 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.888+324T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 11/12 | chr2 | 70215047 | ||||||
chr2:70215184
|
G | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0180 | 3 | HG03704.hp2 NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.888+187C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 11/12 | chr2 | 70215184 | ||||||
chr2:70215590
|
ACAGTTTG | A | 17 | a0001c0001t0001g0342a0001c0001t0001g0344a0001c0001t0001g0345others(14): Show | 17 | HG01243.hp1 HG01884.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.765-103_765-97delC others(6): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70215590 | ||||||
chr2:70215598
|
C | T | 1 | a0001c0001t0018g0286 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.765-104G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70215598 | ||||||
chr2:70215660
|
T | C | 58 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(55): Show | 60 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.765-166A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70215660 | ||||||
chr2:70215706
|
G | C | 2 | a0001c0001t0001g0129a0001c0001t0001g0158 | 2 | HG00609.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.765-212C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70215706 | ||||||
chr2:70215720
|
G | C | 3 | a0001c0001t0002g0305a0001c0001t0002g0309a0001c0001t0002g0310 | 3 | NA18959.hp1 NA18965.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.765-226C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70215720 | ||||||
chr2:70215753
|
A | T | 1 | a0001c0001t0006g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.765-259T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70215753 | ||||||
chr2:70215822
|
C | A | 3 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0248 | 3 | NA18943.hp1 NA18962.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.765-328G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70215822 | ||||||
chr2:70215880
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.764+328G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70215880 | ||||||
chr2:70215900
|
C | T | 15 | a0001c0001t0001g0278a0001c0001t0003g0045a0001c0001t0003g0049others(12): Show | 15 | HG01257.hp2 HG01258.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.764+308G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70215900 | ||||||
chr2:70215998
|
C | T | 1 | a0001c0001t0002g0331 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.764+210G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70215998 | ||||||
chr2:70216003
|
C | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | NA18945.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.764+205G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70216003 | ||||||
chr2:70216033
|
T | C | 17 | a0001c0001t0001g0342a0001c0001t0001g0344a0001c0001t0001g0345others(14): Show | 17 | HG01243.hp1 HG01884.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.764+175A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70216033 | ||||||
chr2:70216115
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.764+93A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70216115 | ||||||
chr2:70216191
|
T | A | 1 | a0001c0001t0001g0215 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.764+17A>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70216191 | ||||||
chr2:70216596
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.584-97G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 8/12 | chr2 | 70216596 | ||||||
chr2:70217184
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.475-190A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217184 | ||||||
chr2:70217202
|
C | T | 1 | a0001c0001t0020g0202 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.475-208G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217202 | ||||||
chr2:70217303
|
C | T | 3 | a0001c0001t0009g0339a0001c0001t0009g0341a0001c0001t0024g0340 | 3 | HG01884.hp1 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.475-309G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217303 | ||||||
chr2:70217304
|
G | T | 60 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0002g0019others(57): Show | 62 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.475-310C>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217304 | ||||||
chr2:70217369
|
G | A | 2 | a0001c0001t0001g0084a0001c0001t0022g0085 | 2 | HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.475-375C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217369 | ||||||
chr2:70217404
|
CTTT | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(87): Show | 103 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.475-413_475-411del others(3): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217404 | ||||||
chr2:70217558
|
T | C | 38 | a0001c0001t0001g0075a0001c0001t0003g0004a0001c0001t0003g0027others(35): Show | 39 | HG00609.hp2 HG00735.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.475-564A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217558 | ||||||
chr2:70217562
|
T | TCATTTTT others(329): Show |
1 | a0001c0001t0002g0313 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.475-569_475-568ins others(336): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217562 | ||||||
chr2:70217651
|
C | A | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-657G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217651 | ||||||
chr2:70217656
|
C | G | 3 | a0001c0001t0001g0207a0001c0001t0001g0229a0001c0001t0001g0256 | 3 | HG01106.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.475-662G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217656 | ||||||
chr2:70217716
|
C | A | 3 | a0001c0001t0001g0220a0001c0001t0001g0225a0001c0001t0001g0231 | 3 | HG01070.hp1 HG01175.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.475-722G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217716 | ||||||
chr2:70217866
|
G | A | 58 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(55): Show | 60 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.475-872C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217866 | ||||||
chr2:70217888
|
T | C | 49 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(46): Show | 50 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.475-894A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217888 | ||||||
chr2:70217908
|
A | ATC | 3 | a0001c0001t0001g0204a0001c0001t0001g0228a0001c0001t0001g0247 | 3 | HG02602.hp1 HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.475-915_475-914ins others(2): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217908 | ||||||
chr2:70217920
|
A | G | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-926T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217920 | ||||||
chr2:70218051
|
C | A | 1 | a0001c0001t0002g0326 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.475-1057G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70218051 | ||||||
chr2:70218104
|
G | GT | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-1111dupA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70218104 | ||||||
chr2:70218114
|
T | G | 1 | a0001c0001t0001g0352 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.475-1120A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70218114 | ||||||
chr2:70218119
|
G | C | 50 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(47): Show | 51 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.475-1125C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70218119 | ||||||
chr2:70218267
|
A | G | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(248): Show | 269 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.475-1273T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70218267 | ||||||
chr2:70218403
|
C | G | 45 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(42): Show | 46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.475-1409G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70218403 | ||||||
chr2:70218449
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0173 | 2 | NA18979.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.475-1455G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70218449 | ||||||
chr2:70218530
|
C | A | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-1536G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70218530 | ||||||
chr2:70218804
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.475-1810A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70218804 | ||||||
chr2:70218832
|
A | T | 1 | a0001c0001t0002g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.475-1838T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70218832 | ||||||
chr2:70218973
|
G | C | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-1979C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70218973 | ||||||
chr2:70219187
|
A | T | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-2193T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219187 | ||||||
chr2:70219193
|
A | G | 45 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(42): Show | 46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.475-2199T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219193 | ||||||
chr2:70219199
|
G | C | 1 | a0001c0001t0013g0354 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.475-2205C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219199 | ||||||
chr2:70219239
|
GGGA | G | 45 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(42): Show | 46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.475-2248_475-2246d others(5): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219239 | ||||||
chr2:70219392
|
A | T | 1 | a0001c0001t0020g0202 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.475-2398T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219392 | ||||||
chr2:70219625
|
C | G | 1 | a0001c0001t0004g0336 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.475-2631G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219625 | ||||||
chr2:70219653
|
A | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(80): Show | 96 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.475-2659T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219653 | ||||||
chr2:70219738
|
C | CT | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 210 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(207): Show |
intron_variant | MODIFIER | c.475-2745dupA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219738 | ||||||
chr2:70219738
|
C | CTT | 5 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 6 | HG02074.hp2 HG02083.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.475-2746_475-2745d others(4): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219738 | ||||||
chr2:70219738
|
CT | C | 7 | a0001c0001t0001g0186a0001c0001t0001g0201a0001c0001t0001g0204others(4): Show | 8 | HG00642.hp1 HG01943.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.475-2745delA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219738 | ||||||
chr2:70219759
|
A | G | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-2765T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219759 | ||||||
chr2:70219867
|
A | G | 2 | a0001c0001t0002g0305a0001c0001t0002g0310 | 2 | NA18959.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.475-2873T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219867 | ||||||
chr2:70219891
|
T | C | 1 | a0001c0001t0001g0231 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.475-2897A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219891 | ||||||
chr2:70219943
|
C | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.475-2949G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219943 | ||||||
chr2:70219968
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.475-2974A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219968 | ||||||
chr2:70219984
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.475-2990C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219984 | ||||||
chr2:70220023
|
CT | C | 37 | a0001c0001t0003g0004a0001c0001t0003g0027a0001c0001t0003g0038others(34): Show | 38 | HG00609.hp2 HG00735.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.475-3030delA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220023 | ||||||
chr2:70220072
|
T | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG02040.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.475-3078A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220072 | ||||||
chr2:70220134
|
G | C | 1 | a0001c0001t0022g0085 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.475-3140C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220134 | ||||||
chr2:70220250
|
A | T | 1 | a0003c0006t0001g0116 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.475-3256T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220250 | ||||||
chr2:70220342
|
A | G | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-3348T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220342 | ||||||
chr2:70220453
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.475-3459A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220453 | ||||||
chr2:70220467
|
T | C | 1 | a0001c0001t0001g0010 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.475-3473A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220467 | ||||||
chr2:70220540
|
G | T | 1 | a0001c0001t0001g0236 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.475-3546C>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220540 | ||||||
chr2:70220604
|
A | C | 2 | a0001c0001t0001g0154a0001c0001t0001g0177 | 2 | HG03669.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.475-3610T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220604 | ||||||
chr2:70220605
|
T | C | 2 | a0001c0005t0012g0087a0001c0005t0012g0100 | 2 | HG02280.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.475-3611A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220605 | ||||||
chr2:70220648
|
G | T | 15 | a0001c0001t0001g0069a0001c0001t0001g0080a0001c0001t0001g0081others(12): Show | 16 | HG01192.hp1 HG01433.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.475-3654C>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220648 | ||||||
chr2:70220743
|
G | A | 2 | a0001c0001t0001g0226a0001c0001t0001g0259 | 2 | HG01192.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.475-3749C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220743 | ||||||
chr2:70220894
|
G | T | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+3660C>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220894 | ||||||
chr2:70220964
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.474+3590C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220964 | ||||||
chr2:70220983
|
A | G | 1 | a0001c0001t0001g0114 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.474+3571T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220983 | ||||||
chr2:70221006
|
A | T | 4 | a0001c0001t0001g0272a0001c0001t0004g0269a0001c0001t0004g0270others(1): Show | 4 | HG01433.hp1 HG02257.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+3548T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221006 | ||||||
chr2:70221008
|
T | A | 1 | a0001c0001t0001g0075 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.474+3546A>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221008 | ||||||
chr2:70221030
|
G | A | 8 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.474+3524C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221030 | ||||||
chr2:70221061
|
C | T | 8 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.474+3493G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221061 | ||||||
chr2:70221080
|
C | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0177 | 2 | HG03669.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.474+3474G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221080 | ||||||
chr2:70221141
|
T | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.474+3413A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221141 | ||||||
chr2:70221151
|
C | T | 1 | a0001c0001t0018g0286 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.474+3403G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221151 | ||||||
chr2:70221198
|
G | C | 4 | a0001c0001t0008g0363a0001c0001t0008g0364a0001c0001t0008g0366others(1): Show | 4 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+3356C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221198 | ||||||
chr2:70221202
|
T | G | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+3352A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221202 | ||||||
chr2:70221311
|
T | TA | 14 | a0001c0001t0003g0045a0001c0001t0003g0049a0001c0001t0003g0050others(11): Show | 14 | HG01257.hp2 HG01258.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.474+3242dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221311 | ||||||
chr2:70221470
|
C | CA | 46 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(43): Show | 47 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.474+3083dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221470 | ||||||
chr2:70221474
|
A | T | 4 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(1): Show | 5 | HG02109.hp1 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.474+3080T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221474 | ||||||
chr2:70221488
|
C | T | 1 | a0001c0001t0002g0318 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.474+3066G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221488 | ||||||
chr2:70221601
|
G | A | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+2953C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221601 | ||||||
chr2:70221798
|
A | AT | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(87): Show | 103 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.474+2755dupA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221798 | ||||||
chr2:70221798
|
A | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0272a0001c0001t0004g0271 | 3 | HG02257.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.474+2756T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221798 | ||||||
chr2:70221799
|
T | A | 1 | a0001c0001t0001g0227 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.474+2755A>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221799 | ||||||
chr2:70221827
|
G | A | 5 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.474+2727C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221827 | ||||||
chr2:70221863
|
C | T | 1 | a0001c0001t0004g0333 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.474+2691G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221863 | ||||||
chr2:70221935
|
G | A | 1 | a0001c0001t0019g0198 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.474+2619C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221935 | ||||||
chr2:70221981
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.474+2573A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221981 | ||||||
chr2:70221992
|
C | G | 1 | a0001c0001t0003g0063 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.474+2562G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221992 | ||||||
chr2:70222056
|
A | C | 8 | a0001c0001t0001g0005a0001c0001t0001g0036a0001c0001t0001g0088others(5): Show | 9 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+2498T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222056 | ||||||
chr2:70222062
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.474+2492C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222062 | ||||||
chr2:70222136
|
AAAAC | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0026a0001c0001t0001g0197others(5): Show | 9 | HG00423.hp2 NA18941.hp2 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.474+2414_474+2417d others(6): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222136 | ||||||
chr2:70222148
|
C | A | 5 | a0001c0001t0001g0069a0001c0001t0001g0170a0001c0001t0003g0038others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.474+2406G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222148 | ||||||
chr2:70222148
|
C | CA | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(84): Show | 100 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.474+2405dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222148 | ||||||
chr2:70222152
|
A | C | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0274others(4): Show | 7 | HG00544.hp1 HG01884.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.474+2402T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222152 | ||||||
chr2:70222207
|
A | C | 1 | a0001c0002t0007g0288 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.474+2347T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222207 | ||||||
chr2:70222398
|
C | T | 3 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181 | 3 | HG02630.hp1 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.474+2156G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222398 | ||||||
chr2:70222470
|
G | A | 1 | a0001c0001t0026g0360 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.474+2084C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222470 | ||||||
chr2:70222557
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.474+1997C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222557 | ||||||
chr2:70222602
|
T | C | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.474+1952A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222602 | ||||||
chr2:70222644
|
A | G | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 272 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(269): Show |
intron_variant | MODIFIER | c.474+1910T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222644 | ||||||
chr2:70222648
|
G | A | 45 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(42): Show | 46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.474+1906C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222648 | ||||||
chr2:70222731
|
T | C | 1 | a0001c0001t0001g0265 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.474+1823A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222731 | ||||||
chr2:70222863
|
G | A | 3 | a0001c0001t0001g0249a0001c0001t0001g0264a0001c0001t0001g0267 | 3 | NA18963.hp2 NA19055.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.474+1691C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222863 | ||||||
chr2:70222873
|
C | A | 1 | a0001c0001t0019g0198 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.474+1681G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222873 | ||||||
chr2:70222876
|
T | G | 10 | a0001c0001t0001g0272a0001c0001t0004g0020a0001c0001t0004g0269others(7): Show | 11 | HG01192.hp1 HG01433.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.474+1678A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222876 | ||||||
chr2:70222878
|
C | T | 3 | a0001c0001t0001g0133a0001c0001t0001g0180a0001c0001t0001g0356 | 3 | HG01257.hp1 HG02735.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.474+1676G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222878 | ||||||
chr2:70222894
|
A | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.474+1660T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222894 | ||||||
chr2:70222900
|
C | T | 1 | a0001c0001t0004g0334 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.474+1654G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222900 | ||||||
chr2:70222916
|
A | G | 4 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0096others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.474+1638T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222916 | ||||||
chr2:70222926
|
ATAT | A | 9 | a0001c0001t0001g0272a0001c0001t0004g0020a0001c0001t0004g0269others(6): Show | 10 | HG01192.hp1 HG01433.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.474+1625_474+1627d others(5): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222926 | ||||||
chr2:70222929
|
T | G | 1 | a0001c0001t0004g0336 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.474+1625A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222929 | ||||||
chr2:70223008
|
A | G | 1 | a0001c0001t0006g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.474+1546T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70223008 | ||||||
chr2:70223064
|
T | C | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.474+1490A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70223064 | ||||||
chr2:70223154
|
A | C | 3 | a0001c0001t0001g0024a0001c0001t0001g0234a0001c0001t0001g0268 | 3 | HG00280.hp1 HG00642.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.474+1400T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70223154 | ||||||
chr2:70223253
|
T | C | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+1301A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70223253 | ||||||
chr2:70223297
|
G | C | 60 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0002g0019others(57): Show | 62 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.474+1257C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70223297 | ||||||
chr2:70223315
|
CTTAATTT | C | 45 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(42): Show | 46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.474+1232_474+1238d others(9): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70223315 | ||||||
chr2:70223577
|
A | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.474+977T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70223577 | ||||||
chr2:70223710
|
G | A | 1 | a0001c0001t0018g0286 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.474+844C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70223710 | ||||||
chr2:70224042
|
C | T | 8 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.474+512G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70224042 | ||||||
chr2:70224075
|
G | A | 1 | a0001c0001t0003g0048 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.474+479C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70224075 | ||||||
chr2:70224164
|
C | T | 8 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.474+390G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70224164 | ||||||
chr2:70224209
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.474+345G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70224209 | ||||||
chr2:70224270
|
G | C | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(157): Show | 175 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.474+284C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70224270 | ||||||
chr2:70224349
|
C | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.474+205G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70224349 | ||||||
chr2:70224349
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.474+205G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70224349 | ||||||
chr2:70224370
|
G | A | 3 | a0001c0001t0001g0103a0001c0001t0001g0163a0001c0001t0001g0164 | 3 | HG02976.hp2 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.474+184C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70224370 | ||||||
chr2:70224471
|
C | T | 1 | a0001c0001t0001g0243 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.474+83G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70224471 | ||||||
chr2:70224472
|
GA | G | 29 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0030others(26): Show | 30 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.474+81delT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70224472 | ||||||
chr2:70224473
|
A | G | 1 | a0001c0001t0001g0146 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.474+81T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70224473 | ||||||
chr2:70224652
|
G | A | 17 | a0001c0001t0001g0342a0001c0001t0001g0344a0001c0001t0001g0345others(14): Show | 17 | HG01243.hp1 HG01884.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.399-23C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70224652 | ||||||
chr2:70224945
|
T | C | 1 | a0001c0001t0001g0266 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.399-316A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70224945 | ||||||
chr2:70225285
|
A | C | 1 | a0001c0001t0001g0081 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.399-656T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70225285 | ||||||
chr2:70225478
|
A | C | 1 | a0001c0001t0001g0274 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.399-849T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70225478 | ||||||
chr2:70226251
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0173 | 2 | NA18979.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.398+1484G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70226251 | ||||||
chr2:70226252
|
G | A | 5 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0279others(2): Show | 5 | NA18962.hp1 NA18966.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.398+1483C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70226252 | ||||||
chr2:70226290
|
C | T | 3 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181 | 3 | HG02630.hp1 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.398+1445G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70226290 | ||||||
chr2:70226348
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.398+1387G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70226348 | ||||||
chr2:70226351
|
G | A | 1 | a0001c0001t0013g0354 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.398+1384C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70226351 | ||||||
chr2:70226631
|
G | A | 8 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(5): Show | 8 | HG02622.hp1 HG02630.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.398+1104C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70226631 | ||||||
chr2:70226685
|
C | T | 1 | a0001c0001t0003g0054 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.398+1050G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70226685 | ||||||
chr2:70226820
|
T | C | 4 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0086others(1): Show | 4 | HG02572.hp1 HG02818.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.398+915A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70226820 | ||||||
chr2:70226853
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0022g0085 | 2 | HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.398+882G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70226853 | ||||||
chr2:70226894
|
C | T | 1 | a0001c0001t0001g0205 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.398+841G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70226894 | ||||||
chr2:70227073
|
T | A | 8 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.398+662A>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70227073 | ||||||
chr2:70227113
|
T | G | 13 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0030others(10): Show | 14 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.398+622A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70227113 | ||||||
chr2:70227151
|
T | A | 2 | a0001c0001t0001g0272a0001c0001t0004g0271 | 2 | HG02257.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.398+584A>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70227151 | ||||||
chr2:70227234
|
T | C | 37 | a0001c0001t0003g0004a0001c0001t0003g0027a0001c0001t0003g0038others(34): Show | 38 | HG00609.hp2 HG00735.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.398+501A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70227234 | ||||||
chr2:70227662
|
G | C | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(90): Show | 106 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.398+73C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70227662 | ||||||
chr2:70228072
|
C | T | 46 | a0001c0001t0001g0132a0001c0001t0002g0019a0001c0001t0002g0285others(43): Show | 47 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.311-250G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 5/12 | chr2 | 70228072 | ||||||
chr2:70228482
|
A | AACAGTAA others(5): Show |
1 | a0001c0001t0002g0314 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.310+565_310+576dup others(12): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 5/12 | chr2 | 70228482 | ||||||
chr2:70228681
|
T | A | 1 | a0001c0008t0001g0218 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.310+378A>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 5/12 | chr2 | 70228681 | ||||||
chr2:70228775
|
A | G | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(248): Show | 269 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.310+284T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 5/12 | chr2 | 70228775 | ||||||
chr2:70228809
|
C | T | 1 | a0001c0001t0004g0334 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.310+250G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 5/12 | chr2 | 70228809 | ||||||
chr2:70229206
|
C | T | 30 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0030others(27): Show | 31 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.277+58G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 4/12 | chr2 | 70229206 | ||||||
chr2:70229237
|
T | C | 8 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.277+27A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 4/12 | chr2 | 70229237 | ||||||
chr2:70229352
|
C | T | 8 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.223-34G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70229352 | ||||||
chr2:70229395
|
G | C | 1 | a0001c0001t0014g0023 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.223-77C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70229395 | ||||||
chr2:70229400
|
A | G | 1 | a0001c0001t0001g0277 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.223-82T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70229400 | ||||||
chr2:70229454
|
C | T | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 277 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.223-136G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70229454 | ||||||
chr2:70229565
|
T | C | 3 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0006g0070 | 3 | HG02055.hp2 HG02257.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.223-247A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70229565 | ||||||
chr2:70229583
|
C | T | 7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0183others(4): Show | 9 | HG00558.hp2 HG02015.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.223-265G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70229583 | ||||||
chr2:70229647
|
G | A | 3 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0006g0070 | 3 | HG02055.hp2 HG02257.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.223-329C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70229647 | ||||||
chr2:70229802
|
A | G | 1 | a0001c0001t0003g0062 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.223-484T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70229802 | ||||||
chr2:70229937
|
C | CA | 18 | a0001c0001t0001g0069a0001c0001t0001g0159a0001c0001t0001g0169others(15): Show | 19 | HG00741.hp2 HG01109.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.223-620dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70229937 | ||||||
chr2:70229945
|
A | G | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.223-627T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70229945 | ||||||
chr2:70229966
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.223-648G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70229966 | ||||||
chr2:70229987
|
G | C | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(248): Show | 269 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.223-669C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70229987 | ||||||
chr2:70230018
|
C | T | 2 | a0001c0001t0003g0048a0001c0001t0003g0053 | 2 | HG02129.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.223-700G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230018 | ||||||
chr2:70230059
|
C | T | 1 | a0001c0002t0007g0284 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.222+697G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230059 | ||||||
chr2:70230073
|
T | C | 58 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(55): Show | 60 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.222+683A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230073 | ||||||
chr2:70230083
|
A | T | 1 | a0001c0001t0001g0103 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.222+673T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230083 | ||||||
chr2:70230116
|
G | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG02735.hp1 HG02738.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+640C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230116 | ||||||
chr2:70230170
|
A | G | 60 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0002g0019others(57): Show | 62 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.222+586T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230170 | ||||||
chr2:70230181
|
T | G | 2 | a0001c0001t0003g0048a0001c0001t0003g0053 | 2 | HG02129.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.222+575A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230181 | ||||||
chr2:70230198
|
G | A | 15 | a0001c0001t0001g0069a0001c0001t0001g0080a0001c0001t0001g0081others(12): Show | 16 | HG01192.hp1 HG01433.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.222+558C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230198 | ||||||
chr2:70230203
|
G | A | 1 | a0001c0001t0002g0314 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.222+553C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230203 | ||||||
chr2:70230241
|
C | CA | 32 | a0001c0001t0001g0033a0001c0001t0001g0078a0001c0001t0001g0080others(29): Show | 33 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.222+514dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230241 | ||||||
chr2:70230241
|
CA | C | 6 | a0001c0001t0001g0030a0001c0001t0001g0127a0001c0001t0001g0146others(3): Show | 6 | HG01167.hp2 HG02129.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.222+514delT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230241 | ||||||
chr2:70230376
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.222+380G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230376 | ||||||
chr2:70230477
|
C | T | 3 | a0001c0001t0001g0024a0001c0001t0001g0234a0001c0001t0001g0268 | 3 | HG00280.hp1 HG00642.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.222+279G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230477 | ||||||
chr2:70230496
|
C | T | 4 | a0001c0001t0004g0020a0001c0001t0004g0333a0001c0001t0004g0335others(1): Show | 5 | HG01192.hp1 HG02922.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+260G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230496 | ||||||
chr2:70230523
|
G | A | 1 | a0001c0001t0002g0315 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.222+233C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230523 | ||||||
chr2:70230608
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 218 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.222+148A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230608 | ||||||
chr2:70230652
|
C | CA | 94 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(91): Show | 96 | HG00544.hp2 HG00609.hp2 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.222+103dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230652 | ||||||
chr2:70230652
|
C | CAA | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(117): Show | 134 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.222+102_222+103dup others(2): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230652 | ||||||
chr2:70230652
|
C | CAAA | 11 | a0001c0001t0001g0009a0001c0001t0001g0112a0001c0001t0001g0118others(8): Show | 12 | HG00621.hp2 HG02155.hp1 NA18953.hp1 others(9): Show |
intron_variant | MODIFIER | c.222+101_222+103dup others(3): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230652 | ||||||
chr2:70230693
|
C | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.222+63G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230693 | ||||||
chr2:70231135
|
T | TA | 5 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0233others(2): Show | 5 | HG01069.hp2 HG01169.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-282dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70231135 | ||||||
chr2:70231226
|
C | T | 45 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(42): Show | 46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.124-372G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70231226 | ||||||
chr2:70231234
|
G | A | 8 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.124-380C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70231234 | ||||||
chr2:70231324
|
A | G | 2 | a0001c0001t0001g0186a0001c0001t0001g0244 | 2 | HG02074.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.124-470T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70231324 | ||||||
chr2:70231448
|
T | TA | 47 | a0001c0001t0001g0136a0001c0001t0002g0019a0001c0001t0002g0285others(44): Show | 48 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.124-595dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70231448 | ||||||
chr2:70231632
|
A | T | 4 | a0001c0001t0001g0272a0001c0001t0004g0269a0001c0001t0004g0270others(1): Show | 4 | HG01433.hp1 HG02257.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-778T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70231632 | ||||||
chr2:70231877
|
A | T | 8 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.124-1023T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70231877 | ||||||
chr2:70231881
|
A | G | 1 | a0001c0001t0001g0010 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.124-1027T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70231881 | ||||||
chr2:70232018
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0145 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.124-1164G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232018 | ||||||
chr2:70232030
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.124-1176C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232030 | ||||||
chr2:70232095
|
A | G | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(248): Show | 269 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.124-1241T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232095 | ||||||
chr2:70232137
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.124-1283C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232137 | ||||||
chr2:70232196
|
G | A | 1 | a0001c0001t0001g0265 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.124-1342C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232196 | ||||||
chr2:70232208
|
C | CA | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(81): Show | 97 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.124-1355dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232208 | ||||||
chr2:70232208
|
CA | C | 7 | a0001c0001t0001g0267a0001c0001t0002g0323a0001c0001t0003g0062others(4): Show | 7 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.124-1355delT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232208 | ||||||
chr2:70232265
|
G | A | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-1411C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232265 | ||||||
chr2:70232335
|
G | GT | 2 | a0001c0001t0001g0010a0001c0001t0001g0172 | 3 | HG01070.hp2 HG01071.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.124-1482dupA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232335 | ||||||
chr2:70232432
|
C | A | 45 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(42): Show | 46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.124-1578G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232432 | ||||||
chr2:70232432
|
C | T | 1 | a0001c0001t0001g0255 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.124-1578G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232432 | ||||||
chr2:70232526
|
G | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0212 | 5 | HG01256.hp2 HG01258.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.124-1672C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232526 | ||||||
chr2:70232540
|
C | CA | 15 | a0001c0001t0001g0016a0001c0001t0001g0187a0001c0001t0001g0201others(12): Show | 16 | HG00558.hp2 HG02132.hp2 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.124-1687dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232540 | ||||||
chr2:70232540
|
C | CAAA | 9 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0195others(6): Show | 9 | HG02083.hp2 NA18943.hp1 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.124-1689_124-1687d others(5): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232540 | ||||||
chr2:70232540
|
C | CAAAA | 6 | a0001c0001t0001g0014a0001c0001t0001g0186a0001c0001t0001g0216others(3): Show | 7 | NA18747.hp1 NA18947.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-1690_124-1687d others(6): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232540 | ||||||
chr2:70232540
|
CA | C | 52 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(49): Show | 59 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.124-1687delT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232540 | ||||||
chr2:70232540
|
CAA | C | 58 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0028others(55): Show | 60 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.124-1688_124-1687d others(4): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232540 | ||||||
chr2:70232540
|
CAAA | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(91): Show | 106 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.124-1689_124-1687d others(5): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232540 | ||||||
chr2:70232540
|
CAAAA | C | 31 | a0001c0001t0001g0075a0001c0001t0001g0096a0001c0001t0001g0114others(28): Show | 32 | HG00735.hp2 HG01099.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.124-1690_124-1687d others(6): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232540 | ||||||
chr2:70232540
|
CAAAAAAA others(3): Show |
C | 7 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(4): Show | 8 | HG02109.hp1 HG02145.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.124-1696_124-1687d others(12): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232540 | ||||||
chr2:70232540
|
CAAAAAAA others(5): Show |
C | 5 | a0001c0001t0002g0292a0001c0001t0002g0299a0001c0001t0002g0300others(2): Show | 5 | HG00741.hp2 HG02165.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.124-1698_124-1687d others(14): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232540 | ||||||
chr2:70232540
|
CAAAAAAA others(6): Show |
C | 38 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(35): Show | 39 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.124-1699_124-1687d others(15): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232540 | ||||||
chr2:70232540
|
CAAAAAAA others(7): Show |
C | 7 | a0001c0001t0002g0290a0001c0001t0002g0311a0001c0001t0002g0323others(4): Show | 7 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.124-1700_124-1687d others(16): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232540 | ||||||
chr2:70232616
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.124-1762G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232616 | ||||||
chr2:70232654
|
A | G | 2 | a0001c0001t0001g0140a0001c0001t0001g0145 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.124-1800T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232654 | ||||||
chr2:70232693
|
A | C | 1 | a0001c0002t0007g0287 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.124-1839T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232693 | ||||||
chr2:70232706
|
T | C | 3 | a0001c0001t0001g0009a0001c0001t0001g0138a0001c0001t0001g0171 | 4 | NA18971.hp2 NA18981.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-1852A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232706 | ||||||
chr2:70232721
|
C | T | 1 | a0001c0001t0014g0023 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.124-1867G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232721 | ||||||
chr2:70232813
|
G | A | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.124-1959C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232813 | ||||||
chr2:70232847
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0356 | 2 | HG02735.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.124-1993G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232847 | ||||||
chr2:70232854
|
C | T | 4 | a0001c0001t0008g0363a0001c0001t0008g0364a0001c0001t0008g0366others(1): Show | 4 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-2000G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232854 | ||||||
chr2:70232867
|
C | CA | 7 | a0001c0001t0001g0113a0001c0001t0001g0213a0001c0001t0001g0216others(4): Show | 7 | HG00741.hp1 HG03225.hp1 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.124-2014dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232867 | ||||||
chr2:70233144
|
A | AT | 38 | a0001c0001t0001g0075a0001c0001t0003g0004a0001c0001t0003g0027others(35): Show | 39 | HG00609.hp2 HG00735.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.124-2291dupA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233144 | ||||||
chr2:70233174
|
T | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(150): Show | 168 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.124-2320A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233174 | ||||||
chr2:70233179
|
C | G | 45 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(42): Show | 46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.124-2325G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233179 | ||||||
chr2:70233264
|
C | T | 58 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(55): Show | 60 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.124-2410G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233264 | ||||||
chr2:70233279
|
T | C | 8 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.124-2425A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233279 | ||||||
chr2:70233434
|
C | T | 1 | a0001c0001t0001g0352 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.124-2580G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233434 | ||||||
chr2:70233456
|
C | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.124-2602G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233456 | ||||||
chr2:70233562
|
A | T | 1 | a0001c0001t0001g0342 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.123+2517T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233562 | ||||||
chr2:70233565
|
A | G | 1 | a0001c0001t0001g0342 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.123+2514T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233565 | ||||||
chr2:70233590
|
A | C | 45 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(42): Show | 46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.123+2489T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233590 | ||||||
chr2:70233634
|
C | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0228a0001c0001t0001g0240others(1): Show | 4 | HG02602.hp1 HG03239.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+2445G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233634 | ||||||
chr2:70233764
|
T | TA | 46 | a0001c0001t0001g0227a0001c0001t0002g0019a0001c0001t0002g0285others(43): Show | 47 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.123+2314dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233764 | ||||||
chr2:70233885
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0172 | 3 | HG01070.hp2 HG01071.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.123+2194T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233885 | ||||||
chr2:70233896
|
C | A | 1 | a0001c0001t0018g0286 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.123+2183G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233896 | ||||||
chr2:70233911
|
T | C | 4 | a0001c0001t0008g0363a0001c0001t0008g0364a0001c0001t0008g0366others(1): Show | 4 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+2168A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233911 | ||||||
chr2:70234223
|
T | G | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+1856A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234223 | ||||||
chr2:70234319
|
T | C | 1 | a0001c0001t0001g0239 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.123+1760A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234319 | ||||||
chr2:70234354
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.123+1725A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234354 | ||||||
chr2:70234446
|
G | T | 45 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(42): Show | 46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.123+1633C>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234446 | ||||||
chr2:70234491
|
C | G | 1 | a0001c0001t0001g0069 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.123+1588G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234491 | ||||||
chr2:70234513
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.123+1566T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234513 | ||||||
chr2:70234562
|
T | C | 37 | a0001c0001t0003g0004a0001c0001t0003g0027a0001c0001t0003g0038others(34): Show | 38 | HG00609.hp2 HG00735.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.123+1517A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234562 | ||||||
chr2:70234597
|
T | C | 3 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0006g0070 | 3 | HG02055.hp2 HG02257.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.123+1482A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234597 | ||||||
chr2:70234607
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.123+1472C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234607 | ||||||
chr2:70234626
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.123+1453T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234626 | ||||||
chr2:70234642
|
A | T | 1 | a0001c0001t0001g0203 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.123+1437T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234642 | ||||||
chr2:70234643
|
C | A | 45 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(42): Show | 46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.123+1436G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234643 | ||||||
chr2:70234723
|
G | A | 1 | a0001c0001t0018g0286 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.123+1356C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234723 | ||||||
chr2:70234781
|
C | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(87): Show | 103 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.123+1298G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234781 | ||||||
chr2:70234782
|
G | A | 1 | a0001c0001t0002g0311 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.123+1297C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234782 | ||||||
chr2:70234844
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0224 | 2 | NA18979.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.123+1235C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234844 | ||||||
chr2:70234881
|
T | C | 1 | a0002c0004t0001g0353 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.123+1198A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234881 | ||||||
chr2:70235031
|
GACAAACA others(5): Show |
G | 1 | a0001c0001t0001g0086 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.123+1036_123+1047d others(14): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235031 | ||||||
chr2:70235058
|
G | A | 1 | a0001c0001t0001g0255 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.123+1021C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235058 | ||||||
chr2:70235107
|
A | T | 3 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362 | 4 | HG02109.hp1 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+972T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235107 | ||||||
chr2:70235111
|
A | T | 60 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0002g0019others(57): Show | 62 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.123+968T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235111 | ||||||
chr2:70235151
|
C | G | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+928G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235151 | ||||||
chr2:70235206
|
G | A | 4 | a0001c0001t0001g0103a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG00544.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+873C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235206 | ||||||
chr2:70235303
|
T | C | 2 | a0001c0001t0001g0083a0001c0001t0001g0086 | 2 | HG02572.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.123+776A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235303 | ||||||
chr2:70235333
|
T | C | 38 | a0001c0001t0001g0075a0001c0001t0003g0004a0001c0001t0003g0027others(35): Show | 39 | HG00609.hp2 HG00735.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.123+746A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235333 | ||||||
chr2:70235346
|
C | T | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+733G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235346 | ||||||
chr2:70235415
|
C | G | 46 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(43): Show | 47 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.123+664G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235415 | ||||||
chr2:70235485
|
C | T | 8 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.123+594G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235485 | ||||||
chr2:70235541
|
A | AGT | 8 | a0001c0001t0001g0143a0001c0001t0001g0187a0001c0001t0001g0226others(5): Show | 8 | HG02155.hp2 HG02293.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.123+536_123+537dup others(2): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235541 | ||||||
chr2:70235541
|
A | AGTGT | 40 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0037others(37): Show | 42 | HG00558.hp1 HG01109.hp1 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.123+534_123+537dup others(4): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235541 | ||||||
chr2:70235541
|
A | AGTGTGT | 65 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(62): Show | 66 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.123+532_123+537dup others(6): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235541 | ||||||
chr2:70235541
|
A | AGTGTGTG others(1): Show |
74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(71): Show | 85 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.123+530_123+537dup others(8): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235541 | ||||||
chr2:70235541
|
A | AGTGTGTG others(3): Show |
49 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0025others(46): Show | 52 | HG00423.hp1 HG00621.hp1 HG01167.hp2 others(49): Show |
intron_variant | MODIFIER | c.123+528_123+537dup others(10): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235541 | ||||||
chr2:70235541
|
A | AGTGTGTG others(5): Show |
13 | a0001c0001t0001g0103a0001c0001t0001g0110a0001c0001t0001g0122others(10): Show | 14 | HG00544.hp2 HG01074.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.123+526_123+537dup others(12): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235541 | ||||||
chr2:70235541
|
A | AGTGTGTG others(7): Show |
1 | a0001c0001t0008g0363 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.123+524_123+537dup others(14): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235541 | ||||||
chr2:70235541
|
A | AGTGTGTG others(17): Show |
1 | a0001c0002t0007g0284 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.123+514_123+537dup others(24): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235541 | ||||||
chr2:70235541
|
A | AGTGTGTG others(21): Show |
1 | a0001c0002t0007g0332 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.123+510_123+537dup others(28): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235541 | ||||||
chr2:70235541
|
A | AGTGTGTG others(29): Show |
1 | a0001c0002t0007g0288 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.123+537_123+538ins others(36): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235541 | ||||||
chr2:70235541
|
A | AGTGTGTG others(31): Show |
1 | a0001c0002t0007g0287 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.123+537_123+538ins others(38): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235541 | ||||||
chr2:70235541
|
AGT | A | 10 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0069others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.123+536_123+537del others(2): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235541 | ||||||
chr2:70235572
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.123+507T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235572 | ||||||
chr2:70235575
|
T | C | 45 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(42): Show | 46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.123+504A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235575 | ||||||
chr2:70235588
|
T | C | 45 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(42): Show | 46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.123+491A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235588 | ||||||
chr2:70235603
|
A | G | 4 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(1): Show | 5 | HG02109.hp1 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+476T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235603 | ||||||
chr2:70235765
|
T | C | 1 | a0001c0001t0004g0020 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.123+314A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235765 | ||||||
chr2:70235796
|
CAT | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0191 | 3 | HG03017.hp1 HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.123+281_123+282del others(2): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235796 | ||||||
chr2:70235852
|
A | G | 1 | a0001c0002t0007g0284 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.123+227T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235852 | ||||||
chr2:70235917
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.123+162A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235917 | ||||||
chr2:70235985
|
A | G | 1 | a0002c0004t0001g0346 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.123+94T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235985 | ||||||
chr2:70236036
|
T | TA | 11 | a0001c0001t0001g0272a0001c0001t0002g0300a0001c0001t0004g0020others(8): Show | 12 | HG01192.hp1 HG01433.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.123+42dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70236036 | ||||||
chr2:70236202
|
C | CT | 15 | a0001c0001t0001g0121a0001c0001t0001g0162a0001c0001t0001g0192others(12): Show | 15 | HG01099.hp2 HG01243.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.27-28dupA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70236202 | ||||||
chr2:70236219
|
A | G | 4 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(1): Show | 5 | HG02109.hp1 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.27-44T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70236219 | ||||||
chr2:70236233
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.27-58A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70236233 | ||||||
chr2:70236460
|
A | T | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-285T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70236460 | ||||||
chr2:70236507
|
T | C | 2 | a0001c0001t0003g0038a0001c0001t0003g0040 | 2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.27-332A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70236507 | ||||||
chr2:70236669
|
C | T | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-494G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70236669 | ||||||
chr2:70236688
|
G | A | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.27-513C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70236688 | ||||||
chr2:70236712
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.27-537G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70236712 | ||||||
chr2:70236901
|
A | C | 29 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0030others(26): Show | 30 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.27-726T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70236901 | ||||||
chr2:70237126
|
G | A | 17 | a0001c0001t0001g0342a0001c0001t0001g0344a0001c0001t0001g0345others(14): Show | 17 | HG01243.hp1 HG01884.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.27-951C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70237126 | ||||||
chr2:70237379
|
C | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.27-1204G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70237379 | ||||||
chr2:70237619
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.27-1444G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70237619 | ||||||
chr2:70237721
|
G | A | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-1546C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70237721 | ||||||
chr2:70237870
|
G | A | 1 | a0001c0001t0003g0043 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.27-1695C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70237870 | ||||||
chr2:70237870
|
G | GA | 6 | a0001c0001t0001g0272a0001c0001t0001g0357a0001c0001t0001g0358others(3): Show | 6 | HG01433.hp1 HG02257.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.27-1696dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70237870 | ||||||
chr2:70237940
|
T | C | 1 | a0001c0001t0002g0320 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.27-1765A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70237940 | ||||||
chr2:70238164
|
T | TA | 37 | a0001c0001t0003g0004a0001c0001t0003g0027a0001c0001t0003g0038others(34): Show | 38 | HG00609.hp2 HG00735.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.27-1990dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238164 | ||||||
chr2:70238165
|
A | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.27-1990T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238165 | ||||||
chr2:70238245
|
T | C | 47 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0002g0019others(44): Show | 48 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.27-2070A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238245 | ||||||
chr2:70238249
|
C | T | 1 | a0001c0001t0018g0286 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.27-2074G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238249 | ||||||
chr2:70238249
|
CGTTCCCC others(32): Show |
C | 1 | a0001c0001t0002g0326 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.27-2113_27-2075del others(39): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238249 | ||||||
chr2:70238260
|
G | GT | 102 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(99): Show | 107 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.27-2086dupA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238260 | ||||||
chr2:70238260
|
G | GTT | 9 | a0001c0001t0001g0264a0001c0001t0001g0273a0001c0001t0001g0274others(6): Show | 9 | HG00544.hp1 HG02071.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.27-2087_27-2086dup others(2): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238260 | ||||||
chr2:70238260
|
G | GTTTT | 17 | a0001c0001t0002g0292a0001c0001t0002g0294a0001c0001t0002g0301others(14): Show | 17 | HG00621.hp1 HG01943.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.27-2089_27-2086dup others(4): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238260 | ||||||
chr2:70238260
|
G | GTTTTT | 17 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0290others(14): Show | 18 | HG00673.hp1 HG00741.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.27-2090_27-2086dup others(5): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238260 | ||||||
chr2:70238260
|
G | GTTTTTT | 6 | a0001c0001t0002g0289a0001c0001t0002g0293a0001c0001t0002g0297others(3): Show | 6 | HG01934.hp2 HG02071.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-2091_27-2086dup others(6): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238260 | ||||||
chr2:70238260
|
G | GTTTTTTT others(18): Show |
1 | a0001c0001t0001g0102 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-2110_27-2086dup others(25): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238260 | ||||||
chr2:70238260
|
G | GTTTTTTT others(45): Show |
1 | a0001c0001t0001g0099 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.27-2086_27-2085ins others(52): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238260 | ||||||
chr2:70238260
|
GT | G | 25 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0031others(22): Show | 26 | HG01109.hp1 HG01167.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.27-2086delA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238260 | ||||||
chr2:70238260
|
GTTTTTTT others(5): Show |
G | 3 | a0001c0001t0001g0103a0001c0001t0001g0163a0001c0001t0001g0164 | 3 | HG02976.hp2 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.27-2097_27-2086del others(12): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238260 | ||||||
chr2:70238260
|
GTTTTTTT others(11): Show |
G | 1 | a0001c0002t0007g0332 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.27-2103_27-2086del others(18): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238260 | ||||||
chr2:70238263
|
T | TG | 3 | a0001c0001t0005g0361a0001c0001t0005g0362a0001c0001t0005g0365 | 3 | HG02109.hp1 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.27-2089_27-2088ins others(1): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238263 | ||||||
chr2:70238264
|
T | G | 1 | a0001c0001t0005g0022 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.27-2089A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238264 | ||||||
chr2:70238428
|
G | A | 5 | a0001c0001t0001g0094a0001c0001t0008g0363a0001c0001t0008g0364others(2): Show | 5 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.27-2253C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238428 | ||||||
chr2:70238472
|
C | T | 3 | a0001c0001t0001g0103a0001c0001t0001g0163a0001c0001t0001g0164 | 3 | HG02976.hp2 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.27-2297G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238472 | ||||||
chr2:70238497
|
A | T | 1 | a0001c0001t0002g0326 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.27-2322T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238497 | ||||||
chr2:70238574
|
A | C | 3 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0006g0070 | 3 | HG02055.hp2 HG02257.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.27-2399T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238574 | ||||||
chr2:70238625
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.27-2450G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238625 | ||||||
chr2:70238698
|
T | A | 60 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0002g0019others(57): Show | 62 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.27-2523A>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238698 | ||||||
chr2:70238842
|
G | T | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-2667C>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238842 | ||||||
chr2:70238918
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.27-2743G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238918 | ||||||
chr2:70238921
|
A | G | 6 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.27-2746T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238921 | ||||||
chr2:70238939
|
C | T | 8 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-2764G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238939 | ||||||
chr2:70239155
|
T | C | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-2980A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239155 | ||||||
chr2:70239156
|
G | A | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-2981C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239156 | ||||||
chr2:70239157
|
A | G | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-2982T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239157 | ||||||
chr2:70239178
|
C | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(188): Show | 207 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.27-3003G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239178 | ||||||
chr2:70239206
|
C | A | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-3031G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239206 | ||||||
chr2:70239251
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.27-3076G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239251 | ||||||
chr2:70239360
|
T | C | 58 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(55): Show | 60 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.27-3185A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239360 | ||||||
chr2:70239388
|
G | A | 8 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-3213C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239388 | ||||||
chr2:70239417
|
T | C | 1 | a0001c0001t0019g0198 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.27-3242A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239417 | ||||||
chr2:70239495
|
C | A | 1 | a0001c0001t0002g0321 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.27-3320G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239495 | ||||||
chr2:70239694
|
G | A | 5 | a0001c0001t0001g0192a0001c0001t0001g0201a0001c0001t0001g0250others(2): Show | 5 | NA18953.hp2 NA18967.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.27-3519C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239694 | ||||||
chr2:70239863
|
A | T | 1 | a0001c0001t0001g0149 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.27-3688T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239863 | ||||||
chr2:70239904
|
C | A | 1 | a0001c0001t0001g0241 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.27-3729G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239904 | ||||||
chr2:70240039
|
T | G | 58 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(55): Show | 60 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.27-3864A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70240039 | ||||||
chr2:70240136
|
A | C | 4 | a0001c0001t0001g0272a0001c0001t0004g0269a0001c0001t0004g0270others(1): Show | 4 | HG01433.hp1 HG02257.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-3961T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70240136 | ||||||
chr2:70240271
|
T | C | 1 | a0001c0001t0003g0041 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.27-4096A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70240271 | ||||||
chr2:70240489
|
C | T | 8 | a0001c0001t0001g0014a0001c0001t0001g0215a0001c0001t0001g0216others(5): Show | 9 | HG02083.hp2 NA18747.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-4314G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70240489 | ||||||
chr2:70240881
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.27-4706G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70240881 | ||||||
chr2:70240886
|
CA | C | 8 | a0001c0001t0001g0078a0001c0001t0001g0090a0001c0001t0001g0091others(5): Show | 8 | HG01891.hp1 HG02486.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.27-4712delT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70240886 | ||||||
chr2:70240920
|
A | C | 1 | a0001c0001t0002g0296 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.27-4745T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70240920 | ||||||
chr2:70241265
|
C | A | 1 | a0001c0001t0006g0108 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.27-5090G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241265 | ||||||
chr2:70241281
|
A | G | 8 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-5106T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241281 | ||||||
chr2:70241305
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.27-5130C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241305 | ||||||
chr2:70241390
|
C | T | 8 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-5215G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241390 | ||||||
chr2:70241393
|
G | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG02040.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.27-5218C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241393 | ||||||
chr2:70241435
|
T | A | 1 | a0001c0001t0001g0031 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.27-5260A>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241435 | ||||||
chr2:70241453
|
A | AAAAAAGT others(52): Show |
1 | a0001c0001t0002g0326 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.27-5337_27-5279dup others(59): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241453 | ||||||
chr2:70241558
|
C | A | 1 | a0001c0001t0001g0148 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.27-5383G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241558 | ||||||
chr2:70241561
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0102 | 2 | HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.27-5386C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241561 | ||||||
chr2:70241566
|
G | A | 8 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-5391C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241566 | ||||||
chr2:70241590
|
G | GT | 10 | a0001c0001t0001g0272a0001c0001t0004g0020a0001c0001t0004g0269others(7): Show | 11 | HG01192.hp1 HG01433.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.27-5416dupA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241590 | ||||||
chr2:70241658
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.27-5483C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241658 | ||||||
chr2:70241697
|
T | G | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.27-5522A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241697 | ||||||
chr2:70241835
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.27-5660A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241835 | ||||||
chr2:70241850
|
G | C | 37 | a0001c0001t0003g0004a0001c0001t0003g0027a0001c0001t0003g0038others(34): Show | 38 | HG00609.hp2 HG00735.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.27-5675C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241850 | ||||||
chr2:70241897
|
C | T | 23 | a0001c0001t0002g0019a0001c0001t0002g0289a0001c0001t0002g0290others(20): Show | 24 | HG00544.hp2 HG00621.hp1 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.27-5722G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241897 | ||||||
chr2:70242025
|
A | G | 6 | a0001c0001t0004g0020a0001c0001t0004g0333a0001c0001t0004g0334others(3): Show | 7 | HG01192.hp1 HG01884.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.27-5850T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242025 | ||||||
chr2:70242054
|
A | G | 1 | a0001c0001t0002g0328 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.27-5879T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242054 | ||||||
chr2:70242087
|
C | T | 3 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0006g0070 | 3 | HG02055.hp2 HG02257.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.27-5912G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242087 | ||||||
chr2:70242256
|
G | A | 8 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-6081C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242256 | ||||||
chr2:70242310
|
T | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0214 | 2 | HG00099.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.26+6095A>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242310 | ||||||
chr2:70242423
|
C | T | 45 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(42): Show | 46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.26+5982G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242423 | ||||||
chr2:70242485
|
A | G | 1 | a0001c0001t0002g0306 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.26+5920T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242485 | ||||||
chr2:70242494
|
C | CA | 155 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(152): Show | 161 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.26+5910dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242494 | ||||||
chr2:70242494
|
C | CAA | 35 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0035others(32): Show | 37 | HG00544.hp2 HG00741.hp2 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.26+5909_26+5910dup others(2): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242494 | ||||||
chr2:70242494
|
C | CAAA | 24 | a0001c0001t0002g0323a0001c0001t0002g0324a0001c0001t0003g0004others(21): Show | 27 | HG00621.hp1 HG00642.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.26+5908_26+5910dup others(3): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242494 | ||||||
chr2:70242494
|
C | CAAAA | 18 | a0001c0001t0001g0082a0001c0001t0001g0272a0001c0001t0003g0045others(15): Show | 18 | HG00609.hp2 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.26+5907_26+5910dup others(4): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242494 | ||||||
chr2:70242494
|
C | CAAAAA | 8 | a0001c0001t0001g0083a0001c0001t0003g0049a0001c0001t0003g0051others(5): Show | 8 | HG01934.hp1 HG01993.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.26+5906_26+5910dup others(5): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242494 | ||||||
chr2:70242494
|
C | CAAAAAAA others(3): Show |
8 | a0001c0001t0001g0078a0001c0001t0001g0090a0001c0001t0001g0091others(5): Show | 8 | HG01891.hp1 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.26+5901_26+5910dup others(10): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242494 | ||||||
chr2:70242494
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0096 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.26+5900_26+5910dup others(11): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242494 | ||||||
chr2:70242562
|
G | A | 4 | a0001c0001t0001g0197a0001c0001t0001g0249a0001c0001t0001g0264others(1): Show | 4 | NA18963.hp2 NA19055.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.26+5843C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242562 | ||||||
chr2:70242659
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.26+5746G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242659 | ||||||
chr2:70242681
|
C | T | 1 | a0001c0001t0018g0286 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.26+5724G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242681 | ||||||
chr2:70242818
|
T | C | 3 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0006g0070 | 3 | HG02055.hp2 HG02257.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.26+5587A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242818 | ||||||
chr2:70242968
|
T | C | 29 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0030others(26): Show | 30 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.26+5437A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242968 | ||||||
chr2:70243187
|
AGG | A | 2 | a0001c0001t0004g0020a0001c0001t0004g0337 | 3 | HG02922.hp1 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.26+5216_26+5217del others(2): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70243187 | ||||||
chr2:70243194
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.26+5211C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70243194 | ||||||
chr2:70243221
|
T | G | 1 | a0001c0001t0001g0250 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.26+5184A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70243221 | ||||||
chr2:70243226
|
G | A | 58 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(55): Show | 60 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.26+5179C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70243226 | ||||||
chr2:70243305
|
T | C | 50 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(47): Show | 51 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.26+5100A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70243305 | ||||||
chr2:70243331
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.26+5074C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70243331 | ||||||
chr2:70243542
|
A | C | 4 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(1): Show | 5 | HG02109.hp1 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.26+4863T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70243542 | ||||||
chr2:70243671
|
T | C | 1 | a0001c0001t0001g0251 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.26+4734A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70243671 | ||||||
chr2:70243748
|
T | C | 1 | a0001c0002t0007g0287 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.26+4657A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70243748 | ||||||
chr2:70243877
|
T | G | 1 | a0001c0001t0003g0071 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.26+4528A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70243877 | ||||||
chr2:70243891
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.26+4514G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70243891 | ||||||
chr2:70243897
|
T | C | 5 | a0001c0001t0001g0036a0001c0001t0001g0097a0001c0001t0001g0098others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.26+4508A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70243897 | ||||||
chr2:70244122
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.26+4283T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244122 | ||||||
chr2:70244363
|
C | T | 8 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.26+4042G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244363 | ||||||
chr2:70244503
|
T | C | 1 | a0001c0002t0007g0332 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.26+3902A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244503 | ||||||
chr2:70244569
|
T | C | 1 | a0001c0001t0018g0286 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.26+3836A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244569 | ||||||
chr2:70244608
|
G | A | 1 | a0001c0001t0018g0286 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.26+3797C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244608 | ||||||
chr2:70244611
|
G | A | 1 | a0001c0001t0003g0072 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.26+3794C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244611 | ||||||
chr2:70244625
|
GGAGATC | G | 3 | a0001c0001t0001g0103a0001c0001t0001g0163a0001c0001t0001g0164 | 3 | HG02976.hp2 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.26+3774_26+3779del others(6): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244625 | ||||||
chr2:70244701
|
G | C | 3 | a0001c0001t0001g0103a0001c0001t0001g0163a0001c0001t0001g0164 | 3 | HG02976.hp2 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.26+3704C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244701 | ||||||
chr2:70244704
|
G | A | 8 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.26+3701C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244704 | ||||||
chr2:70244767
|
A | G | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 277 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.26+3638T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244767 | ||||||
chr2:70244782
|
C | G | 45 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(42): Show | 46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.26+3623G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244782 | ||||||
chr2:70244829
|
T | C | 60 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0002g0019others(57): Show | 62 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.26+3576A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244829 | ||||||
chr2:70244834
|
C | CA | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(112): Show | 128 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.26+3570dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244834 | ||||||
chr2:70244834
|
C | CAA | 24 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(21): Show | 25 | HG00558.hp1 HG01109.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.26+3569_26+3570dup others(2): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244834 | ||||||
chr2:70244834
|
CA | C | 36 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0030others(33): Show | 37 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.26+3570delT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244834 | ||||||
chr2:70244834
|
CAA | C | 39 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(36): Show | 40 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.26+3569_26+3570del others(2): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244834 | ||||||
chr2:70244865
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.26+3540G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244865 | ||||||
chr2:70245031
|
G | C | 1 | a0001c0001t0002g0328 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.26+3374C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245031 | ||||||
chr2:70245246
|
C | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0028 | 3 | HG00735.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.26+3159G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245246 | ||||||
chr2:70245247
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.26+3158T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245247 | ||||||
chr2:70245350
|
G | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(86): Show | 102 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.26+3055C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245350 | ||||||
chr2:70245353
|
C | T | 4 | a0001c0002t0007g0284a0001c0002t0007g0287a0001c0002t0007g0288others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+3052G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245353 | ||||||
chr2:70245391
|
C | G | 30 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0030others(27): Show | 31 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.26+3014G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245391 | ||||||
chr2:70245453
|
T | A | 1 | a0001c0001t0004g0020 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.26+2952A>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245453 | ||||||
chr2:70245803
|
A | G | 1 | a0001c0001t0025g0304 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.26+2602T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245803 | ||||||
chr2:70245816
|
C | T | 1 | a0001c0001t0002g0303 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.26+2589G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245816 | ||||||
chr2:70245860
|
A | G | 1 | a0001c0001t0020g0202 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.26+2545T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245860 | ||||||
chr2:70245898
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0028 | 3 | HG00735.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.26+2507G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245898 | ||||||
chr2:70245914
|
A | AT | 27 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0075others(24): Show | 29 | HG00544.hp1 HG01358.hp2 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.26+2490dupA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245914 | ||||||
chr2:70245914
|
A | ATT | 14 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(11): Show | 15 | HG01192.hp1 HG01433.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.26+2489_26+2490dup others(2): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245914 | ||||||
chr2:70245914
|
A | ATTT | 28 | a0001c0001t0001g0069a0001c0001t0003g0004a0001c0001t0003g0027others(25): Show | 29 | HG00735.hp2 HG01175.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.26+2488_26+2490dup others(3): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245914 | ||||||
chr2:70245914
|
A | ATTTT | 12 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0040others(9): Show | 12 | HG00609.hp2 HG01099.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.26+2487_26+2490dup others(4): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245914 | ||||||
chr2:70245914
|
AT | A | 48 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0266others(45): Show | 49 | HG00621.hp1 HG00673.hp1 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.26+2490delA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245914 | ||||||
chr2:70245914
|
ATT | A | 10 | a0001c0001t0005g0022a0001c0001t0005g0365a0001c0001t0008g0366others(7): Show | 11 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.26+2489_26+2490del others(2): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245914 | ||||||
chr2:70245914
|
ATTTTTTT others(2): Show |
A | 28 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0030others(25): Show | 29 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.26+2482_26+2490del others(9): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245914 | ||||||
chr2:70245914
|
ATTTTTTT others(7): Show |
A | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(86): Show | 102 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.26+2477_26+2490del others(14): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245914 | ||||||
chr2:70245954
|
C | T | 1 | a0001c0002t0007g0287 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.26+2451G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245954 | ||||||
chr2:70245985
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.26+2420C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245985 | ||||||
chr2:70246048
|
C | T | 5 | a0001c0001t0001g0037a0001c0002t0007g0284a0001c0002t0007g0287others(2): Show | 5 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.26+2357G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246048 | ||||||
chr2:70246058
|
G | C | 2 | a0001c0001t0011g0329a0001c0001t0011g0330 | 2 | NA18948.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.26+2347C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246058 | ||||||
chr2:70246178
|
C | G | 8 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.26+2227G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246178 | ||||||
chr2:70246284
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.26+2121A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246284 | ||||||
chr2:70246321
|
C | G | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(248): Show | 269 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.26+2084G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246321 | ||||||
chr2:70246435
|
GTCAAGGT others(10): Show |
G | 1 | a0001c0001t0002g0331 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1953_26+1969del others(17): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246435 | ||||||
chr2:70246454
|
G | C | 1 | a0001c0001t0002g0331 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1951C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246454 | ||||||
chr2:70246488
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.26+1917G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246488 | ||||||
chr2:70246511
|
A | T | 1 | a0001c0001t0002g0331 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1894T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246511 | ||||||
chr2:70246522
|
G | T | 1 | a0001c0001t0002g0331 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1883C>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246522 | ||||||
chr2:70246527
|
G | T | 1 | a0001c0001t0002g0331 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1878C>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246527 | ||||||
chr2:70246534
|
G | T | 1 | a0001c0001t0002g0331 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1871C>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246534 | ||||||
chr2:70246545
|
A | AAAGCTTA others(3): Show |
1 | a0001c0001t0002g0331 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1859_26+1860ins others(10): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246545 | ||||||
chr2:70246546
|
T | G | 1 | a0001c0001t0002g0331 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1859A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246546 | ||||||
chr2:70246552
|
A | T | 1 | a0001c0001t0002g0331 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1853T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246552 | ||||||
chr2:70246554
|
G | A | 1 | a0001c0001t0002g0331 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1851C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246554 | ||||||
chr2:70246565
|
A | T | 1 | a0001c0001t0002g0331 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1840T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246565 | ||||||
chr2:70246581
|
G | A | 1 | a0001c0001t0002g0331 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1824C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246581 | ||||||
chr2:70246582
|
T | C | 1 | a0001c0001t0002g0331 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1823A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246582 | ||||||
chr2:70246584
|
A | T | 1 | a0001c0001t0002g0331 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1821T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246584 | ||||||
chr2:70246592
|
A | G | 1 | a0001c0001t0002g0331 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1813T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246592 | ||||||
chr2:70246594
|
G | A | 1 | a0001c0001t0002g0331 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1811C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246594 | ||||||
chr2:70246599
|
G | T | 1 | a0001c0001t0002g0331 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1806C>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246599 | ||||||
chr2:70246611
|
C | A | 1 | a0001c0001t0002g0331 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1794G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246611 | ||||||
chr2:70246641
|
T | C | 45 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(42): Show | 46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.26+1764A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246641 | ||||||
chr2:70246805
|
A | G | 60 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0002g0019others(57): Show | 62 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.26+1600T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246805 | ||||||
chr2:70246834
|
C | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG02735.hp1 HG02738.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.26+1571G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246834 | ||||||
chr2:70246926
|
G | A | 4 | a0001c0001t0001g0272a0001c0001t0004g0269a0001c0001t0004g0270others(1): Show | 4 | HG01433.hp1 HG02257.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+1479C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246926 | ||||||
chr2:70246950
|
C | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0028 | 3 | HG00735.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.26+1455G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246950 | ||||||
chr2:70247127
|
T | C | 46 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(43): Show | 47 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.26+1278A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247127 | ||||||
chr2:70247245
|
C | G | 46 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(43): Show | 47 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.26+1160G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247245 | ||||||
chr2:70247295
|
G | A | 11 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(8): Show | 11 | HG00544.hp1 HG02040.hp2 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.26+1110C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247295 | ||||||
chr2:70247365
|
T | C | 45 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(42): Show | 46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.26+1040A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247365 | ||||||
chr2:70247397
|
G | T | 1 | a0001c0001t0002g0285 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.26+1008C>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247397 | ||||||
chr2:70247528
|
A | C | 1 | a0001c0002t0007g0284 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.26+877T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247528 | ||||||
chr2:70247611
|
G | T | 1 | a0001c0001t0003g0027 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.26+794C>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247611 | ||||||
chr2:70247650
|
AAT | A | 8 | a0001c0001t0005g0022a0001c0001t0005g0361a0001c0001t0005g0362others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.26+753_26+754delAT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247650 | ||||||
chr2:70247697
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.26+708T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247697 | ||||||
chr2:70247799
|
G | C | 1 | a0001c0002t0007g0332 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.26+606C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247799 | ||||||
chr2:70247850
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.26+555T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247850 | ||||||
chr2:70247877
|
T | C | 50 | a0001c0001t0002g0019a0001c0001t0002g0285a0001c0001t0002g0289others(47): Show | 51 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.26+528A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247877 | ||||||
chr2:70247953
|
G | A | 6 | a0001c0001t0004g0020a0001c0001t0004g0333a0001c0001t0004g0334others(3): Show | 7 | HG01192.hp1 HG01884.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.26+452C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247953 | ||||||
chr2:70248018
|
TAAG | T | 9 | a0001c0001t0001g0024a0001c0001t0005g0022a0001c0001t0005g0361others(6): Show | 10 | HG00642.hp2 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.26+384_26+386delCT others(1): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70248018 | ||||||
chr2:70248021
|
G | C | 17 | a0001c0001t0001g0342a0001c0001t0001g0344a0001c0001t0001g0345others(14): Show | 17 | HG01243.hp1 HG01884.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.26+384C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70248021 | ||||||
chr2:70248137
|
G | C | 1 | a0001c0001t0001g0355 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.26+268C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70248137 | ||||||
chr2:70248248
|
G | C | 1 | a0001c0001t0001g0356 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.26+157C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70248248 | ||||||
chr2:70248283
|
G | A | 2 | a0001c0001t0001g0357a0001c0001t0001g0358 | 2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.26+122C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70248283 |