geneid | 7089 |
---|---|
ensemblid | ENSG00000065717.16 |
hgncid | 11838 |
symbol | TLE2 |
name | TLE family member 2, transcriptional corepressor |
refseq_nuc | NM_003260.5 |
refseq_prot | NP_003251.2 |
ensembl_nuc | ENST00000262953.11 |
ensembl_prot | ENSP00000262953.5 |
mane_status | MANE Select |
chr | chr19 |
start | 2997644 |
end | 3029280 |
strand | - |
ver | v1.2 |
region | chr19:2997644-3029280 |
region5000 | chr19:2992644-3034280 |
regionname0 | TLE2_chr19_2997644_3029280 |
regionname5000 | TLE2_chr19_2992644_3034280 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 743 | 387 | 89 | 79 | 159 | 17 | 41 | 114 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0002 | 0/0 | 743 | 9 | 0 | 2 | 7 | 0 | 0 | 5 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0003 | 0/0 | 743 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0004 | 0/0 | 743 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0005 | 0/0 | 743 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0006 | 0/0 | 743 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0007 | 0/0 | 743 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0008 | 0/0 | 743 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0009 | 0/0 | 743 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0010 | 0/0 | 743 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2232 | 266 | 60 | 52 | 107 | 16 | 30 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
c0002 | 0/1 | 2232 | 90 | 9 | 23 | 50 | 0 | 7 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
c0003 | 0/0 | 2232 | 9 | 4 | 3 | 0 | 1 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
c0004 | 0/0 | 2232 | 8 | 0 | 1 | 7 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
c0005 | 0/0 | 2232 | 5 | 5 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
c0006 | 0/0 | 2232 | 3 | 3 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
c0007 | 0/0 | 2232 | 2 | 0 | 1 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
c0008 | 0/0 | 2232 | 2 | 2 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
c0009 | 0/0 | 2232 | 2 | 0 | 0 | 0 | 0 | 2 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
c0010 | 0/0 | 2232 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
c0011 | 0/0 | 2232 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
c0012 | 0/0 | 2232 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
c0013 | 0/0 | 2232 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
c0014 | 0/0 | 2232 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
c0015 | 0/0 | 2232 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
c0016 | 0/0 | 2232 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
c0017 | 0/0 | 2232 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
c0018 | 0/0 | 2232 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
c0019 | 0/0 | 2232 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
c0020 | 0/0 | 2232 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
c0021 | 0/0 | 2232 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
c0022 | 0/0 | 2232 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
c0023 | 0/0 | 2232 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
c0024 | 0/0 | 2232 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
c0025 | 0/0 | 2232 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
c0026 | 0/0 | 2232 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 581 | 347 | 50 | 72 | 165 | 18 | 40 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
t0002 | 0/0 | 581 | 35 | 29 | 5 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
t0003 | 0/0 | 581 | 7 | 0 | 5 | 1 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
t0004 | 0/0 | 581 | 5 | 5 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
t0005 | 0/0 | 581 | 2 | 2 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
t0006 | 0/0 | 581 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
t0007 | 0/0 | 581 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
t0008 | 0/0 | 581 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
t0009 | 0/0 | 581 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
t0010 | 0/0 | 581 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
t0011 | 0/0 | 581 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
t0012 | 0/0 | 581 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
t0013 | 0/0 | 581 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0037 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0173 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0355 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2232 | 266 | 60 | 52 | 107 | 16 | 30 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0002 | 0/1 | 2232 | 90 | 9 | 23 | 50 | 0 | 7 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0003 | 0/0 | 2232 | 9 | 4 | 3 | 0 | 1 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0005 | 0/0 | 2232 | 5 | 5 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0006 | 0/0 | 2232 | 3 | 3 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0007 | 0/0 | 2232 | 2 | 0 | 1 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0008 | 0/0 | 2232 | 2 | 2 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0009 | 0/0 | 2232 | 2 | 0 | 0 | 0 | 0 | 2 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0010 | 0/0 | 2232 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0013 | 0/0 | 2232 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0015 | 0/0 | 2232 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0016 | 0/0 | 2232 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0017 | 0/0 | 2232 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0018 | 0/0 | 2232 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0020 | 0/0 | 2232 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0024 | 0/0 | 2232 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0002c0004 | 0/0 | 2232 | 8 | 0 | 1 | 7 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0002c0011 | 0/0 | 2232 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0003c0026 | 0/0 | 2232 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0004c0025 | 0/0 | 2232 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0005c0022 | 0/0 | 2232 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0006c0019 | 0/0 | 2232 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0007c0014 | 0/0 | 2232 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0008c0012 | 0/0 | 2232 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0009c0021 | 0/0 | 2232 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0010c0023 | 0/0 | 2232 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2812 | 229 | 33 | 47 | 104 | 16 | 28 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0001t0002 | 0/0 | 2812 | 25 | 19 | 5 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0001t0003 | 0/0 | 2812 | 2 | 0 | 0 | 1 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0001t0004 | 0/0 | 2812 | 5 | 5 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0001t0005 | 0/0 | 2812 | 2 | 2 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0001t0008 | 0/0 | 2812 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0001t0010 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0001t0013 | 0/0 | 2812 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0002t0001 | 0/1 | 2812 | 84 | 8 | 18 | 50 | 0 | 7 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0002t0003 | 0/0 | 2812 | 5 | 0 | 5 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0002t0007 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0003t0001 | 0/0 | 2812 | 6 | 1 | 3 | 0 | 1 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0003t0002 | 0/0 | 2812 | 3 | 3 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0005t0001 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0005t0002 | 0/0 | 2812 | 3 | 3 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0005t0011 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0006t0001 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0006t0002 | 0/0 | 2812 | 2 | 2 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0007t0001 | 0/0 | 2812 | 2 | 0 | 1 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0008t0001 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0008t0002 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0009t0001 | 0/0 | 2812 | 2 | 0 | 0 | 0 | 0 | 2 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0010t0001 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0013t0001 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0015t0009 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0016t0001 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0017t0001 | 0/0 | 2812 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0018t0001 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0020t0001 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0001c0024t0001 | 0/0 | 2812 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0002c0004t0001 | 0/0 | 2812 | 8 | 0 | 1 | 7 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0002c0011t0001 | 0/0 | 2812 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0003c0026t0006 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0004c0025t0002 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0005c0022t0001 | 0/0 | 2812 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0006c0019t0001 | 0/0 | 2812 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0007c0014t0001 | 0/0 | 2812 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0008c0012t0012 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0009c0021t0001 | 0/0 | 2812 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
a0010c0023t0001 | 0/0 | 2812 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | copy fasta | chr19 | 2992644 | 3034280 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0173 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0001g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0002g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0002g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0002g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0004g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0008g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0010g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0001t0013g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0037 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0001g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0002t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0003t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0003t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0003t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0003t0001g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0003t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0003t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0003t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0005t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0005t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0005t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0005t0002g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0005t0011g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0006t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0006t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0006t0002g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0007t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0007t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0008t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0008t0002g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0009t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0009t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0010t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0013t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0015t0009g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0016t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0017t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0018t0001g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0020t0001g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0001c0024t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0002c0004t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0002c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0002c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0002c0004t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0002c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0002c0004t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0002c0004t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0002c0011t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0003c0026t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0004c0025t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0005c0022t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0006c0019t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0007c0014t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0008c0012t0012g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0009c0021t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
a0010c0023t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0007 | c0014 | t0001 | g0041 | EUR | GBR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00099 | hp2 | a0001 | c0003 | t0001 | g0172 | EUR | GBR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | GBR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | GBR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0355 | EUR | FIN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0148 | EUR | FIN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0074 | EUR | FIN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | FIN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00438 | hp2 | a0002 | c0004 | t0001 | g0125 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00597 | hp1 | a0001 | c0007 | t0001 | g0314 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0312 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0311 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0373 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00733 | hp2 | a0009 | c0021 | t0001 | g0301 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00738 | hp1 | a0001 | c0002 | t0003 | g0027 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0376 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01069 | hp1 | a0001 | c0002 | t0003 | g0021 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01069 | hp2 | a0001 | c0003 | t0001 | g0362 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01071 | hp1 | a0001 | c0003 | t0001 | g0363 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0078 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0175 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0310 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0354 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0327 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0365 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0361 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0178 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0179 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0360 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01496 | hp1 | a0001 | c0003 | t0001 | g0372 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | IBS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | IBS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0228 | EUR | IBS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0258 | EUR | IBS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0259 | EUR | IBS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | IBS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0374 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0370 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01928 | hp1 | a0001 | c0002 | t0003 | g0020 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0335 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0359 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01943 | hp1 | a0001 | c0002 | t0003 | g0022 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0282 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0331 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0108 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01981 | hp1 | a0001 | c0007 | t0001 | g0333 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0330 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0159 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0353 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02015 | hp2 | a0005 | c0022 | t0001 | g0070 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0349 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0260 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0344 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02129 | hp1 | a0002 | c0004 | t0001 | g0300 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02145 | hp2 | a0001 | c0020 | t0001 | g0380 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02148 | hp1 | a0002 | c0011 | t0001 | g0080 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0332 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CDX | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | CDX | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0217 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02258 | hp1 | a0001 | c0003 | t0002 | g0269 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0383 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02273 | hp2 | a0001 | c0002 | t0003 | g0023 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0307 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0382 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0371 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02615 | hp1 | a0001 | c0005 | t0001 | g0149 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0381 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02622 | hp1 | a0001 | c0005 | t0002 | g0241 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0379 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02647 | hp1 | a0001 | c0006 | t0001 | g0377 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02683 | hp1 | a0001 | c0009 | t0001 | g0062 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0063 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0155 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0366 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02717 | hp2 | a0001 | c0002 | t0007 | g0028 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0350 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02723 | hp2 | a0001 | c0001 | t0005 | g0025 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02738 | hp2 | a0010 | c0023 | t0001 | g0237 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02886 | hp1 | a0001 | c0006 | t0002 | g0368 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02922 | hp1 | a0001 | c0003 | t0002 | g0270 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0087 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02965 | hp2 | a0001 | c0005 | t0002 | g0364 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0275 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02970 | hp2 | a0001 | c0005 | t0002 | g0240 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0348 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03041 | hp2 | a0001 | c0006 | t0002 | g0239 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0356 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03130 | hp2 | a0004 | c0025 | t0002 | g0309 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03195 | hp2 | a0001 | c0010 | t0001 | g0231 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03209 | hp1 | a0001 | c0016 | t0001 | g0243 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03225 | hp2 | a0001 | c0003 | t0002 | g0268 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0281 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03453 | hp2 | a0001 | c0001 | t0010 | g0384 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03486 | hp1 | a0008 | c0012 | t0012 | g0386 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03486 | hp2 | a0001 | c0013 | t0001 | g0246 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0024 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0151 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0083 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03516 | hp2 | a0001 | c0003 | t0001 | g0245 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03540 | hp2 | a0001 | c0005 | t0011 | g0385 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0367 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0040 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | STU | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03688 | hp2 | a0001 | c0003 | t0001 | g0222 | SAS | STU | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0082 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03927 | hp1 | a0001 | c0009 | t0001 | g0038 | SAS | BEB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0266 | SAS | BEB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | STU | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0296 | SAS | STU | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | STU | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | STU | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | YRI | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0322 | AFR | YRI | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | CHB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0345 | EAS | CHB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | CHB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0321 | AFR | YRI | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0293 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0343 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18960 | hp1 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0340 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18967 | hp1 | a0002 | c0004 | t0001 | g0093 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18970 | hp1 | a0001 | c0001 | t0013 | g0387 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18973 | hp1 | a0002 | c0004 | t0001 | g0096 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18986 | hp1 | a0001 | c0001 | t0008 | g0341 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0305 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0342 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19010 | hp1 | a0006 | c0019 | t0001 | g0186 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19011 | hp2 | a0002 | c0004 | t0001 | g0127 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19030 | hp1 | a0001 | c0018 | t0001 | g0375 | AFR | LWK | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19030 | hp2 | a0001 | c0015 | t0009 | g0129 | AFR | LWK | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0026 | AFR | LWK | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19043 | hp2 | a0001 | c0008 | t0001 | g0369 | AFR | LWK | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19080 | hp2 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19083 | hp1 | a0001 | c0024 | t0001 | g0073 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19084 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0352 | AFR | YRI | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | YRI | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA20129 | hp1 | a0003 | c0026 | t0006 | g0018 | AFR | ASW | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | ASW | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0358 | EUR | TSI | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0325 | EUR | TSI | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0357 | EUR | TSI | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0079 | EUR | TSI | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | GIH | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA20905 | hp2 | a0001 | c0017 | t0001 | g0324 | SAS | GIH | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01123 | hp1 | a0002 | c0004 | t0001 | g0257 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02109 | hp2 | a0001 | c0008 | t0002 | g0378 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0317 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0351 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0244 | AFR | USA | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | USA | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | USA | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0215 | AFR | USA | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | LWK | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | LWK | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0037 | REF | REF | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0173 | REF | REF | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:3000657
|
C | T | 1 | a0008 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.2114G>A | p.Ser705Asn | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/20 | 2490/2812 | 2114/2232 | 705/743 | chr19 | 3000657 | ||
chr19:3009574
|
T | C | 1 | a0006 | 1 | NA19010.hp1 | missense_variant | MODERATE | c.1141A>G | p.Ser381Gly | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 13/20 | 1517/2812 | 1141/2232 | 381/743 | chr19 | 3009574 | ||
chr19:3011088
|
C | T | 1 | a0007 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.946G>A | p.Gly316Arg | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/20 | 1322/2812 | 946/2232 | 316/743 | chr19 | 3011088 | ||
chr19:3011148
|
C | T | 2 | a0002a0008 | 10 | HG00438.hp2 HG01123.hp1 HG02129.hp1 others(7): Show |
missense_variant | MODERATE | c.886G>A | p.Ala296Thr | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/20 | 1262/2812 | 886/2232 | 296/743 | chr19 | 3011148 | ||
chr19:3011151
|
G | A | 1 | a0009 | 1 | HG00733.hp2 | missense_variant | MODERATE | c.883C>T | p.Pro295Ser | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/20 | 1259/2812 | 883/2232 | 295/743 | chr19 | 3011151 | ||
chr19:3013697
|
G | A | 1 | a0005 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.845C>T | p.Pro282Leu | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/20 | 1221/2812 | 845/2232 | 282/743 | chr19 | 3013697 | ||
chr19:3015742
|
G | A | 1 | a0010 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.589C>T | p.Pro197Ser | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/20 | 965/2812 | 589/2232 | 197/743 | chr19 | 3015742 | ||
chr19:3019381
|
G | A | 1 | a0004 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.452C>T | p.Thr151Met | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/20 | 828/2812 | 452/2232 | 151/743 | chr19 | 3019381 | ||
chr19:3019430
|
G | C | 1 | a0003 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.403C>G | p.Pro135Ala | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/20 | 779/2812 | 403/2232 | 135/743 | chr19 | 3019430 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:2997899
|
G | A | 6 | a0001c0002a0001c0010a0001c0013others(3): Show | 95 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(92): Show |
synonymous_variant | LOW | c.2181C>T | p.Ile727Ile | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 20/20 | 2557/2812 | 2181/2232 | 727/743 | chr19 | 2997899 | ||
chr19:3000665
|
G | A | 4 | a0001c0007a0001c0015a0002c0004others(1): Show | 12 | HG00438.hp2 HG00597.hp1 HG01123.hp1 others(9): Show |
synonymous_variant | LOW | c.2106C>T | p.Tyr702Tyr | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/20 | 2482/2812 | 2106/2232 | 702/743 | chr19 | 3000665 | ||
chr19:3005476
|
C | T | 1 | a0001c0003 | 9 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(6): Show |
synonymous_variant | LOW | c.1857G>A | p.Arg619Arg | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/20 | 2233/2812 | 1857/2232 | 619/743 | chr19 | 3005476 | ||
chr19:3005557
|
G | A | 1 | a0001c0008 | 2 | HG02109.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.1776C>T | p.Ala592Ala | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/20 | 2152/2812 | 1776/2232 | 592/743 | chr19 | 3005557 | ||
chr19:3005768
|
G | A | 1 | a0001c0017 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.1701C>T | p.Ser567Ser | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 16/20 | 2077/2812 | 1701/2232 | 567/743 | chr19 | 3005768 | ||
chr19:3005885
|
G | A | 1 | a0001c0015 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1584C>T | p.Ser528Ser | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 16/20 | 1960/2812 | 1584/2232 | 528/743 | chr19 | 3005885 | ||
chr19:3006450
|
G | C | 1 | a0001c0018 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1470C>G | p.Ala490Ala | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 15/20 | 1846/2812 | 1470/2232 | 490/743 | chr19 | 3006450 | ||
chr19:3006561
|
C | G | 1 | a0001c0016 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.1359G>C | p.Thr453Thr | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 15/20 | 1735/2812 | 1359/2232 | 453/743 | chr19 | 3006561 | ||
chr19:3008907
|
G | A | 1 | a0001c0009 | 2 | HG02683.hp1 HG03927.hp1 |
synonymous_variant | LOW | c.1212C>T | p.Ser404Ser | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/20 | 1588/2812 | 1212/2232 | 404/743 | chr19 | 3008907 | ||
chr19:3011032
|
C | T | 2 | a0001c0005a0001c0015 | 6 | HG02615.hp1 HG02622.hp1 HG02965.hp2 others(3): Show |
synonymous_variant | LOW | c.1002G>A | p.Thr334Thr | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/20 | 1378/2812 | 1002/2232 | 334/743 | chr19 | 3011032 | ||
chr19:3011062
|
G | A | 1 | a0001c0020 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.972C>T | p.Cys324Cys | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/20 | 1348/2812 | 972/2232 | 324/743 | chr19 | 3011062 | ||
chr19:3011110
|
C | T | 1 | a0001c0013 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.924G>A | p.Pro308Pro | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/20 | 1300/2812 | 924/2232 | 308/743 | chr19 | 3011110 | ||
chr19:3019308
|
C | A | 1 | a0001c0024 | 1 | NA19083.hp1 | synonymous_variant | LOW | c.525G>T | p.Ala175Ala | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/20 | 901/2812 | 525/2232 | 175/743 | chr19 | 3019308 | ||
chr19:3025059
|
G | A | 1 | a0001c0006 | 3 | HG02647.hp1 HG02886.hp1 HG03041.hp2 |
synonymous_variant | LOW | c.255C>T | p.Ser85Ser | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/20 | 631/2812 | 255/2232 | 85/743 | chr19 | 3025059 | ||
chr19:3028768
|
C | T | 1 | a0001c0010 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.60G>A | p.Ser20Ser | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 2/20 | 436/2812 | 60/2232 | 20/743 | chr19 | 3028768 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:2997710
|
G | A | 1 | a0001c0015t0009 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*138C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 20/20 | 138 | chr19 | 2997710 | |||||
chr19:2997741
|
G | A | 1 | a0001c0001t0008 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*107C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 20/20 | 107 | chr19 | 2997741 | |||||
chr19:2997792
|
T | C | 10 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(7): Show | 44 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*56A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 20/20 | 56 | chr19 | 2997792 | |||||
chr19:3028914
|
C | T | 3 | a0001c0001t0004a0001c0002t0007a0003c0026t0006 | 7 | HG01891.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-10G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 1/20 | 10 | chr19 | 3028914 | |||||
chr19:3028981
|
G | A | 1 | a0001c0001t0010 | 1 | HG03453.hp2 | 5_prime_UTR_variant | MODIFIER | c.-77C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 1/20 | 77 | chr19 | 3028981 | |||||
chr19:3029042
|
G | A | 1 | a0001c0005t0011 | 1 | HG03540.hp2 | 5_prime_UTR_variant | MODIFIER | c.-138C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 1/20 | 138 | chr19 | 3029042 | |||||
chr19:3029060
|
C | T | 5 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(2): Show | 15 | HG00738.hp1 HG01069.hp1 HG01891.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-156G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 1/20 | 156 | chr19 | 3029060 | |||||
chr19:3029248
|
G | A | 1 | a0008c0012t0012 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-344C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 1/20 | 344 | chr19 | 3029248 | |||||
chr19:3029258
|
G | A | 1 | a0001c0001t0013 | 1 | NA18970.hp1 | 5_prime_UTR_variant | MODIFIER | c.-354C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 1/20 | 354 | chr19 | 3029258 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:2997972
|
G | A | 1 | a0001c0002t0001g0191 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2125-17C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2997972 | ||||||
chr19:2997972
|
G | T | 1 | a0001c0008t0001g0369 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2125-17C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2997972 | ||||||
chr19:2997978
|
A | G | 38 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0072others(35): Show | 39 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.2125-23T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2997978 | ||||||
chr19:2998080
|
C | G | 7 | a0001c0001t0002g0205a0001c0001t0002g0321a0001c0001t0002g0348others(4): Show | 7 | HG01891.hp1 HG02559.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2125-125G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998080 | ||||||
chr19:2998105
|
T | C | 2 | a0001c0006t0002g0239a0001c0006t0002g0368 | 2 | HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2125-150A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998105 | ||||||
chr19:2998150
|
A | C | 1 | a0001c0002t0001g0206 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2125-195T>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998150 | ||||||
chr19:2998177
|
T | A | 3 | a0001c0001t0001g0304a0001c0001t0001g0306a0006c0019t0001g0186 | 3 | HG02040.hp1 NA18979.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.2125-222A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998177 | ||||||
chr19:2998236
|
AATGTGTG others(15): Show |
A | 6 | a0001c0005t0001g0149a0001c0005t0002g0240a0001c0005t0002g0241others(3): Show | 6 | HG02109.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2125-303_2125-282d others(24): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998236 | ||||||
chr19:2998237
|
A | ATG | 23 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0001g0076others(20): Show | 23 | HG00280.hp2 HG00741.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.2125-284_2125-283d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | ||||||
chr19:2998237
|
A | ATGTG | 9 | a0001c0001t0001g0074a0001c0001t0001g0109a0001c0001t0001g0152others(6): Show | 9 | HG00099.hp1 HG00323.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.2125-286_2125-283d others(6): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | ||||||
chr19:2998237
|
A | ATGTGTGT others(1): Show |
4 | a0001c0001t0002g0014a0001c0001t0004g0001a0001c0001t0004g0016others(1): Show | 7 | HG01891.hp2 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2125-290_2125-283d others(10): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | ||||||
chr19:2998237
|
A | ATGTGTGT others(3): Show |
2 | a0001c0001t0002g0013a0001c0001t0002g0352 | 3 | HG03041.hp1 HG03540.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2125-292_2125-283d others(12): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | ||||||
chr19:2998237
|
A | ATGTGTGT others(5): Show |
2 | a0001c0001t0002g0322a0001c0001t0005g0025 | 2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2125-294_2125-283d others(14): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | ||||||
chr19:2998237
|
A | ATGTGTGT others(13): Show |
1 | a0001c0001t0004g0017 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2125-302_2125-283d others(22): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | ||||||
chr19:2998237
|
ATGTG | A | 11 | a0001c0001t0001g0288a0001c0001t0001g0294a0001c0001t0001g0347others(8): Show | 11 | HG00597.hp2 HG01934.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.2125-286_2125-283d others(6): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | ||||||
chr19:2998237
|
ATGTGTG | A | 83 | a0001c0001t0001g0236a0001c0002t0001g0007a0001c0002t0001g0010others(80): Show | 85 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.2125-288_2125-283d others(8): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | ||||||
chr19:2998237
|
ATGTGTGT others(1): Show |
A | 11 | a0001c0007t0001g0314a0001c0007t0001g0333a0001c0015t0009g0129others(8): Show | 12 | HG00438.hp2 HG00597.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.2125-290_2125-283d others(10): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | ||||||
chr19:2998237
|
ATGTGTGT others(3): Show |
A | 1 | a0001c0001t0002g0307 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2125-292_2125-283d others(12): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | ||||||
chr19:2998237
|
ATGTGTGT others(5): Show |
A | 5 | a0001c0001t0001g0050a0001c0001t0001g0174a0001c0006t0001g0377others(2): Show | 5 | HG02145.hp1 HG02145.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2125-294_2125-283d others(14): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | ||||||
chr19:2998237
|
ATGTGTGT others(7): Show |
A | 1 | a0001c0016t0001g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2125-296_2125-283d others(16): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | ||||||
chr19:2998237
|
ATGTGTGT others(9): Show |
A | 1 | a0009c0021t0001g0301 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2125-298_2125-283d others(18): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | ||||||
chr19:2998237
|
ATGTGTGT others(11): Show |
A | 5 | a0001c0003t0001g0172a0001c0003t0001g0222a0001c0003t0001g0362others(2): Show | 5 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.2125-300_2125-283d others(20): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | ||||||
chr19:2998237
|
ATGTGTGT others(15): Show |
A | 5 | a0001c0001t0001g0308a0001c0001t0002g0238a0001c0001t0002g0317others(2): Show | 5 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2125-304_2125-283d others(24): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | ||||||
chr19:2998237
|
ATGTGTGT others(17): Show |
A | 1 | a0001c0003t0001g0245 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2125-306_2125-283d others(26): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | ||||||
chr19:2998243
|
GTGTGT | G | 3 | a0001c0003t0002g0268a0001c0003t0002g0269a0001c0003t0002g0270 | 3 | HG02258.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2125-293_2125-289d others(7): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998243 | ||||||
chr19:2998243
|
GTGTGTGT | G | 13 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0090others(10): Show | 14 | HG00738.hp2 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.2125-295_2125-289d others(9): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998243 | ||||||
chr19:2998263
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2125-308C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998263 | ||||||
chr19:2998264
|
T | A | 1 | a0001c0001t0001g0225 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2125-309A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998264 | ||||||
chr19:2998264
|
TGTGTGTG others(4): Show |
T | 2 | a0001c0001t0001g0304a0001c0001t0001g0306 | 2 | HG02040.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.2125-320_2125-310d others(13): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998264 | ||||||
chr19:2998265
|
G | T | 1 | a0001c0001t0001g0225 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2125-310C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998265 | ||||||
chr19:2998266
|
TGTGTGTG others(5): Show |
T | 1 | a0001c0001t0001g0225 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2125-323_2125-312d others(14): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998266 | ||||||
chr19:2998268
|
TGTGTGTG | T | 3 | a0001c0001t0001g0034a0001c0001t0001g0104a0001c0001t0001g0156 | 3 | HG00140.hp1 HG01346.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2125-320_2125-314d others(9): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998268 | ||||||
chr19:2998270
|
TGTGTG | T | 5 | a0001c0001t0001g0164a0001c0001t0001g0295a0001c0001t0001g0298others(2): Show | 5 | HG01934.hp2 HG02523.hp2 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.2125-320_2125-316d others(7): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998270 | ||||||
chr19:2998271
|
G | A | 8 | a0001c0001t0001g0381a0001c0001t0002g0033a0001c0001t0002g0036others(5): Show | 8 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.2125-316C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998271 | ||||||
chr19:2998272
|
TGTG | T | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(126): Show | 137 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.2125-320_2125-318d others(5): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998272 | ||||||
chr19:2998273
|
G | A | 10 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0119others(7): Show | 10 | HG01257.hp1 HG02129.hp2 HG03225.hp1 others(7): Show |
intron_variant | MODIFIER | c.2125-318C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998273 | ||||||
chr19:2998274
|
T | A | 7 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0119others(4): Show | 7 | HG01257.hp1 HG02129.hp2 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.2125-319A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998274 | ||||||
chr19:2998274
|
TG | T | 19 | a0001c0001t0001g0123a0001c0001t0001g0157a0001c0001t0001g0158others(16): Show | 19 | HG01516.hp1 HG01516.hp2 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2125-320delC | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998274 | ||||||
chr19:2998275
|
G | A | 149 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0050others(146): Show | 153 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.2125-320C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998275 | ||||||
chr19:2998275
|
G | GTA | 7 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0085others(4): Show | 8 | HG01109.hp2 HG02055.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.2125-322_2125-321d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998275 | ||||||
chr19:2998275
|
G | GTGTGTGT others(3): Show |
1 | a0001c0001t0002g0351 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2125-321_2125-320i others(12): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998275 | ||||||
chr19:2998275
|
G | GTGTGTGT others(5): Show |
1 | a0004c0025t0002g0309 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2125-321_2125-320i others(14): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998275 | ||||||
chr19:2998275
|
G | GTGTGTGT others(7): Show |
2 | a0001c0001t0002g0205a0001c0001t0002g0348 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2125-321_2125-320i others(16): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998275 | ||||||
chr19:2998275
|
G | GTGTGTGT others(9): Show |
1 | a0001c0001t0002g0370 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2125-321_2125-320i others(18): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998275 | ||||||
chr19:2998275
|
G | GTGTGTGT others(11): Show |
1 | a0001c0001t0002g0350 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2125-321_2125-320i others(20): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998275 | ||||||
chr19:2998275
|
G | GTGTGTGT others(15): Show |
1 | a0001c0001t0002g0321 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2125-321_2125-320i others(24): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998275 | ||||||
chr19:2998275
|
G | T | 7 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0119others(4): Show | 7 | HG01257.hp1 HG02129.hp2 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.2125-320C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998275 | ||||||
chr19:2998276
|
T | A | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.2125-321A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998276 | ||||||
chr19:2998276
|
TAA | T | 7 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0119others(4): Show | 7 | HG01257.hp1 HG02129.hp2 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.2125-323_2125-322d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998276 | ||||||
chr19:2998277
|
A | T | 1 | a0001c0001t0001g0060 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2125-322T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998277 | ||||||
chr19:2998278
|
A | T | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.2125-323T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998278 | ||||||
chr19:2998278
|
AT | A | 13 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0090others(10): Show | 14 | HG00738.hp2 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.2125-324delA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998278 | ||||||
chr19:2998279
|
T | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0185 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2125-324A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998279 | ||||||
chr19:2998288
|
T | G | 3 | a0001c0003t0002g0268a0001c0003t0002g0269a0001c0003t0002g0270 | 3 | HG02258.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2125-333A>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998288 | ||||||
chr19:2998290
|
T | G | 17 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0090others(14): Show | 18 | HG00738.hp2 HG02258.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.2125-335A>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998290 | ||||||
chr19:2998292
|
T | G | 18 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0090others(15): Show | 19 | HG00738.hp2 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.2125-337A>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998292 | ||||||
chr19:2998293
|
T | G | 1 | a0001c0001t0002g0205 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2125-338A>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998293 | ||||||
chr19:2998307
|
T | G | 1 | a0001c0001t0001g0224 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2125-352A>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998307 | ||||||
chr19:2998406
|
C | A | 143 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0050others(140): Show | 147 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(144): Show |
intron_variant | MODIFIER | c.2125-451G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998406 | ||||||
chr19:2998483
|
GGC | G | 132 | a0001c0001t0001g0050a0001c0001t0001g0209a0001c0001t0001g0216others(129): Show | 135 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.2125-530_2125-529d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998483 | ||||||
chr19:2998556
|
G | A | 1 | a0001c0006t0001g0377 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2125-601C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998556 | ||||||
chr19:2998651
|
C | T | 14 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0090others(11): Show | 15 | HG00738.hp2 HG02559.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2125-696G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998651 | ||||||
chr19:2998709
|
G | A | 1 | a0001c0002t0001g0310 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2125-754C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998709 | ||||||
chr19:2999034
|
C | T | 7 | a0001c0001t0002g0205a0001c0001t0002g0321a0001c0001t0002g0348others(4): Show | 7 | HG02559.hp2 HG02723.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.2125-1079G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999034 | ||||||
chr19:2999040
|
C | G | 162 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0050others(159): Show | 166 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.2125-1085G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999040 | ||||||
chr19:2999047
|
C | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0216a0001c0001t0010g0384 | 3 | HG03225.hp1 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2125-1092G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999047 | ||||||
chr19:2999054
|
G | A | 1 | a0001c0006t0002g0239 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2125-1099C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999054 | ||||||
chr19:2999109
|
C | G | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.2125-1154G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999109 | ||||||
chr19:2999261
|
G | A | 14 | a0001c0001t0001g0209a0001c0001t0001g0216a0001c0001t0010g0384others(11): Show | 15 | HG00438.hp2 HG00597.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.2125-1306C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999261 | ||||||
chr19:2999277
|
G | A | 23 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0029others(20): Show | 25 | HG00738.hp2 HG01109.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.2125-1322C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999277 | ||||||
chr19:2999482
|
C | T | 1 | a0001c0001t0008g0341 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2124+1165G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999482 | ||||||
chr19:2999494
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2124+1153T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999494 | ||||||
chr19:2999499
|
G | A | 2 | a0001c0002t0001g0374a0001c0006t0001g0377 | 2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2124+1148C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999499 | ||||||
chr19:2999554
|
C | T | 1 | a0001c0002t0001g0102 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2124+1093G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999554 | ||||||
chr19:2999555
|
G | A | 104 | a0001c0001t0001g0050a0001c0001t0001g0216a0001c0001t0001g0236others(101): Show | 106 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.2124+1092C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999555 | ||||||
chr19:2999595
|
C | T | 14 | a0001c0001t0002g0205a0001c0001t0002g0321a0001c0001t0002g0348others(11): Show | 14 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.2124+1052G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999595 | ||||||
chr19:2999626
|
C | A | 4 | a0001c0001t0001g0052a0001c0001t0001g0058a0001c0001t0001g0103others(1): Show | 4 | NA18747.hp1 NA18975.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.2124+1021G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999626 | ||||||
chr19:2999671
|
A | G | 14 | a0001c0001t0001g0055a0001c0001t0001g0126a0001c0001t0001g0164others(11): Show | 14 | HG00408.hp1 HG00642.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.2124+976T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999671 | ||||||
chr19:2999687
|
G | A | 1 | a0001c0003t0001g0222 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2124+960C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999687 | ||||||
chr19:2999726
|
C | CA | 181 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 194 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.2124+920dupT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999726 | ||||||
chr19:2999737
|
AAAG | A | 140 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0050others(137): Show | 144 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.2124+907_2124+909d others(5): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999737 | ||||||
chr19:2999759
|
G | A | 11 | a0001c0001t0001g0236a0001c0002t0001g0078a0001c0002t0001g0175others(8): Show | 11 | HG00639.hp2 HG01099.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.2124+888C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999759 | ||||||
chr19:2999761
|
A | G | 148 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0050others(145): Show | 152 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.2124+886T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999761 | ||||||
chr19:2999806
|
G | C | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.2124+841C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999806 | ||||||
chr19:2999868
|
A | G | 1 | a0001c0006t0002g0368 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2124+779T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999868 | ||||||
chr19:2999987
|
C | T | 7 | a0001c0001t0002g0205a0001c0001t0002g0321a0001c0001t0002g0348others(4): Show | 7 | HG02559.hp2 HG02723.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.2124+660G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999987 | ||||||
chr19:3000012
|
G | C | 148 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0050others(145): Show | 152 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.2124+635C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 3000012 | ||||||
chr19:3000164
|
T | C | 158 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0029others(155): Show | 163 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.2124+483A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 3000164 | ||||||
chr19:3000217
|
G | A | 18 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0090others(15): Show | 19 | HG00738.hp2 HG01891.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.2124+430C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 3000217 | ||||||
chr19:3000218
|
C | T | 1 | a0001c0016t0001g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2124+429G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 3000218 | ||||||
chr19:3000276
|
C | T | 1 | a0001c0020t0001g0380 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2124+371G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 3000276 | ||||||
chr19:3000289
|
G | A | 156 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0050others(153): Show | 160 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(157): Show |
intron_variant | MODIFIER | c.2124+358C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 3000289 | ||||||
chr19:3000366
|
T | G | 1 | a0001c0002t0001g0373 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2124+281A>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 3000366 | ||||||
chr19:3000374
|
T | C | 149 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0050others(146): Show | 153 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(150): Show |
intron_variant | MODIFIER | c.2124+273A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 3000374 | ||||||
chr19:3000434
|
C | G | 1 | a0001c0006t0002g0368 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2124+213G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 3000434 | ||||||
chr19:3000493
|
G | C | 9 | a0001c0001t0001g0263a0001c0001t0001g0381a0001c0001t0002g0033others(6): Show | 9 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.2124+154C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 3000493 | ||||||
chr19:3000502
|
C | T | 1 | a0001c0008t0002g0378 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2124+145G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 3000502 | ||||||
chr19:3000601
|
C | T | 2 | a0001c0001t0001g0209a0001c0001t0010g0384 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2124+46G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 3000601 | ||||||
chr19:3000767
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2048-44C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3000767 | ||||||
chr19:3000785
|
G | A | 1 | a0001c0001t0001g0201 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2048-62C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3000785 | ||||||
chr19:3000824
|
C | CT | 226 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(223): Show | 239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.2048-102dupA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3000824 | ||||||
chr19:3000824
|
C | CTT | 99 | a0001c0001t0001g0060a0001c0001t0001g0085a0001c0001t0001g0116others(96): Show | 102 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.2048-103_2048-102d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3000824 | ||||||
chr19:3000841
|
T | TTC | 6 | a0001c0001t0002g0205a0001c0001t0002g0321a0001c0001t0002g0348others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2048-119_2048-118i others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3000841 | ||||||
chr19:3000969
|
C | T | 11 | a0001c0001t0001g0236a0001c0002t0001g0078a0001c0002t0001g0175others(8): Show | 11 | HG00639.hp2 HG01099.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.2048-246G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3000969 | ||||||
chr19:3000970
|
G | C | 1 | a0001c0016t0001g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2048-247C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3000970 | ||||||
chr19:3001130
|
G | A | 1 | a0004c0025t0002g0309 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2048-407C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001130 | ||||||
chr19:3001230
|
G | A | 1 | a0001c0008t0002g0378 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2048-507C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001230 | ||||||
chr19:3001272
|
CA | C | 327 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(324): Show | 343 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.2048-550delT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001272 | ||||||
chr19:3001272
|
CAA | C | 9 | a0001c0001t0001g0120a0001c0001t0001g0265a0001c0001t0002g0067others(6): Show | 9 | HG01169.hp1 HG02615.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2048-551_2048-550d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001272 | ||||||
chr19:3001286
|
A | T | 1 | a0001c0002t0007g0028 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2048-563T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001286 | ||||||
chr19:3001352
|
C | T | 3 | a0001c0002t0001g0183a0001c0002t0001g0188a0001c0002t0001g0311 | 3 | HG00558.hp2 HG00609.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2048-629G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001352 | ||||||
chr19:3001364
|
C | T | 1 | a0009c0021t0001g0301 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2048-641G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001364 | ||||||
chr19:3001365
|
G | A | 1 | a0001c0015t0009g0129 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2048-642C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001365 | ||||||
chr19:3001392
|
G | C | 84 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(81): Show | 90 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.2048-669C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001392 | ||||||
chr19:3001419
|
T | TTTTG | 13 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0072others(10): Show | 14 | HG00323.hp2 HG00735.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2048-700_2048-697d others(6): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001419 | ||||||
chr19:3001419
|
TTTTG | T | 10 | a0001c0001t0001g0209a0001c0001t0001g0272a0001c0001t0001g0273others(7): Show | 10 | HG02572.hp2 HG02647.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.2048-700_2048-697d others(6): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001419 | ||||||
chr19:3001498
|
T | A | 5 | a0001c0001t0001g0100a0001c0001t0001g0150a0001c0002t0001g0183others(2): Show | 5 | HG00733.hp1 HG02109.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.2048-775A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001498 | ||||||
chr19:3001499
|
A | T | 3 | a0001c0002t0001g0115a0001c0002t0001g0184a0001c0002t0001g0283 | 3 | NA18967.hp2 NA19083.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.2048-776T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001499 | ||||||
chr19:3001613
|
G | A | 6 | a0001c0001t0002g0151a0001c0002t0001g0087a0001c0002t0001g0215others(3): Show | 6 | HG02257.hp2 HG02717.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2047+740C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001613 | ||||||
chr19:3001649
|
A | C | 24 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0072others(21): Show | 25 | HG00323.hp2 HG00735.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2047+704T>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001649 | ||||||
chr19:3001704
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2047+649C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001704 | ||||||
chr19:3001791
|
C | CT | 17 | a0001c0001t0001g0029a0001c0001t0001g0166a0001c0001t0001g0267others(14): Show | 17 | HG00099.hp2 HG00621.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.2047+561dupA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001791 | ||||||
chr19:3001791
|
C | CTT | 18 | a0001c0001t0001g0009a0001c0001t0001g0090a0001c0001t0001g0271others(15): Show | 19 | HG00738.hp2 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.2047+560_2047+561d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001791 | ||||||
chr19:3001791
|
CT | C | 45 | a0001c0001t0001g0167a0001c0001t0001g0198a0001c0001t0001g0209others(42): Show | 50 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.2047+561delA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001791 | ||||||
chr19:3001791
|
CTT | C | 164 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.2047+560_2047+561d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001791 | ||||||
chr19:3001791
|
CTTT | C | 15 | a0001c0001t0001g0046a0001c0001t0001g0058a0001c0001t0001g0077others(12): Show | 15 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.2047+559_2047+561d others(5): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001791 | ||||||
chr19:3001797
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2047+556A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001797 | ||||||
chr19:3001876
|
C | T | 16 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0090others(13): Show | 17 | HG00738.hp2 HG01891.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.2047+477G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001876 | ||||||
chr19:3001877
|
G | A | 3 | a0001c0003t0002g0268a0001c0003t0002g0269a0001c0003t0002g0270 | 3 | HG02258.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2047+476C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001877 | ||||||
chr19:3001957
|
C | A | 6 | a0001c0001t0002g0238a0001c0001t0002g0317a0001c0001t0002g0382others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2047+396G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001957 | ||||||
chr19:3002000
|
G | A | 1 | a0001c0016t0001g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2047+353C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3002000 | ||||||
chr19:3002013
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2047+340C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3002013 | ||||||
chr19:3002082
|
G | C | 1 | a0001c0001t0001g0110 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2047+271C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3002082 | ||||||
chr19:3002115
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2047+238T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3002115 | ||||||
chr19:3002150
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2047+203G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3002150 | ||||||
chr19:3002288
|
T | C | 1 | a0001c0016t0001g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2047+65A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3002288 | ||||||
chr19:3002655
|
C | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0339 | 2 | NA18945.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1897-152G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3002655 | ||||||
chr19:3002690
|
C | T | 4 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0146others(1): Show | 4 | HG02027.hp2 NA18953.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1897-187G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3002690 | ||||||
chr19:3002703
|
C | CTT | 19 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0072others(16): Show | 20 | HG00323.hp2 HG00735.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1897-202_1897-201d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3002703 | ||||||
chr19:3002899
|
G | A | 34 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0072others(31): Show | 35 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1897-396C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3002899 | ||||||
chr19:3002946
|
G | A | 1 | a0001c0001t0001g0337 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1897-443C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3002946 | ||||||
chr19:3003000
|
C | T | 2 | a0001c0001t0001g0164a0001c0001t0001g0295 | 2 | NA19084.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1897-497G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003000 | ||||||
chr19:3003025
|
G | A | 1 | a0001c0002t0001g0371 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1897-522C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003025 | ||||||
chr19:3003072
|
C | G | 1 | a0001c0016t0001g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1897-569G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003072 | ||||||
chr19:3003079
|
A | AC | 9 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0322others(6): Show | 13 | HG01891.hp2 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1897-577dupG | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003079 | ||||||
chr19:3003080
|
C | A | 1 | a0001c0016t0001g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1897-577G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003080 | ||||||
chr19:3003142
|
C | T | 92 | a0001c0001t0001g0060a0001c0001t0001g0236a0001c0002t0001g0007others(89): Show | 94 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1897-639G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003142 | ||||||
chr19:3003168
|
A | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0162 | 2 | HG01928.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1897-665T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003168 | ||||||
chr19:3003178
|
C | G | 1 | a0001c0002t0001g0083 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1897-675G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003178 | ||||||
chr19:3003340
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1897-837A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003340 | ||||||
chr19:3003353
|
C | T | 1 | a0001c0002t0001g0087 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1897-850G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003353 | ||||||
chr19:3003444
|
C | A | 1 | a0001c0015t0009g0129 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1897-941G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003444 | ||||||
chr19:3003650
|
C | CA | 14 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0090others(11): Show | 15 | HG00738.hp2 HG01891.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1897-1148dupT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003650 | ||||||
chr19:3003693
|
A | T | 1 | a0001c0001t0001g0224 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1897-1190T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003693 | ||||||
chr19:3003729
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1897-1226C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003729 | ||||||
chr19:3003758
|
G | A | 1 | a0001c0016t0001g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1897-1255C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003758 | ||||||
chr19:3003958
|
C | T | 1 | a0001c0002t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1897-1455G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003958 | ||||||
chr19:3003975
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1896+1462C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003975 | ||||||
chr19:3003987
|
G | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0072others(16): Show | 20 | HG00323.hp2 HG00735.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1896+1450C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003987 | ||||||
chr19:3003995
|
C | T | 9 | a0001c0003t0001g0172a0001c0003t0001g0222a0001c0003t0001g0245others(6): Show | 9 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1896+1442G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003995 | ||||||
chr19:3004032
|
G | A | 1 | a0001c0016t0001g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1896+1405C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004032 | ||||||
chr19:3004041
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1896+1396G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004041 | ||||||
chr19:3004255
|
G | C | 4 | a0001c0003t0001g0172a0001c0003t0001g0362a0001c0003t0001g0363others(1): Show | 4 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1896+1182C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004255 | ||||||
chr19:3004336
|
GTTGGACA others(102): Show |
G | 1 | a0001c0016t0001g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1896+992_1896+1100 others(3): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004336 | ||||||
chr19:3004366
|
G | A | 1 | a0001c0015t0009g0129 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1896+1071C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004366 | ||||||
chr19:3004501
|
T | C | 12 | a0001c0001t0001g0050a0001c0001t0001g0367a0001c0001t0002g0238others(9): Show | 12 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1896+936A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004501 | ||||||
chr19:3004509
|
C | T | 4 | a0001c0002t0001g0094a0001c0002t0001g0095a0001c0002t0001g0099others(1): Show | 4 | NA18944.hp2 NA18964.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.1896+928G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004509 | ||||||
chr19:3004614
|
C | CA | 28 | a0001c0001t0001g0050a0001c0001t0001g0109a0001c0001t0001g0119others(25): Show | 28 | HG01167.hp2 HG01169.hp1 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.1896+822dupT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004614 | ||||||
chr19:3004614
|
CA | C | 52 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0046others(49): Show | 58 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.1896+822delT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004614 | ||||||
chr19:3004643
|
C | G | 45 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0072others(42): Show | 50 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.1896+794G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004643 | ||||||
chr19:3004794
|
G | A | 60 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0029others(57): Show | 66 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.1896+643C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004794 | ||||||
chr19:3004798
|
T | G | 1 | a0001c0002t0001g0289 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1896+639A>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004798 | ||||||
chr19:3004843
|
G | C | 63 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0029others(60): Show | 69 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.1896+594C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004843 | ||||||
chr19:3004894
|
C | T | 2 | a0001c0002t0001g0366a0001c0002t0001g0371 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1896+543G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004894 | ||||||
chr19:3005062
|
T | C | 1 | a0001c0003t0001g0222 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1896+375A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3005062 | ||||||
chr19:3005110
|
C | G | 37 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0029others(34): Show | 39 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.1896+327G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3005110 | ||||||
chr19:3005147
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1896+290C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3005147 | ||||||
chr19:3005198
|
G | T | 1 | a0001c0009t0001g0062 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1896+239C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3005198 | ||||||
chr19:3005233
|
G | C | 22 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0072others(19): Show | 23 | HG00323.hp2 HG00735.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1896+204C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3005233 | ||||||
chr19:3005278
|
G | A | 161 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(158): Show | 169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.1896+159C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3005278 | ||||||
chr19:3005290
|
A | G | 9 | a0001c0003t0001g0172a0001c0003t0001g0222a0001c0003t0001g0245others(6): Show | 9 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1896+147T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3005290 | ||||||
chr19:3005349
|
G | A | 1 | a0001c0002t0001g0244 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1896+88C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3005349 | ||||||
chr19:3005413
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1896+24G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3005413 | ||||||
chr19:3005427
|
C | T | 4 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0297others(1): Show | 4 | HG00673.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1896+10G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3005427 | ||||||
chr19:3005691
|
G | C | 1 | a0001c0001t0001g0261 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1748+30C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 16/19 | chr19 | 3005691 | ||||||
chr19:3006134
|
C | T | 1 | a0001c0002t0001g0010 | 2 | NA18947.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1501-166G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 15/19 | chr19 | 3006134 | ||||||
chr19:3006149
|
A | G | 1 | a0001c0002t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1501-181T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 15/19 | chr19 | 3006149 | ||||||
chr19:3006179
|
C | A | 1 | a0009c0021t0001g0301 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1501-211G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 15/19 | chr19 | 3006179 | ||||||
chr19:3006229
|
A | T | 73 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0029others(70): Show | 79 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.1500+191T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 15/19 | chr19 | 3006229 | ||||||
chr19:3006238
|
A | AAT | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.1500+181_1500+182i others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 15/19 | chr19 | 3006238 | ||||||
chr19:3006276
|
C | T | 344 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(341): Show | 361 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(358): Show |
intron_variant | MODIFIER | c.1500+144G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 15/19 | chr19 | 3006276 | ||||||
chr19:3006302
|
T | C | 1 | a0001c0015t0009g0129 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1500+118A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 15/19 | chr19 | 3006302 | ||||||
chr19:3006710
|
C | A | 1 | a0001c0015t0009g0129 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1251-41G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3006710 | ||||||
chr19:3006773
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1251-104C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3006773 | ||||||
chr19:3006773
|
G | GTGTTTTT others(12): Show |
3 | a0001c0003t0001g0172a0001c0003t0001g0362a0001c0003t0001g0363 | 3 | HG00099.hp2 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1251-123_1251-105d others(21): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3006773 | ||||||
chr19:3006946
|
C | A | 6 | a0001c0001t0002g0205a0001c0001t0002g0321a0001c0001t0002g0348others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1251-277G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3006946 | ||||||
chr19:3007054
|
G | C | 5 | a0001c0001t0002g0033a0001c0001t0002g0036a0001c0001t0002g0067others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.1251-385C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3007054 | ||||||
chr19:3007119
|
G | A | 3 | a0001c0003t0002g0268a0001c0003t0002g0269a0001c0003t0002g0270 | 3 | HG02258.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1251-450C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3007119 | ||||||
chr19:3007321
|
T | C | 250 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.1251-652A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3007321 | ||||||
chr19:3007338
|
C | T | 2 | a0001c0005t0001g0149a0001c0005t0002g0364 | 2 | HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1251-669G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3007338 | ||||||
chr19:3007359
|
G | C | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0065others(1): Show | 4 | HG01993.hp2 HG02080.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1251-690C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3007359 | ||||||
chr19:3007370
|
A | G | 348 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(345): Show | 365 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.1251-701T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3007370 | ||||||
chr19:3007429
|
T | C | 1 | a0001c0002t0001g0176 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1251-760A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3007429 | ||||||
chr19:3007646
|
C | T | 6 | a0001c0001t0001g0141a0001c0001t0001g0198a0001c0001t0001g0318others(3): Show | 6 | NA18944.hp1 NA18952.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.1251-977G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3007646 | ||||||
chr19:3007677
|
G | A | 1 | a0001c0002t0001g0340 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1251-1008C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3007677 | ||||||
chr19:3007700
|
A | C | 250 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.1251-1031T>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3007700 | ||||||
chr19:3007807
|
C | A | 10 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0322others(7): Show | 14 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1250+1062G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3007807 | ||||||
chr19:3007942
|
G | A | 8 | a0001c0001t0002g0033a0001c0001t0002g0036a0001c0001t0002g0067others(5): Show | 8 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.1250+927C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3007942 | ||||||
chr19:3008069
|
G | A | 1 | a0001c0001t0001g0329 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1250+800C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008069 | ||||||
chr19:3008083
|
GAAAAC | G | 98 | a0001c0001t0001g0060a0001c0001t0001g0236a0001c0001t0001g0249others(95): Show | 100 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.1250+781_1250+785d others(7): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008083 | ||||||
chr19:3008151
|
A | G | 1 | a0001c0006t0002g0368 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1250+718T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008151 | ||||||
chr19:3008153
|
G | A | 8 | a0001c0001t0002g0033a0001c0001t0002g0036a0001c0001t0002g0067others(5): Show | 8 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.1250+716C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008153 | ||||||
chr19:3008197
|
A | G | 1 | a0001c0016t0001g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1250+672T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008197 | ||||||
chr19:3008321
|
G | A | 2 | a0001c0008t0001g0369a0001c0008t0002g0378 | 2 | HG02109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1250+548C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008321 | ||||||
chr19:3008352
|
G | T | 1 | a0001c0001t0001g0290 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1250+517C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008352 | ||||||
chr19:3008455
|
C | CT | 32 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0090others(29): Show | 33 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1250+413dupA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008455 | ||||||
chr19:3008455
|
C | CTT | 86 | a0001c0001t0001g0060a0001c0001t0001g0236a0001c0001t0001g0381others(83): Show | 88 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.1250+412_1250+413d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008455 | ||||||
chr19:3008462
|
T | C | 1 | a0001c0001t0001g0201 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1250+407A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008462 | ||||||
chr19:3008490
|
G | T | 1 | a0001c0001t0001g0225 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1250+379C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008490 | ||||||
chr19:3008500
|
G | A | 164 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.1250+369C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008500 | ||||||
chr19:3008507
|
A | G | 1 | a0001c0015t0009g0129 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1250+362T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008507 | ||||||
chr19:3008598
|
C | G | 89 | a0001c0001t0001g0060a0001c0001t0001g0236a0001c0001t0001g0381others(86): Show | 91 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.1250+271G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008598 | ||||||
chr19:3008599
|
C | T | 164 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.1250+270G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008599 | ||||||
chr19:3008604
|
C | A | 1 | a0001c0001t0002g0370 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1250+265G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008604 | ||||||
chr19:3008695
|
C | A | 97 | a0001c0001t0001g0060a0001c0001t0001g0236a0001c0001t0001g0381others(94): Show | 99 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.1250+174G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008695 | ||||||
chr19:3008854
|
C | CA | 3 | a0001c0001t0001g0128a0001c0001t0001g0357a0001c0001t0001g0376 | 3 | HG00741.hp1 HG04228.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1250+14dupT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008854 | ||||||
chr19:3008991
|
C | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0072others(12): Show | 16 | HG00323.hp2 HG00735.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1174-46G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 13/19 | chr19 | 3008991 | ||||||
chr19:3008992
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1174-47G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 13/19 | chr19 | 3008992 | ||||||
chr19:3009010
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1174-65G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 13/19 | chr19 | 3009010 | ||||||
chr19:3009011
|
G | A | 16 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0090others(13): Show | 17 | HG00738.hp2 HG01884.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1174-66C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 13/19 | chr19 | 3009011 | ||||||
chr19:3009083
|
A | C | 1 | a0001c0006t0001g0377 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1174-138T>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 13/19 | chr19 | 3009083 | ||||||
chr19:3009163
|
C | G | 1 | a0001c0001t0001g0123 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1174-218G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 13/19 | chr19 | 3009163 | ||||||
chr19:3009222
|
T | G | 96 | a0001c0001t0001g0060a0001c0001t0001g0236a0001c0001t0001g0381others(93): Show | 98 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.1174-277A>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 13/19 | chr19 | 3009222 | ||||||
chr19:3009287
|
C | T | 1 | a0001c0002t0001g0142 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1173+255G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 13/19 | chr19 | 3009287 | ||||||
chr19:3009336
|
G | A | 8 | a0001c0003t0001g0172a0001c0003t0001g0222a0001c0003t0001g0362others(5): Show | 8 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1173+206C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 13/19 | chr19 | 3009336 | ||||||
chr19:3009340
|
T | C | 4 | a0001c0001t0001g0050a0001c0001t0001g0367a0001c0001t0002g0307others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1173+202A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 13/19 | chr19 | 3009340 | ||||||
chr19:3009517
|
C | G | 1 | a0001c0006t0002g0368 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1173+25G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 13/19 | chr19 | 3009517 | ||||||
chr19:3009707
|
G | A | 1 | a0001c0003t0001g0245 | 1 | HG03516.hp2 | splice_region_variant&intron_variant | LOW | c.1013-5C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009707 | ||||||
chr19:3009734
|
C | T | 1 | a0001c0006t0002g0368 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1013-32G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009734 | ||||||
chr19:3009735
|
G | A | 9 | a0001c0003t0001g0172a0001c0003t0001g0222a0001c0003t0001g0245others(6): Show | 9 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1013-33C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009735 | ||||||
chr19:3009755
|
C | T | 5 | a0001c0001t0002g0321a0001c0001t0002g0348a0001c0001t0002g0350others(2): Show | 5 | HG02559.hp2 HG02723.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1013-53G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009755 | ||||||
chr19:3009772
|
G | A | 9 | a0001c0006t0001g0377a0002c0004t0001g0008a0002c0004t0001g0093others(6): Show | 10 | HG00438.hp2 HG01123.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.1013-70C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009772 | ||||||
chr19:3009776
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1013-74G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009776 | ||||||
chr19:3009790
|
T | C | 332 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(329): Show | 349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.1013-88A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009790 | ||||||
chr19:3009836
|
C | G | 97 | a0001c0001t0001g0050a0001c0001t0001g0060a0001c0001t0001g0131others(94): Show | 99 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.1013-134G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009836 | ||||||
chr19:3009872
|
C | T | 97 | a0001c0001t0001g0050a0001c0001t0001g0060a0001c0001t0001g0131others(94): Show | 99 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.1013-170G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009872 | ||||||
chr19:3009885
|
C | CT | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(243): Show | 261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1013-184dupA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009885 | ||||||
chr19:3009887
|
C | CTCTTTTT | 8 | a0001c0001t0002g0033a0001c0001t0002g0036a0001c0001t0002g0067others(5): Show | 8 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.1013-186_1013-185i others(9): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009887 | ||||||
chr19:3009887
|
C | CTCTTTTT others(1): Show |
87 | a0001c0001t0001g0050a0001c0001t0001g0060a0001c0001t0001g0131others(84): Show | 89 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.1013-186_1013-185i others(10): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009887 | ||||||
chr19:3009887
|
C | T | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(249): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.1013-185G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009887 | ||||||
chr19:3009900
|
G | T | 97 | a0001c0001t0001g0050a0001c0001t0001g0060a0001c0001t0001g0131others(94): Show | 99 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.1013-198C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009900 | ||||||
chr19:3009904
|
G | T | 97 | a0001c0001t0001g0050a0001c0001t0001g0060a0001c0001t0001g0131others(94): Show | 99 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.1013-202C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009904 | ||||||
chr19:3009954
|
G | A | 95 | a0001c0001t0001g0050a0001c0001t0001g0060a0001c0001t0001g0131others(92): Show | 97 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.1013-252C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009954 | ||||||
chr19:3009970
|
T | C | 95 | a0001c0001t0001g0050a0001c0001t0001g0060a0001c0001t0001g0131others(92): Show | 97 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.1013-268A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009970 | ||||||
chr19:3010061
|
C | T | 4 | a0001c0003t0001g0245a0001c0003t0002g0268a0001c0003t0002g0269others(1): Show | 4 | HG02258.hp1 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1013-359G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010061 | ||||||
chr19:3010087
|
A | T | 1 | a0001c0001t0001g0193 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1013-385T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010087 | ||||||
chr19:3010101
|
C | T | 3 | a0001c0001t0001g0367a0001c0001t0002g0307a0001c0002t0001g0371 | 3 | HG02280.hp2 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1013-399G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010101 | ||||||
chr19:3010117
|
A | C | 1 | a0001c0001t0001g0103 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1013-415T>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010117 | ||||||
chr19:3010220
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1013-518A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010220 | ||||||
chr19:3010235
|
A | C | 6 | a0001c0001t0001g0141a0001c0001t0001g0198a0001c0001t0001g0318others(3): Show | 6 | NA18944.hp1 NA18952.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.1013-533T>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010235 | ||||||
chr19:3010294
|
C | T | 4 | a0001c0001t0001g0079a0001c0001t0001g0100a0001c0001t0001g0325others(1): Show | 4 | HG00639.hp2 HG00733.hp1 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.1013-592G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010294 | ||||||
chr19:3010295
|
G | A | 12 | a0001c0001t0001g0009a0001c0001t0001g0090a0001c0001t0001g0267others(9): Show | 13 | HG00738.hp2 HG01891.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1013-593C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010295 | ||||||
chr19:3010325
|
T | C | 1 | a0001c0001t0005g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1013-623A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010325 | ||||||
chr19:3010368
|
A | G | 91 | a0001c0001t0001g0050a0001c0001t0001g0060a0001c0001t0001g0131others(88): Show | 93 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.1012+654T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010368 | ||||||
chr19:3010369
|
A | G | 1 | a0001c0002t0001g0330 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1012+653T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010369 | ||||||
chr19:3010370
|
A | T | 1 | a0001c0008t0001g0369 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1012+652T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010370 | ||||||
chr19:3010372
|
AAG | A | 90 | a0001c0001t0001g0050a0001c0001t0001g0060a0001c0001t0001g0131others(87): Show | 92 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1012+648_1012+649d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010372 | ||||||
chr19:3010375
|
G | GA | 14 | a0001c0001t0001g0101a0001c0001t0001g0119a0001c0001t0001g0197others(11): Show | 14 | HG01123.hp2 HG01884.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.1012+646dupT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010375 | ||||||
chr19:3010376
|
A | G | 91 | a0001c0001t0001g0050a0001c0001t0001g0060a0001c0001t0001g0131others(88): Show | 93 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.1012+646T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010376 | ||||||
chr19:3010399
|
C | G | 1 | a0001c0001t0001g0381 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1012+623G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010399 | ||||||
chr19:3010500
|
A | T | 4 | a0001c0003t0001g0245a0001c0003t0002g0268a0001c0003t0002g0269others(1): Show | 4 | HG02258.hp1 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012+522T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010500 | ||||||
chr19:3010650
|
T | C | 100 | a0001c0001t0001g0050a0001c0001t0001g0060a0001c0001t0001g0131others(97): Show | 102 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.1012+372A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010650 | ||||||
chr19:3010805
|
C | T | 91 | a0001c0001t0001g0050a0001c0001t0001g0060a0001c0001t0001g0131others(88): Show | 93 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.1012+217G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010805 | ||||||
chr19:3010842
|
G | A | 6 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0322others(3): Show | 8 | HG02280.hp1 HG02486.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1012+180C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010842 | ||||||
chr19:3011174
|
G | T | 1 | a0001c0016t0001g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.874-14C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011174 | ||||||
chr19:3011247
|
G | A | 1 | a0001c0001t0001g0381 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.874-87C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011247 | ||||||
chr19:3011282
|
C | G | 6 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0322others(3): Show | 8 | HG02280.hp1 HG02486.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.874-122G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011282 | ||||||
chr19:3011319
|
G | C | 1 | a0001c0006t0002g0368 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.874-159C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011319 | ||||||
chr19:3011353
|
C | T | 5 | a0001c0001t0001g0050a0001c0001t0001g0367a0001c0001t0002g0307others(2): Show | 5 | HG02145.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.874-193G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011353 | ||||||
chr19:3011389
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.874-229C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011389 | ||||||
chr19:3011414
|
C | T | 93 | a0001c0001t0001g0050a0001c0001t0001g0060a0001c0001t0001g0131others(90): Show | 95 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.874-254G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011414 | ||||||
chr19:3011519
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.874-359C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011519 | ||||||
chr19:3011529
|
C | CA | 19 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0054others(16): Show | 20 | HG00323.hp2 HG00735.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.874-370dupT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011529 | ||||||
chr19:3011529
|
CA | C | 104 | a0001c0001t0001g0050a0001c0001t0001g0060a0001c0001t0001g0090others(101): Show | 106 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.874-370delT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011529 | ||||||
chr19:3011567
|
A | G | 94 | a0001c0001t0001g0050a0001c0001t0001g0060a0001c0001t0001g0131others(91): Show | 96 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.874-407T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011567 | ||||||
chr19:3011599
|
C | A | 1 | a0009c0021t0001g0301 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.874-439G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011599 | ||||||
chr19:3011606
|
T | C | 1 | a0001c0001t0001g0140 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.874-446A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011606 | ||||||
chr19:3011621
|
C | T | 2 | a0001c0005t0001g0149a0001c0005t0002g0364 | 2 | HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.874-461G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011621 | ||||||
chr19:3011662
|
G | A | 94 | a0001c0001t0001g0050a0001c0001t0001g0060a0001c0001t0001g0131others(91): Show | 96 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.874-502C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011662 | ||||||
chr19:3011749
|
C | A | 6 | a0001c0005t0001g0149a0001c0005t0002g0240a0001c0005t0002g0241others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.874-589G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011749 | ||||||
chr19:3011777
|
G | C | 1 | a0001c0001t0001g0141 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.874-617C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011777 | ||||||
chr19:3011811
|
T | C | 1 | a0001c0001t0001g0337 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.874-651A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011811 | ||||||
chr19:3011952
|
C | G | 2 | a0001c0001t0002g0067a0001c0001t0002g0202 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.874-792G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011952 | ||||||
chr19:3012107
|
G | A | 99 | a0001c0001t0001g0050a0001c0001t0001g0060a0001c0001t0001g0131others(96): Show | 101 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.874-947C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012107 | ||||||
chr19:3012240
|
G | A | 22 | a0001c0001t0001g0009a0001c0001t0001g0090a0001c0001t0001g0267others(19): Show | 26 | HG00438.hp2 HG00738.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.874-1080C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012240 | ||||||
chr19:3012261
|
A | AAAAC | 99 | a0001c0001t0001g0050a0001c0001t0001g0060a0001c0001t0001g0131others(96): Show | 101 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.874-1105_874-1102d others(6): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012261 | ||||||
chr19:3012314
|
C | T | 2 | a0001c0002t0001g0361a0001c0005t0001g0149 | 2 | HG01255.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.874-1154G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012314 | ||||||
chr19:3012328
|
G | A | 4 | a0001c0001t0001g0050a0001c0001t0001g0367a0001c0001t0002g0307others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.874-1168C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012328 | ||||||
chr19:3012365
|
G | A | 1 | a0001c0016t0001g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.874-1205C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012365 | ||||||
chr19:3012450
|
C | T | 1 | a0001c0001t0002g0205 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.873+1219G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012450 | ||||||
chr19:3012515
|
C | A | 1 | a0001c0002t0001g0082 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.873+1154G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012515 | ||||||
chr19:3012528
|
T | C | 103 | a0001c0001t0001g0050a0001c0001t0001g0060a0001c0001t0001g0131others(100): Show | 107 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.873+1141A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012528 | ||||||
chr19:3012559
|
A | G | 18 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0054others(15): Show | 19 | HG00323.hp2 HG00735.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.873+1110T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012559 | ||||||
chr19:3012649
|
A | C | 1 | a0001c0001t0001g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.873+1020T>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012649 | ||||||
chr19:3012668
|
C | A | 1 | a0001c0001t0001g0381 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.873+1001G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012668 | ||||||
chr19:3012748
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.873+921C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012748 | ||||||
chr19:3012760
|
C | T | 7 | a0001c0001t0001g0381a0001c0001t0004g0001a0001c0001t0004g0016others(4): Show | 9 | HG01891.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.873+909G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012760 | ||||||
chr19:3012885
|
G | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0054others(14): Show | 18 | HG00323.hp2 HG00735.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.873+784C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012885 | ||||||
chr19:3012892
|
C | T | 14 | a0001c0001t0001g0250a0001c0001t0001g0381a0001c0001t0002g0033others(11): Show | 16 | HG01074.hp2 HG01255.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.873+777G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012892 | ||||||
chr19:3012916
|
C | T | 1 | a0001c0001t0001g0349 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.873+753G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012916 | ||||||
chr19:3012940
|
A | G | 3 | a0001c0003t0001g0245a0001c0003t0002g0268a0001c0003t0002g0269 | 3 | HG02258.hp1 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.873+729T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012940 | ||||||
chr19:3012971
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.873+698C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012971 | ||||||
chr19:3013020
|
G | A | 7 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(4): Show | 7 | HG02572.hp2 HG02647.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.873+649C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013020 | ||||||
chr19:3013060
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.873+609G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013060 | ||||||
chr19:3013112
|
G | C | 1 | a0001c0020t0001g0380 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.873+557C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013112 | ||||||
chr19:3013173
|
G | A | 1 | a0001c0003t0002g0270 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.873+496C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013173 | ||||||
chr19:3013220
|
G | T | 7 | a0001c0001t0001g0250a0001c0001t0002g0033a0001c0001t0002g0036others(4): Show | 7 | HG01074.hp2 HG01255.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.873+449C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013220 | ||||||
chr19:3013229
|
A | G | 160 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0029others(157): Show | 169 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(166): Show |
intron_variant | MODIFIER | c.873+440T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013229 | ||||||
chr19:3013288
|
G | A | 1 | a0009c0021t0001g0301 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.873+381C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013288 | ||||||
chr19:3013289
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.873+380C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013289 | ||||||
chr19:3013376
|
A | G | 105 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 110 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.873+293T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013376 | ||||||
chr19:3013523
|
T | TA | 5 | a0001c0001t0001g0052a0001c0001t0001g0066a0001c0001t0001g0315others(2): Show | 7 | HG01891.hp2 HG02818.hp2 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.873+145dupT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013523 | ||||||
chr19:3013538
|
A | C | 4 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0146others(1): Show | 4 | HG02027.hp2 NA18953.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.873+131T>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013538 | ||||||
chr19:3013551
|
A | G | 1 | a0001c0006t0002g0368 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.873+118T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013551 | ||||||
chr19:3013618
|
G | A | 178 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0009others(175): Show | 188 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(185): Show |
intron_variant | MODIFIER | c.873+51C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013618 | ||||||
chr19:3013625
|
C | T | 2 | a0001c0001t0001g0381a0001c0003t0001g0245 | 2 | HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.873+44G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013625 | ||||||
chr19:3013626
|
G | A | 18 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0042others(15): Show | 19 | HG00609.hp2 HG02109.hp1 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.873+43C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013626 | ||||||
chr19:3013948
|
G | A | 3 | a0001c0001t0001g0367a0001c0001t0002g0307a0001c0002t0001g0371 | 3 | HG02280.hp2 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.724-130C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 10/19 | chr19 | 3013948 | ||||||
chr19:3013973
|
T | A | 128 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0050others(125): Show | 132 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.724-155A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 10/19 | chr19 | 3013973 | ||||||
chr19:3013988
|
A | AT | 18 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0054others(15): Show | 19 | HG00323.hp2 HG00735.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.724-171dupA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 10/19 | chr19 | 3013988 | ||||||
chr19:3013988
|
AT | A | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.724-171delA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 10/19 | chr19 | 3013988 | ||||||
chr19:3014015
|
G | A | 2 | a0001c0001t0005g0026a0001c0002t0001g0082 | 2 | HG03710.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.724-197C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 10/19 | chr19 | 3014015 | ||||||
chr19:3014275
|
T | C | 7 | a0001c0001t0001g0250a0001c0001t0002g0033a0001c0001t0002g0036others(4): Show | 7 | HG01074.hp2 HG01255.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.723+295A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 10/19 | chr19 | 3014275 | ||||||
chr19:3014428
|
C | T | 2 | a0001c0001t0002g0382a0001c0001t0002g0383 | 2 | HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.723+142G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 10/19 | chr19 | 3014428 | ||||||
chr19:3014433
|
C | T | 1 | a0001c0008t0002g0378 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.723+137G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 10/19 | chr19 | 3014433 | ||||||
chr19:3014557
|
C | T | 1 | a0001c0009t0001g0038 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.723+13G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 10/19 | chr19 | 3014557 | ||||||
chr19:3014641
|
A | G | 142 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0050others(139): Show | 150 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.679-27T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3014641 | ||||||
chr19:3014649
|
C | A | 169 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(166): Show | 176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.679-35G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3014649 | ||||||
chr19:3014666
|
A | T | 2 | a0001c0001t0001g0091a0001c0001t0001g0208 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.679-52T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3014666 | ||||||
chr19:3014677
|
G | A | 5 | a0001c0001t0001g0180a0001c0001t0001g0354a0001c0001t0001g0358others(2): Show | 5 | HG01168.hp2 HG01361.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.679-63C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3014677 | ||||||
chr19:3014868
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.679-254A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3014868 | ||||||
chr19:3014875
|
C | G | 1 | a0001c0001t0001g0034 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.679-261G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3014875 | ||||||
chr19:3015022
|
T | TAATA | 4 | a0001c0003t0002g0268a0001c0003t0002g0269a0001c0003t0002g0270others(1): Show | 4 | HG02258.hp1 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.679-412_679-409dup others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3015022 | ||||||
chr19:3015058
|
C | CA | 82 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0042others(79): Show | 86 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.679-445dupT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3015058 | ||||||
chr19:3015058
|
C | CAA | 96 | a0001c0001t0001g0050a0001c0001t0001g0060a0001c0001t0001g0131others(93): Show | 98 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.679-446_679-445dup others(2): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3015058 | ||||||
chr19:3015058
|
CAA | C | 170 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(167): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.679-446_679-445del others(2): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3015058 | ||||||
chr19:3015058
|
CAAA | C | 10 | a0001c0001t0001g0009a0001c0001t0001g0090a0001c0001t0001g0091others(7): Show | 11 | HG00738.hp2 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.679-447_679-445del others(3): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3015058 | ||||||
chr19:3015152
|
C | T | 1 | a0001c0002t0001g0361 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.678+501G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3015152 | ||||||
chr19:3015285
|
T | C | 1 | a0001c0001t0002g0238 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.678+368A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3015285 | ||||||
chr19:3015453
|
C | T | 1 | a0002c0011t0001g0080 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.678+200G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3015453 | ||||||
chr19:3015483
|
C | A | 7 | a0001c0001t0001g0250a0001c0001t0002g0033a0001c0001t0002g0036others(4): Show | 7 | HG01074.hp2 HG01255.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.678+170G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3015483 | ||||||
chr19:3015517
|
C | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.678+136G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3015517 | ||||||
chr19:3015547
|
C | T | 7 | a0001c0001t0001g0250a0001c0001t0002g0033a0001c0001t0002g0036others(4): Show | 7 | HG01074.hp2 HG01255.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.678+106G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3015547 | ||||||
chr19:3015548
|
G | A | 1 | a0001c0016t0001g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.678+105C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3015548 | ||||||
chr19:3015870
|
C | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0339 | 2 | NA18945.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.571-110G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3015870 | ||||||
chr19:3015905
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0100 | 2 | HG00733.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.571-145G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3015905 | ||||||
chr19:3015939
|
CTGTTT | C | 7 | a0001c0001t0001g0250a0001c0001t0002g0033a0001c0001t0002g0036others(4): Show | 7 | HG01074.hp2 HG01255.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.571-184_571-180del others(5): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3015939 | ||||||
chr19:3016054
|
A | G | 5 | a0001c0005t0001g0149a0001c0005t0002g0241a0001c0005t0002g0364others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-294T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016054 | ||||||
chr19:3016208
|
T | C | 1 | a0001c0003t0001g0245 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.571-448A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016208 | ||||||
chr19:3016419
|
C | CA | 94 | a0001c0001t0001g0009a0001c0001t0001g0042a0001c0001t0001g0060others(91): Show | 97 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.571-660dupT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016419 | ||||||
chr19:3016419
|
C | CAA | 146 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(143): Show | 155 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.571-661_571-660dup others(2): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016419 | ||||||
chr19:3016419
|
C | CAAA | 30 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0058others(27): Show | 30 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.571-662_571-660dup others(3): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016419 | ||||||
chr19:3016419
|
CA | C | 19 | a0001c0001t0001g0250a0001c0001t0001g0286a0001c0001t0002g0033others(16): Show | 20 | HG00738.hp1 HG01069.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.571-660delT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016419 | ||||||
chr19:3016419
|
CAA | C | 22 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0054others(19): Show | 23 | HG00323.hp2 HG00735.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.571-661_571-660del others(2): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016419 | ||||||
chr19:3016504
|
C | T | 1 | a0001c0001t0002g0350 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.571-744G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016504 | ||||||
chr19:3016589
|
CA | C | 316 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 328 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.571-830delT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016589 | ||||||
chr19:3016589
|
CAA | C | 47 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0054others(44): Show | 49 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.571-831_571-830del others(2): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016589 | ||||||
chr19:3016589
|
CAAA | C | 8 | a0001c0001t0001g0009a0001c0001t0001g0053a0001c0001t0001g0077others(5): Show | 9 | HG00639.hp1 HG00738.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.571-832_571-830del others(3): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016589 | ||||||
chr19:3016707
|
G | A | 6 | a0001c0005t0001g0149a0001c0005t0002g0240a0001c0005t0002g0241others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-947C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016707 | ||||||
chr19:3016715
|
G | T | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168 | 3 | HG00741.hp2 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.571-955C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016715 | ||||||
chr19:3016725
|
A | G | 143 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0050others(140): Show | 149 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.571-965T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016725 | ||||||
chr19:3016793
|
T | C | 2 | a0001c0005t0001g0149a0001c0005t0002g0240 | 2 | HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.571-1033A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016793 | ||||||
chr19:3016879
|
C | T | 8 | a0001c0001t0001g0250a0001c0001t0002g0033a0001c0001t0002g0036others(5): Show | 8 | HG01074.hp2 HG01255.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.570+961G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016879 | ||||||
chr19:3016900
|
T | A | 8 | a0001c0001t0001g0250a0001c0001t0002g0033a0001c0001t0002g0036others(5): Show | 8 | HG01074.hp2 HG01255.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.570+940A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016900 | ||||||
chr19:3016923
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.570+917G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016923 | ||||||
chr19:3016935
|
C | A | 1 | a0001c0018t0001g0375 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.570+905G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016935 | ||||||
chr19:3016954
|
T | G | 78 | a0001c0001t0001g0060a0001c0001t0001g0131a0001c0001t0001g0209others(75): Show | 80 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.570+886A>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016954 | ||||||
chr19:3017010
|
T | C | 1 | a0001c0002t0001g0206 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.570+830A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017010 | ||||||
chr19:3017049
|
G | GTTATAGG others(32): Show |
44 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0054others(41): Show | 47 | HG00323.hp2 HG00735.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.570+790_570+791ins others(39): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017049 | ||||||
chr19:3017079
|
C | G | 1 | a0001c0002t0001g0051 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.570+761G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017079 | ||||||
chr19:3017143
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.570+697A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017143 | ||||||
chr19:3017160
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.570+680G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017160 | ||||||
chr19:3017195
|
T | TGGTGCAA others(9): Show |
2 | a0001c0001t0001g0126a0001c0001t0001g0177 | 2 | HG00642.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.570+629_570+644dup others(16): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017195 | ||||||
chr19:3017232
|
GGTC | G | 3 | a0001c0001t0001g0381a0001c0008t0001g0369a0001c0008t0002g0378 | 3 | HG02109.hp2 HG02615.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.570+605_570+607del others(3): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017232 | ||||||
chr19:3017241
|
G | A | 1 | a0001c0002t0001g0047 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.570+599C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017241 | ||||||
chr19:3017241
|
G | GA | 165 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0043others(162): Show | 173 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(170): Show |
intron_variant | MODIFIER | c.570+598dupT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017241 | ||||||
chr19:3017297
|
T | C | 3 | a0001c0001t0002g0352a0001c0001t0004g0001a0001c0001t0004g0016 | 5 | HG01891.hp2 HG02818.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+543A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017297 | ||||||
chr19:3017317
|
T | C | 30 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0054others(27): Show | 31 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.570+523A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017317 | ||||||
chr19:3017432
|
G | GT | 21 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0072others(18): Show | 21 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.570+407dupA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017432 | ||||||
chr19:3017439
|
T | C | 1 | a0001c0002t0001g0155 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.570+401A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017439 | ||||||
chr19:3017444
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.570+396G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017444 | ||||||
chr19:3017452
|
C | CT | 52 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0034others(49): Show | 57 | HG00140.hp1 HG00323.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.570+387dupA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017452 | ||||||
chr19:3017452
|
C | CTT | 38 | a0001c0001t0001g0043a0001c0001t0001g0050a0001c0001t0001g0060others(35): Show | 39 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.570+386_570+387dup others(2): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017452 | ||||||
chr19:3017452
|
C | CTTT | 75 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0011others(72): Show | 79 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.570+385_570+387dup others(3): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017452 | ||||||
chr19:3017452
|
CT | C | 6 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0235others(3): Show | 6 | HG01099.hp2 HG01256.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+387delA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017452 | ||||||
chr19:3017483
|
C | G | 2 | a0001c0001t0001g0200a0001c0001t0001g0263 | 2 | HG03017.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.570+357G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017483 | ||||||
chr19:3017514
|
G | A | 1 | a0001c0001t0002g0205 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.570+326C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017514 | ||||||
chr19:3017522
|
C | T | 1 | a0001c0016t0001g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.570+318G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017522 | ||||||
chr19:3017607
|
C | T | 5 | a0001c0001t0001g0058a0001c0001t0001g0103a0001c0001t0001g0164others(2): Show | 5 | NA18747.hp1 NA18747.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+233G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017607 | ||||||
chr19:3017615
|
C | T | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(165): Show | 178 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(175): Show |
intron_variant | MODIFIER | c.570+225G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017615 | ||||||
chr19:3017624
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0379 | 2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.570+216C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017624 | ||||||
chr19:3017818
|
T | C | 2 | a0001c0001t0001g0126a0001c0001t0001g0177 | 2 | HG00642.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.570+22A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017818 | ||||||
chr19:3017822
|
A | G | 11 | a0001c0001t0001g0216a0001c0001t0001g0328a0001c0002t0001g0083others(8): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.570+18T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017822 | ||||||
chr19:3017826
|
T | C | 2 | a0001c0002t0001g0371a0001c0003t0001g0245 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.570+14A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017826 | ||||||
chr19:3017890
|
G | C | 3 | a0001c0001t0001g0302a0001c0001t0002g0067a0001c0001t0002g0202 | 3 | HG01167.hp2 HG01169.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.551-31C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3017890 | ||||||
chr19:3017920
|
C | T | 1 | a0001c0001t0001g0251 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.551-61G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3017920 | ||||||
chr19:3017931
|
G | A | 22 | a0001c0001t0001g0009a0001c0001t0001g0209a0001c0001t0001g0272others(19): Show | 23 | HG00738.hp2 HG02145.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.551-72C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3017931 | ||||||
chr19:3017955
|
CCCCCCGC others(8): Show |
C | 1 | a0001c0024t0001g0073 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.551-111_551-97delT others(14): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3017955 | ||||||
chr19:3017958
|
C | T | 2 | a0001c0001t0001g0068a0001c0002t0001g0082 | 2 | HG03704.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.551-99G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3017958 | ||||||
chr19:3017960
|
C | T | 26 | a0001c0001t0001g0009a0001c0001t0001g0050a0001c0001t0001g0209others(23): Show | 27 | HG00738.hp2 HG02145.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.551-101G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3017960 | ||||||
chr19:3017961
|
G | A | 25 | a0001c0001t0001g0029a0001c0001t0001g0054a0001c0001t0001g0084others(22): Show | 27 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.551-102C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3017961 | ||||||
chr19:3017965
|
C | T | 12 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(9): Show | 12 | HG00280.hp2 HG00323.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.551-106G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3017965 | ||||||
chr19:3017978
|
CAG | C | 19 | a0001c0001t0001g0034a0001c0001t0001g0060a0001c0001t0001g0077others(16): Show | 19 | HG00639.hp1 HG00639.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.551-121_551-120del others(2): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3017978 | ||||||
chr19:3018085
|
C | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0085others(6): Show | 10 | HG01109.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.551-226G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018085 | ||||||
chr19:3018164
|
C | A | 7 | a0001c0001t0001g0011a0001c0001t0001g0263a0001c0001t0002g0033others(4): Show | 8 | HG01257.hp1 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.551-305G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018164 | ||||||
chr19:3018233
|
G | C | 127 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0011others(124): Show | 137 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.551-374C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018233 | ||||||
chr19:3018257
|
G | A | 1 | a0001c0006t0001g0377 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.551-398C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018257 | ||||||
chr19:3018295
|
C | CATTT | 13 | a0001c0001t0001g0103a0001c0001t0001g0150a0001c0001t0001g0152others(10): Show | 13 | HG00280.hp1 HG01168.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.551-440_551-437dup others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018295 | ||||||
chr19:3018371
|
C | G | 1 | a0001c0001t0001g0079 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.551-512G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018371 | ||||||
chr19:3018485
|
G | A | 16 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0085others(13): Show | 17 | HG01109.hp2 HG01891.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.551-626C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018485 | ||||||
chr19:3018524
|
C | G | 1 | a0001c0005t0001g0149 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.551-665G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018524 | ||||||
chr19:3018653
|
C | T | 1 | a0001c0005t0001g0149 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.550+630G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018653 | ||||||
chr19:3018727
|
G | A | 1 | a0001c0002t0001g0244 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.550+556C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018727 | ||||||
chr19:3018742
|
G | C | 1 | a0001c0001t0001g0050 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.550+541C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018742 | ||||||
chr19:3018763
|
C | T | 1 | a0001c0001t0001g0334 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.550+520G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018763 | ||||||
chr19:3018837
|
C | G | 1 | a0001c0001t0001g0356 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.550+446G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018837 | ||||||
chr19:3018838
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.550+445C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018838 | ||||||
chr19:3018899
|
T | A | 1 | a0006c0019t0001g0186 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.550+384A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018899 | ||||||
chr19:3019087
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.550+196C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3019087 | ||||||
chr19:3019095
|
G | A | 1 | a0001c0001t0001g0381 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.550+188C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3019095 | ||||||
chr19:3019125
|
T | G | 6 | a0001c0001t0001g0379a0001c0001t0004g0001a0001c0001t0004g0016others(3): Show | 8 | HG01891.hp2 HG02630.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.550+158A>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3019125 | ||||||
chr19:3019135
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.550+148G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3019135 | ||||||
chr19:3019268
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.550+15C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3019268 | ||||||
chr19:3019490
|
G | A | 1 | a0001c0010t0001g0231 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.370-27C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 6/19 | chr19 | 3019490 | ||||||
chr19:3019499
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.370-36C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 6/19 | chr19 | 3019499 | ||||||
chr19:3019539
|
A | G | 1 | a0001c0013t0001g0246 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.370-76T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 6/19 | chr19 | 3019539 | ||||||
chr19:3019662
|
G | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(31): Show | 35 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.369+37C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 6/19 | chr19 | 3019662 | ||||||
chr19:3019857
|
G | A | 1 | a0001c0002t0001g0310 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.295-84C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3019857 | ||||||
chr19:3019901
|
T | C | 8 | a0001c0001t0001g0228a0001c0001t0001g0354a0001c0001t0001g0355others(5): Show | 8 | HG00280.hp1 HG01168.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.295-128A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3019901 | ||||||
chr19:3019988
|
T | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(94): Show | 103 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.295-215A>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3019988 | ||||||
chr19:3019994
|
C | T | 1 | a0001c0001t0001g0381 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.295-221G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3019994 | ||||||
chr19:3020008
|
C | T | 8 | a0001c0001t0001g0228a0001c0001t0001g0354a0001c0001t0001g0355others(5): Show | 8 | HG00280.hp1 HG01168.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.295-235G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020008 | ||||||
chr19:3020116
|
A | T | 48 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0209others(45): Show | 50 | HG00280.hp1 HG00738.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.295-343T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020116 | ||||||
chr19:3020191
|
G | A | 1 | a0001c0010t0001g0231 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.295-418C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020191 | ||||||
chr19:3020230
|
T | C | 204 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(201): Show | 216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.295-457A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020230 | ||||||
chr19:3020354
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.295-581G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020354 | ||||||
chr19:3020377
|
C | G | 1 | a0001c0001t0001g0030 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.295-604G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020377 | ||||||
chr19:3020401
|
A | G | 1 | a0001c0024t0001g0073 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.295-628T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020401 | ||||||
chr19:3020543
|
C | A | 1 | a0001c0002t0001g0281 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.295-770G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020543 | ||||||
chr19:3020592
|
T | C | 1 | a0001c0001t0001g0079 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.295-819A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020592 | ||||||
chr19:3020616
|
C | T | 7 | a0001c0001t0001g0242a0001c0001t0003g0024a0001c0002t0003g0020others(4): Show | 7 | HG00738.hp1 HG01069.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.295-843G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020616 | ||||||
chr19:3020617
|
G | A | 2 | a0001c0001t0001g0103a0001c0002t0001g0188 | 2 | HG00558.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.295-844C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020617 | ||||||
chr19:3020644
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.295-871A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020644 | ||||||
chr19:3020649
|
G | A | 3 | a0001c0001t0001g0146a0001c0001t0001g0189a0001c0001t0001g0201 | 3 | NA18939.hp1 NA18986.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.295-876C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020649 | ||||||
chr19:3020680
|
A | T | 50 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0050others(47): Show | 52 | HG00280.hp1 HG00738.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.295-907T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020680 | ||||||
chr19:3020693
|
A | G | 204 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(201): Show | 216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.295-920T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020693 | ||||||
chr19:3020784
|
G | A | 1 | a0001c0001t0002g0317 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.295-1011C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020784 | ||||||
chr19:3020881
|
T | C | 3 | a0001c0005t0002g0240a0001c0005t0002g0241a0001c0005t0011g0385 | 3 | HG02622.hp1 HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.295-1108A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020881 | ||||||
chr19:3021088
|
C | CA | 26 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(23): Show | 26 | HG00621.hp2 HG01243.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.295-1316dupT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021088 | ||||||
chr19:3021088
|
CA | C | 39 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0059others(36): Show | 41 | HG01255.hp2 HG02055.hp2 HG02273.hp1 others(38): Show |
intron_variant | MODIFIER | c.295-1316delT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021088 | ||||||
chr19:3021088
|
CAA | C | 10 | a0001c0001t0001g0030a0001c0001t0001g0271a0001c0001t0001g0379others(7): Show | 12 | HG00140.hp2 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.295-1317_295-1316d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021088 | ||||||
chr19:3021090
|
A | AAC | 12 | a0001c0001t0001g0009a0001c0001t0001g0225a0001c0001t0001g0230others(9): Show | 13 | HG00738.hp2 HG01943.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.295-1318_295-1317i others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021090 | ||||||
chr19:3021111
|
AAAAG | A | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(83): Show | 93 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.295-1342_295-1339d others(6): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021111 | ||||||
chr19:3021112
|
AAAG | A | 12 | a0001c0001t0001g0032a0001c0001t0001g0050a0001c0001t0001g0313others(9): Show | 12 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.295-1342_295-1340d others(5): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021112 | ||||||
chr19:3021113
|
AAG | A | 6 | a0001c0001t0001g0286a0001c0001t0002g0348a0001c0001t0002g0382others(3): Show | 6 | HG02258.hp2 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.295-1342_295-1341d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021113 | ||||||
chr19:3021114
|
A | AAAAAAAA others(5): Show |
1 | a0001c0002t0003g0023 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.295-1342_295-1341i others(14): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021114 | ||||||
chr19:3021114
|
A | AAAAAAAA others(6): Show |
2 | a0001c0001t0001g0242a0001c0002t0003g0020 | 2 | HG01928.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.295-1342_295-1341i others(15): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021114 | ||||||
chr19:3021114
|
A | AAAAAAAA others(4): Show |
3 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0027 | 3 | HG00738.hp1 HG01069.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.295-1342_295-1341i others(13): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021114 | ||||||
chr19:3021114
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0003g0019 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.295-1342_295-1341i others(14): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021114 | ||||||
chr19:3021114
|
A | AG | 22 | a0001c0001t0001g0006a0001c0001t0001g0116a0001c0001t0001g0117others(19): Show | 23 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.295-1342dupC | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021114 | ||||||
chr19:3021114
|
A | G | 18 | a0001c0001t0001g0056a0001c0001t0001g0106a0001c0001t0001g0109others(15): Show | 18 | HG00544.hp2 HG00609.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.295-1341T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021114 | ||||||
chr19:3021114
|
AG | A | 32 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0044others(29): Show | 33 | HG00639.hp1 HG00642.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.295-1342delC | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021114 | ||||||
chr19:3021115
|
G | A | 11 | a0001c0001t0001g0081a0001c0001t0001g0088a0001c0001t0001g0089others(8): Show | 11 | HG01109.hp1 HG01109.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.295-1342C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021115 | ||||||
chr19:3021116
|
G | C | 1 | a0001c0002t0001g0203 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.295-1343C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021116 | ||||||
chr19:3021118
|
G | T | 87 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(84): Show | 93 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.295-1345C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021118 | ||||||
chr19:3021122
|
G | C | 2 | a0001c0003t0001g0245a0001c0013t0001g0246 | 2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.295-1349C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021122 | ||||||
chr19:3021122
|
G | GT | 17 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0225others(14): Show | 18 | HG00738.hp2 HG00741.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.295-1350_295-1349i others(3): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021122 | ||||||
chr19:3021123
|
G | T | 5 | a0001c0001t0001g0029a0001c0001t0002g0370a0001c0002t0001g0244others(2): Show | 5 | HG01891.hp1 HG02109.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.295-1350C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021123 | ||||||
chr19:3021128
|
T | C | 48 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0209others(45): Show | 50 | HG00280.hp1 HG00738.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.295-1355A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021128 | ||||||
chr19:3021144
|
C | G | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(197): Show | 212 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.295-1371G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021144 | ||||||
chr19:3021235
|
T | C | 1 | a0001c0001t0001g0221 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.295-1462A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021235 | ||||||
chr19:3021338
|
G | C | 17 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0225others(14): Show | 18 | HG00738.hp2 HG00741.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.295-1565C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021338 | ||||||
chr19:3021359
|
C | T | 1 | a0001c0002t0001g0244 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.295-1586G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021359 | ||||||
chr19:3021360
|
G | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(84): Show | 93 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.295-1587C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021360 | ||||||
chr19:3021436
|
T | A | 1 | a0001c0001t0001g0265 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.295-1663A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021436 | ||||||
chr19:3021534
|
A | G | 1 | a0001c0016t0001g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.295-1761T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021534 | ||||||
chr19:3021548
|
C | T | 1 | a0001c0001t0001g0055 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.295-1775G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021548 | ||||||
chr19:3021571
|
T | C | 1 | a0001c0001t0001g0328 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.295-1798A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021571 | ||||||
chr19:3021606
|
G | A | 3 | a0001c0001t0001g0069a0001c0002t0001g0204a0001c0024t0001g0073 | 3 | NA18961.hp1 NA19074.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.295-1833C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021606 | ||||||
chr19:3021652
|
G | A | 2 | a0001c0001t0001g0318a0001c0001t0001g0319 | 2 | NA18944.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.295-1879C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021652 | ||||||
chr19:3021771
|
C | T | 9 | a0001c0001t0001g0242a0001c0001t0003g0019a0001c0001t0003g0024others(6): Show | 9 | HG00738.hp1 HG01069.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.295-1998G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021771 | ||||||
chr19:3021798
|
G | C | 43 | a0001c0001t0001g0009a0001c0001t0001g0225a0001c0001t0001g0228others(40): Show | 45 | HG00280.hp1 HG00738.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.295-2025C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021798 | ||||||
chr19:3021835
|
A | T | 2 | a0001c0001t0002g0382a0001c0001t0002g0383 | 2 | HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.295-2062T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021835 | ||||||
chr19:3021926
|
T | C | 10 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(7): Show | 11 | HG01123.hp1 HG01243.hp2 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.295-2153A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021926 | ||||||
chr19:3021931
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.295-2158G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021931 | ||||||
chr19:3021968
|
T | C | 106 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0009others(103): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.295-2195A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021968 | ||||||
chr19:3021988
|
G | A | 1 | a0001c0001t0002g0370 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.295-2215C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021988 | ||||||
chr19:3022053
|
A | G | 46 | a0001c0001t0001g0009a0001c0001t0001g0225a0001c0001t0001g0228others(43): Show | 48 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.295-2280T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3022053 | ||||||
chr19:3022067
|
A | G | 62 | a0001c0001t0001g0009a0001c0001t0001g0053a0001c0001t0001g0074others(59): Show | 64 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.295-2294T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3022067 | ||||||
chr19:3022109
|
C | T | 17 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0054others(14): Show | 20 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.295-2336G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3022109 | ||||||
chr19:3022176
|
G | C | 19 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(16): Show | 20 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.295-2403C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3022176 | ||||||
chr19:3022288
|
G | A | 1 | a0001c0016t0001g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.295-2515C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3022288 | ||||||
chr19:3022349
|
A | AC | 11 | a0001c0001t0001g0046a0001c0001t0001g0101a0001c0001t0001g0103others(8): Show | 11 | HG00621.hp2 HG00741.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.295-2577dupG | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3022349 | ||||||
chr19:3022356
|
C | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(99): Show | 109 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.295-2583G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3022356 | ||||||
chr19:3022434
|
T | C | 115 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0009others(112): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.294+2586A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3022434 | ||||||
chr19:3022477
|
T | C | 127 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0012others(124): Show | 135 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.294+2543A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3022477 | ||||||
chr19:3022542
|
A | T | 21 | a0001c0001t0001g0050a0001c0001t0001g0100a0001c0001t0001g0247others(18): Show | 22 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.294+2478T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3022542 | ||||||
chr19:3022738
|
G | A | 1 | a0001c0002t0001g0244 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.294+2282C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3022738 | ||||||
chr19:3022987
|
G | C | 8 | a0001c0001t0001g0320a0001c0001t0001g0349a0001c0001t0002g0321others(5): Show | 8 | HG02055.hp1 HG02559.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.294+2033C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3022987 | ||||||
chr19:3023054
|
A | ATCT | 33 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0030others(30): Show | 35 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.294+1963_294+1965d others(5): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023054 | ||||||
chr19:3023057
|
T | TTC | 39 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0230others(36): Show | 41 | HG00639.hp2 HG00738.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.294+1962_294+1963i others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023057 | ||||||
chr19:3023059
|
T | C | 124 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(121): Show | 132 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.294+1961A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023059 | ||||||
chr19:3023099
|
G | A | 3 | a0001c0006t0001g0377a0001c0006t0002g0239a0001c0006t0002g0368 | 3 | HG02647.hp1 HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.294+1921C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023099 | ||||||
chr19:3023120
|
A | T | 131 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(128): Show | 138 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.294+1900T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023120 | ||||||
chr19:3023145
|
C | T | 7 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.294+1875G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023145 | ||||||
chr19:3023146
|
C | A | 1 | a0001c0002t0001g0253 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.294+1874G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023146 | ||||||
chr19:3023147
|
C | G | 17 | a0001c0001t0001g0228a0001c0001t0001g0354a0001c0001t0001g0355others(14): Show | 17 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.294+1873G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023147 | ||||||
chr19:3023273
|
T | C | 1 | a0001c0001t0001g0284 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.294+1747A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023273 | ||||||
chr19:3023276
|
C | A | 5 | a0001c0001t0004g0001a0001c0001t0004g0016a0001c0001t0004g0017others(2): Show | 7 | HG01891.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.294+1744G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023276 | ||||||
chr19:3023276
|
C | T | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(156): Show | 168 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.294+1744G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023276 | ||||||
chr19:3023370
|
G | A | 1 | a0001c0006t0002g0239 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.294+1650C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023370 | ||||||
chr19:3023378
|
C | T | 1 | a0001c0002t0001g0037 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.294+1642G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023378 | ||||||
chr19:3023537
|
T | C | 1 | a0001c0002t0001g0371 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.294+1483A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023537 | ||||||
chr19:3023552
|
A | G | 134 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(131): Show | 143 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.294+1468T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023552 | ||||||
chr19:3023566
|
C | T | 17 | a0001c0001t0001g0228a0001c0001t0001g0354a0001c0001t0001g0355others(14): Show | 17 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.294+1454G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023566 | ||||||
chr19:3023672
|
T | C | 118 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(115): Show | 125 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.294+1348A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023672 | ||||||
chr19:3023683
|
G | A | 2 | a0001c0001t0001g0091a0001c0001t0001g0208 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.294+1337C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023683 | ||||||
chr19:3023690
|
C | T | 8 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0002t0001g0092others(5): Show | 8 | HG02293.hp2 NA18944.hp2 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.294+1330G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023690 | ||||||
chr19:3023753
|
G | A | 132 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(129): Show | 139 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.294+1267C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023753 | ||||||
chr19:3023812
|
C | A | 132 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(129): Show | 139 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.294+1208G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023812 | ||||||
chr19:3023863
|
G | A | 115 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(112): Show | 122 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.294+1157C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023863 | ||||||
chr19:3023873
|
CAG | C | 16 | a0001c0001t0001g0242a0001c0001t0003g0019a0001c0001t0003g0024others(13): Show | 18 | HG00738.hp1 HG01069.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.294+1145_294+1146d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023873 | ||||||
chr19:3023888
|
T | TCA | 62 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0030others(59): Show | 63 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.294+1130_294+1131d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023888 | ||||||
chr19:3023888
|
T | TCACA | 2 | a0001c0001t0001g0009a0001c0013t0001g0246 | 3 | HG00738.hp2 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.294+1128_294+1131d others(6): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023888 | ||||||
chr19:3023897
|
C | T | 1 | a0001c0002t0001g0244 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.294+1123G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023897 | ||||||
chr19:3023907
|
CAAAAGAA others(4): Show |
C | 100 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(97): Show | 106 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.294+1102_294+1112d others(13): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023907 | ||||||
chr19:3023908
|
AAAAGAAA others(2): Show |
A | 15 | a0001c0001t0001g0050a0001c0001t0001g0247a0001c0001t0001g0248others(12): Show | 16 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.294+1103_294+1111d others(11): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023908 | ||||||
chr19:3023918
|
A | C | 15 | a0001c0001t0001g0050a0001c0001t0001g0247a0001c0001t0001g0248others(12): Show | 16 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.294+1102T>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023918 | ||||||
chr19:3023994
|
C | CT | 47 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(44): Show | 51 | HG00323.hp1 HG00639.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.294+1025dupA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023994 | ||||||
chr19:3023994
|
CT | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(95): Show | 104 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.294+1025delA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023994 | ||||||
chr19:3023994
|
CTT | C | 7 | a0001c0001t0001g0233a0001c0001t0001g0276a0001c0001t0001g0323others(4): Show | 7 | HG01358.hp1 HG01975.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+1024_294+1025d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023994 | ||||||
chr19:3024020
|
G | C | 2 | a0001c0003t0001g0245a0001c0013t0001g0246 | 2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.294+1000C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024020 | ||||||
chr19:3024052
|
G | C | 2 | a0001c0003t0001g0245a0001c0013t0001g0246 | 2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.294+968C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024052 | ||||||
chr19:3024053
|
C | T | 132 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(129): Show | 139 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.294+967G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024053 | ||||||
chr19:3024079
|
C | T | 101 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(98): Show | 107 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.294+941G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024079 | ||||||
chr19:3024167
|
A | AT | 24 | a0001c0001t0001g0242a0001c0001t0003g0019a0001c0001t0003g0024others(21): Show | 26 | HG00738.hp1 HG01069.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.294+852dupA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024167 | ||||||
chr19:3024315
|
T | C | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(183): Show | 197 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.294+705A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024315 | ||||||
chr19:3024382
|
C | A | 3 | a0001c0001t0001g0216a0001c0002t0001g0215a0001c0002t0001g0217 | 3 | HG02257.hp2 HG03453.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.294+638G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024382 | ||||||
chr19:3024437
|
A | G | 180 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(177): Show | 191 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.294+583T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024437 | ||||||
chr19:3024456
|
C | T | 6 | a0001c0001t0001g0365a0001c0002t0001g0374a0001c0005t0002g0364others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+564G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024456 | ||||||
chr19:3024546
|
T | C | 5 | a0001c0002t0001g0282a0001c0002t0001g0330a0001c0002t0001g0331others(2): Show | 5 | HG01975.hp1 HG01978.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.294+474A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024546 | ||||||
chr19:3024599
|
G | A | 21 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0030others(18): Show | 23 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.294+421C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024599 | ||||||
chr19:3024626
|
G | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(88): Show | 97 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.294+394C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024626 | ||||||
chr19:3024665
|
C | CA | 3 | a0001c0006t0001g0377a0001c0006t0002g0239a0001c0006t0002g0368 | 3 | HG02647.hp1 HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.294+354_294+355ins others(1): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024665 | ||||||
chr19:3024751
|
G | A | 1 | a0001c0016t0001g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.294+269C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024751 | ||||||
chr19:3024876
|
G | C | 21 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0030others(18): Show | 23 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.294+144C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024876 | ||||||
chr19:3024905
|
C | T | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG01358.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.294+115G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024905 | ||||||
chr19:3024954
|
G | A | 1 | a0001c0006t0002g0368 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.294+66C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024954 | ||||||
chr19:3024979
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.294+41C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024979 | ||||||
chr19:3025191
|
A | G | 9 | a0001c0001t0001g0365a0001c0002t0001g0366a0001c0002t0001g0374others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.232-109T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025191 | ||||||
chr19:3025269
|
T | A | 2 | a0001c0001t0001g0226a0001c0002t0001g0218 | 2 | NA19012.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.232-187A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025269 | ||||||
chr19:3025369
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.232-287C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025369 | ||||||
chr19:3025382
|
GGCAGACG others(20): Show |
G | 2 | a0001c0001t0002g0370a0001c0008t0001g0369 | 2 | HG01891.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.232-327_232-301del others(27): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025382 | ||||||
chr19:3025434
|
C | T | 1 | a0001c0002t0001g0244 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.232-352G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025434 | ||||||
chr19:3025481
|
G | T | 11 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0357others(8): Show | 11 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.232-399C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025481 | ||||||
chr19:3025659
|
C | T | 22 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0030others(19): Show | 24 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.232-577G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025659 | ||||||
chr19:3025705
|
G | C | 16 | a0001c0001t0001g0015a0001c0001t0001g0284a0001c0001t0001g0334others(13): Show | 17 | HG00558.hp1 HG01934.hp1 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.232-623C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025705 | ||||||
chr19:3025707
|
A | G | 49 | a0001c0001t0001g0029a0001c0001t0001g0050a0001c0001t0001g0242others(46): Show | 52 | HG00642.hp2 HG00738.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.232-625T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025707 | ||||||
chr19:3025806
|
G | A | 2 | a0001c0003t0001g0245a0001c0013t0001g0246 | 2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.232-724C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025806 | ||||||
chr19:3025817
|
A | AG | 49 | a0001c0001t0001g0029a0001c0001t0001g0050a0001c0001t0001g0242others(46): Show | 52 | HG00642.hp2 HG00738.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.232-736dupC | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025817 | ||||||
chr19:3025823
|
G | T | 1 | a0001c0016t0001g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.232-741C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025823 | ||||||
chr19:3025902
|
C | A | 7 | a0001c0001t0001g0365a0001c0002t0001g0366a0001c0002t0001g0374others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.232-820G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025902 | ||||||
chr19:3025920
|
G | T | 1 | a0001c0002t0001g0260 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.232-838C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025920 | ||||||
chr19:3025997
|
C | A | 1 | a0001c0001t0001g0220 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.232-915G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025997 | ||||||
chr19:3025998
|
A | C | 1 | a0001c0001t0001g0220 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.232-916T>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025998 | ||||||
chr19:3026010
|
T | C | 12 | a0001c0001t0001g0228a0001c0001t0001g0354a0001c0001t0001g0355others(9): Show | 12 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.232-928A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026010 | ||||||
chr19:3026065
|
T | G | 1 | a0001c0001t0001g0011 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.232-983A>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026065 | ||||||
chr19:3026104
|
C | T | 7 | a0001c0001t0001g0365a0001c0002t0001g0366a0001c0002t0001g0374others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.232-1022G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026104 | ||||||
chr19:3026228
|
C | A | 13 | a0001c0001t0001g0050a0001c0001t0001g0247a0001c0001t0001g0248others(10): Show | 14 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.232-1146G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026228 | ||||||
chr19:3026281
|
T | C | 10 | a0001c0001t0001g0029a0001c0001t0001g0379a0001c0001t0001g0381others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.232-1199A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026281 | ||||||
chr19:3026363
|
G | A | 1 | a0001c0002t0001g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.232-1281C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026363 | ||||||
chr19:3026401
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.232-1319A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026401 | ||||||
chr19:3026403
|
A | G | 52 | a0001c0001t0001g0029a0001c0001t0001g0050a0001c0001t0001g0242others(49): Show | 55 | HG00642.hp2 HG00738.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.232-1321T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026403 | ||||||
chr19:3026452
|
AT | A | 9 | a0001c0001t0001g0357a0001c0001t0001g0358a0001c0001t0001g0359others(6): Show | 9 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.232-1371delA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026452 | ||||||
chr19:3026454
|
T | TAA | 5 | a0001c0001t0001g0029a0001c0001t0001g0379a0001c0001t0002g0370others(2): Show | 5 | HG01891.hp1 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.232-1373_232-1372i others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026454 | ||||||
chr19:3026454
|
TTA | T | 3 | a0001c0001t0001g0228a0001c0001t0001g0354a0001c0001t0001g0355 | 3 | HG00280.hp1 HG01168.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.231+1373_232-1373d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026454 | ||||||
chr19:3026455
|
T | A | 11 | a0001c0001t0001g0029a0001c0001t0001g0267a0001c0001t0001g0379others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.232-1373A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026455 | ||||||
chr19:3026455
|
T | TA | 12 | a0001c0001t0001g0050a0001c0001t0001g0220a0001c0001t0001g0221others(9): Show | 12 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.231+1373dupT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026455 | ||||||
chr19:3026455
|
TA | T | 56 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0042others(53): Show | 59 | HG00099.hp1 HG00609.hp1 HG01074.hp1 others(56): Show |
intron_variant | MODIFIER | c.231+1373delT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026455 | ||||||
chr19:3026455
|
TAA | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0012others(79): Show | 89 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.231+1372_231+1373d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026455 | ||||||
chr19:3026455
|
TAAA | T | 15 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(12): Show | 15 | HG00544.hp1 HG01975.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.231+1371_231+1373d others(5): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026455 | ||||||
chr19:3026456
|
A | T | 1 | a0001c0002t0001g0051 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.231+1373T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026456 | ||||||
chr19:3026481
|
C | T | 1 | a0001c0016t0001g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.231+1348G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026481 | ||||||
chr19:3026570
|
G | GCAGAACC others(13): Show |
5 | a0001c0001t0001g0365a0001c0002t0001g0366a0001c0002t0001g0374others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+1239_231+1258d others(22): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026570 | ||||||
chr19:3026586
|
T | TATCTCAG others(33): Show |
9 | a0001c0001t0001g0029a0001c0001t0001g0381a0001c0001t0002g0382others(6): Show | 9 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.231+1242_231+1243i others(42): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026586 | ||||||
chr19:3026586
|
T | TATCTCAG others(53): Show |
4 | a0001c0001t0001g0379a0001c0001t0002g0370a0001c0008t0001g0369others(1): Show | 4 | HG01891.hp1 HG02109.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+1242_231+1243i others(62): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026586 | ||||||
chr19:3026592
|
T | A | 13 | a0001c0001t0001g0029a0001c0001t0001g0379a0001c0001t0001g0381others(10): Show | 13 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.231+1237A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026592 | ||||||
chr19:3026592
|
TGAACCCT others(13): Show |
T | 110 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(107): Show | 116 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.231+1217_231+1236d others(22): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026592 | ||||||
chr19:3026596
|
C | T | 1 | a0001c0005t0002g0364 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.231+1233G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026596 | ||||||
chr19:3026606
|
A | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0379a0001c0001t0002g0370others(2): Show | 5 | HG01891.hp1 HG02109.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+1223T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026606 | ||||||
chr19:3026650
|
G | A | 10 | a0001c0001t0001g0029a0001c0001t0001g0379a0001c0001t0001g0381others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.231+1179C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026650 | ||||||
chr19:3026812
|
G | A | 13 | a0001c0001t0001g0029a0001c0001t0001g0379a0001c0001t0001g0381others(10): Show | 13 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.231+1017C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026812 | ||||||
chr19:3026868
|
C | T | 3 | a0001c0003t0002g0268a0001c0003t0002g0269a0001c0003t0002g0270 | 3 | HG02258.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.231+961G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026868 | ||||||
chr19:3026869
|
T | C | 184 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(181): Show | 195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.231+960A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026869 | ||||||
chr19:3026921
|
C | T | 1 | a0001c0002t0001g0010 | 2 | NA18947.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.231+908G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026921 | ||||||
chr19:3026926
|
GACCTTGA others(93): Show |
G | 6 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0046others(3): Show | 7 | HG01256.hp2 HG01361.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.231+803_231+902del others(100): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026926 | ||||||
chr19:3026987
|
A | G | 34 | a0001c0001t0001g0050a0001c0001t0001g0242a0001c0001t0001g0247others(31): Show | 37 | HG00642.hp2 HG00738.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.231+842T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026987 | ||||||
chr19:3027034
|
G | A | 1 | a0001c0001t0002g0229 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.231+795C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3027034 | ||||||
chr19:3027124
|
T | C | 17 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0030others(14): Show | 19 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.231+705A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3027124 | ||||||
chr19:3027190
|
T | C | 1 | a0001c0001t0001g0381 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.231+639A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3027190 | ||||||
chr19:3027234
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG02080.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.231+595T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3027234 | ||||||
chr19:3027345
|
A | T | 14 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(11): Show | 15 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.231+484T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3027345 | ||||||
chr19:3027560
|
C | T | 19 | a0001c0001t0001g0242a0001c0001t0003g0019a0001c0001t0003g0024others(16): Show | 21 | HG00738.hp1 HG01069.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.231+269G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3027560 | ||||||
chr19:3027760
|
C | A | 1 | a0001c0003t0001g0372 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.231+69G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3027760 | ||||||
chr19:3028011
|
G | A | 1 | a0001c0002t0001g0373 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.187-138C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 3/19 | chr19 | 3028011 | ||||||
chr19:3028109
|
G | A | 2 | a0001c0002t0001g0374a0001c0018t0001g0375 | 2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.186+210C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 3/19 | chr19 | 3028109 | ||||||
chr19:3028199
|
G | C | 1 | a0001c0001t0001g0230 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.186+120C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 3/19 | chr19 | 3028199 | ||||||
chr19:3028213
|
C | T | 9 | a0001c0001t0001g0379a0001c0001t0001g0381a0001c0001t0002g0382others(6): Show | 9 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.186+106G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 3/19 | chr19 | 3028213 | ||||||
chr19:3028225
|
G | A | 1 | a0001c0001t0001g0376 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.186+94C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 3/19 | chr19 | 3028225 | ||||||
chr19:3028254
|
G | A | 1 | a0001c0006t0001g0377 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.186+65C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 3/19 | chr19 | 3028254 | ||||||
chr19:3028403
|
A | G | 1 | a0001c0001t0002g0238 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.123-21T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 2/19 | chr19 | 3028403 | ||||||
chr19:3028465
|
C | A | 2 | a0001c0001t0001g0379a0001c0008t0002g0378 | 2 | HG02109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.123-83G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 2/19 | chr19 | 3028465 | ||||||
chr19:3028574
|
C | T | 6 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(3): Show | 6 | HG01358.hp1 HG02602.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+132G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 2/19 | chr19 | 3028574 | ||||||
chr19:3028604
|
C | A | 3 | a0001c0001t0001g0381a0001c0010t0001g0231a0001c0020t0001g0380 | 3 | HG02145.hp2 HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.122+102G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 2/19 | chr19 | 3028604 | ||||||
chr19:3028821
|
G | A | 2 | a0001c0001t0002g0382a0001c0001t0002g0383 | 2 | HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.25-18C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 1/19 | chr19 | 3028821 | ||||||
chr19:3028873
|
G | C | 163 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(160): Show | 171 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(168): Show |
splice_region_variant&intron_variant | LOW | c.24+8C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 1/19 | chr19 | 3028873 | ||||||
chr19:3028875
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG02896.hp1 | splice_region_variant&intron_variant | LOW | c.24+6T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 1/19 | chr19 | 3028875 |