geneid | 158248 |
---|---|
ensemblid | ENSG00000167094.16 |
hgncid | 26536 |
symbol | TTC16 |
name | tetratricopeptide repeat domain 16 |
refseq_nuc | NM_144965.3 |
refseq_prot | NP_659402.1 |
ensembl_nuc | ENST00000373289.4 |
ensembl_prot | ENSP00000362386.3 |
mane_status | MANE Select |
chr | chr9 |
start | 127716079 |
end | 127731590 |
strand | + |
ver | v1.2 |
region | chr9:127716079-127731590 |
region5000 | chr9:127711079-127736590 |
regionname0 | TTC16_chr9_127716079_127731590 |
regionname5000 | TTC16_chr9_127711079_127736590 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 873 | 201 | 57 | 39 | 76 | 5 | 23 | 52 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0002 | 0/1 | 873 | 77 | 7 | 20 | 25 | 5 | 19 | 17 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0003 | 0/0 | 873 | 9 | 7 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0004 | 0/0 | 873 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0005 | 0/0 | 873 | 7 | 0 | 6 | 1 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0006 | 0/0 | 873 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0007 | 0/0 | 873 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0008 | 0/0 | 873 | 3 | 0 | 0 | 3 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0009 | 0/0 | 873 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0010 | 0/0 | 873 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0011 | 0/0 | 143 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0012 | 0/0 | 873 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0013 | 0/0 | 873 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0014 | 0/0 | 873 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0015 | 0/0 | 873 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0016 | 0/0 | 873 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0017 | 0/0 | 873 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0018 | 0/0 | 873 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0019 | 0/0 | 873 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0020 | 0/0 | 873 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0021 | 0/0 | 873 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0022 | 0/0 | 873 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0023 | 0/0 | 873 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0024 | 0/0 | 873 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2622 | 122 | 17 | 28 | 59 | 4 | 13 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0002 | 0/0 | 2622 | 77 | 38 | 11 | 17 | 1 | 10 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0003 | 0/1 | 2622 | 72 | 3 | 20 | 24 | 5 | 19 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0004 | 0/0 | 2622 | 9 | 7 | 2 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0005 | 0/0 | 2622 | 9 | 9 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0006 | 0/0 | 2622 | 7 | 0 | 6 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0007 | 0/0 | 2622 | 5 | 5 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0008 | 0/0 | 2622 | 5 | 0 | 0 | 5 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0009 | 0/0 | 2622 | 3 | 0 | 0 | 3 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0010 | 0/0 | 2622 | 3 | 3 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0011 | 0/0 | 2622 | 2 | 0 | 2 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0012 | 0/0 | 2622 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0013 | 0/0 | 2622 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0014 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0015 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0016 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0017 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0018 | 0/0 | 2622 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0019 | 0/0 | 2622 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0020 | 0/0 | 2622 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0021 | 0/0 | 2622 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0022 | 0/0 | 2622 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0023 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0024 | 0/0 | 2622 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0025 | 0/0 | 2622 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0026 | 0/0 | 2611 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0027 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0028 | 0/0 | 2622 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
c0029 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 253 | 174 | 52 | 30 | 73 | 4 | 14 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
t0002 | 0/1 | 253 | 160 | 42 | 42 | 37 | 6 | 32 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/1 | 16 | 1 | 7 | 5 | 1 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0002 | 0/0 | 13 | 1 | 3 | 9 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0003 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0004 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0005 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0006 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0007 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0008 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0012 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0235 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2622 | 122 | 17 | 28 | 59 | 4 | 13 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0001c0002 | 0/0 | 2622 | 77 | 38 | 11 | 17 | 1 | 10 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0001c0013 | 0/0 | 2622 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0002c0003 | 0/1 | 2622 | 72 | 3 | 20 | 24 | 5 | 19 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0002c0010 | 0/0 | 2622 | 3 | 3 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0002c0023 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0002c0024 | 0/0 | 2622 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0003c0004 | 0/0 | 2622 | 9 | 7 | 2 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0004c0005 | 0/0 | 2622 | 9 | 9 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0005c0006 | 0/0 | 2622 | 7 | 0 | 6 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0006c0008 | 0/0 | 2622 | 5 | 0 | 0 | 5 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0007c0007 | 0/0 | 2622 | 5 | 5 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0008c0009 | 0/0 | 2622 | 3 | 0 | 0 | 3 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0009c0012 | 0/0 | 2622 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0010c0011 | 0/0 | 2622 | 2 | 0 | 2 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0011c0026 | 0/0 | 2611 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0012c0025 | 0/0 | 2622 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0013c0016 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0014c0017 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0015c0020 | 0/0 | 2622 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0016c0018 | 0/0 | 2622 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0017c0022 | 0/0 | 2622 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0018c0021 | 0/0 | 2622 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0019c0019 | 0/0 | 2622 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0020c0015 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0021c0014 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0022c0029 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0023c0028 | 0/0 | 2622 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0024c0027 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2874 | 122 | 17 | 28 | 59 | 4 | 13 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0001c0002t0001 | 0/0 | 2874 | 24 | 14 | 0 | 10 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0001c0002t0002 | 0/0 | 2874 | 53 | 24 | 11 | 7 | 1 | 10 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0001c0013t0001 | 0/0 | 2874 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0002c0003t0002 | 0/1 | 2874 | 72 | 3 | 20 | 24 | 5 | 19 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0002c0010t0002 | 0/0 | 2874 | 3 | 3 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0002c0023t0002 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0002c0024t0001 | 0/0 | 2874 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0003c0004t0002 | 0/0 | 2874 | 9 | 7 | 2 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0004c0005t0001 | 0/0 | 2874 | 9 | 9 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0005c0006t0002 | 0/0 | 2874 | 7 | 0 | 6 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0006c0008t0002 | 0/0 | 2874 | 5 | 0 | 0 | 5 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0007c0007t0001 | 0/0 | 2874 | 5 | 5 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0008c0009t0001 | 0/0 | 2874 | 3 | 0 | 0 | 3 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0009c0012t0001 | 0/0 | 2874 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0010c0011t0002 | 0/0 | 2874 | 2 | 0 | 2 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0011c0026t0002 | 0/0 | 2863 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0012c0025t0001 | 0/0 | 2874 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0013c0016t0001 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0014c0017t0001 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0015c0020t0002 | 0/0 | 2874 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0016c0018t0001 | 0/0 | 2874 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0017c0022t0002 | 0/0 | 2874 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0018c0021t0002 | 0/0 | 2874 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0019c0019t0002 | 0/0 | 2874 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0020c0015t0002 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0021c0014t0002 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0022c0029t0002 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0023c0028t0001 | 0/0 | 2874 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
a0024c0027t0001 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | copy fasta | chr9 | 127711079 | 127736590 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 12 | 0 | 3 | 9 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0235 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0008 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0002t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0013t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0001c0013t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0001 | 0/1 | 10 | 0 | 3 | 4 | 1 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0004 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0005 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0006 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0003t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0010t0002g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0010t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0010t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0023t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0002c0024t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0003c0004t0002g0007 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0003c0004t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0003c0004t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0003c0004t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0003c0004t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0003c0004t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0004c0005t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0004c0005t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0004c0005t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0004c0005t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0004c0005t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0004c0005t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0004c0005t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0005c0006t0002g0001 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0005c0006t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0005c0006t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0006c0008t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0006c0008t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0006c0008t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0006c0008t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0007c0007t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0007c0007t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0007c0007t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0007c0007t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0008c0009t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0008c0009t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0008c0009t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0009c0012t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0009c0012t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0010c0011t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0010c0011t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0011c0026t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0012c0025t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0013c0016t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0014c0017t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0015c0020t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0016c0018t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0017c0022t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0018c0021t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0019c0019t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0020c0015t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0021c0014t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0022c0029t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0023c0028t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
a0024c0027t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0245 | EUR | GBR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00099 | hp2 | a0002 | c0003 | t0002 | g0004 | EUR | GBR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00280 | hp1 | a0002 | c0003 | t0002 | g0001 | EUR | FIN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | FIN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0008 | EUR | FIN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00323 | hp2 | a0002 | c0003 | t0002 | g0124 | EUR | FIN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00423 | hp2 | a0002 | c0003 | t0002 | g0075 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00438 | hp1 | a0002 | c0003 | t0002 | g0043 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00438 | hp2 | a0008 | c0009 | t0001 | g0205 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00544 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00597 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00621 | hp1 | a0002 | c0003 | t0002 | g0006 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00642 | hp1 | a0010 | c0011 | t0002 | g0065 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00673 | hp2 | a0002 | c0003 | t0002 | g0040 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00735 | hp2 | a0002 | c0003 | t0002 | g0004 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00738 | hp1 | a0002 | c0003 | t0002 | g0054 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG00741 | hp2 | a0001 | c0002 | t0002 | g0135 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01069 | hp2 | a0003 | c0004 | t0002 | g0007 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01070 | hp2 | a0001 | c0002 | t0002 | g0136 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01074 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01099 | hp2 | a0003 | c0004 | t0002 | g0085 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01106 | hp1 | a0001 | c0002 | t0002 | g0032 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01106 | hp2 | a0002 | c0003 | t0002 | g0063 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01109 | hp1 | a0012 | c0025 | t0001 | g0249 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01109 | hp2 | a0023 | c0028 | t0001 | g0101 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01169 | hp2 | a0002 | c0003 | t0002 | g0001 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01175 | hp1 | a0002 | c0003 | t0002 | g0062 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01243 | hp2 | a0002 | c0003 | t0002 | g0004 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01256 | hp1 | a0001 | c0002 | t0002 | g0259 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01256 | hp2 | a0002 | c0003 | t0002 | g0001 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01257 | hp1 | a0002 | c0003 | t0002 | g0004 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01258 | hp1 | a0002 | c0003 | t0002 | g0004 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01258 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01261 | hp1 | a0002 | c0003 | t0002 | g0016 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01346 | hp2 | a0002 | c0003 | t0002 | g0064 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01358 | hp1 | a0002 | c0003 | t0002 | g0037 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01361 | hp1 | a0002 | c0003 | t0002 | g0006 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01361 | hp2 | a0005 | c0006 | t0002 | g0001 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01433 | hp1 | a0002 | c0003 | t0002 | g0061 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0133 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0246 | EUR | IBS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01515 | hp2 | a0002 | c0003 | t0002 | g0052 | EUR | IBS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01517 | hp1 | a0002 | c0003 | t0002 | g0060 | EUR | IBS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0229 | EUR | IBS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01884 | hp1 | a0007 | c0007 | t0001 | g0018 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0152 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01891 | hp1 | a0004 | c0005 | t0001 | g0020 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01891 | hp2 | a0001 | c0002 | t0002 | g0058 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01928 | hp1 | a0002 | c0003 | t0002 | g0045 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0153 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01943 | hp1 | a0015 | c0020 | t0002 | g0131 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01952 | hp1 | a0002 | c0003 | t0002 | g0067 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01975 | hp1 | a0002 | c0003 | t0002 | g0001 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01975 | hp2 | a0005 | c0006 | t0002 | g0001 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01978 | hp1 | a0002 | c0003 | t0002 | g0005 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01978 | hp2 | a0002 | c0003 | t0002 | g0050 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01981 | hp2 | a0005 | c0006 | t0002 | g0039 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01993 | hp1 | a0002 | c0003 | t0002 | g0005 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0156 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02015 | hp1 | a0008 | c0009 | t0001 | g0209 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02055 | hp1 | a0004 | c0005 | t0001 | g0102 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0250 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02080 | hp1 | a0001 | c0002 | t0002 | g0146 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02083 | hp1 | a0002 | c0003 | t0002 | g0009 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02132 | hp2 | a0008 | c0009 | t0001 | g0027 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02148 | hp1 | a0005 | c0006 | t0002 | g0042 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | CDX | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CDX | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0254 | EAS | CDX | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02165 | hp2 | a0002 | c0003 | t0002 | g0076 | EAS | CDX | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02258 | hp1 | a0001 | c0002 | t0002 | g0024 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0068 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02273 | hp1 | a0001 | c0002 | t0002 | g0157 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02280 | hp1 | a0001 | c0002 | t0002 | g0022 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02280 | hp2 | a0002 | c0010 | t0002 | g0001 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02293 | hp2 | a0010 | c0011 | t0002 | g0014 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0137 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02300 | hp2 | a0005 | c0006 | t0002 | g0001 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02451 | hp1 | a0003 | c0004 | t0002 | g0007 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02572 | hp1 | a0004 | c0005 | t0001 | g0098 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0122 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02602 | hp1 | a0002 | c0003 | t0002 | g0001 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02615 | hp2 | a0011 | c0026 | t0002 | g0086 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02622 | hp1 | a0001 | c0002 | t0002 | g0126 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02622 | hp2 | a0003 | c0004 | t0002 | g0083 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0113 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02647 | hp1 | a0001 | c0002 | t0002 | g0162 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0139 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02683 | hp2 | a0002 | c0003 | t0002 | g0080 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02698 | hp1 | a0002 | c0003 | t0002 | g0036 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0138 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02717 | hp1 | a0001 | c0002 | t0002 | g0132 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0112 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02723 | hp2 | a0009 | c0012 | t0001 | g0145 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0129 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02735 | hp2 | a0002 | c0003 | t0002 | g0014 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02809 | hp2 | a0014 | c0017 | t0001 | g0147 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02818 | hp2 | a0002 | c0003 | t0002 | g0123 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02895 | hp1 | a0002 | c0010 | t0002 | g0078 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0121 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0111 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02896 | hp2 | a0001 | c0002 | t0002 | g0134 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02922 | hp1 | a0002 | c0003 | t0002 | g0044 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02922 | hp2 | a0004 | c0005 | t0001 | g0100 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02965 | hp1 | a0003 | c0004 | t0002 | g0007 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02965 | hp2 | a0004 | c0005 | t0001 | g0019 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02976 | hp1 | a0007 | c0007 | t0001 | g0018 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03017 | hp1 | a0002 | c0003 | t0002 | g0046 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03017 | hp2 | a0002 | c0003 | t0002 | g0070 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03041 | hp1 | a0004 | c0005 | t0001 | g0019 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03041 | hp2 | a0002 | c0010 | t0002 | g0077 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03098 | hp1 | a0002 | c0023 | t0002 | g0088 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0107 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0114 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03130 | hp2 | a0001 | c0002 | t0002 | g0150 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03139 | hp1 | a0004 | c0005 | t0001 | g0020 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03139 | hp2 | a0001 | c0002 | t0002 | g0125 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03195 | hp2 | a0024 | c0027 | t0001 | g0103 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0161 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03225 | hp1 | a0001 | c0013 | t0001 | g0165 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03225 | hp2 | a0001 | c0002 | t0002 | g0108 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0118 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03239 | hp2 | a0002 | c0003 | t0002 | g0006 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0160 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03453 | hp2 | a0003 | c0004 | t0002 | g0084 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03486 | hp1 | a0007 | c0007 | t0001 | g0096 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03486 | hp2 | a0001 | c0002 | t0002 | g0021 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03491 | hp1 | a0002 | c0003 | t0002 | g0047 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03491 | hp2 | a0002 | c0003 | t0002 | g0013 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03492 | hp1 | a0002 | c0003 | t0002 | g0013 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03516 | hp1 | a0020 | c0015 | t0002 | g0163 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03516 | hp2 | a0009 | c0012 | t0001 | g0144 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03540 | hp1 | a0001 | c0002 | t0002 | g0158 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03540 | hp2 | a0001 | c0002 | t0002 | g0117 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0120 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03579 | hp2 | a0002 | c0003 | t0002 | g0115 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03654 | hp1 | a0017 | c0022 | t0002 | g0228 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03654 | hp2 | a0019 | c0019 | t0002 | g0127 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03669 | hp2 | a0002 | c0003 | t0002 | g0005 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03688 | hp1 | a0002 | c0003 | t0002 | g0015 | SAS | STU | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0130 | SAS | STU | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0155 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0109 | SAS | BEB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03831 | hp2 | a0002 | c0003 | t0002 | g0056 | SAS | BEB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03834 | hp2 | a0018 | c0021 | t0002 | g0023 | SAS | BEB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03927 | hp1 | a0001 | c0002 | t0002 | g0008 | SAS | BEB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03927 | hp2 | a0002 | c0003 | t0002 | g0079 | SAS | BEB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG04115 | hp1 | a0002 | c0003 | t0002 | g0006 | SAS | STU | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | STU | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG04184 | hp2 | a0002 | c0003 | t0002 | g0055 | SAS | BEB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG04199 | hp1 | a0002 | c0003 | t0002 | g0005 | SAS | STU | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | STU | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG04204 | hp1 | a0002 | c0003 | t0002 | g0035 | SAS | STU | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG04204 | hp2 | a0002 | c0003 | t0002 | g0034 | SAS | STU | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0119 | SAS | STU | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | STU | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18522 | hp1 | a0004 | c0005 | t0001 | g0099 | AFR | YRI | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0140 | AFR | YRI | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18612 | hp2 | a0006 | c0008 | t0002 | g0009 | EAS | CHB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18906 | hp1 | a0021 | c0014 | t0002 | g0128 | AFR | YRI | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18942 | hp2 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18943 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18952 | hp2 | a0002 | c0003 | t0002 | g0074 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18956 | hp2 | a0002 | c0003 | t0002 | g0087 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18963 | hp1 | a0002 | c0003 | t0002 | g0051 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18964 | hp2 | a0002 | c0003 | t0002 | g0203 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18966 | hp2 | a0002 | c0003 | t0002 | g0016 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18973 | hp1 | a0002 | c0003 | t0002 | g0053 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18978 | hp2 | a0002 | c0003 | t0002 | g0038 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18979 | hp1 | a0006 | c0008 | t0002 | g0041 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18982 | hp2 | a0002 | c0003 | t0002 | g0015 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18983 | hp2 | a0005 | c0006 | t0002 | g0001 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18984 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19004 | hp2 | a0002 | c0003 | t0002 | g0048 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19007 | hp2 | a0002 | c0003 | t0002 | g0049 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19012 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19030 | hp1 | a0003 | c0004 | t0002 | g0081 | AFR | LWK | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19030 | hp2 | a0001 | c0002 | t0002 | g0166 | AFR | LWK | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19043 | hp1 | a0001 | c0002 | t0002 | g0024 | AFR | LWK | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19043 | hp2 | a0001 | c0013 | t0001 | g0164 | AFR | LWK | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19054 | hp2 | a0002 | c0003 | t0002 | g0069 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19059 | hp1 | a0002 | c0024 | t0001 | g0033 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19060 | hp2 | a0006 | c0008 | t0002 | g0009 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19067 | hp1 | a0006 | c0008 | t0002 | g0071 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19075 | hp1 | a0006 | c0008 | t0002 | g0073 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19075 | hp2 | a0001 | c0002 | t0002 | g0143 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19077 | hp2 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19081 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19083 | hp2 | a0002 | c0003 | t0002 | g0059 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19084 | hp1 | a0002 | c0003 | t0002 | g0072 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19088 | hp2 | a0002 | c0003 | t0002 | g0066 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19240 | hp1 | a0001 | c0002 | t0002 | g0057 | AFR | YRI | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA19240 | hp2 | a0022 | c0029 | t0002 | g0094 | AFR | YRI | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ASW | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA20129 | hp2 | a0013 | c0016 | t0001 | g0002 | AFR | ASW | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0149 | SAS | GIH | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA20905 | hp2 | a0016 | c0018 | t0001 | g0193 | SAS | GIH | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG01123 | hp2 | a0005 | c0006 | t0002 | g0001 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0021 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02109 | hp2 | a0007 | c0007 | t0001 | g0104 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG02486 | hp2 | a0003 | c0004 | t0002 | g0082 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03471 | hp1 | a0004 | c0005 | t0001 | g0097 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG03471 | hp2 | a0001 | c0002 | t0002 | g0022 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG06807 | hp1 | a0007 | c0007 | t0001 | g0095 | AFR | USA | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0239 | AFR | USA | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | USA | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA20300 | hp2 | a0001 | c0002 | t0002 | g0151 | AFR | USA | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | LWK | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
NA21309 | hp2 | a0003 | c0004 | t0002 | g0007 | AFR | LWK | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
homoSapiens_chm13v2 | hp1 | a0002 | c0003 | t0002 | g0001 | REF | REF | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0235 | REF | REF | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:127716911
|
A | G | 4 | a0004a0022a0023others(1): Show | 12 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
missense_variant | MODERATE | c.86A>G | p.Lys29Arg | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 2/14 | 153/2874 | 86/2622 | 29/873 | chr9 | 127716911 | ||
chr9:127716931
|
T | G | 1 | a0021 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.106T>G | p.Phe36Val | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 2/14 | 173/2874 | 106/2622 | 36/873 | chr9 | 127716931 | ||
chr9:127717689
|
G | A | 1 | a0024 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.343G>A | p.Ala115Thr | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/14 | 410/2874 | 343/2622 | 115/873 | chr9 | 127717689 | ||
chr9:127717746
|
C | T | 1 | a0008 | 3 | HG00438.hp2 HG02015.hp1 HG02132.hp2 |
missense_variant | MODERATE | c.400C>T | p.Arg134Cys | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/14 | 467/2874 | 400/2622 | 134/873 | chr9 | 127717746 | ||
chr9:127720075
|
CAGGGACA others(6): Show |
C | 1 | a0011 | 1 | HG02615.hp2 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.427-2_437delAGGGAC others(7): Show |
p.Gly143fs | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 5/14 | 427/2622 | 143/873 | chr9 | 127720075 | |||
chr9:127720162
|
T | C | 1 | a0010 | 2 | HG00642.hp1 HG02293.hp2 |
missense_variant | MODERATE | c.511T>C | p.Cys171Arg | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 5/14 | 578/2874 | 511/2622 | 171/873 | chr9 | 127720162 | ||
chr9:127723169
|
G | C | 1 | a0011 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.708G>C | p.Lys236Asn | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/14 | 775/2874 | 708/2622 | 236/873 | chr9 | 127723169 | ||
chr9:127723197
|
A | C | 1 | a0003 | 9 | HG01069.hp2 HG01099.hp2 HG02451.hp1 others(6): Show |
missense_variant | MODERATE | c.736A>C | p.Lys246Gln | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/14 | 803/2874 | 736/2622 | 246/873 | chr9 | 127723197 | ||
chr9:127724190
|
G | T | 1 | a0012 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.943G>T | p.Val315Leu | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 8/14 | 1010/2874 | 943/2622 | 315/873 | chr9 | 127724190 | ||
chr9:127724196
|
G | A | 1 | a0009 | 2 | HG02723.hp2 HG03516.hp2 |
missense_variant | MODERATE | c.949G>A | p.Glu317Lys | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 8/14 | 1016/2874 | 949/2622 | 317/873 | chr9 | 127724196 | ||
chr9:127724854
|
G | A | 4 | a0004a0020a0023others(1): Show | 12 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
missense_variant | MODERATE | c.1216G>A | p.Gly406Ser | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/14 | 1283/2874 | 1216/2622 | 406/873 | chr9 | 127724854 | ||
chr9:127724878
|
T | G | 1 | a0007 | 5 | HG01884.hp1 HG02109.hp2 HG02976.hp1 others(2): Show |
missense_variant | MODERATE | c.1240T>G | p.Phe414Val | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/14 | 1307/2874 | 1240/2622 | 414/873 | chr9 | 127724878 | ||
chr9:127726328
|
G | A | 1 | a0005 | 7 | HG01123.hp2 HG01361.hp2 HG01975.hp2 others(4): Show |
missense_variant | MODERATE | c.1349G>A | p.Arg450Gln | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/14 | 1416/2874 | 1349/2622 | 450/873 | chr9 | 127726328 | ||
chr9:127726352
|
G | C | 1 | a0013 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.1373G>C | p.Gly458Ala | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/14 | 1440/2874 | 1373/2622 | 458/873 | chr9 | 127726352 | ||
chr9:127727281
|
G | C | 1 | a0014 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1580G>C | p.Arg527Pro | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/14 | 1647/2874 | 1580/2622 | 527/873 | chr9 | 127727281 | ||
chr9:127727358
|
G | A | 1 | a0019 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.1657G>A | p.Glu553Lys | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/14 | 1724/2874 | 1657/2622 | 553/873 | chr9 | 127727358 | ||
chr9:127727382
|
A | T | 1 | a0023 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.1681A>T | p.Ile561Phe | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/14 | 1748/2874 | 1681/2622 | 561/873 | chr9 | 127727382 | ||
chr9:127727464
|
A | G | 6 | a0002a0003a0005others(3): Show | 101 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(98): Show |
missense_variant&splice_region_variant | MODERATE | c.1763A>G | p.Glu588Gly | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/14 | 1830/2874 | 1763/2622 | 588/873 | chr9 | 127727464 | ||
chr9:127730725
|
T | G | 1 | a0006 | 5 | NA18612.hp2 NA18979.hp1 NA19060.hp2 others(2): Show |
missense_variant | MODERATE | c.1942T>G | p.Ser648Ala | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 14/14 | 2009/2874 | 1942/2622 | 648/873 | chr9 | 127730725 | ||
chr9:127730861
|
G | A | 1 | a0015 | 1 | HG01943.hp1 | missense_variant | MODERATE | c.2078G>A | p.Arg693Gln | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 14/14 | 2145/2874 | 2078/2622 | 693/873 | chr9 | 127730861 | ||
chr9:127731182
|
G | A | 1 | a0016 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.2399G>A | p.Arg800Gln | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 14/14 | 2466/2874 | 2399/2622 | 800/873 | chr9 | 127731182 | ||
chr9:127731209
|
A | G | 1 | a0017 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.2426A>G | p.Tyr809Cys | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 14/14 | 2493/2874 | 2426/2622 | 809/873 | chr9 | 127731209 | ||
chr9:127731348
|
C | A | 1 | a0018 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.2565C>A | p.Ser855Arg | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 14/14 | 2632/2874 | 2565/2622 | 855/873 | chr9 | 127731348 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:127716954
|
A | G | 1 | a0002c0010 | 3 | HG02280.hp2 HG02895.hp1 HG03041.hp2 |
synonymous_variant | LOW | c.129A>G | p.Gln43Gln | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 2/14 | 196/2874 | 129/2622 | 43/873 | chr9 | 127716954 | ||
chr9:127727279
|
A | G | 19 | a0001c0002a0001c0013a0002c0003others(16): Show | 189 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
synonymous_variant | LOW | c.1578A>G | p.Lys526Lys | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/14 | 1645/2874 | 1578/2622 | 526/873 | chr9 | 127727279 | ||
chr9:127729589
|
A | G | 1 | a0001c0013 | 2 | HG03225.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.1773A>G | p.Lys591Lys | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/14 | 1840/2874 | 1773/2622 | 591/873 | chr9 | 127729589 | ||
chr9:127731192
|
C | A | 1 | a0002c0023 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.2409C>A | p.Thr803Thr | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 14/14 | 2476/2874 | 2409/2622 | 803/873 | chr9 | 127731192 | ||
chr9:127731234
|
A | G | 19 | a0001c0002a0001c0013a0002c0003others(16): Show | 189 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
synonymous_variant | LOW | c.2451A>G | p.Lys817Lys | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 14/14 | 2518/2874 | 2451/2622 | 817/873 | chr9 | 127731234 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:127731445
|
C | T | 16 | a0001c0002t0002a0002c0003t0002a0002c0010t0002others(13): Show | 160 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*40C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 14/14 | 40 | chr9 | 127731445 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:127716191
|
AAGGCAGA others(51): Show |
A | 1 | a0001c0002t0002g0259 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.18+29_18+86delAGGC others(54): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 1/13 | chr9 | 127716191 | ||||||
chr9:127716240
|
T | A | 1 | a0001c0002t0002g0032 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.18+77T>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 1/13 | chr9 | 127716240 | ||||||
chr9:127716246
|
C | T | 9 | a0001c0002t0001g0031a0001c0002t0001g0251a0001c0002t0001g0252others(6): Show | 10 | HG02135.hp1 HG02155.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.18+83C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 1/13 | chr9 | 127716246 | ||||||
chr9:127716374
|
G | A | 70 | a0001c0002t0002g0057a0001c0002t0002g0058a0001c0002t0002g0068others(67): Show | 100 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.18+211G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 1/13 | chr9 | 127716374 | ||||||
chr9:127716580
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | NA18956.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.19-264G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 1/13 | chr9 | 127716580 | ||||||
chr9:127717080
|
C | T | 1 | a0001c0002t0001g0250 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.191+64C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 2/13 | chr9 | 127717080 | ||||||
chr9:127717139
|
T | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0091a0001c0001t0001g0092 | 4 | HG01123.hp1 HG01346.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.191+123T>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 2/13 | chr9 | 127717139 | ||||||
chr9:127717168
|
C | T | 1 | a0002c0023t0002g0088 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.191+152C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 2/13 | chr9 | 127717168 | ||||||
chr9:127717209
|
T | C | 1 | a0002c0024t0001g0033 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.192-125T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 2/13 | chr9 | 127717209 | ||||||
chr9:127717229
|
T | C | 9 | a0001c0002t0001g0031a0001c0002t0001g0251a0001c0002t0001g0252others(6): Show | 10 | HG02135.hp1 HG02155.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.192-105T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 2/13 | chr9 | 127717229 | ||||||
chr9:127717299
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.192-35G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 2/13 | chr9 | 127717299 | ||||||
chr9:127717500
|
C | T | 1 | a0012c0025t0001g0249 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.282+76C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 3/13 | chr9 | 127717500 | ||||||
chr9:127717534
|
T | C | 1 | a0022c0029t0002g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.283-95T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 3/13 | chr9 | 127717534 | ||||||
chr9:127717602
|
T | C | 24 | a0001c0002t0001g0031a0001c0002t0001g0251a0001c0002t0001g0252others(21): Show | 28 | HG01109.hp1 HG01109.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.283-27T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 3/13 | chr9 | 127717602 | ||||||
chr9:127717961
|
A | G | 9 | a0001c0002t0001g0031a0001c0002t0001g0251a0001c0002t0001g0252others(6): Show | 10 | HG02135.hp1 HG02155.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.426+189A>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127717961 | ||||||
chr9:127717969
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.426+197T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127717969 | ||||||
chr9:127718043
|
A | C | 10 | a0001c0001t0001g0012a0001c0001t0001g0240a0001c0001t0001g0241others(7): Show | 12 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.426+271A>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127718043 | ||||||
chr9:127718087
|
T | TTTA | 14 | a0004c0005t0001g0019a0004c0005t0001g0020a0004c0005t0001g0097others(11): Show | 17 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.426+330_426+332dup others(3): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr9 | 127718087 | |||||
chr9:127718105
|
T | A | 1 | a0001c0001t0001g0106 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.426+333T>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127718105 | ||||||
chr9:127718156
|
C | T | 15 | a0004c0005t0001g0019a0004c0005t0001g0020a0004c0005t0001g0097others(12): Show | 18 | HG01109.hp1 HG01109.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.426+384C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127718156 | ||||||
chr9:127718739
|
G | A | 4 | a0002c0003t0002g0005a0002c0003t0002g0034a0002c0003t0002g0035others(1): Show | 7 | HG01978.hp1 HG01993.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.426+967G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127718739 | ||||||
chr9:127718864
|
T | G | 1 | a0002c0024t0001g0033 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.426+1092T>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127718864 | ||||||
chr9:127718867
|
C | T | 1 | a0001c0002t0001g0239 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.426+1095C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127718867 | ||||||
chr9:127719083
|
T | C | 167 | a0001c0001t0001g0026a0001c0001t0001g0116a0001c0001t0001g0148others(164): Show | 211 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.427-995T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127719083 | ||||||
chr9:127719123
|
A | T | 1 | a0001c0002t0002g0166 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.427-955A>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127719123 | ||||||
chr9:127719210
|
C | CA | 40 | a0001c0001t0001g0027a0001c0001t0001g0105a0001c0001t0001g0167others(37): Show | 45 | HG00673.hp2 HG01106.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.427-853dupA | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr9 | 127719210 | |||||
chr9:127719235
|
TA | T | 3 | a0001c0001t0001g0238a0002c0003t0002g0087a0002c0024t0001g0033 | 3 | NA18956.hp2 NA18984.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.427-838delA | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr9 | 127719235 | |||||
chr9:127719243
|
A | C | 1 | a0001c0001t0001g0238 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.427-835A>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127719243 | ||||||
chr9:127719291
|
ATGTCCTG others(26): Show |
A | 1 | a0005c0006t0002g0042 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.427-786_427-754del others(33): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127719291 | ||||||
chr9:127719339
|
C | A | 1 | a0002c0003t0002g0043 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.427-739C>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127719339 | ||||||
chr9:127719467
|
T | A | 6 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(3): Show | 6 | HG02630.hp2 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.427-611T>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127719467 | ||||||
chr9:127719557
|
A | T | 1 | a0001c0001t0001g0090 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.427-521A>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127719557 | ||||||
chr9:127719562
|
G | A | 1 | a0012c0025t0001g0249 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.427-516G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127719562 | ||||||
chr9:127719586
|
A | G | 15 | a0004c0005t0001g0019a0004c0005t0001g0020a0004c0005t0001g0097others(12): Show | 18 | HG01109.hp1 HG01109.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.427-492A>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127719586 | ||||||
chr9:127719876
|
C | T | 1 | a0024c0027t0001g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.427-202C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127719876 | ||||||
chr9:127719984
|
T | A | 1 | a0001c0001t0001g0238 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.427-94T>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127719984 | ||||||
chr9:127720223
|
C | T | 1 | a0003c0004t0002g0085 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.528-43C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 5/13 | chr9 | 127720223 | ||||||
chr9:127720598
|
A | T | 1 | a0001c0001t0001g0090 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.657+203A>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720598 | ||||||
chr9:127720629
|
C | A | 2 | a0022c0029t0002g0094a0024c0027t0001g0103 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.657+234C>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720629 | ||||||
chr9:127720636
|
G | A | 1 | a0002c0003t0002g0115 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.657+241G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720636 | ||||||
chr9:127720687
|
C | G | 168 | a0001c0001t0001g0026a0001c0001t0001g0148a0001c0001t0001g0154others(165): Show | 212 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.657+292C>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720687 | ||||||
chr9:127720705
|
T | C | 1 | a0001c0001t0001g0170 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.657+310T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720705 | ||||||
chr9:127720706
|
G | T | 1 | a0001c0001t0001g0170 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.657+311G>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720706 | ||||||
chr9:127720805
|
T | A | 1 | a0001c0002t0002g0117 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.657+410T>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720805 | ||||||
chr9:127720817
|
T | C | 1 | a0002c0003t0002g0044 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.657+422T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720817 | ||||||
chr9:127720818
|
C | T | 1 | a0002c0003t0002g0044 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.657+423C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720818 | ||||||
chr9:127720820
|
T | C | 1 | a0002c0003t0002g0044 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.657+425T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720820 | ||||||
chr9:127720828
|
G | C | 1 | a0001c0002t0002g0118 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.657+433G>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720828 | ||||||
chr9:127720831
|
T | TGCCCCGT others(514): Show |
1 | a0002c0003t0002g0044 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.657+436_657+437ins others(521): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720831 | ||||||
chr9:127720831
|
T | TTCCCCCC others(597): Show |
1 | a0001c0002t0002g0119 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(604): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(414): Show |
1 | a0001c0002t0002g0118 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(421): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(515): Show |
1 | a0011c0026t0002g0086 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(522): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(493): Show |
1 | a0001c0001t0001g0236 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(500): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(427): Show |
1 | a0001c0001t0001g0171 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(434): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(477): Show |
1 | a0001c0001t0001g0172 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(484): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(440): Show |
1 | a0001c0001t0001g0173 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(447): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(456): Show |
1 | a0001c0001t0001g0174 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(463): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(426): Show |
1 | a0001c0001t0001g0175 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(433): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(888): Show |
1 | a0001c0002t0001g0120 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(895): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(490): Show |
1 | a0001c0002t0001g0251 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(497): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(566): Show |
1 | a0002c0003t0002g0123 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(573): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(411): Show |
1 | a0001c0001t0001g0167 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(418): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(513): Show |
3 | a0001c0001t0001g0017a0001c0001t0001g0091a0001c0001t0001g0092 | 4 | HG01123.hp1 HG01346.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(520): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(491): Show |
1 | a0001c0001t0001g0237 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(498): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(454): Show |
1 | a0001c0001t0001g0176 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(461): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(426): Show |
1 | a0001c0001t0001g0240 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(433): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(405): Show |
1 | a0001c0001t0001g0090 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(412): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(390): Show |
2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG00642.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.657+440_657+441ins others(397): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(389): Show |
1 | a0001c0001t0001g0179 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(396): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(681): Show |
1 | a0001c0001t0001g0180 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(688): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(456): Show |
1 | a0001c0001t0001g0181 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(463): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(730): Show |
1 | a0001c0001t0001g0170 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(737): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(680): Show |
2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG00544.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.657+440_657+441ins others(687): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(695): Show |
1 | a0001c0001t0001g0168 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(702): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(679): Show |
1 | a0001c0001t0001g0184 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(686): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(441): Show |
1 | a0001c0001t0001g0185 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(448): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(469): Show |
2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | NA18943.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.657+440_657+441ins others(476): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(410): Show |
1 | a0001c0001t0001g0188 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(417): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(447): Show |
3 | a0001c0001t0001g0116a0001c0001t0001g0189a0001c0001t0001g0190 | 3 | HG02145.hp2 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.657+440_657+441ins others(454): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(426): Show |
1 | a0001c0001t0001g0191 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(433): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(426): Show |
1 | a0001c0001t0001g0241 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(433): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(410): Show |
1 | a0001c0001t0001g0192 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(417): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(775): Show |
1 | a0016c0018t0001g0193 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(782): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(448): Show |
1 | a0001c0001t0001g0194 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(455): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(625): Show |
1 | a0001c0001t0001g0195 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(632): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(425): Show |
33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(30): Show | 55 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(432): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(440): Show |
1 | a0001c0001t0001g0030 | 2 | HG01069.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.657+440_657+441ins others(447): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(455): Show |
2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | NA19004.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.657+440_657+441ins others(462): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(468): Show |
1 | a0001c0001t0001g0213 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(475): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(380): Show |
1 | a0001c0002t0002g0021 | 2 | HG02109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.657+440_657+441ins others(387): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(395): Show |
2 | a0001c0002t0002g0125a0001c0002t0002g0126 | 2 | HG02622.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.657+440_657+441ins others(402): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(403): Show |
1 | a0001c0001t0001g0214 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(410): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(403): Show |
5 | a0001c0001t0001g0089a0001c0001t0001g0215a0001c0001t0001g0216others(2): Show | 5 | HG00609.hp1 HG02717.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(410): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(381): Show |
1 | a0001c0002t0002g0166 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(388): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(708): Show |
2 | a0001c0002t0001g0110a0001c0002t0001g0111 | 2 | HG02818.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.657+440_657+441ins others(715): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(723): Show |
1 | a0001c0002t0001g0112 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(730): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(396): Show |
2 | a0001c0002t0001g0113a0001c0002t0001g0239 | 2 | HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.657+440_657+441ins others(403): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(424): Show |
6 | a0001c0001t0001g0093a0001c0001t0001g0169a0001c0001t0001g0219others(3): Show | 6 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(431): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(483): Show |
1 | a0001c0001t0001g0223 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(490): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(461): Show |
1 | a0001c0001t0001g0224 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(468): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(389): Show |
1 | a0001c0001t0001g0225 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(396): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(709): Show |
2 | a0007c0007t0001g0018a0007c0007t0001g0095 | 3 | HG01884.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.657+440_657+441ins others(716): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(425): Show |
1 | a0001c0001t0001g0226 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(432): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(424): Show |
1 | a0001c0001t0001g0227 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(431): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(723): Show |
1 | a0007c0007t0001g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(730): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(822): Show |
1 | a0007c0007t0001g0104 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(829): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(582): Show |
1 | a0019c0019t0002g0127 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(589): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(522): Show |
3 | a0002c0003t0002g0045a0002c0003t0002g0115a0021c0014t0002g0128 | 3 | HG01928.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.657+440_657+441ins others(529): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(666): Show |
1 | a0002c0003t0002g0046 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(673): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(492): Show |
1 | a0002c0024t0001g0033 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(499): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(381): Show |
1 | a0017c0022t0002g0228 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(388): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(419): Show |
1 | a0001c0001t0001g0229 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(426): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(418): Show |
1 | a0012c0025t0001g0249 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(425): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(396): Show |
1 | a0001c0001t0001g0105 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(403): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(360): Show |
1 | a0001c0002t0001g0258 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(367): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(338): Show |
1 | a0001c0001t0001g0230 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(345): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(359): Show |
1 | a0001c0002t0001g0252 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(366): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(410): Show |
4 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(1): Show | 4 | NA18947.hp1 NA18982.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(417): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(336): Show |
1 | a0001c0002t0001g0253 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(343): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(358): Show |
3 | a0001c0002t0001g0031a0001c0002t0001g0254a0001c0002t0001g0255 | 4 | HG02155.hp1 HG02165.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(365): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(512): Show |
2 | a0001c0002t0001g0256a0001c0002t0001g0257 | 2 | NA18957.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.657+440_657+441ins others(519): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(467): Show |
1 | a0002c0003t0002g0035 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(474): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(563): Show |
1 | a0002c0003t0002g0037 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(570): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(610): Show |
1 | a0001c0002t0002g0129 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(617): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(523): Show |
2 | a0002c0003t0002g0004a0002c0003t0002g0047 | 6 | HG00099.hp2 HG00735.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(530): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(603): Show |
1 | a0002c0003t0002g0048 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(610): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(611): Show |
1 | a0001c0002t0002g0130 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(618): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(499): Show |
1 | a0002c0003t0002g0049 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(506): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(588): Show |
1 | a0015c0020t0002g0131 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(595): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(644): Show |
1 | a0002c0003t0002g0050 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(651): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(503): Show |
1 | a0002c0003t0002g0051 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(510): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(907): Show |
1 | a0002c0003t0002g0052 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(914): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(501): Show |
1 | a0001c0002t0002g0132 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(508): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(582): Show |
1 | a0001c0002t0002g0108 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(589): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(552): Show |
2 | a0001c0002t0002g0022a0001c0002t0002g0133 | 3 | HG01496.hp2 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.657+440_657+441ins others(559): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(537): Show |
1 | a0001c0002t0002g0134 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(544): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(709): Show |
1 | a0002c0003t0002g0053 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(716): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(522): Show |
1 | a0002c0003t0002g0054 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(529): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(508): Show |
1 | a0002c0003t0002g0038 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(515): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(508): Show |
1 | a0002c0003t0002g0055 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(515): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(485): Show |
1 | a0002c0003t0002g0056 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(492): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(598): Show |
1 | a0001c0002t0002g0135 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(605): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(596): Show |
5 | a0001c0002t0002g0008a0001c0002t0002g0032a0001c0002t0002g0057others(2): Show | 8 | HG00323.hp1 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(603): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(582): Show |
1 | a0001c0002t0002g0058 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(589): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(510): Show |
1 | a0002c0003t0002g0059 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(517): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(908): Show |
1 | a0002c0003t0002g0060 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(915): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(909): Show |
1 | a0002c0003t0002g0061 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(916): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(540): Show |
1 | a0005c0006t0002g0042 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(547): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(507): Show |
18 | a0001c0002t0002g0023a0001c0002t0002g0068a0002c0003t0002g0001others(15): Show | 35 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(514): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(1071): Show |
1 | a0001c0002t0002g0138 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(1078): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(507): Show |
1 | a0002c0003t0002g0040 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(514): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(500): Show |
2 | a0001c0002t0002g0024a0022c0029t0002g0094 | 3 | HG02258.hp1 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.657+440_657+441ins others(507): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(511): Show |
1 | a0002c0003t0002g0069 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(518): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(507): Show |
1 | a0001c0002t0001g0250 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(514): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(536): Show |
1 | a0002c0003t0002g0070 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(543): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(507): Show |
1 | a0006c0008t0002g0071 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(514): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(507): Show |
4 | a0002c0003t0002g0009a0002c0003t0002g0043a0006c0008t0002g0009others(1): Show | 5 | HG00438.hp1 HG02083.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(514): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(506): Show |
1 | a0002c0003t0002g0072 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(513): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(507): Show |
1 | a0006c0008t0002g0073 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(514): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(506): Show |
1 | a0002c0003t0002g0016 | 2 | HG01261.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.657+440_657+441ins others(513): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(506): Show |
1 | a0002c0003t0002g0074 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(513): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(506): Show |
1 | a0002c0003t0002g0075 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(513): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(552): Show |
1 | a0001c0002t0002g0109 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(559): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(506): Show |
1 | a0002c0023t0002g0088 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(513): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(503): Show |
1 | a0002c0003t0002g0076 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(510): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(594): Show |
1 | a0001c0002t0002g0139 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(601): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(549): Show |
1 | a0002c0003t0002g0013 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.657+440_657+441ins others(556): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(507): Show |
1 | a0003c0004t0002g0085 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(514): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(324): Show |
4 | a0004c0005t0001g0019a0004c0005t0001g0097a0004c0005t0001g0098others(1): Show | 5 | HG02572.hp1 HG02965.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(331): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(302): Show |
1 | a0004c0005t0001g0100 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(309): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(223): Show |
2 | a0004c0005t0001g0020a0023c0028t0001g0101 | 3 | HG01109.hp2 HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.657+440_657+441ins others(230): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(464): Show |
3 | a0002c0003t0002g0005a0002c0003t0002g0034a0002c0003t0002g0036 | 6 | HG01978.hp1 HG01993.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(471): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(408): Show |
1 | a0001c0002t0002g0140 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(415): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(284): Show |
1 | a0024c0027t0001g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(291): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(397): Show |
1 | a0004c0005t0001g0102 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(404): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(479): Show |
1 | a0002c0010t0002g0077 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(486): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(475): Show |
1 | a0002c0010t0002g0078 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(482): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(535): Show |
1 | a0001c0002t0002g0141 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(542): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(535): Show |
1 | a0001c0002t0002g0142 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(542): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(534): Show |
2 | a0001c0002t0002g0025a0001c0002t0002g0143 | 3 | NA18980.hp2 NA18984.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.657+440_657+441ins others(541): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(492): Show |
1 | a0009c0012t0001g0145 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(499): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(883): Show |
1 | a0009c0012t0001g0144 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(890): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(493): Show |
1 | a0001c0002t0002g0146 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(500): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(537): Show |
1 | a0002c0003t0002g0079 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(544): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(536): Show |
4 | a0001c0001t0001g0026a0001c0001t0001g0148a0002c0003t0002g0080others(1): Show | 5 | HG02615.hp1 HG02683.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(543): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(479): Show |
1 | a0001c0002t0002g0149 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(486): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(493): Show |
1 | a0001c0002t0002g0150 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(500): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(514): Show |
2 | a0001c0002t0002g0151a0001c0002t0002g0152 | 2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.657+440_657+441ins others(521): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(492): Show |
6 | a0001c0001t0001g0154a0001c0002t0002g0153a0001c0002t0002g0155others(3): Show | 6 | HG01928.hp2 HG01993.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(499): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(477): Show |
1 | a0001c0002t0002g0117 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(484): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(535): Show |
1 | a0001c0001t0001g0159 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(542): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(438): Show |
1 | a0001c0002t0002g0160 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(445): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(479): Show |
1 | a0003c0004t0002g0081 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(486): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(478): Show |
6 | a0001c0002t0002g0161a0001c0002t0002g0162a0003c0004t0002g0007others(3): Show | 9 | HG01069.hp2 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(485): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(474): Show |
1 | a0020c0015t0002g0163 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(481): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(22): Show |
2 | a0001c0013t0001g0164a0001c0013t0001g0165 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.657+440_657+441ins others(29): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCCCT others(737): Show |
1 | a0001c0002t0001g0114 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(744): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720831
|
T | TTCCCTTC others(467): Show |
1 | a0001c0001t0001g0238 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.657+441_657+442ins others(474): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | |||||
chr9:127720832
|
T | TCCCCCTT others(633): Show |
1 | a0001c0002t0002g0259 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(640): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720832 | |||||
chr9:127720835
|
C | CCCT | 4 | a0001c0002t0001g0010a0001c0002t0001g0107a0001c0002t0001g0121others(1): Show | 6 | HG02572.hp2 HG02630.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(3): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720835 | ||||||
chr9:127720839
|
T | TCCCTCCC others(443): Show |
3 | a0001c0002t0001g0010a0001c0002t0001g0121a0001c0002t0001g0122 | 5 | HG02572.hp2 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.657+448_657+449ins others(450): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720839 | |||||
chr9:127720839
|
T | TCCCTCCC others(444): Show |
1 | a0001c0002t0001g0107 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.657+448_657+449ins others(451): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720839 | |||||
chr9:127720847
|
T | G | 1 | a0024c0027t0001g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.657+452T>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720847 | ||||||
chr9:127720874
|
T | C | 1 | a0001c0002t0002g0259 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.657+479T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720874 | ||||||
chr9:127720881
|
T | TCCCCTTT others(7): Show |
12 | a0001c0002t0001g0031a0001c0002t0001g0251a0001c0002t0001g0252others(9): Show | 13 | HG01109.hp1 HG02135.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.657+492_657+493ins others(14): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720881 | |||||
chr9:127720881
|
T | TCCCCTTT others(27): Show |
2 | a0001c0002t0001g0253a0001c0002t0001g0254 | 2 | HG02165.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.657+492_657+493ins others(34): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720881 | |||||
chr9:127720888
|
C | T | 12 | a0004c0005t0001g0019a0004c0005t0001g0020a0004c0005t0001g0097others(9): Show | 15 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.657+493C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720888 | ||||||
chr9:127720897
|
T | C | 12 | a0004c0005t0001g0019a0004c0005t0001g0020a0004c0005t0001g0097others(9): Show | 15 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.657+502T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720897 | ||||||
chr9:127720914
|
C | T | 12 | a0004c0005t0001g0019a0004c0005t0001g0020a0004c0005t0001g0097others(9): Show | 15 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.657+519C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720914 | ||||||
chr9:127720922
|
T | TCCTCCC | 12 | a0004c0005t0001g0019a0004c0005t0001g0020a0004c0005t0001g0097others(9): Show | 15 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.657+527_657+528ins others(6): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720922 | ||||||
chr9:127720934
|
C | T | 13 | a0004c0005t0001g0019a0004c0005t0001g0020a0004c0005t0001g0097others(10): Show | 16 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.657+539C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720934 | ||||||
chr9:127720972
|
C | T | 1 | a0007c0007t0001g0095 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.657+577C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720972 | ||||||
chr9:127721006
|
A | G | 1 | a0001c0002t0002g0158 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.657+611A>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127721006 | ||||||
chr9:127721123
|
G | A | 1 | a0002c0003t0002g0062 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.657+728G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127721123 | ||||||
chr9:127721263
|
G | C | 14 | a0004c0005t0001g0019a0004c0005t0001g0020a0004c0005t0001g0097others(11): Show | 17 | HG01109.hp1 HG01109.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.657+868G>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127721263 | ||||||
chr9:127721283
|
A | G | 1 | a0007c0007t0001g0104 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.657+888A>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127721283 | ||||||
chr9:127721342
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02738.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.657+947C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127721342 | ||||||
chr9:127721413
|
G | C | 9 | a0004c0005t0001g0019a0004c0005t0001g0020a0004c0005t0001g0097others(6): Show | 11 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.657+1018G>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127721413 | ||||||
chr9:127721548
|
C | T | 1 | a0001c0002t0001g0122 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.657+1153C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127721548 | ||||||
chr9:127721552
|
C | T | 172 | a0001c0001t0001g0026a0001c0001t0001g0116a0001c0001t0001g0148others(169): Show | 216 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.657+1157C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127721552 | ||||||
chr9:127721649
|
G | A | 2 | a0001c0013t0001g0164a0001c0013t0001g0165 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.657+1254G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127721649 | ||||||
chr9:127721666
|
T | A | 1 | a0001c0002t0002g0259 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.657+1271T>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127721666 | ||||||
chr9:127721667
|
C | T | 1 | a0001c0002t0002g0259 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.657+1272C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127721667 | ||||||
chr9:127721738
|
CTG | C | 9 | a0001c0002t0001g0031a0001c0002t0001g0251a0001c0002t0001g0252others(6): Show | 10 | HG02135.hp1 HG02155.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.657+1345_657+1346d others(4): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127721738 | |||||
chr9:127721791
|
C | T | 6 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(3): Show | 6 | HG02630.hp2 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.658-1328C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127721791 | ||||||
chr9:127722170
|
C | T | 1 | a0001c0002t0001g0107 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.658-949C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127722170 | ||||||
chr9:127722171
|
T | G | 1 | a0001c0002t0001g0107 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.658-948T>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127722171 | ||||||
chr9:127722243
|
C | G | 2 | a0001c0002t0002g0068a0011c0026t0002g0086 | 2 | HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.658-876C>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127722243 | ||||||
chr9:127722263
|
G | T | 2 | a0009c0012t0001g0144a0009c0012t0001g0145 | 2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.658-856G>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127722263 | ||||||
chr9:127722378
|
A | G | 1 | a0001c0001t0001g0192 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.658-741A>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127722378 | ||||||
chr9:127722416
|
T | G | 1 | a0001c0001t0001g0196 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.658-703T>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127722416 | ||||||
chr9:127722499
|
T | C | 14 | a0004c0005t0001g0019a0004c0005t0001g0020a0004c0005t0001g0097others(11): Show | 17 | HG01109.hp1 HG01109.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.658-620T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127722499 | ||||||
chr9:127722749
|
A | G | 1 | a0001c0013t0001g0165 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.658-370A>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127722749 | ||||||
chr9:127722807
|
A | C | 1 | a0001c0002t0001g0107 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.658-312A>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127722807 | ||||||
chr9:127722816
|
A | T | 1 | a0001c0002t0001g0107 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.658-303A>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127722816 | ||||||
chr9:127722967
|
C | CA | 24 | a0001c0001t0001g0154a0001c0001t0001g0170a0001c0001t0001g0175others(21): Show | 24 | HG01106.hp2 HG01243.hp1 HG01517.hp1 others(21): Show |
intron_variant | MODIFIER | c.658-137dupA | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127722967 | |||||
chr9:127722967
|
CA | C | 11 | a0004c0005t0001g0019a0004c0005t0001g0020a0004c0005t0001g0097others(8): Show | 14 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.658-137delA | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127722967 | |||||
chr9:127723084
|
T | C | 14 | a0004c0005t0001g0019a0004c0005t0001g0020a0004c0005t0001g0097others(11): Show | 17 | HG01109.hp1 HG01109.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.658-35T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127723084 | ||||||
chr9:127723339
|
G | A | 122 | a0001c0002t0001g0250a0001c0002t0002g0008a0001c0002t0002g0021others(119): Show | 159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
splice_region_variant&intron_variant | LOW | c.872+6G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | chr9 | 127723339 | ||||||
chr9:127723582
|
G | A | 2 | a0001c0001t0001g0214a0016c0018t0001g0193 | 2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.872+249G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | chr9 | 127723582 | ||||||
chr9:127723632
|
C | G | 1 | a0007c0007t0001g0104 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.872+299C>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | chr9 | 127723632 | ||||||
chr9:127723676
|
G | A | 9 | a0001c0002t0001g0031a0001c0002t0001g0251a0001c0002t0001g0252others(6): Show | 10 | HG02135.hp1 HG02155.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.872+343G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | chr9 | 127723676 | ||||||
chr9:127723794
|
C | T | 1 | a0002c0003t0002g0035 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.873-326C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | chr9 | 127723794 | ||||||
chr9:127723838
|
T | G | 3 | a0007c0007t0001g0018a0007c0007t0001g0095a0007c0007t0001g0096 | 4 | HG01884.hp1 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.873-282T>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | chr9 | 127723838 | ||||||
chr9:127723842
|
G | C | 4 | a0007c0007t0001g0018a0007c0007t0001g0095a0007c0007t0001g0096others(1): Show | 5 | HG01884.hp1 HG02109.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.873-278G>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | chr9 | 127723842 | ||||||
chr9:127723905
|
C | CA | 127 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0186others(124): Show | 164 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.873-202dupA | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 127723905 | |||||
chr9:127723905
|
C | CAA | 20 | a0001c0002t0001g0120a0001c0002t0002g0021a0001c0002t0002g0125others(17): Show | 22 | HG01346.hp2 HG01358.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.873-203_873-202dup others(2): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 127723905 | |||||
chr9:127723905
|
C | CAAAA | 8 | a0001c0002t0001g0031a0001c0002t0001g0251a0001c0002t0001g0252others(5): Show | 9 | HG02155.hp1 HG02165.hp1 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.873-205_873-202dup others(4): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 127723905 | |||||
chr9:127723983
|
A | G | 1 | a0002c0003t0002g0067 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.873-137A>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | chr9 | 127723983 | ||||||
chr9:127724104
|
A | ATG | 3 | a0001c0002t0002g0118a0002c0003t0002g0037a0022c0029t0002g0094 | 3 | HG01358.hp1 HG03239.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.873-16_873-15insTG | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | chr9 | 127724104 | ||||||
chr9:127724105
|
C | T | 119 | a0001c0002t0001g0250a0001c0002t0002g0008a0001c0002t0002g0021others(116): Show | 156 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.873-15C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | chr9 | 127724105 | ||||||
chr9:127724106
|
G | C | 3 | a0001c0002t0002g0118a0002c0003t0002g0037a0022c0029t0002g0094 | 3 | HG01358.hp1 HG03239.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.873-14G>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | chr9 | 127724106 | ||||||
chr9:127724106
|
G | GC | 117 | a0001c0001t0001g0177a0001c0001t0001g0225a0001c0002t0001g0107others(114): Show | 153 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
splice_region_variant&intron_variant | LOW | c.873-6dupC | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 127724106 | |||||
chr9:127724617
|
A | T | 1 | a0012c0025t0001g0249 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1118-139A>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 8/13 | chr9 | 127724617 | ||||||
chr9:127724636
|
T | C | 148 | a0001c0002t0001g0010a0001c0002t0001g0031a0001c0002t0001g0107others(145): Show | 188 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1118-120T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 8/13 | chr9 | 127724636 | ||||||
chr9:127724901
|
C | T | 1 | a0002c0003t0002g0069 | 1 | NA19054.hp2 | splice_region_variant&intron_variant | LOW | c.1259+4C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127724901 | ||||||
chr9:127724935
|
C | T | 1 | a0002c0003t0002g0047 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1259+38C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127724935 | ||||||
chr9:127724973
|
C | T | 1 | a0001c0002t0002g0166 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1259+76C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127724973 | ||||||
chr9:127724997
|
C | G | 1 | a0001c0001t0001g0210 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1259+100C>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127724997 | ||||||
chr9:127725028
|
C | A | 2 | a0001c0001t0001g0201a0001c0001t0001g0226 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1259+131C>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127725028 | ||||||
chr9:127725115
|
AATTTAAA others(6): Show |
A | 1 | a0001c0002t0002g0166 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1259+219_1259+231d others(15): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127725115 | ||||||
chr9:127725273
|
C | CA | 24 | a0001c0001t0001g0091a0001c0001t0001g0168a0001c0001t0001g0169others(21): Show | 24 | HG00544.hp1 HG00642.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1259+385dupA | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 127725273 | |||||
chr9:127725411
|
A | C | 1 | a0001c0002t0001g0121 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1259+514A>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127725411 | ||||||
chr9:127725437
|
G | A | 3 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0114 | 3 | HG02818.hp1 HG02896.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1259+540G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127725437 | ||||||
chr9:127725525
|
C | G | 6 | a0004c0005t0001g0020a0004c0005t0001g0098a0004c0005t0001g0099others(3): Show | 7 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1259+628C>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127725525 | ||||||
chr9:127725540
|
G | A | 123 | a0001c0002t0001g0250a0001c0002t0002g0008a0001c0002t0002g0021others(120): Show | 160 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.1259+643G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127725540 | ||||||
chr9:127725563
|
C | CA | 38 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0092others(35): Show | 42 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.1260-653dupA | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 127725563 | |||||
chr9:127725563
|
CA | C | 16 | a0001c0001t0001g0030a0001c0001t0001g0176a0001c0002t0001g0031others(13): Show | 20 | HG01069.hp1 HG01070.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1260-653delA | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 127725563 | |||||
chr9:127725563
|
CAA | C | 44 | a0001c0002t0001g0110a0001c0002t0001g0120a0001c0002t0001g0122others(41): Show | 50 | HG00423.hp2 HG00621.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.1260-654_1260-653d others(4): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 127725563 | |||||
chr9:127725563
|
CAAA | C | 90 | a0001c0002t0001g0010a0001c0002t0001g0111a0001c0002t0001g0112others(87): Show | 123 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1260-655_1260-653d others(5): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 127725563 | |||||
chr9:127725590
|
T | G | 8 | a0004c0005t0001g0019a0004c0005t0001g0020a0004c0005t0001g0097others(5): Show | 10 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1260-649T>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127725590 | ||||||
chr9:127725626
|
G | A | 8 | a0004c0005t0001g0019a0004c0005t0001g0020a0004c0005t0001g0097others(5): Show | 10 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1260-613G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127725626 | ||||||
chr9:127725906
|
GCTTTTCT others(17): Show |
G | 1 | a0023c0028t0001g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1260-330_1260-307d others(26): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 127725906 | |||||
chr9:127725932
|
T | A | 1 | a0023c0028t0001g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1260-307T>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127725932 | ||||||
chr9:127725954
|
T | A | 1 | a0023c0028t0001g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1260-285T>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127725954 | ||||||
chr9:127726007
|
C | T | 2 | a0004c0005t0001g0020a0023c0028t0001g0101 | 3 | HG01109.hp2 HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1260-232C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127726007 | ||||||
chr9:127726091
|
G | A | 1 | a0012c0025t0001g0249 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1260-148G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127726091 | ||||||
chr9:127726215
|
C | T | 148 | a0001c0002t0001g0010a0001c0002t0001g0031a0001c0002t0001g0107others(145): Show | 188 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1260-24C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127726215 | ||||||
chr9:127726614
|
C | A | 9 | a0004c0005t0001g0019a0004c0005t0001g0020a0004c0005t0001g0097others(6): Show | 11 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1425+210C>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | chr9 | 127726614 | ||||||
chr9:127726643
|
C | G | 9 | a0001c0002t0001g0031a0001c0002t0001g0251a0001c0002t0001g0252others(6): Show | 10 | HG02135.hp1 HG02155.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.1425+239C>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | chr9 | 127726643 | ||||||
chr9:127726652
|
G | A | 26 | a0001c0002t0001g0250a0001c0002t0002g0008a0001c0002t0002g0022others(23): Show | 31 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.1425+248G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | chr9 | 127726652 | ||||||
chr9:127726712
|
CG | C | 3 | a0001c0002t0001g0107a0001c0002t0002g0141a0023c0028t0001g0101 | 3 | HG01109.hp2 HG03098.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1426-255delG | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 127726712 | |||||
chr9:127726728
|
C | T | 1 | a0002c0024t0001g0033 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1426-242C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | chr9 | 127726728 | ||||||
chr9:127726766
|
C | T | 13 | a0001c0002t0001g0010a0001c0002t0001g0107a0001c0002t0001g0110others(10): Show | 15 | HG02572.hp2 HG02630.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.1426-204C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | chr9 | 127726766 | ||||||
chr9:127726782
|
T | A | 1 | a0023c0028t0001g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1426-188T>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | chr9 | 127726782 | ||||||
chr9:127726787
|
CA | C | 46 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0027others(43): Show | 53 | HG00280.hp2 HG00423.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.1426-149delA | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 127726787 | |||||
chr9:127726787
|
CAA | C | 35 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(32): Show | 51 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.1426-150_1426-149d others(4): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 127726787 | |||||
chr9:127726787
|
CAAA | C | 6 | a0001c0001t0001g0026a0001c0001t0001g0093a0001c0001t0001g0172others(3): Show | 7 | HG02145.hp2 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1426-151_1426-149d others(5): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 127726787 | |||||
chr9:127726787
|
CAAAAA | C | 9 | a0004c0005t0001g0019a0004c0005t0001g0020a0004c0005t0001g0097others(6): Show | 11 | HG01109.hp1 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1426-153_1426-149d others(7): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 127726787 | |||||
chr9:127726787
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0183a0001c0001t0001g0208 | 2 | HG00621.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.1426-160_1426-149d others(14): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 127726787 | |||||
chr9:127726787
|
CAAAAAAA others(6): Show |
C | 1 | a0008c0009t0001g0209 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1426-161_1426-149d others(15): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 127726787 | |||||
chr9:127726787
|
CAAAAAAA others(16): Show |
C | 149 | a0001c0002t0001g0010a0001c0002t0001g0031a0001c0002t0001g0107others(146): Show | 189 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1426-171_1426-149d others(25): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 127726787 | |||||
chr9:127726805
|
A | C | 1 | a0012c0025t0001g0249 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1426-165A>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | chr9 | 127726805 | ||||||
chr9:127726807
|
A | C | 1 | a0023c0028t0001g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1426-163A>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | chr9 | 127726807 | ||||||
chr9:127726808
|
A | C | 8 | a0004c0005t0001g0019a0004c0005t0001g0020a0004c0005t0001g0097others(5): Show | 10 | HG01891.hp1 HG02055.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1426-162A>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | chr9 | 127726808 | ||||||
chr9:127726817
|
A | C | 160 | a0001c0002t0001g0010a0001c0002t0001g0031a0001c0002t0001g0107others(157): Show | 202 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.1426-153A>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | chr9 | 127726817 | ||||||
chr9:127726890
|
G | A | 2 | a0001c0001t0001g0245a0001c0001t0001g0248 | 2 | HG00099.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1426-80G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | chr9 | 127726890 | ||||||
chr9:127726910
|
C | T | 149 | a0001c0002t0001g0010a0001c0002t0001g0031a0001c0002t0001g0107others(146): Show | 189 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1426-60C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | chr9 | 127726910 | ||||||
chr9:127726953
|
A | AC | 8 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0002t0002g0135others(5): Show | 8 | HG00741.hp2 HG01358.hp1 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.1426-12dupC | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 127726953 | |||||
chr9:127727482
|
C | A | 1 | a0001c0002t0002g0166 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1764+17C>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727482 | ||||||
chr9:127727498
|
T | A | 1 | a0023c0028t0001g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1764+33T>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727498 | ||||||
chr9:127727515
|
G | T | 1 | a0023c0028t0001g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1764+50G>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727515 | ||||||
chr9:127727625
|
G | A | 1 | a0002c0003t0002g0066 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1764+160G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727625 | ||||||
chr9:127727701
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1764+236C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727701 | ||||||
chr9:127727763
|
A | T | 1 | a0023c0028t0001g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1764+298A>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727763 | ||||||
chr9:127727765
|
T | A | 1 | a0002c0024t0001g0033 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1764+300T>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727765 | ||||||
chr9:127727781
|
C | T | 1 | a0001c0002t0002g0139 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1764+316C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727781 | ||||||
chr9:127727797
|
CA | C | 149 | a0001c0002t0001g0010a0001c0002t0001g0031a0001c0002t0001g0107others(146): Show | 189 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1764+334delA | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr9 | 127727797 | |||||
chr9:127727821
|
A | C | 1 | a0023c0028t0001g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1764+356A>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727821 | ||||||
chr9:127727829
|
G | A | 1 | a0002c0003t0002g0013 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1764+364G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727829 | ||||||
chr9:127727845
|
C | T | 4 | a0001c0002t0002g0137a0001c0002t0002g0153a0001c0002t0002g0156others(1): Show | 4 | HG01928.hp2 HG01993.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1764+380C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727845 | ||||||
chr9:127727846
|
G | A | 1 | a0001c0002t0002g0133 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1764+381G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727846 | ||||||
chr9:127727914
|
C | A | 1 | a0023c0028t0001g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1764+449C>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727914 | ||||||
chr9:127727933
|
G | A | 5 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0001t0001g0210others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1764+468G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727933 | ||||||
chr9:127728087
|
A | C | 1 | a0023c0028t0001g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1764+622A>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127728087 | ||||||
chr9:127728112
|
A | AC | 13 | a0001c0001t0001g0154a0001c0001t0001g0197a0001c0001t0001g0198others(10): Show | 13 | HG00423.hp2 HG00438.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1764+649dupC | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr9 | 127728112 | |||||
chr9:127728113
|
C | A | 2 | a0009c0012t0001g0144a0009c0012t0001g0145 | 2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1764+648C>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127728113 | ||||||
chr9:127728115
|
G | C | 1 | a0023c0028t0001g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1764+650G>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127728115 | ||||||
chr9:127728134
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02738.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1764+669A>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127728134 | ||||||
chr9:127728229
|
G | A | 12 | a0001c0001t0001g0206a0001c0002t0001g0031a0001c0002t0001g0251others(9): Show | 13 | HG01934.hp1 HG02135.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.1764+764G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127728229 | ||||||
chr9:127728350
|
T | C | 4 | a0001c0002t0002g0021a0001c0002t0002g0125a0001c0002t0002g0126others(1): Show | 5 | HG02109.hp1 HG02622.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1764+885T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127728350 | ||||||
chr9:127728362
|
C | T | 1 | a0001c0002t0001g0257 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1764+897C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127728362 | ||||||
chr9:127728381
|
C | T | 1 | a0002c0003t0002g0036 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1764+916C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127728381 | ||||||
chr9:127728414
|
TCTA | T | 13 | a0001c0002t0001g0010a0001c0002t0001g0107a0001c0002t0001g0110others(10): Show | 15 | HG02572.hp2 HG02630.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.1764+952_1764+954d others(5): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr9 | 127728414 | |||||
chr9:127728639
|
A | G | 1 | a0017c0022t0002g0228 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1765-942A>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127728639 | ||||||
chr9:127728813
|
A | G | 5 | a0001c0001t0001g0026a0001c0001t0001g0148a0001c0001t0001g0154others(2): Show | 6 | HG02615.hp1 HG02809.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1765-768A>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127728813 | ||||||
chr9:127728958
|
C | T | 9 | a0001c0002t0001g0031a0001c0002t0001g0251a0001c0002t0001g0252others(6): Show | 10 | HG02135.hp1 HG02155.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.1765-623C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127728958 | ||||||
chr9:127729082
|
G | A | 11 | a0001c0002t0001g0010a0001c0002t0001g0107a0001c0002t0001g0110others(8): Show | 13 | HG02572.hp2 HG02630.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1765-499G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127729082 | ||||||
chr9:127729204
|
G | A | 145 | a0001c0002t0001g0010a0001c0002t0001g0031a0001c0002t0001g0107others(142): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.1765-377G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127729204 | ||||||
chr9:127729259
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1765-322T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127729259 | ||||||
chr9:127729260
|
C | T | 1 | a0002c0003t0002g0036 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1765-321C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127729260 | ||||||
chr9:127729354
|
T | C | 164 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0002t0001g0010others(161): Show | 207 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1765-227T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127729354 | ||||||
chr9:127729364
|
C | T | 2 | a0001c0013t0001g0164a0001c0013t0001g0165 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1765-217C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127729364 | ||||||
chr9:127729447
|
T | C | 149 | a0001c0002t0001g0010a0001c0002t0001g0031a0001c0002t0001g0107others(146): Show | 189 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1765-134T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127729447 | ||||||
chr9:127729719
|
A | G | 149 | a0001c0002t0001g0010a0001c0002t0001g0031a0001c0002t0001g0107others(146): Show | 189 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1852+51A>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/13 | chr9 | 127729719 | ||||||
chr9:127729760
|
G | A | 124 | a0001c0002t0001g0250a0001c0002t0002g0008a0001c0002t0002g0021others(121): Show | 161 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1852+92G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/13 | chr9 | 127729760 | ||||||
chr9:127729782
|
TG | T | 5 | a0001c0002t0001g0010a0001c0002t0001g0107a0001c0002t0001g0120others(2): Show | 7 | HG02572.hp2 HG02630.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1852+117delG | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr9 | 127729782 | |||||
chr9:127729812
|
G | A | 2 | a0001c0013t0001g0164a0001c0013t0001g0165 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1852+144G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/13 | chr9 | 127729812 | ||||||
chr9:127729924
|
C | G | 1 | a0001c0002t0001g0257 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1852+256C>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/13 | chr9 | 127729924 | ||||||
chr9:127730042
|
G | C | 1 | a0024c0027t0001g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1852+374G>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/13 | chr9 | 127730042 | ||||||
chr9:127730105
|
A | C | 1 | a0024c0027t0001g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1852+437A>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/13 | chr9 | 127730105 | ||||||
chr9:127730115
|
A | G | 2 | a0009c0012t0001g0144a0009c0012t0001g0145 | 2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1852+447A>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/13 | chr9 | 127730115 | ||||||
chr9:127730299
|
G | A | 11 | a0001c0002t0001g0010a0001c0002t0001g0107a0001c0002t0001g0110others(8): Show | 13 | HG02572.hp2 HG02630.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1853-337G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/13 | chr9 | 127730299 | ||||||
chr9:127730345
|
G | A | 2 | a0007c0007t0001g0018a0007c0007t0001g0095 | 3 | HG01884.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1853-291G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/13 | chr9 | 127730345 | ||||||
chr9:127730492
|
C | T | 11 | a0001c0002t0001g0010a0001c0002t0001g0107a0001c0002t0001g0110others(8): Show | 13 | HG02572.hp2 HG02630.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1853-144C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/13 | chr9 | 127730492 | ||||||
chr9:127730518
|
T | C | 2 | a0001c0002t0002g0057a0001c0002t0002g0058 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1853-118T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/13 | chr9 | 127730518 |