geneid | 7265 |
---|---|
ensemblid | ENSG00000113312.12 |
hgncid | 12391 |
symbol | TTC1 |
name | tetratricopeptide repeat domain 1 |
refseq_nuc | NM_003314.3 |
refseq_prot | NP_003305.1 |
ensembl_nuc | ENST00000231238.10 |
ensembl_prot | ENSP00000231238.4 |
mane_status | MANE Select |
chr | chr5 |
start | 160009139 |
end | 160065543 |
strand | + |
ver | v1.2 |
region | chr5:160009139-160065543 |
region5000 | chr5:160004139-160070543 |
regionname0 | TTC1_chr5_160009139_160065543 |
regionname5000 | TTC1_chr5_160004139_160070543 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 292 | 375 | 77 | 62 | 187 | 11 | 36 | 143 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
a0002 | 0/0 | 292 | 6 | 2 | 1 | 0 | 1 | 2 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
a0003 | 0/0 | 292 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
a0004 | 0/0 | 292 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
a0005 | 0/0 | 292 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 879 | 375 | 77 | 62 | 187 | 11 | 36 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
c0002 | 0/0 | 879 | 6 | 2 | 1 | 0 | 1 | 2 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
c0003 | 0/0 | 879 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
c0004 | 0/0 | 879 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
c0005 | 0/0 | 879 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 563 | 317 | 76 | 50 | 143 | 10 | 36 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
t0002 | 0/0 | 563 | 62 | 1 | 14 | 43 | 2 | 2 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
t0003 | 0/0 | 563 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
t0004 | 0/0 | 563 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
t0005 | 0/0 | 563 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
t0006 | 0/0 | 563 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
t0007 | 0/0 | 563 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0027 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0047 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 879 | 375 | 77 | 62 | 187 | 11 | 36 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
a0002c0002 | 0/0 | 879 | 6 | 2 | 1 | 0 | 1 | 2 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
a0003c0004 | 0/0 | 879 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
a0004c0003 | 0/0 | 879 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
a0005c0005 | 0/0 | 879 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1441 | 309 | 73 | 48 | 143 | 9 | 34 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
a0001c0001t0002 | 0/0 | 1441 | 61 | 1 | 14 | 42 | 2 | 2 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
a0001c0001t0003 | 0/0 | 1441 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
a0001c0001t0004 | 0/0 | 1441 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
a0001c0001t0005 | 0/0 | 1441 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
a0001c0001t0006 | 0/0 | 1441 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
a0001c0001t0007 | 0/0 | 1441 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
a0002c0002t0001 | 0/0 | 1441 | 6 | 2 | 1 | 0 | 1 | 2 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
a0003c0004t0002 | 0/0 | 1441 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
a0004c0003t0001 | 0/0 | 1441 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
a0005c0005t0001 | 0/0 | 1441 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | copy fasta | chr5 | 160004139 | 160070543 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0027 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0047 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0001g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0006g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0001c0001t0007g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0002c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0002c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0003c0004t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0004c0003t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
a0005c0005t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | GBR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0229 | EUR | GBR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | GBR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | GBR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | FIN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | FIN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00642 | hp2 | a0004 | c0003 | t0001 | g0123 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0315 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0358 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0299 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0341 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0306 | AMR | CLM | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0302 | EUR | IBS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | IBS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0249 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0371 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0343 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0307 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0319 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0340 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0298 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0366 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02056 | hp1 | a0001 | c0001 | t0007 | g0206 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0332 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0316 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CDX | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | CDX | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CDX | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CDX | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02258 | hp2 | a0001 | c0001 | t0006 | g0283 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0313 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0331 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0359 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0354 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0361 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0248 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0363 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ESN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0360 | AFR | ESN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ESN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ESN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0364 | AFR | MSL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0365 | AFR | MSL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0251 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | BEB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | BEB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | STU | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0300 | SAS | STU | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0362 | SAS | BEB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0250 | SAS | STU | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | STU | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | STU | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | STU | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | YRI | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0345 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0347 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0367 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0346 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0368 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0350 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18959 | hp1 | a0003 | c0004 | t0002 | g0355 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0370 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0337 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0356 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0344 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0352 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0351 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0349 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0348 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0353 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | LWK | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | LWK | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0342 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0369 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19081 | hp1 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0357 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | YRI | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | YRI | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ASW | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ASW | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0010 | EUR | TSI | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | TSI | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0252 | EUR | TSI | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | TSI | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | GIH | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | GIH | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0146 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0329 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02486 | hp2 | a0005 | c0005 | t0001 | g0013 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | MSL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | USA | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | USA | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0027 | REF | REF | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0047 | REF | REF | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:160010614
|
C | G | 2 | a0002a0005 | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
missense_variant | MODERATE | c.86C>G | p.Ala29Gly | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/8 | 170/1441 | 86/879 | 29/292 | chr5 | 160010614 | ||
chr5:160036712
|
C | T | 1 | a0005 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.413C>T | p.Ser138Phe | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/8 | 497/1441 | 413/879 | 138/292 | chr5 | 160036712 | ||
chr5:160036742
|
C | T | 1 | a0003 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.443C>T | p.Ser148Phe | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/8 | 527/1441 | 443/879 | 148/292 | chr5 | 160036742 | ||
chr5:160065034
|
A | G | 1 | a0004 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.848A>G | p.Asn283Ser | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 8/8 | 932/1441 | 848/879 | 283/292 | chr5 | 160065034 |
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 |
---|
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:160009154
|
C | T | 2 | a0001c0001t0002a0003c0004t0002 | 62 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(59): Show |
5_prime_UTR_variant | MODIFIER | c.-69C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/8 | 1375 | chr5 | 160009154 | |||||
chr5:160009176
|
C | T | 1 | a0001c0001t0007 | 1 | HG02056.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-47C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/8 | chr5 | 160009176 | ||||||
chr5:160065120
|
A | T | 1 | a0001c0001t0006 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*55A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 8/8 | 55 | chr5 | 160065120 | |||||
chr5:160065211
|
C | G | 1 | a0001c0001t0005 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*146C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 8/8 | 146 | chr5 | 160065211 | |||||
chr5:160065478
|
C | T | 1 | a0001c0001t0004 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*413C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 8/8 | 413 | chr5 | 160065478 | |||||
chr5:160065486
|
G | A | 1 | a0001c0001t0003 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*421G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 8/8 | 421 | chr5 | 160065486 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:160009472
|
A | T | 1 | a0001c0001t0001g0371 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-30+279A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160009472 | ||||||
chr5:160009491
|
A | G | 4 | a0001c0001t0001g0367a0001c0001t0001g0368a0001c0001t0001g0369others(1): Show | 4 | NA18948.hp1 NA18954.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+298A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160009491 | ||||||
chr5:160009517
|
C | G | 3 | a0001c0001t0001g0364a0001c0001t0001g0365a0001c0001t0001g0366 | 3 | HG02055.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-30+324C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160009517 | ||||||
chr5:160009539
|
C | T | 6 | a0001c0001t0001g0011a0001c0001t0001g0359a0001c0001t0001g0360others(3): Show | 7 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30+346C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160009539 | ||||||
chr5:160009597
|
C | CATAA | 65 | a0001c0001t0001g0305a0001c0001t0001g0320a0001c0001t0001g0334others(62): Show | 66 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(63): Show |
intron_variant | MODIFIER | c.-30+422_-30+425dup others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 160009597 | |||||
chr5:160009606
|
A | G | 1 | a0001c0001t0001g0358 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-30+413A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160009606 | ||||||
chr5:160009763
|
G | A | 2 | a0002c0002t0001g0012a0005c0005t0001g0013 | 2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-30+570G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160009763 | ||||||
chr5:160009816
|
A | C | 118 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0253others(115): Show | 122 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.-30+623A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160009816 | ||||||
chr5:160009862
|
G | A | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-638G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160009862 | ||||||
chr5:160009899
|
C | A | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-601C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160009899 | ||||||
chr5:160009918
|
T | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-29-582T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160009918 | ||||||
chr5:160010001
|
G | T | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-499G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160010001 | ||||||
chr5:160010113
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-29-387C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160010113 | ||||||
chr5:160010124
|
G | A | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-376G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160010124 | ||||||
chr5:160010218
|
A | ACTG | 4 | a0002c0002t0001g0249a0002c0002t0001g0250a0002c0002t0001g0251others(1): Show | 4 | HG01928.hp1 HG03669.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-280_-29-278dup others(3): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 160010218 | |||||
chr5:160010257
|
C | CA | 55 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0014others(52): Show | 58 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.-29-221dupA | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 160010257 | |||||
chr5:160010257
|
CA | C | 11 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(8): Show | 11 | HG00609.hp1 HG02523.hp1 HG02735.hp1 others(8): Show |
intron_variant | MODIFIER | c.-29-221delA | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 160010257 | |||||
chr5:160010282
|
A | C | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG02735.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-29-218A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160010282 | ||||||
chr5:160010396
|
C | T | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-104C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160010396 | ||||||
chr5:160010414
|
T | G | 1 | a0001c0001t0001g0029 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-29-86T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160010414 | ||||||
chr5:160010459
|
C | T | 113 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0253others(110): Show | 117 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-29-41C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160010459 | ||||||
chr5:160011088
|
T | C | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.330+230T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160011088 | ||||||
chr5:160011124
|
G | T | 1 | a0002c0002t0001g0252 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.330+266G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160011124 | ||||||
chr5:160011187
|
G | A | 1 | a0001c0001t0001g0253 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.330+329G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160011187 | ||||||
chr5:160011245
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.330+387A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160011245 | ||||||
chr5:160011439
|
A | G | 3 | a0001c0001t0001g0364a0001c0001t0001g0365a0001c0001t0001g0366 | 3 | HG02055.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.330+581A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160011439 | ||||||
chr5:160011863
|
G | A | 1 | a0001c0001t0006g0283 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.330+1005G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160011863 | ||||||
chr5:160012030
|
A | C | 33 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0260others(30): Show | 36 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.330+1172A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160012030 | ||||||
chr5:160012193
|
C | G | 1 | a0001c0001t0001g0237 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.330+1335C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160012193 | ||||||
chr5:160012209
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.330+1351C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160012209 | ||||||
chr5:160012290
|
T | C | 13 | a0001c0001t0001g0003a0001c0001t0001g0032a0001c0001t0001g0033others(10): Show | 14 | HG01928.hp1 HG01981.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.330+1432T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160012290 | ||||||
chr5:160012359
|
A | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 6 | HG01981.hp1 HG02723.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.330+1501A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160012359 | ||||||
chr5:160012368
|
A | AT | 17 | a0001c0001t0001g0003a0001c0001t0001g0032a0001c0001t0001g0033others(14): Show | 18 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.330+1524dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160012368 | |||||
chr5:160012832
|
G | C | 1 | a0001c0001t0001g0014 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.330+1974G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160012832 | ||||||
chr5:160012955
|
C | T | 65 | a0001c0001t0001g0305a0001c0001t0001g0320a0001c0001t0001g0334others(62): Show | 66 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(63): Show |
intron_variant | MODIFIER | c.330+2097C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160012955 | ||||||
chr5:160012957
|
A | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0260others(28): Show | 34 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.330+2099A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160012957 | ||||||
chr5:160013010
|
T | A | 68 | a0001c0001t0001g0305a0001c0001t0001g0320a0001c0001t0001g0334others(65): Show | 69 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(66): Show |
intron_variant | MODIFIER | c.330+2152T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160013010 | ||||||
chr5:160013013
|
T | C | 1 | a0001c0001t0001g0260 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.330+2155T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160013013 | ||||||
chr5:160013306
|
A | G | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+2448A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160013306 | ||||||
chr5:160013308
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.330+2450A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160013308 | ||||||
chr5:160013398
|
T | TA | 8 | a0001c0001t0001g0241a0002c0002t0001g0012a0002c0002t0001g0248others(5): Show | 8 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.330+2552dupA | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160013398 | |||||
chr5:160013458
|
G | A | 117 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(114): Show | 122 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.330+2600G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160013458 | ||||||
chr5:160013509
|
C | G | 11 | a0001c0001t0001g0003a0001c0001t0001g0032a0001c0001t0001g0033others(8): Show | 12 | HG01928.hp1 HG01981.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.330+2651C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160013509 | ||||||
chr5:160013540
|
C | T | 33 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0260others(30): Show | 36 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.330+2682C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160013540 | ||||||
chr5:160013541
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.330+2683G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160013541 | ||||||
chr5:160013627
|
C | G | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+2769C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160013627 | ||||||
chr5:160013658
|
G | A | 2 | a0001c0001t0002g0298a0001c0001t0002g0299 | 2 | HG01106.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.330+2800G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160013658 | ||||||
chr5:160013742
|
C | CA | 109 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0036others(106): Show | 113 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.330+2901dupA | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160013742 | |||||
chr5:160013742
|
CA | C | 6 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0026others(3): Show | 6 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.330+2901delA | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160013742 | |||||
chr5:160013742
|
CAA | C | 10 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0006g0283others(7): Show | 10 | HG01928.hp1 HG02258.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.330+2900_330+2901d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160013742 | |||||
chr5:160014007
|
A | G | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+3149A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014007 | ||||||
chr5:160014039
|
A | C | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+3181A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014039 | ||||||
chr5:160014070
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.330+3212T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014070 | ||||||
chr5:160014114
|
A | G | 2 | a0001c0001t0001g0228a0001c0001t0001g0229 | 2 | HG00099.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.330+3256A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014114 | ||||||
chr5:160014171
|
A | G | 1 | a0005c0005t0001g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.330+3313A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014171 | ||||||
chr5:160014226
|
C | T | 1 | a0001c0001t0002g0354 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.330+3368C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014226 | ||||||
chr5:160014241
|
G | C | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+3383G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014241 | ||||||
chr5:160014241
|
G | T | 1 | a0001c0001t0001g0227 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.330+3383G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014241 | ||||||
chr5:160014335
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.330+3477G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014335 | ||||||
chr5:160014391
|
A | G | 32 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0260others(29): Show | 35 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.330+3533A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014391 | ||||||
chr5:160014493
|
G | A | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+3635G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014493 | ||||||
chr5:160014514
|
T | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0230others(105): Show | 112 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.330+3656T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014514 | ||||||
chr5:160014515
|
T | A | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+3657T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014515 | ||||||
chr5:160014674
|
G | A | 33 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0260others(30): Show | 36 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.330+3816G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014674 | ||||||
chr5:160014683
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.330+3825A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014683 | ||||||
chr5:160014835
|
A | G | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+3977A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014835 | ||||||
chr5:160015305
|
G | A | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+4447G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160015305 | ||||||
chr5:160015569
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.330+4711A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160015569 | ||||||
chr5:160015590
|
G | A | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+4732G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160015590 | ||||||
chr5:160015593
|
G | A | 1 | a0001c0001t0001g0015 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.330+4735G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160015593 | ||||||
chr5:160015628
|
C | T | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+4770C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160015628 | ||||||
chr5:160015755
|
A | G | 9 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0002t0001g0012others(6): Show | 9 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.330+4897A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160015755 | ||||||
chr5:160015910
|
A | G | 68 | a0001c0001t0001g0305a0001c0001t0001g0320a0001c0001t0001g0334others(65): Show | 69 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(66): Show |
intron_variant | MODIFIER | c.330+5052A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160015910 | ||||||
chr5:160015927
|
T | C | 9 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0002t0001g0012others(6): Show | 9 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.330+5069T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160015927 | ||||||
chr5:160015929
|
C | T | 4 | a0001c0001t0001g0367a0001c0001t0001g0368a0001c0001t0001g0369others(1): Show | 4 | NA18948.hp1 NA18954.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+5071C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160015929 | ||||||
chr5:160016056
|
A | G | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0237 | 3 | HG00438.hp1 NA18999.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.330+5198A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016056 | ||||||
chr5:160016073
|
T | C | 3 | a0002c0002t0001g0249a0002c0002t0001g0250a0002c0002t0001g0251 | 3 | HG01928.hp1 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.330+5215T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016073 | ||||||
chr5:160016080
|
G | A | 3 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0006g0283 | 3 | HG02258.hp2 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.330+5222G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016080 | ||||||
chr5:160016167
|
C | T | 65 | a0001c0001t0001g0305a0001c0001t0001g0320a0001c0001t0001g0334others(62): Show | 66 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(63): Show |
intron_variant | MODIFIER | c.330+5309C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016167 | ||||||
chr5:160016285
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.330+5427C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016285 | ||||||
chr5:160016318
|
C | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.330+5460C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016318 | ||||||
chr5:160016321
|
A | T | 369 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(366): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.330+5463A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016321 | ||||||
chr5:160016398
|
A | T | 8 | a0001c0001t0002g0297a0001c0001t0002g0347a0001c0001t0002g0348others(5): Show | 8 | NA18946.hp1 NA18956.hp2 NA18983.hp2 others(5): Show |
intron_variant | MODIFIER | c.330+5540A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016398 | ||||||
chr5:160016403
|
A | T | 1 | a0002c0002t0001g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.330+5545A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016403 | ||||||
chr5:160016423
|
C | T | 1 | a0001c0001t0001g0366 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.330+5565C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016423 | ||||||
chr5:160016585
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.330+5727A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016585 | ||||||
chr5:160016659
|
T | C | 2 | a0001c0001t0001g0284a0001c0001t0006g0283 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.330+5801T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016659 | ||||||
chr5:160016799
|
G | T | 113 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0255others(110): Show | 117 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.330+5941G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016799 | ||||||
chr5:160016918
|
T | C | 4 | a0002c0002t0001g0249a0002c0002t0001g0250a0002c0002t0001g0251others(1): Show | 4 | HG01928.hp1 HG03669.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.330+6060T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016918 | ||||||
chr5:160016977
|
A | T | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+6119A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016977 | ||||||
chr5:160016991
|
C | CAA | 9 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0002t0001g0012others(6): Show | 9 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.330+6134_330+6135i others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160016991 | |||||
chr5:160017010
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.330+6152G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160017010 | ||||||
chr5:160017179
|
G | C | 1 | a0001c0001t0001g0049 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.330+6321G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160017179 | ||||||
chr5:160017189
|
A | G | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.330+6331A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160017189 | ||||||
chr5:160017192
|
A | G | 6 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0027others(3): Show | 6 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.330+6334A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160017192 | ||||||
chr5:160017213
|
T | G | 9 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0002t0001g0012others(6): Show | 9 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.330+6355T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160017213 | ||||||
chr5:160017221
|
A | C | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+6363A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160017221 | ||||||
chr5:160017621
|
A | G | 2 | a0001c0001t0001g0284a0001c0001t0006g0283 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.330+6763A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160017621 | ||||||
chr5:160017629
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.330+6771C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160017629 | ||||||
chr5:160017681
|
A | C | 1 | a0001c0001t0001g0285 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.330+6823A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160017681 | ||||||
chr5:160017858
|
T | C | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+7000T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160017858 | ||||||
chr5:160017924
|
G | A | 2 | a0001c0001t0001g0284a0001c0001t0006g0283 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.330+7066G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160017924 | ||||||
chr5:160018209
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.330+7351G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018209 | ||||||
chr5:160018224
|
C | T | 3 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0246 | 3 | HG02523.hp1 NA19010.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.330+7366C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018224 | ||||||
chr5:160018239
|
C | A | 1 | a0001c0001t0001g0286 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.330+7381C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018239 | ||||||
chr5:160018303
|
C | G | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+7445C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018303 | ||||||
chr5:160018341
|
A | G | 13 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(10): Show | 13 | HG00609.hp1 HG02074.hp2 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.330+7483A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018341 | ||||||
chr5:160018452
|
G | A | 5 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.330+7594G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018452 | ||||||
chr5:160018618
|
A | G | 2 | a0001c0001t0001g0207a0001c0001t0007g0206 | 2 | HG02056.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.330+7760A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018618 | ||||||
chr5:160018632
|
A | G | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+7774A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018632 | ||||||
chr5:160018654
|
C | G | 1 | a0001c0001t0001g0219 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.330+7796C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018654 | ||||||
chr5:160018772
|
G | A | 1 | a0001c0001t0002g0300 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.330+7914G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018772 | ||||||
chr5:160018795
|
C | A | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+7937C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018795 | ||||||
chr5:160018799
|
A | G | 2 | a0001c0001t0002g0345a0001c0001t0002g0346 | 2 | NA18941.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.330+7941A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018799 | ||||||
chr5:160018822
|
A | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0253others(110): Show | 117 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.330+7964A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018822 | ||||||
chr5:160018874
|
T | C | 118 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0253others(115): Show | 122 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.330+8016T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018874 | ||||||
chr5:160018923
|
T | C | 1 | a0001c0001t0001g0263 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.330+8065T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018923 | ||||||
chr5:160018928
|
G | A | 1 | a0001c0001t0001g0364 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.330+8070G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018928 | ||||||
chr5:160018970
|
C | G | 1 | a0001c0001t0001g0205 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.330+8112C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018970 | ||||||
chr5:160018974
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.330+8116A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018974 | ||||||
chr5:160018977
|
G | C | 5 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(2): Show | 5 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.330+8119G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018977 | ||||||
chr5:160019107
|
A | G | 7 | a0001c0001t0001g0203a0001c0001t0001g0230a0001c0001t0001g0231others(4): Show | 7 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+8249A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160019107 | ||||||
chr5:160019204
|
A | C | 5 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.330+8346A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160019204 | ||||||
chr5:160019235
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.330+8377T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160019235 | ||||||
chr5:160019410
|
A | G | 68 | a0001c0001t0001g0305a0001c0001t0001g0320a0001c0001t0001g0334others(65): Show | 69 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(66): Show |
intron_variant | MODIFIER | c.330+8552A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160019410 | ||||||
chr5:160019451
|
A | G | 118 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0253others(115): Show | 122 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.330+8593A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160019451 | ||||||
chr5:160019491
|
T | G | 33 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0260others(30): Show | 36 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.330+8633T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160019491 | ||||||
chr5:160019492
|
C | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0253others(109): Show | 116 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.330+8634C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160019492 | ||||||
chr5:160019495
|
A | G | 1 | a0001c0001t0006g0283 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.330+8637A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160019495 | ||||||
chr5:160019533
|
C | T | 2 | a0001c0001t0001g0364a0001c0001t0001g0365 | 2 | HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.330+8675C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160019533 | ||||||
chr5:160019545
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.330+8687C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160019545 | ||||||
chr5:160019580
|
C | CT | 20 | a0001c0001t0001g0029a0001c0001t0001g0185a0001c0001t0001g0186others(17): Show | 20 | HG01175.hp2 HG01192.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.330+8745dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160019580 | |||||
chr5:160019580
|
CT | C | 10 | a0001c0001t0001g0016a0001c0001t0001g0051a0001c0001t0001g0052others(7): Show | 10 | HG01952.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.330+8745delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160019580 | |||||
chr5:160019580
|
CTT | C | 66 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0285others(63): Show | 67 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.330+8744_330+8745d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160019580 | |||||
chr5:160019580
|
CTTT | C | 6 | a0001c0001t0002g0301a0001c0001t0002g0302a0001c0001t0002g0347others(3): Show | 6 | HG01515.hp1 HG02486.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.330+8743_330+8745d others(5): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160019580 | |||||
chr5:160019580
|
CTTTT | C | 8 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(5): Show | 8 | HG01928.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+8742_330+8745d others(6): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160019580 | |||||
chr5:160019580
|
CTTTTTTT others(7): Show |
C | 33 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0260others(30): Show | 36 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.330+8732_330+8745d others(16): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160019580 | |||||
chr5:160019644
|
G | A | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.330+8786G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160019644 | ||||||
chr5:160019669
|
CCTCCGCC others(22): Show |
C | 1 | a0001c0001t0001g0184 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.330+8815_330+8843d others(31): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160019669 | |||||
chr5:160019722
|
C | T | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+8864C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160019722 | ||||||
chr5:160020055
|
A | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.330+9197A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160020055 | ||||||
chr5:160020206
|
A | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.330+9348A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160020206 | ||||||
chr5:160020302
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.330+9444A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160020302 | ||||||
chr5:160020390
|
C | T | 3 | a0002c0002t0001g0249a0002c0002t0001g0250a0002c0002t0001g0251 | 3 | HG01928.hp1 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.330+9532C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160020390 | ||||||
chr5:160020480
|
G | A | 33 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0260others(30): Show | 36 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.330+9622G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160020480 | ||||||
chr5:160020663
|
C | G | 1 | a0001c0001t0001g0181 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.330+9805C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160020663 | ||||||
chr5:160020693
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.330+9835G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160020693 | ||||||
chr5:160020707
|
T | A | 1 | a0001c0001t0001g0284 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.330+9849T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160020707 | ||||||
chr5:160020754
|
C | G | 1 | a0001c0001t0001g0362 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.330+9896C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160020754 | ||||||
chr5:160020770
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.330+9912A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160020770 | ||||||
chr5:160020776
|
A | G | 4 | a0001c0001t0002g0342a0001c0001t0002g0356a0001c0001t0002g0357others(1): Show | 4 | NA18959.hp1 NA18969.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.330+9918A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160020776 | ||||||
chr5:160020912
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.330+10054C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160020912 | ||||||
chr5:160021129
|
C | T | 68 | a0001c0001t0001g0305a0001c0001t0001g0320a0001c0001t0001g0334others(65): Show | 69 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(66): Show |
intron_variant | MODIFIER | c.330+10271C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160021129 | ||||||
chr5:160021508
|
A | C | 68 | a0001c0001t0001g0305a0001c0001t0001g0320a0001c0001t0001g0334others(65): Show | 69 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(66): Show |
intron_variant | MODIFIER | c.330+10650A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160021508 | ||||||
chr5:160021570
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.330+10712C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160021570 | ||||||
chr5:160021620
|
C | G | 7 | a0001c0001t0001g0203a0001c0001t0001g0230a0001c0001t0001g0231others(4): Show | 7 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+10762C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160021620 | ||||||
chr5:160021793
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.330+10935G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160021793 | ||||||
chr5:160021834
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.330+10976A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160021834 | ||||||
chr5:160021959
|
T | A | 71 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0305others(68): Show | 72 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(69): Show |
intron_variant | MODIFIER | c.330+11101T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160021959 | ||||||
chr5:160022068
|
C | T | 1 | a0001c0001t0002g0341 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.330+11210C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160022068 | ||||||
chr5:160022092
|
CCT | C | 6 | a0001c0001t0001g0179a0002c0002t0001g0248a0002c0002t0001g0249others(3): Show | 6 | HG01928.hp1 HG02723.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.330+11235_330+1123 others(6): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160022092 | ||||||
chr5:160022293
|
T | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.330+11435T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160022293 | ||||||
chr5:160022435
|
A | G | 1 | a0001c0001t0001g0362 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.330+11577A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160022435 | ||||||
chr5:160022677
|
A | G | 1 | a0001c0001t0001g0184 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.330+11819A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160022677 | ||||||
chr5:160022695
|
G | C | 1 | a0001c0001t0002g0303 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.330+11837G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160022695 | ||||||
chr5:160022978
|
G | A | 16 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0056others(13): Show | 17 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.330+12120G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160022978 | ||||||
chr5:160023188
|
G | A | 2 | a0002c0002t0001g0012a0005c0005t0001g0013 | 2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.331-11952G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160023188 | ||||||
chr5:160023255
|
C | CA | 105 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0050others(102): Show | 109 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.331-11869dupA | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160023255 | |||||
chr5:160023255
|
C | CAA | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.331-11870_331-1186 others(6): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160023255 | |||||
chr5:160023351
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.331-11789A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160023351 | ||||||
chr5:160023406
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.331-11734C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160023406 | ||||||
chr5:160023428
|
A | G | 1 | a0001c0001t0001g0015 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.331-11712A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160023428 | ||||||
chr5:160023526
|
T | C | 3 | a0001c0001t0001g0364a0001c0001t0001g0365a0001c0001t0001g0366 | 3 | HG02055.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.331-11614T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160023526 | ||||||
chr5:160023745
|
T | G | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.331-11395T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160023745 | ||||||
chr5:160024056
|
C | CT | 9 | a0001c0001t0001g0058a0001c0001t0001g0171a0001c0001t0001g0172others(6): Show | 9 | HG01981.hp2 HG02155.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.331-11083dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160024056 | |||||
chr5:160024203
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.331-10937C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160024203 | ||||||
chr5:160024266
|
A | G | 1 | a0005c0005t0001g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.331-10874A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160024266 | ||||||
chr5:160024588
|
A | T | 68 | a0001c0001t0001g0305a0001c0001t0001g0320a0001c0001t0001g0334others(65): Show | 69 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(66): Show |
intron_variant | MODIFIER | c.331-10552A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160024588 | ||||||
chr5:160024589
|
C | T | 113 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0253others(110): Show | 117 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.331-10551C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160024589 | ||||||
chr5:160024664
|
AT | A | 69 | a0001c0001t0001g0255a0001c0001t0001g0284a0001c0001t0001g0285others(66): Show | 70 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(67): Show |
intron_variant | MODIFIER | c.331-10461delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160024664 | |||||
chr5:160024725
|
G | A | 1 | a0002c0002t0001g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.331-10415G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160024725 | ||||||
chr5:160024799
|
C | CTTG | 33 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0260others(30): Show | 36 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.331-10340_331-1033 others(7): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160024799 | |||||
chr5:160025050
|
C | T | 101 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0029others(98): Show | 102 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.331-10090C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160025050 | ||||||
chr5:160025092
|
A | G | 1 | a0005c0005t0001g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.331-10048A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160025092 | ||||||
chr5:160025265
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.331-9875C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160025265 | ||||||
chr5:160025316
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0101a0001c0001t0001g0155 | 3 | HG01884.hp1 HG03927.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.331-9824C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160025316 | ||||||
chr5:160025371
|
A | G | 3 | a0001c0001t0001g0364a0001c0001t0001g0365a0001c0001t0001g0366 | 3 | HG02055.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.331-9769A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160025371 | ||||||
chr5:160025427
|
G | A | 5 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(2): Show | 5 | HG01071.hp2 HG02055.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.331-9713G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160025427 | ||||||
chr5:160025575
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.331-9565A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160025575 | ||||||
chr5:160025898
|
A | T | 1 | a0001c0001t0001g0221 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.331-9242A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160025898 | ||||||
chr5:160026005
|
A | C | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0293 | 3 | NA18946.hp2 NA18975.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.331-9135A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160026005 | ||||||
chr5:160026155
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0063 | 2 | NA18962.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.331-8985G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160026155 | ||||||
chr5:160026208
|
G | C | 1 | a0001c0001t0001g0025 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.331-8932G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160026208 | ||||||
chr5:160026216
|
G | A | 2 | a0001c0001t0001g0284a0001c0001t0006g0283 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.331-8924G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160026216 | ||||||
chr5:160026219
|
G | A | 65 | a0001c0001t0001g0305a0001c0001t0001g0320a0001c0001t0001g0334others(62): Show | 66 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(63): Show |
intron_variant | MODIFIER | c.331-8921G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160026219 | ||||||
chr5:160026291
|
A | G | 1 | a0002c0002t0001g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.331-8849A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160026291 | ||||||
chr5:160026322
|
T | G | 65 | a0001c0001t0001g0305a0001c0001t0001g0320a0001c0001t0001g0334others(62): Show | 66 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(63): Show |
intron_variant | MODIFIER | c.331-8818T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160026322 | ||||||
chr5:160026415
|
A | G | 5 | a0001c0001t0001g0008a0001c0001t0001g0057a0001c0001t0001g0152others(2): Show | 6 | HG00140.hp2 HG01074.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.331-8725A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160026415 | ||||||
chr5:160026450
|
A | G | 1 | a0002c0002t0001g0252 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.331-8690A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160026450 | ||||||
chr5:160026595
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.331-8545C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160026595 | ||||||
chr5:160026789
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.331-8351T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160026789 | ||||||
chr5:160026848
|
T | G | 66 | a0001c0001t0001g0157a0001c0001t0001g0305a0001c0001t0001g0320others(63): Show | 67 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.331-8292T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160026848 | ||||||
chr5:160027128
|
C | G | 1 | a0001c0001t0001g0151 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.331-8012C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160027128 | ||||||
chr5:160027541
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.331-7599A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160027541 | ||||||
chr5:160027561
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.331-7579C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160027561 | ||||||
chr5:160027622
|
C | T | 47 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0253others(44): Show | 50 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.331-7518C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160027622 | ||||||
chr5:160027643
|
A | G | 118 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0253others(115): Show | 122 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.331-7497A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160027643 | ||||||
chr5:160027879
|
C | T | 5 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.331-7261C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160027879 | ||||||
chr5:160028014
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.331-7126C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160028014 | ||||||
chr5:160028095
|
C | G | 1 | a0001c0001t0001g0366 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.331-7045C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160028095 | ||||||
chr5:160028109
|
C | T | 4 | a0001c0001t0002g0342a0001c0001t0002g0356a0001c0001t0002g0357others(1): Show | 4 | NA18959.hp1 NA18969.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.331-7031C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160028109 | ||||||
chr5:160028293
|
C | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(42): Show | 48 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.331-6847C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160028293 | ||||||
chr5:160028298
|
C | CA | 79 | a0001c0001t0001g0037a0001c0001t0001g0053a0001c0001t0001g0065others(76): Show | 80 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.331-6823dupA | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160028298 | |||||
chr5:160028298
|
CA | C | 35 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0099others(32): Show | 38 | HG00609.hp2 HG01433.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.331-6823delA | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160028298 | |||||
chr5:160028460
|
C | T | 1 | a0001c0001t0001g0359 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.331-6680C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160028460 | ||||||
chr5:160028510
|
G | T | 1 | a0001c0001t0001g0240 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.331-6630G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160028510 | ||||||
chr5:160028512
|
C | T | 30 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0029others(27): Show | 30 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.331-6628C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160028512 | ||||||
chr5:160028646
|
T | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.331-6494T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160028646 | ||||||
chr5:160028666
|
G | C | 3 | a0001c0001t0001g0036a0001c0001t0001g0067a0001c0001t0001g0068 | 3 | HG00738.hp1 HG01975.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.331-6474G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160028666 | ||||||
chr5:160028672
|
C | T | 1 | a0001c0001t0002g0295 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.331-6468C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160028672 | ||||||
chr5:160029032
|
C | G | 1 | a0001c0001t0001g0218 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.331-6108C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160029032 | ||||||
chr5:160029200
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.331-5940G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160029200 | ||||||
chr5:160029285
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.331-5855C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160029285 | ||||||
chr5:160029466
|
A | AC | 68 | a0001c0001t0001g0118a0001c0001t0001g0305a0001c0001t0001g0320others(65): Show | 69 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(66): Show |
intron_variant | MODIFIER | c.331-5667dupC | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160029466 | |||||
chr5:160029481
|
C | CA | 14 | a0001c0001t0001g0070a0001c0001t0001g0119a0001c0001t0001g0133others(11): Show | 14 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.331-5641dupA | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160029481 | |||||
chr5:160029481
|
C | CAA | 48 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0009others(45): Show | 52 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.331-5642_331-5641d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160029481 | |||||
chr5:160029481
|
C | CAAA | 73 | a0001c0001t0001g0018a0001c0001t0001g0105a0001c0001t0001g0106others(70): Show | 74 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(71): Show |
intron_variant | MODIFIER | c.331-5643_331-5641d others(5): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160029481 | |||||
chr5:160029580
|
T | A | 1 | a0001c0001t0001g0120 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.331-5560T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160029580 | ||||||
chr5:160029583
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.331-5557G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160029583 | ||||||
chr5:160029680
|
G | T | 1 | a0001c0001t0001g0285 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.331-5460G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160029680 | ||||||
chr5:160029751
|
AC | A | 4 | a0002c0002t0001g0249a0002c0002t0001g0250a0002c0002t0001g0251others(1): Show | 4 | HG01928.hp1 HG03669.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.331-5387delC | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160029751 | |||||
chr5:160029771
|
C | T | 1 | a0001c0001t0002g0333 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.331-5369C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160029771 | ||||||
chr5:160029980
|
C | T | 1 | a0001c0001t0002g0332 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.331-5160C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160029980 | ||||||
chr5:160030025
|
A | C | 1 | a0005c0005t0001g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.331-5115A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030025 | ||||||
chr5:160030090
|
A | G | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | NA18986.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.331-5050A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030090 | ||||||
chr5:160030095
|
C | A | 1 | a0001c0001t0001g0267 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.331-5045C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030095 | ||||||
chr5:160030265
|
G | T | 1 | a0001c0001t0001g0285 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.331-4875G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030265 | ||||||
chr5:160030293
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.331-4847G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030293 | ||||||
chr5:160030376
|
G | C | 30 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0036others(27): Show | 31 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.331-4764G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030376 | ||||||
chr5:160030392
|
G | A | 6 | a0001c0001t0001g0285a0002c0002t0001g0012a0002c0002t0001g0249others(3): Show | 6 | HG01928.hp1 HG02486.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.331-4748G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030392 | ||||||
chr5:160030450
|
A | G | 1 | a0001c0001t0001g0263 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.331-4690A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030450 | ||||||
chr5:160030616
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.331-4524C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030616 | ||||||
chr5:160030637
|
G | C | 3 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211 | 3 | NA18986.hp1 NA19057.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.331-4503G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030637 | ||||||
chr5:160030836
|
A | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0169a0001c0001t0001g0170others(1): Show | 4 | NA18968.hp2 NA18993.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.331-4304A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030836 | ||||||
chr5:160030868
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.331-4272T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030868 | ||||||
chr5:160030980
|
T | A | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.331-4160T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030980 | ||||||
chr5:160031040
|
T | C | 1 | a0001c0001t0001g0268 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.331-4100T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160031040 | ||||||
chr5:160031048
|
T | C | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.331-4092T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160031048 | ||||||
chr5:160031085
|
A | G | 1 | a0002c0002t0001g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.331-4055A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160031085 | ||||||
chr5:160031152
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.331-3988C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160031152 | ||||||
chr5:160031165
|
T | A | 57 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0009others(54): Show | 61 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.331-3975T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160031165 | ||||||
chr5:160031622
|
T | A | 1 | a0002c0002t0001g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.331-3518T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160031622 | ||||||
chr5:160031715
|
A | T | 1 | a0001c0001t0001g0148 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.331-3425A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160031715 | ||||||
chr5:160031753
|
A | G | 6 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG00558.hp1 HG02027.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.331-3387A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160031753 | ||||||
chr5:160032285
|
A | G | 4 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(1): Show | 4 | HG02165.hp1 NA18612.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-2855A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160032285 | ||||||
chr5:160032427
|
C | G | 1 | a0001c0001t0001g0019 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.331-2713C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160032427 | ||||||
chr5:160032619
|
T | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0159 | 2 | NA18966.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.331-2521T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160032619 | ||||||
chr5:160032702
|
C | CT | 66 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(63): Show | 67 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.331-2408dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160032702 | |||||
chr5:160032702
|
C | CTT | 13 | a0001c0001t0001g0038a0001c0001t0001g0070a0001c0001t0001g0095others(10): Show | 13 | HG02055.hp1 HG02135.hp1 HG02300.hp1 others(10): Show |
intron_variant | MODIFIER | c.331-2409_331-2408d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160032702 | |||||
chr5:160032702
|
C | CTTT | 40 | a0001c0001t0001g0118a0001c0001t0001g0190a0001c0001t0001g0218others(37): Show | 41 | HG00408.hp2 HG01081.hp1 HG01256.hp1 others(38): Show |
intron_variant | MODIFIER | c.331-2410_331-2408d others(5): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160032702 | |||||
chr5:160032702
|
C | CTTTT | 18 | a0001c0001t0001g0334a0001c0001t0002g0295a0001c0001t0002g0297others(15): Show | 18 | HG00597.hp2 HG01192.hp1 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.331-2411_331-2408d others(6): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160032702 | |||||
chr5:160032702
|
C | CTTTTT | 10 | a0001c0001t0002g0294a0001c0001t0002g0298a0001c0001t0002g0299others(7): Show | 10 | HG01106.hp2 HG01175.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.331-2412_331-2408d others(7): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160032702 | |||||
chr5:160032702
|
CT | C | 18 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0059others(15): Show | 18 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.331-2408delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160032702 | |||||
chr5:160032702
|
CTT | C | 13 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0113others(10): Show | 16 | HG00423.hp2 HG00609.hp2 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.331-2409_331-2408d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160032702 | |||||
chr5:160032702
|
CTTT | C | 18 | a0001c0001t0001g0185a0001c0001t0001g0261a0001c0001t0001g0263others(15): Show | 18 | HG01175.hp2 HG01433.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.331-2410_331-2408d others(5): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160032702 | |||||
chr5:160032702
|
CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.331-2422_331-2408d others(17): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160032702 | |||||
chr5:160032754
|
G | A | 5 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.331-2386G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160032754 | ||||||
chr5:160032880
|
AT | A | 127 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0118others(124): Show | 131 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.331-2249delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160032880 | |||||
chr5:160032891
|
T | G | 42 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0133others(39): Show | 45 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.331-2249T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160032891 | ||||||
chr5:160033281
|
G | A | 74 | a0001c0001t0001g0118a0001c0001t0001g0253a0001c0001t0001g0254others(71): Show | 75 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(72): Show |
intron_variant | MODIFIER | c.331-1859G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160033281 | ||||||
chr5:160033336
|
T | C | 277 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(274): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.331-1804T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160033336 | ||||||
chr5:160033365
|
C | G | 1 | a0001c0001t0002g0342 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.331-1775C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160033365 | ||||||
chr5:160033484
|
A | G | 66 | a0001c0001t0001g0118a0001c0001t0001g0305a0001c0001t0001g0320others(63): Show | 67 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.331-1656A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160033484 | ||||||
chr5:160033550
|
A | C | 1 | a0001c0001t0006g0283 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.331-1590A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160033550 | ||||||
chr5:160033758
|
C | T | 2 | a0001c0001t0001g0284a0001c0001t0006g0283 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.331-1382C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160033758 | ||||||
chr5:160033794
|
C | T | 5 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.331-1346C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160033794 | ||||||
chr5:160034126
|
CT | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0026others(54): Show | 60 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.331-993delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160034126 | |||||
chr5:160034303
|
C | T | 120 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0118others(117): Show | 124 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.331-837C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160034303 | ||||||
chr5:160034711
|
A | AACTAAGG others(13): Show |
1 | a0001c0001t0001g0278 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.331-428_331-409dup others(20): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160034711 | |||||
chr5:160034731
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.331-409C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160034731 | ||||||
chr5:160034782
|
G | C | 4 | a0002c0002t0001g0249a0002c0002t0001g0250a0002c0002t0001g0251others(1): Show | 4 | HG01928.hp1 HG03669.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.331-358G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160034782 | ||||||
chr5:160034883
|
T | C | 2 | a0001c0001t0001g0284a0001c0001t0006g0283 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.331-257T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160034883 | ||||||
chr5:160034932
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.331-208T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160034932 | ||||||
chr5:160034938
|
C | A | 1 | a0001c0001t0002g0328 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.331-202C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160034938 | ||||||
chr5:160034976
|
T | C | 4 | a0001c0001t0002g0295a0001c0001t0002g0302a0001c0001t0002g0329others(1): Show | 4 | HG01175.hp1 HG01192.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.331-164T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160034976 | ||||||
chr5:160035413
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.391+213C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160035413 | ||||||
chr5:160035415
|
T | C | 20 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0014others(17): Show | 22 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(19): Show |
intron_variant | MODIFIER | c.391+215T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160035415 | ||||||
chr5:160035650
|
C | A | 5 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.391+450C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160035650 | ||||||
chr5:160035753
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.391+553G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160035753 | ||||||
chr5:160035952
|
G | GT | 23 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0018others(20): Show | 24 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.392-726dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 160035952 | |||||
chr5:160035953
|
T | G | 73 | a0001c0001t0001g0118a0001c0001t0001g0253a0001c0001t0001g0254others(70): Show | 74 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(71): Show |
intron_variant | MODIFIER | c.392-738T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160035953 | ||||||
chr5:160035954
|
T | G | 1 | a0003c0004t0002g0355 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.392-737T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160035954 | ||||||
chr5:160036115
|
A | C | 1 | a0001c0001t0001g0287 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.392-576A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160036115 | ||||||
chr5:160036357
|
T | G | 1 | a0001c0001t0002g0339 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.392-334T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160036357 | ||||||
chr5:160036358
|
G | A | 1 | a0001c0001t0002g0339 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.392-333G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160036358 | ||||||
chr5:160036400
|
A | G | 1 | a0002c0002t0001g0252 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.392-291A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160036400 | ||||||
chr5:160036534
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.392-157A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160036534 | ||||||
chr5:160036549
|
G | C | 74 | a0001c0001t0001g0118a0001c0001t0001g0253a0001c0001t0001g0254others(71): Show | 75 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(72): Show |
intron_variant | MODIFIER | c.392-142G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160036549 | ||||||
chr5:160036680
|
C | T | 4 | a0001c0001t0001g0020a0001c0001t0001g0135a0001c0001t0001g0196others(1): Show | 4 | HG01071.hp1 HG02109.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.392-11C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160036680 | ||||||
chr5:160037163
|
G | T | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG02735.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.504+360G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160037163 | ||||||
chr5:160037296
|
A | T | 3 | a0001c0001t0001g0127a0001c0001t0001g0192a0001c0001t0001g0193 | 3 | HG02258.hp1 HG02559.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.504+493A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160037296 | ||||||
chr5:160037666
|
A | G | 74 | a0001c0001t0001g0118a0001c0001t0001g0253a0001c0001t0001g0254others(71): Show | 75 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(72): Show |
intron_variant | MODIFIER | c.504+863A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160037666 | ||||||
chr5:160037742
|
C | A | 3 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211 | 3 | NA18986.hp1 NA19057.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.504+939C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160037742 | ||||||
chr5:160037743
|
G | T | 369 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(366): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.504+940G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160037743 | ||||||
chr5:160037781
|
G | GT | 11 | a0001c0001t0001g0050a0001c0001t0001g0147a0001c0001t0001g0226others(8): Show | 11 | HG00099.hp2 HG02074.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.504+992dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160037781 | |||||
chr5:160037899
|
G | T | 3 | a0001c0001t0001g0364a0001c0001t0001g0365a0001c0001t0001g0366 | 3 | HG02055.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.504+1096G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160037899 | ||||||
chr5:160037962
|
A | G | 1 | a0001c0001t0001g0178 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.504+1159A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160037962 | ||||||
chr5:160038013
|
G | T | 118 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0118others(115): Show | 122 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.504+1210G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160038013 | ||||||
chr5:160038016
|
T | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0076 | 2 | HG01099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.504+1213T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160038016 | ||||||
chr5:160038044
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0359a0001c0001t0001g0360others(2): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.504+1241G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160038044 | ||||||
chr5:160038086
|
G | GT | 16 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0034others(13): Show | 16 | HG01981.hp1 HG01981.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.504+1295dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160038086 | |||||
chr5:160038317
|
T | G | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.504+1514T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160038317 | ||||||
chr5:160038359
|
C | T | 1 | a0001c0001t0002g0339 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.504+1556C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160038359 | ||||||
chr5:160038659
|
C | CT | 74 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0043others(71): Show | 75 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(72): Show |
intron_variant | MODIFIER | c.504+1877dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160038659 | |||||
chr5:160038659
|
C | CTT | 7 | a0001c0001t0001g0320a0001c0001t0002g0294a0001c0001t0002g0319others(4): Show | 7 | HG01175.hp1 HG01978.hp1 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.504+1876_504+1877d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160038659 | |||||
chr5:160038659
|
CT | C | 6 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0106others(3): Show | 6 | HG02896.hp2 HG03041.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.504+1877delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160038659 | |||||
chr5:160038659
|
CTTTTTTT | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0185others(42): Show | 48 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.504+1871_504+1877d others(9): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160038659 | |||||
chr5:160038686
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.504+1883G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160038686 | ||||||
chr5:160038721
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.504+1918G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160038721 | ||||||
chr5:160038791
|
T | G | 115 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0118others(112): Show | 119 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.504+1988T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160038791 | ||||||
chr5:160038809
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.504+2006C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160038809 | ||||||
chr5:160038875
|
C | T | 4 | a0002c0002t0001g0249a0002c0002t0001g0250a0002c0002t0001g0251others(1): Show | 4 | HG01928.hp1 HG03669.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.504+2072C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160038875 | ||||||
chr5:160038882
|
C | T | 4 | a0002c0002t0001g0249a0002c0002t0001g0250a0002c0002t0001g0251others(1): Show | 4 | HG01928.hp1 HG03669.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.504+2079C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160038882 | ||||||
chr5:160038947
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.504+2144C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160038947 | ||||||
chr5:160039050
|
A | T | 1 | a0001c0001t0001g0022 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.504+2247A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160039050 | ||||||
chr5:160039207
|
T | C | 1 | a0002c0002t0001g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.504+2404T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160039207 | ||||||
chr5:160039221
|
AGTTTCAG others(48): Show |
A | 1 | a0001c0001t0001g0320 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.504+2419_504+2473d others(57): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160039221 | ||||||
chr5:160039247
|
A | G | 2 | a0001c0001t0001g0284a0001c0001t0006g0283 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.504+2444A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160039247 | ||||||
chr5:160039280
|
C | CT | 31 | a0001c0001t0001g0185a0001c0001t0001g0261a0001c0001t0001g0263others(28): Show | 31 | HG00423.hp2 HG00438.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.504+2494dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160039280 | |||||
chr5:160039280
|
C | CTT | 8 | a0001c0001t0001g0009a0001c0001t0001g0260a0001c0001t0001g0266others(5): Show | 9 | HG00609.hp2 NA18959.hp2 NA18965.hp2 others(6): Show |
intron_variant | MODIFIER | c.504+2493_504+2494d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160039280 | |||||
chr5:160039280
|
CT | C | 21 | a0001c0001t0001g0039a0001c0001t0001g0077a0001c0001t0001g0099others(18): Show | 21 | HG00639.hp1 HG01167.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.504+2494delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160039280 | |||||
chr5:160039306
|
T | C | 5 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.504+2503T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160039306 | ||||||
chr5:160039386
|
C | T | 46 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0185others(43): Show | 49 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.504+2583C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160039386 | ||||||
chr5:160039459
|
T | C | 1 | a0001c0001t0001g0287 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.504+2656T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160039459 | ||||||
chr5:160039532
|
C | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0088a0001c0001t0001g0089others(1): Show | 4 | HG00597.hp1 NA18747.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.504+2729C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160039532 | ||||||
chr5:160039539
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.504+2736G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160039539 | ||||||
chr5:160039643
|
A | G | 1 | a0001c0001t0001g0216 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.504+2840A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160039643 | ||||||
chr5:160039744
|
T | C | 46 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0185others(43): Show | 49 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.504+2941T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160039744 | ||||||
chr5:160039794
|
T | G | 73 | a0001c0001t0001g0118a0001c0001t0001g0203a0001c0001t0001g0230others(70): Show | 74 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.504+2991T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160039794 | ||||||
chr5:160040078
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.505-3055A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160040078 | ||||||
chr5:160040264
|
A | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0105a0001c0001t0001g0106others(4): Show | 7 | HG01109.hp1 HG01943.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.505-2869A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160040264 | ||||||
chr5:160040265
|
T | TAC | 8 | a0001c0001t0001g0008a0001c0001t0001g0057a0001c0001t0001g0152others(5): Show | 9 | HG00140.hp2 HG01074.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.505-2852_505-2851d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160040265 | |||||
chr5:160040323
|
G | A | 1 | a0001c0001t0001g0224 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.505-2810G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160040323 | ||||||
chr5:160040406
|
T | C | 46 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0185others(43): Show | 49 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.505-2727T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160040406 | ||||||
chr5:160040434
|
A | T | 66 | a0001c0001t0001g0118a0001c0001t0001g0305a0001c0001t0001g0320others(63): Show | 67 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.505-2699A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160040434 | ||||||
chr5:160040467
|
G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.505-2666G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160040467 | ||||||
chr5:160040475
|
G | A | 5 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(2): Show | 5 | HG01071.hp2 HG02055.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.505-2658G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160040475 | ||||||
chr5:160040482
|
G | C | 5 | a0001c0001t0001g0046a0001c0001t0001g0119a0001c0001t0001g0124others(2): Show | 5 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.505-2651G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160040482 | ||||||
chr5:160040494
|
AACTTT | A | 6 | a0002c0002t0001g0248a0002c0002t0001g0249a0002c0002t0001g0250others(3): Show | 6 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.505-2638_505-2634d others(7): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160040494 | ||||||
chr5:160040768
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.505-2365C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160040768 | ||||||
chr5:160040806
|
T | A | 1 | a0001c0001t0001g0076 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.505-2327T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160040806 | ||||||
chr5:160040870
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.505-2263G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160040870 | ||||||
chr5:160040945
|
AT | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0058others(48): Show | 54 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.505-2174delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160040945 | |||||
chr5:160041040
|
A | T | 1 | a0001c0001t0001g0320 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.505-2093A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160041040 | ||||||
chr5:160041091
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.505-2042G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160041091 | ||||||
chr5:160041247
|
T | C | 1 | a0001c0001t0001g0285 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.505-1886T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160041247 | ||||||
chr5:160041313
|
C | CT | 104 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0020others(101): Show | 107 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.505-1804dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160041313 | |||||
chr5:160041313
|
C | CTT | 7 | a0001c0001t0001g0144a0001c0001t0001g0253a0001c0001t0001g0254others(4): Show | 7 | HG00408.hp2 HG00673.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.505-1805_505-1804d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160041313 | |||||
chr5:160041372
|
G | A | 39 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0185others(36): Show | 42 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.505-1761G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160041372 | ||||||
chr5:160041496
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.505-1637A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160041496 | ||||||
chr5:160041686
|
A | G | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG02055.hp1 HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.505-1447A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160041686 | ||||||
chr5:160041800
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.505-1333C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160041800 | ||||||
chr5:160041827
|
C | T | 1 | a0001c0001t0002g0349 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.505-1306C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160041827 | ||||||
chr5:160041851
|
C | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.505-1282C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160041851 | ||||||
chr5:160042076
|
C | T | 1 | a0001c0001t0001g0366 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.505-1057C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160042076 | ||||||
chr5:160042178
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.505-955C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160042178 | ||||||
chr5:160042216
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.505-917C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160042216 | ||||||
chr5:160042222
|
G | A | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.505-911G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160042222 | ||||||
chr5:160042261
|
G | A | 5 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0284others(2): Show | 5 | HG02258.hp2 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.505-872G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160042261 | ||||||
chr5:160042270
|
T | A | 115 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0118others(112): Show | 119 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.505-863T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160042270 | ||||||
chr5:160042368
|
C | G | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.505-765C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160042368 | ||||||
chr5:160042440
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.505-693C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160042440 | ||||||
chr5:160042678
|
C | T | 2 | a0001c0001t0002g0308a0001c0001t0002g0336 | 2 | NA18962.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.505-455C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160042678 | ||||||
chr5:160042993
|
A | G | 10 | a0001c0001t0001g0023a0001c0001t0001g0045a0001c0001t0001g0157others(7): Show | 10 | HG00621.hp2 HG02027.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.505-140A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160042993 | ||||||
chr5:160043127
|
T | C | 5 | a0002c0002t0001g0248a0002c0002t0001g0249a0002c0002t0001g0250others(2): Show | 5 | HG01928.hp1 HG02723.hp2 HG03669.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.505-6T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160043127 | ||||||
chr5:160043240
|
G | T | 1 | a0005c0005t0001g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.541+71G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160043240 | ||||||
chr5:160043354
|
C | G | 1 | a0002c0002t0001g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.541+185C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160043354 | ||||||
chr5:160043408
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.541+239G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160043408 | ||||||
chr5:160043455
|
T | C | 1 | a0001c0001t0001g0243 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.541+286T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160043455 | ||||||
chr5:160043542
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.541+373G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160043542 | ||||||
chr5:160043572
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.541+403A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160043572 | ||||||
chr5:160043876
|
A | G | 1 | a0001c0001t0006g0283 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.541+707A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160043876 | ||||||
chr5:160043886
|
TA | T | 3 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0006g0283 | 3 | HG02258.hp2 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.541+719delA | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160043886 | |||||
chr5:160043932
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.541+763C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160043932 | ||||||
chr5:160043962
|
G | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.541+793G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160043962 | ||||||
chr5:160044052
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.541+883T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160044052 | ||||||
chr5:160044053
|
G | A | 127 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0118others(124): Show | 131 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.541+884G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160044053 | ||||||
chr5:160044575
|
G | GTGGGGGA others(6): Show |
1 | a0001c0001t0001g0320 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.541+1411_541+1412i others(15): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160044575 | |||||
chr5:160044798
|
G | A | 7 | a0002c0002t0001g0012a0002c0002t0001g0248a0002c0002t0001g0249others(4): Show | 7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.541+1629G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160044798 | ||||||
chr5:160044804
|
C | T | 6 | a0002c0002t0001g0248a0002c0002t0001g0249a0002c0002t0001g0250others(3): Show | 6 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.541+1635C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160044804 | ||||||
chr5:160045124
|
C | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0032others(8): Show | 13 | HG00140.hp2 HG00642.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.541+1955C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045124 | ||||||
chr5:160045163
|
C | T | 32 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0185others(29): Show | 35 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.541+1994C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045163 | ||||||
chr5:160045241
|
C | T | 1 | a0001c0001t0006g0283 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.541+2072C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045241 | ||||||
chr5:160045402
|
T | C | 9 | a0001c0001t0001g0015a0001c0001t0001g0029a0001c0001t0001g0163others(6): Show | 9 | HG00408.hp1 NA18949.hp2 NA18964.hp1 others(6): Show |
intron_variant | MODIFIER | c.541+2233T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045402 | ||||||
chr5:160045438
|
C | T | 72 | a0001c0001t0001g0118a0001c0001t0001g0284a0001c0001t0001g0285others(69): Show | 73 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.541+2269C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045438 | ||||||
chr5:160045443
|
T | G | 1 | a0001c0001t0001g0137 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.541+2274T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045443 | ||||||
chr5:160045449
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.541+2280A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045449 | ||||||
chr5:160045450
|
C | A | 1 | a0001c0001t0001g0137 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.541+2281C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045450 | ||||||
chr5:160045452
|
C | A | 1 | a0001c0001t0001g0137 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.541+2283C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045452 | ||||||
chr5:160045454
|
C | CCA | 16 | a0001c0001t0001g0045a0001c0001t0001g0059a0001c0001t0001g0060others(13): Show | 16 | HG01943.hp2 HG02040.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.541+2344_541+2345d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | |||||
chr5:160045454
|
C | CCACA | 12 | a0001c0001t0001g0049a0001c0001t0001g0092a0001c0001t0001g0096others(9): Show | 12 | HG00423.hp1 HG00609.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.541+2342_541+2345d others(6): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | |||||
chr5:160045454
|
C | CCACACA | 10 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(7): Show | 10 | HG00738.hp2 HG00741.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.541+2340_541+2345d others(8): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | |||||
chr5:160045454
|
C | CCACACAC others(1): Show |
6 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0058others(3): Show | 6 | HG00735.hp2 HG01169.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.541+2338_541+2345d others(10): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | |||||
chr5:160045454
|
C | CCACACAC others(3): Show |
1 | a0001c0001t0001g0051 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.541+2336_541+2345d others(12): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | |||||
chr5:160045454
|
C | CCACACAC others(5): Show |
2 | a0001c0001t0001g0022a0001c0001t0001g0173 | 2 | HG01884.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.541+2334_541+2345d others(14): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | |||||
chr5:160045454
|
C | CCACACAC others(7): Show |
1 | a0001c0001t0001g0177 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.541+2332_541+2345d others(16): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | |||||
chr5:160045454
|
CCA | C | 24 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0046others(21): Show | 24 | HG00639.hp2 HG01071.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.541+2344_541+2345d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | |||||
chr5:160045454
|
CCACA | C | 32 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0024others(29): Show | 33 | HG00738.hp1 HG01071.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.541+2342_541+2345d others(6): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | |||||
chr5:160045454
|
CCACACA | C | 31 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0019others(28): Show | 33 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.541+2340_541+2345d others(8): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | |||||
chr5:160045454
|
CCACACAC others(1): Show |
C | 26 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0040others(23): Show | 27 | HG00438.hp1 HG00558.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.541+2338_541+2345d others(10): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | |||||
chr5:160045454
|
CCACACAC others(3): Show |
C | 23 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0029others(20): Show | 25 | HG00140.hp2 HG00621.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.541+2336_541+2345d others(12): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | |||||
chr5:160045454
|
CCACACAC others(5): Show |
C | 18 | a0001c0001t0001g0018a0001c0001t0001g0055a0001c0001t0001g0116others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(15): Show |
intron_variant | MODIFIER | c.541+2334_541+2345d others(14): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | |||||
chr5:160045454
|
CCACACAC others(7): Show |
C | 8 | a0001c0001t0001g0011a0001c0001t0001g0044a0001c0001t0001g0075others(5): Show | 9 | HG01167.hp2 HG01169.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.541+2332_541+2345d others(16): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | |||||
chr5:160045454
|
CCACACAC others(9): Show |
C | 5 | a0001c0001t0001g0015a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG01256.hp2 HG01258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.541+2330_541+2345d others(18): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | |||||
chr5:160045454
|
CCACACAC others(11): Show |
C | 2 | a0001c0001t0001g0156a0001c0001t0001g0359 | 2 | HG01515.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.541+2328_541+2345d others(20): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | |||||
chr5:160045454
|
CCACACAC others(13): Show |
C | 4 | a0001c0001t0001g0158a0001c0001t0001g0169a0001c0001t0001g0170others(1): Show | 4 | NA18968.hp2 NA18993.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.541+2326_541+2345d others(22): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | |||||
chr5:160045454
|
CCACACAC others(15): Show |
C | 2 | a0001c0001t0001g0115a0001c0001t0001g0254 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.541+2324_541+2345d others(24): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | |||||
chr5:160045454
|
CCACACAC others(17): Show |
C | 8 | a0001c0001t0001g0009a0001c0001t0001g0271a0001c0001t0001g0286others(5): Show | 9 | HG02717.hp2 HG02723.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.541+2322_541+2345d others(26): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | |||||
chr5:160045454
|
CCACACAC others(19): Show |
C | 31 | a0001c0001t0001g0002a0001c0001t0001g0185a0001c0001t0001g0253others(28): Show | 33 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.541+2320_541+2345d others(28): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | |||||
chr5:160045454
|
CCACACAC others(25): Show |
C | 1 | a0001c0001t0001g0364 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.541+2314_541+2345d others(34): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | |||||
chr5:160045483
|
C | T | 4 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0365others(1): Show | 4 | HG02055.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.541+2314C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045483 | ||||||
chr5:160045485
|
C | T | 2 | a0001c0001t0002g0325a0001c0001t0006g0283 | 2 | HG02258.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.541+2316C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045485 | ||||||
chr5:160045486
|
A | G | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG02735.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.541+2317A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045486 | ||||||
chr5:160045487
|
C | T | 64 | a0001c0001t0001g0118a0001c0001t0001g0305a0001c0001t0001g0320others(61): Show | 65 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(62): Show |
intron_variant | MODIFIER | c.541+2318C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045487 | ||||||
chr5:160045487
|
CACACACA others(21): Show |
C | 2 | a0001c0001t0001g0365a0001c0001t0001g0366 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.541+2325_541+2352d others(30): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045487 | |||||
chr5:160045489
|
C | T | 1 | a0001c0001t0002g0356 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.541+2320C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045489 | ||||||
chr5:160045491
|
CACACACA others(17): Show |
C | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.541+2329_541+2352d others(26): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045491 | |||||
chr5:160045493
|
CACACACA others(15): Show |
C | 3 | a0002c0002t0001g0249a0002c0002t0001g0250a0002c0002t0001g0251 | 3 | HG01928.hp1 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.541+2331_541+2352d others(24): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045493 | |||||
chr5:160045494
|
A | T | 1 | a0001c0001t0006g0283 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.541+2325A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045494 | ||||||
chr5:160045496
|
A | T | 3 | a0001c0001t0002g0301a0001c0001t0002g0325a0001c0001t0006g0283 | 3 | HG02258.hp2 NA19085.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.541+2327A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045496 | ||||||
chr5:160045496
|
ACACACAC others(19): Show |
A | 1 | a0001c0001t0002g0304 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.541+2329_541+2354d others(28): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045496 | |||||
chr5:160045497
|
CACACACA others(11): Show |
C | 4 | a0001c0001t0002g0317a0001c0001t0002g0325a0001c0001t0002g0357others(1): Show | 4 | NA18945.hp1 NA18959.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.541+2335_541+2352d others(20): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045497 | |||||
chr5:160045498
|
A | T | 61 | a0001c0001t0001g0118a0001c0001t0001g0305a0001c0001t0001g0320others(58): Show | 62 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(59): Show |
intron_variant | MODIFIER | c.541+2329A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045498 | ||||||
chr5:160045499
|
CACACACA others(9): Show |
C | 23 | a0001c0001t0001g0335a0001c0001t0002g0296a0001c0001t0002g0297others(20): Show | 23 | HG01175.hp1 HG01256.hp1 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.541+2337_541+2352d others(18): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045499 | |||||
chr5:160045500
|
A | T | 39 | a0001c0001t0001g0118a0001c0001t0001g0305a0001c0001t0001g0320others(36): Show | 40 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.541+2331A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045500 | ||||||
chr5:160045501
|
CACACACA others(7): Show |
C | 28 | a0001c0001t0001g0118a0001c0001t0001g0305a0001c0001t0001g0320others(25): Show | 29 | HG00408.hp2 HG00597.hp2 HG01928.hp2 others(26): Show |
intron_variant | MODIFIER | c.541+2339_541+2352d others(16): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045501 | |||||
chr5:160045502
|
A | T | 11 | a0001c0001t0002g0295a0001c0001t0002g0299a0001c0001t0002g0308others(8): Show | 11 | HG01081.hp1 HG01106.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.541+2333A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045502 | ||||||
chr5:160045503
|
CACACACA others(5): Show |
C | 6 | a0001c0001t0002g0295a0001c0001t0002g0299a0001c0001t0002g0313others(3): Show | 6 | HG01106.hp2 HG01192.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.541+2341_541+2352d others(14): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045503 | |||||
chr5:160045504
|
A | T | 5 | a0001c0001t0002g0308a0001c0001t0002g0315a0001c0001t0002g0316others(2): Show | 5 | HG01081.hp1 HG02148.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.541+2335A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045504 | ||||||
chr5:160045505
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.541+2336C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045505 | ||||||
chr5:160045505
|
CACACACA others(3): Show |
C | 2 | a0001c0001t0001g0368a0001c0001t0002g0315 | 2 | HG01081.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.541+2343_541+2352d others(12): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045505 | |||||
chr5:160045506
|
A | T | 4 | a0001c0001t0002g0308a0001c0001t0002g0316a0001c0001t0002g0333others(1): Show | 4 | HG02148.hp2 NA18972.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.541+2337A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045506 | ||||||
chr5:160045508
|
A | T | 3 | a0001c0001t0002g0308a0001c0001t0002g0316a0001c0001t0002g0333 | 3 | HG02148.hp2 NA19060.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.541+2339A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045508 | ||||||
chr5:160045510
|
A | T | 2 | a0001c0001t0002g0308a0001c0001t0002g0316 | 2 | HG02148.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.541+2341A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045510 | ||||||
chr5:160045511
|
CACAT | C | 3 | a0001c0001t0001g0168a0001c0001t0002g0308a0001c0001t0002g0316 | 3 | HG02148.hp2 NA19005.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.541+2346_541+2349d others(6): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045511 | |||||
chr5:160045512
|
ACATACAC others(5): Show |
A | 1 | a0001c0001t0001g0161 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.541+2345_541+2356d others(14): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045512 | |||||
chr5:160045515
|
T | C | 7 | a0001c0001t0001g0134a0001c0001t0001g0155a0001c0001t0001g0202others(4): Show | 7 | HG00280.hp1 HG00642.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.541+2346T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045515 | ||||||
chr5:160045516
|
A | T | 67 | a0001c0001t0001g0118a0001c0001t0001g0284a0001c0001t0001g0305others(64): Show | 68 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(65): Show |
intron_variant | MODIFIER | c.541+2347A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045516 | ||||||
chr5:160045518
|
A | T | 71 | a0001c0001t0001g0118a0001c0001t0001g0284a0001c0001t0001g0285others(68): Show | 72 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(69): Show |
intron_variant | MODIFIER | c.541+2349A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045518 | ||||||
chr5:160045518
|
ACACTCTC others(7): Show |
A | 1 | a0001c0001t0001g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.541+2351_541+2364d others(16): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045518 | |||||
chr5:160045520
|
A | ACT | 12 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0084others(9): Show | 12 | HG02055.hp1 HG02109.hp1 HG02683.hp1 others(9): Show |
intron_variant | MODIFIER | c.541+2383_541+2384d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045520 | |||||
chr5:160045520
|
A | ACTCT | 37 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0015others(34): Show | 40 | HG00609.hp2 HG01109.hp1 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.541+2381_541+2384d others(6): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045520 | |||||
chr5:160045520
|
A | ACTCTCT | 7 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0269others(4): Show | 7 | HG00423.hp2 HG00438.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.541+2379_541+2384d others(8): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045520 | |||||
chr5:160045520
|
A | ACTCTCTC others(1): Show |
3 | a0001c0001t0001g0185a0001c0001t0001g0266a0001c0001t0001g0270 | 3 | HG01175.hp2 HG02135.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.541+2377_541+2384d others(10): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045520 | |||||
chr5:160045520
|
A | ACTCTCTC others(3): Show |
1 | a0001c0001t0001g0253 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.541+2375_541+2384d others(12): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045520 | |||||
chr5:160045520
|
A | ACTCTCTC others(9): Show |
2 | a0001c0001t0001g0254a0002c0002t0001g0248 | 2 | HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.541+2369_541+2384d others(18): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045520 | |||||
chr5:160045520
|
A | T | 76 | a0001c0001t0001g0050a0001c0001t0001g0118a0001c0001t0001g0134others(73): Show | 77 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.541+2351A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045520 | ||||||
chr5:160045520
|
ACT | A | 17 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0032others(14): Show | 19 | HG00140.hp2 HG00642.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.541+2383_541+2384d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045520 | |||||
chr5:160045520
|
ACTCT | A | 13 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0045others(10): Show | 13 | HG00673.hp1 HG01071.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.541+2381_541+2384d others(6): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045520 | |||||
chr5:160045520
|
ACTCTCTC others(1): Show |
A | 6 | a0001c0001t0001g0035a0001c0001t0001g0120a0001c0001t0001g0125others(3): Show | 6 | HG00741.hp2 HG01952.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.541+2377_541+2384d others(10): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045520 | |||||
chr5:160045520
|
ACTCTCTC others(3): Show |
A | 1 | a0001c0001t0001g0022 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.541+2375_541+2384d others(12): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045520 | |||||
chr5:160045522
|
T | A | 4 | a0001c0001t0001g0023a0001c0001t0001g0160a0001c0001t0001g0162others(1): Show | 4 | HG02027.hp1 HG03098.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.541+2353T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045522 | ||||||
chr5:160045554
|
C | T | 114 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0118others(111): Show | 118 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.541+2385C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045554 | ||||||
chr5:160045556
|
C | T | 72 | a0001c0001t0001g0118a0001c0001t0001g0284a0001c0001t0001g0285others(69): Show | 73 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.541+2387C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045556 | ||||||
chr5:160045558
|
T | C | 1 | a0001c0001t0001g0285 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.541+2389T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045558 | ||||||
chr5:160045558
|
TC | T | 7 | a0001c0001t0001g0305a0001c0001t0002g0308a0001c0001t0002g0331others(4): Show | 7 | HG01952.hp2 HG01993.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.541+2393delC | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045558 | |||||
chr5:160045560
|
C | T | 1 | a0001c0001t0002g0338 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.541+2391C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045560 | ||||||
chr5:160045570
|
A | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0185others(28): Show | 34 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.541+2401A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045570 | ||||||
chr5:160045682
|
C | G | 34 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0185others(31): Show | 37 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.541+2513C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045682 | ||||||
chr5:160045733
|
T | C | 1 | a0001c0001t0001g0366 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.541+2564T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045733 | ||||||
chr5:160045903
|
C | T | 5 | a0002c0002t0001g0248a0002c0002t0001g0249a0002c0002t0001g0250others(2): Show | 5 | HG01928.hp1 HG02723.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.541+2734C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045903 | ||||||
chr5:160046087
|
C | A | 72 | a0001c0001t0001g0118a0001c0001t0001g0284a0001c0001t0001g0285others(69): Show | 73 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.541+2918C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160046087 | ||||||
chr5:160046117
|
C | T | 1 | a0002c0002t0001g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.541+2948C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160046117 | ||||||
chr5:160046270
|
C | T | 5 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.541+3101C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160046270 | ||||||
chr5:160046645
|
T | C | 5 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.542-2869T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160046645 | ||||||
chr5:160046789
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.542-2725G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160046789 | ||||||
chr5:160046826
|
T | G | 1 | a0002c0002t0001g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.542-2688T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160046826 | ||||||
chr5:160046877
|
C | T | 37 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0185others(34): Show | 40 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.542-2637C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160046877 | ||||||
chr5:160046883
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.542-2631G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160046883 | ||||||
chr5:160047152
|
CAACTCTG others(582): Show |
C | 2 | a0001c0001t0001g0264a0001c0001t0001g0265 | 2 | HG00423.hp2 HG00438.hp2 |
intron_variant | MODIFIER | c.542-2360_542-1772d others(2): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160047152 | |||||
chr5:160047186
|
G | T | 1 | a0001c0001t0001g0034 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.542-2328G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160047186 | ||||||
chr5:160047256
|
A | C | 1 | a0001c0001t0001g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.542-2258A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160047256 | ||||||
chr5:160047265
|
C | A | 1 | a0001c0001t0001g0143 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.542-2249C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160047265 | ||||||
chr5:160047378
|
T | C | 1 | a0001c0001t0001g0104 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.542-2136T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160047378 | ||||||
chr5:160047410
|
T | G | 66 | a0001c0001t0001g0118a0001c0001t0001g0305a0001c0001t0001g0320others(63): Show | 67 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.542-2104T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160047410 | ||||||
chr5:160047597
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.542-1917T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160047597 | ||||||
chr5:160047672
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.542-1842C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160047672 | ||||||
chr5:160047779
|
A | C | 3 | a0001c0001t0001g0122a0001c0001t0001g0129a0001c0001t0001g0130 | 3 | HG02615.hp1 HG02886.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.542-1735A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160047779 | ||||||
chr5:160047797
|
C | G | 11 | a0001c0001t0002g0301a0001c0001t0002g0308a0001c0001t0002g0311others(8): Show | 11 | HG02132.hp2 NA18951.hp1 NA18962.hp2 others(8): Show |
intron_variant | MODIFIER | c.542-1717C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160047797 | ||||||
chr5:160047858
|
G | A | 66 | a0001c0001t0001g0118a0001c0001t0001g0305a0001c0001t0001g0320others(63): Show | 67 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.542-1656G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160047858 | ||||||
chr5:160047933
|
G | A | 249 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(246): Show | 259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.542-1581G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160047933 | ||||||
chr5:160048094
|
G | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.542-1420G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048094 | ||||||
chr5:160048126
|
CTT | C | 22 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0115others(19): Show | 24 | HG00423.hp1 HG01106.hp1 HG01515.hp2 others(21): Show |
intron_variant | MODIFIER | c.542-1353_542-1352d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160048126 | |||||
chr5:160048126
|
CTTT | C | 22 | a0001c0001t0001g0046a0001c0001t0001g0058a0001c0001t0001g0113others(19): Show | 22 | HG00280.hp1 HG00673.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.542-1354_542-1352d others(5): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160048126 | |||||
chr5:160048126
|
CTTTTTTT others(1): Show |
C | 22 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0034others(19): Show | 22 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(19): Show |
intron_variant | MODIFIER | c.542-1359_542-1352d others(10): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160048126 | |||||
chr5:160048126
|
CTTTTTTT others(2): Show |
C | 94 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(91): Show | 100 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.542-1360_542-1352d others(11): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160048126 | |||||
chr5:160048126
|
CTTTTTTT others(3): Show |
C | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(184): Show | 192 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.542-1361_542-1352d others(12): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160048126 | |||||
chr5:160048126
|
CTTTTTTT others(4): Show |
C | 6 | a0001c0001t0001g0043a0001c0001t0001g0221a0001c0001t0001g0232others(3): Show | 6 | HG01081.hp1 HG01167.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.542-1362_542-1352d others(13): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160048126 | |||||
chr5:160048126
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0285 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.542-1364_542-1352d others(15): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160048126 | |||||
chr5:160048162
|
T | G | 1 | a0001c0001t0001g0230 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.542-1352T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048162 | ||||||
chr5:160048179
|
T | C | 5 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.542-1335T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048179 | ||||||
chr5:160048186
|
T | G | 1 | a0001c0001t0001g0287 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.542-1328T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048186 | ||||||
chr5:160048197
|
G | A | 1 | a0001c0001t0002g0299 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.542-1317G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048197 | ||||||
chr5:160048309
|
G | A | 1 | a0001c0001t0001g0289 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.542-1205G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048309 | ||||||
chr5:160048391
|
T | C | 3 | a0001c0001t0002g0301a0001c0001t0002g0321a0001c0001t0002g0337 | 3 | NA18951.hp1 NA18967.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.542-1123T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048391 | ||||||
chr5:160048459
|
C | G | 6 | a0002c0002t0001g0248a0002c0002t0001g0249a0002c0002t0001g0250others(3): Show | 6 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.542-1055C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048459 | ||||||
chr5:160048469
|
A | G | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.542-1045A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048469 | ||||||
chr5:160048529
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.542-985A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048529 | ||||||
chr5:160048548
|
G | A | 5 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0284others(2): Show | 5 | HG02258.hp2 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.542-966G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048548 | ||||||
chr5:160048667
|
C | G | 1 | a0001c0001t0001g0068 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.542-847C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048667 | ||||||
chr5:160048686
|
A | G | 2 | a0001c0001t0001g0071a0001c0001t0007g0206 | 2 | HG00558.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.542-828A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048686 | ||||||
chr5:160048746
|
C | G | 1 | a0005c0005t0001g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.542-768C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048746 | ||||||
chr5:160048929
|
T | C | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.542-585T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048929 | ||||||
chr5:160048937
|
C | A | 41 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0185others(38): Show | 44 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.542-577C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048937 | ||||||
chr5:160048949
|
TA | T | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.542-553delA | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160048949 | |||||
chr5:160049020
|
T | C | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.542-494T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160049020 | ||||||
chr5:160049078
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.542-436C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160049078 | ||||||
chr5:160049278
|
G | A | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(168): Show | 176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.542-236G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160049278 | ||||||
chr5:160049369
|
A | G | 1 | a0001c0001t0001g0366 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.542-145A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160049369 | ||||||
chr5:160049488
|
A | G | 2 | a0001c0001t0001g0284a0001c0001t0006g0283 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.542-26A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160049488 | ||||||
chr5:160050161
|
C | A | 46 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0185others(43): Show | 49 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.690+499C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | chr5 | 160050161 | ||||||
chr5:160050185
|
C | T | 46 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0185others(43): Show | 49 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.690+523C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | chr5 | 160050185 | ||||||
chr5:160050193
|
C | A | 46 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0185others(43): Show | 49 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.690+531C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | chr5 | 160050193 | ||||||
chr5:160050214
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.690+552G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | chr5 | 160050214 | ||||||
chr5:160050345
|
G | A | 46 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0185others(43): Show | 49 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.690+683G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | chr5 | 160050345 | ||||||
chr5:160050423
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.691-706G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | chr5 | 160050423 | ||||||
chr5:160050474
|
A | T | 3 | a0001c0001t0001g0048a0001c0001t0001g0103a0001c0001t0001g0157 | 3 | HG00741.hp1 HG04204.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.691-655A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | chr5 | 160050474 | ||||||
chr5:160050510
|
C | CATCTGAT others(4): Show |
1 | a0001c0001t0001g0214 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.691-615_691-605dup others(11): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 160050510 | |||||
chr5:160050510
|
C | T | 1 | a0001c0001t0002g0296 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.691-619C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | chr5 | 160050510 | ||||||
chr5:160050627
|
C | CT | 62 | a0001c0001t0001g0118a0001c0001t0001g0133a0001c0001t0001g0204others(59): Show | 63 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(60): Show |
intron_variant | MODIFIER | c.691-482dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 160050627 | |||||
chr5:160050627
|
C | CTT | 6 | a0001c0001t0001g0320a0001c0001t0001g0334a0001c0001t0001g0335others(3): Show | 6 | HG01993.hp2 HG04115.hp2 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.691-483_691-482dup others(2): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 160050627 | |||||
chr5:160050627
|
CT | C | 226 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(223): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.691-482delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 160050627 | |||||
chr5:160050761
|
G | A | 34 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0185others(31): Show | 37 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.691-368G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | chr5 | 160050761 | ||||||
chr5:160050816
|
G | C | 1 | a0001c0001t0001g0288 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.691-313G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | chr5 | 160050816 | ||||||
chr5:160050905
|
C | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0185others(31): Show | 37 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.691-224C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | chr5 | 160050905 | ||||||
chr5:160050977
|
G | GT | 200 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(197): Show | 207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.691-140dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 160050977 | |||||
chr5:160051082
|
GT | G | 258 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(255): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.691-31delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 160051082 | |||||
chr5:160051082
|
GTT | G | 24 | a0001c0001t0001g0079a0001c0001t0001g0118a0001c0001t0001g0127others(21): Show | 25 | HG01081.hp1 HG01106.hp2 HG01928.hp1 others(22): Show |
intron_variant | MODIFIER | c.691-32_691-31delTT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 160051082 | |||||
chr5:160051087
|
T | G | 2 | a0001c0001t0001g0284a0001c0001t0006g0283 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.691-42T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | chr5 | 160051087 | ||||||
chr5:160051331
|
G | A | 5 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.745+148G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160051331 | ||||||
chr5:160051427
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.745+244A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160051427 | ||||||
chr5:160051534
|
G | A | 319 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(316): Show | 330 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.745+351G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160051534 | ||||||
chr5:160051633
|
C | T | 48 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0116others(45): Show | 51 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.745+450C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160051633 | ||||||
chr5:160051769
|
T | C | 1 | a0001c0001t0002g0310 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.745+586T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160051769 | ||||||
chr5:160051969
|
C | G | 1 | a0001c0001t0001g0075 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.745+786C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160051969 | ||||||
chr5:160052059
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.745+876G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160052059 | ||||||
chr5:160052168
|
C | CA | 48 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0116others(45): Show | 51 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.745+991dupA | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160052168 | |||||
chr5:160052235
|
CG | C | 3 | a0001c0001t0001g0049a0001c0001t0001g0070a0001c0001t0001g0102 | 3 | HG02135.hp1 HG03017.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.745+1054delG | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160052235 | |||||
chr5:160052391
|
ATGGGAGG others(6): Show |
A | 20 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0014others(17): Show | 22 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(19): Show |
intron_variant | MODIFIER | c.745+1211_745+1223d others(15): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160052391 | |||||
chr5:160052548
|
C | A | 1 | a0001c0001t0001g0077 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.745+1365C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160052548 | ||||||
chr5:160052548
|
C | CA | 38 | a0001c0001t0001g0046a0001c0001t0001g0132a0001c0001t0001g0133others(35): Show | 38 | HG00642.hp1 HG00673.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.745+1391dupA | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160052548 | |||||
chr5:160052548
|
C | CAA | 7 | a0001c0001t0001g0017a0001c0001t0001g0141a0001c0001t0001g0147others(4): Show | 7 | HG00597.hp2 HG00642.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.745+1390_745+1391d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160052548 | |||||
chr5:160052548
|
C | CAAA | 120 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(117): Show | 123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.745+1389_745+1391d others(5): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160052548 | |||||
chr5:160052548
|
C | CAAAA | 51 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0018others(48): Show | 53 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.745+1388_745+1391d others(6): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160052548 | |||||
chr5:160052548
|
C | CAAAAA | 14 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0033others(11): Show | 16 | HG01243.hp2 HG01978.hp2 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.745+1387_745+1391d others(7): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160052548 | |||||
chr5:160052548
|
CAAAAA | C | 6 | a0001c0001t0001g0185a0001c0001t0001g0257a0001c0001t0001g0278others(3): Show | 6 | HG01175.hp2 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.745+1387_745+1391d others(7): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160052548 | |||||
chr5:160052548
|
CAAAAAA | C | 40 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0255others(37): Show | 43 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.745+1386_745+1391d others(8): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160052548 | |||||
chr5:160052548
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0065 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.745+1380_745+1391d others(14): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160052548 | |||||
chr5:160052572
|
A | C | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.745+1389A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160052572 | ||||||
chr5:160052893
|
C | T | 1 | a0002c0002t0001g0249 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.745+1710C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160052893 | ||||||
chr5:160053151
|
AT | A | 48 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0116others(45): Show | 51 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.745+1970delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160053151 | |||||
chr5:160053186
|
A | G | 1 | a0001c0001t0004g0262 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.745+2003A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160053186 | ||||||
chr5:160053463
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.745+2280C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160053463 | ||||||
chr5:160053611
|
G | A | 250 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.745+2428G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160053611 | ||||||
chr5:160053691
|
A | G | 32 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0036others(29): Show | 33 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.745+2508A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160053691 | ||||||
chr5:160054026
|
G | A | 3 | a0001c0001t0001g0359a0001c0001t0001g0360a0001c0001t0001g0361 | 3 | HG02630.hp1 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.745+2843G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160054026 | ||||||
chr5:160054069
|
G | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0185others(31): Show | 37 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.745+2886G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160054069 | ||||||
chr5:160054075
|
T | TTTTG | 3 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0287 | 3 | HG01192.hp2 HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.745+2913_745+2916d others(6): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160054075 | |||||
chr5:160054075
|
TTTTG | T | 5 | a0002c0002t0001g0248a0002c0002t0001g0249a0002c0002t0001g0250others(2): Show | 5 | HG01928.hp1 HG02723.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.745+2913_745+2916d others(6): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160054075 | |||||
chr5:160054108
|
C | G | 2 | a0001c0001t0001g0284a0001c0001t0006g0283 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.745+2925C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160054108 | ||||||
chr5:160054287
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.745+3104A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160054287 | ||||||
chr5:160054408
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0363 | 3 | HG02280.hp2 HG02895.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.745+3225G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160054408 | ||||||
chr5:160054625
|
A | T | 1 | a0005c0005t0001g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.745+3442A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160054625 | ||||||
chr5:160054743
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.745+3560A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160054743 | ||||||
chr5:160054777
|
G | A | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.745+3594G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160054777 | ||||||
chr5:160054925
|
G | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0236 | 2 | HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.745+3742G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160054925 | ||||||
chr5:160055034
|
G | A | 6 | a0001c0001t0001g0011a0001c0001t0001g0359a0001c0001t0001g0360others(3): Show | 7 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.745+3851G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160055034 | ||||||
chr5:160055080
|
A | C | 1 | a0001c0001t0001g0290 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.745+3897A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160055080 | ||||||
chr5:160055230
|
T | G | 1 | a0001c0001t0001g0290 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.745+4047T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160055230 | ||||||
chr5:160055493
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.745+4310A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160055493 | ||||||
chr5:160055573
|
G | T | 48 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0116others(45): Show | 51 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.745+4390G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160055573 | ||||||
chr5:160055604
|
T | C | 1 | a0001c0001t0001g0363 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.745+4421T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160055604 | ||||||
chr5:160055735
|
G | T | 1 | a0001c0001t0001g0290 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.745+4552G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160055735 | ||||||
chr5:160055953
|
A | G | 1 | a0001c0001t0002g0336 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.745+4770A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160055953 | ||||||
chr5:160056015
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.745+4832G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160056015 | ||||||
chr5:160056119
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.745+4936C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160056119 | ||||||
chr5:160056134
|
T | C | 48 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0116others(45): Show | 51 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.745+4951T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160056134 | ||||||
chr5:160056354
|
T | A | 1 | a0001c0001t0001g0290 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.745+5171T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160056354 | ||||||
chr5:160056490
|
C | A | 1 | a0001c0001t0001g0290 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.745+5307C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160056490 | ||||||
chr5:160056567
|
A | T | 1 | a0001c0001t0001g0290 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.745+5384A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160056567 | ||||||
chr5:160056568
|
T | A | 1 | a0001c0001t0001g0290 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.745+5385T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160056568 | ||||||
chr5:160056768
|
A | C | 250 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.745+5585A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160056768 | ||||||
chr5:160056928
|
A | C | 1 | a0001c0001t0001g0290 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.745+5745A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160056928 | ||||||
chr5:160056929
|
C | A | 1 | a0001c0001t0001g0290 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.745+5746C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160056929 | ||||||
chr5:160056941
|
C | T | 3 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0246 | 3 | HG02523.hp1 NA19010.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.745+5758C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160056941 | ||||||
chr5:160057040
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.745+5857C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160057040 | ||||||
chr5:160057358
|
T | A | 1 | a0001c0001t0001g0021 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.745+6175T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160057358 | ||||||
chr5:160057418
|
T | A | 48 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0116others(45): Show | 51 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.745+6235T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160057418 | ||||||
chr5:160057809
|
G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.745+6626G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160057809 | ||||||
chr5:160057884
|
C | T | 2 | a0001c0001t0001g0284a0001c0001t0006g0283 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.745+6701C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160057884 | ||||||
chr5:160058047
|
G | A | 34 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0185others(31): Show | 37 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.745+6864G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058047 | ||||||
chr5:160058133
|
G | T | 204 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(201): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.746-6799G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058133 | ||||||
chr5:160058219
|
T | C | 259 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(256): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.746-6713T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058219 | ||||||
chr5:160058240
|
C | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0236 | 2 | HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.746-6692C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058240 | ||||||
chr5:160058262
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.746-6670A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058262 | ||||||
chr5:160058389
|
T | C | 1 | a0001c0001t0001g0285 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.746-6543T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058389 | ||||||
chr5:160058409
|
C | CT | 18 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0019others(15): Show | 20 | HG00140.hp2 HG00642.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.746-6504dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160058409 | |||||
chr5:160058409
|
CT | C | 18 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0077others(15): Show | 18 | HG01071.hp1 HG01167.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.746-6504delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160058409 | |||||
chr5:160058413
|
T | C | 2 | a0001c0001t0001g0284a0001c0001t0006g0283 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.746-6519T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058413 | ||||||
chr5:160058414
|
T | G | 5 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0284others(2): Show | 5 | HG02258.hp2 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.746-6518T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058414 | ||||||
chr5:160058486
|
G | C | 1 | a0001c0001t0006g0283 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.746-6446G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058486 | ||||||
chr5:160058579
|
T | A | 19 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0029others(16): Show | 19 | HG00408.hp1 HG00621.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.746-6353T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058579 | ||||||
chr5:160058616
|
G | A | 195 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(192): Show | 202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.746-6316G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058616 | ||||||
chr5:160058691
|
G | A | 30 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0185others(27): Show | 33 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.746-6241G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058691 | ||||||
chr5:160058702
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.746-6230C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058702 | ||||||
chr5:160058741
|
A | G | 190 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(187): Show | 197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.746-6191A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058741 | ||||||
chr5:160058775
|
T | C | 308 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(305): Show | 319 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.746-6157T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058775 | ||||||
chr5:160058795
|
G | C | 195 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(192): Show | 202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.746-6137G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058795 | ||||||
chr5:160058891
|
C | G | 5 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0284others(2): Show | 5 | HG02258.hp2 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.746-6041C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058891 | ||||||
chr5:160058928
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.746-6004T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058928 | ||||||
chr5:160059012
|
G | A | 66 | a0001c0001t0001g0118a0001c0001t0001g0305a0001c0001t0001g0320others(63): Show | 67 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.746-5920G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160059012 | ||||||
chr5:160059084
|
G | A | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(180): Show | 190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.746-5848G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160059084 | ||||||
chr5:160059193
|
GT | G | 225 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(222): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.746-5735delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160059193 | |||||
chr5:160059252
|
G | C | 1 | a0001c0001t0001g0224 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.746-5680G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160059252 | ||||||
chr5:160059347
|
T | C | 196 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(193): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.746-5585T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160059347 | ||||||
chr5:160059425
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.746-5507G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160059425 | ||||||
chr5:160059687
|
G | T | 1 | a0005c0005t0001g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.746-5245G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160059687 | ||||||
chr5:160059729
|
G | A | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(180): Show | 190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.746-5203G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160059729 | ||||||
chr5:160059809
|
G | A | 5 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(2): Show | 5 | HG01071.hp2 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.746-5123G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160059809 | ||||||
chr5:160059962
|
G | A | 1 | a0001c0001t0001g0221 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.746-4970G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160059962 | ||||||
chr5:160060243
|
C | T | 1 | a0001c0001t0002g0337 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.746-4689C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160060243 | ||||||
chr5:160060316
|
A | G | 196 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(193): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.746-4616A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160060316 | ||||||
chr5:160060323
|
T | A | 190 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(187): Show | 197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.746-4609T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160060323 | ||||||
chr5:160060372
|
C | G | 196 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(193): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.746-4560C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160060372 | ||||||
chr5:160060384
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.746-4548C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160060384 | ||||||
chr5:160060468
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.746-4464C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160060468 | ||||||
chr5:160060618
|
T | A | 196 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(193): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.746-4314T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160060618 | ||||||
chr5:160060639
|
T | G | 1 | a0002c0002t0001g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.746-4293T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160060639 | ||||||
chr5:160060832
|
T | C | 1 | a0002c0002t0001g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.746-4100T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160060832 | ||||||
chr5:160060946
|
G | A | 196 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(193): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.746-3986G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160060946 | ||||||
chr5:160061088
|
C | T | 66 | a0001c0001t0001g0118a0001c0001t0001g0305a0001c0001t0001g0320others(63): Show | 67 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.746-3844C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160061088 | ||||||
chr5:160061329
|
C | T | 1 | a0005c0005t0001g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.746-3603C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160061329 | ||||||
chr5:160061345
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.746-3587C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160061345 | ||||||
chr5:160061358
|
G | A | 44 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0116others(41): Show | 47 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.746-3574G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160061358 | ||||||
chr5:160061550
|
G | A | 2 | a0001c0001t0001g0205a0001c0001t0001g0285 | 2 | HG02622.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.746-3382G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160061550 | ||||||
chr5:160061660
|
CT | C | 46 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0116others(43): Show | 49 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.746-3261delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160061660 | |||||
chr5:160061671
|
T | C | 169 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(166): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.746-3261T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160061671 | ||||||
chr5:160061690
|
G | A | 39 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0116others(36): Show | 42 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.746-3242G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160061690 | ||||||
chr5:160061694
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0057a0001c0001t0001g0153others(1): Show | 5 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.746-3238A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160061694 | ||||||
chr5:160061915
|
C | G | 169 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(166): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.746-3017C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160061915 | ||||||
chr5:160061921
|
A | C | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(169): Show | 179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.746-3011A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160061921 | ||||||
chr5:160061964
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.746-2968C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160061964 | ||||||
chr5:160062062
|
T | C | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | NA18963.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.746-2870T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160062062 | ||||||
chr5:160062203
|
G | A | 2 | a0001c0001t0001g0266a0001c0001t0001g0275 | 2 | HG00609.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.746-2729G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160062203 | ||||||
chr5:160062230
|
C | T | 1 | a0005c0005t0001g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.746-2702C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160062230 | ||||||
chr5:160062448
|
C | T | 28 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0029others(25): Show | 28 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.746-2484C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160062448 | ||||||
chr5:160062543
|
T | C | 234 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(231): Show | 244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.746-2389T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160062543 | ||||||
chr5:160062807
|
GT | G | 35 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0185others(32): Show | 38 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.746-2115delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160062807 | |||||
chr5:160062863
|
G | A | 3 | a0001c0001t0001g0364a0001c0001t0001g0365a0001c0001t0001g0366 | 3 | HG02055.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.746-2069G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160062863 | ||||||
chr5:160062934
|
C | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.746-1998C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160062934 | ||||||
chr5:160062955
|
C | T | 4 | a0001c0001t0001g0091a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG01884.hp2 HG02572.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.746-1977C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160062955 | ||||||
chr5:160063032
|
G | A | 2 | a0001c0001t0001g0253a0001c0001t0006g0283 | 2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.746-1900G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160063032 | ||||||
chr5:160063240
|
T | C | 308 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(305): Show | 319 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.746-1692T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160063240 | ||||||
chr5:160063317
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.746-1615A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160063317 | ||||||
chr5:160063386
|
T | G | 4 | a0002c0002t0001g0249a0002c0002t0001g0250a0002c0002t0001g0251others(1): Show | 4 | HG01928.hp1 HG03669.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.746-1546T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160063386 | ||||||
chr5:160063622
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.746-1310T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160063622 | ||||||
chr5:160063748
|
A | G | 3 | a0001c0001t0001g0364a0001c0001t0001g0365a0001c0001t0001g0366 | 3 | HG02055.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.746-1184A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160063748 | ||||||
chr5:160063966
|
C | CT | 49 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0032others(46): Show | 52 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.746-946dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160063966 | |||||
chr5:160063966
|
C | CTT | 180 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.746-947_746-946dup others(2): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160063966 | |||||
chr5:160063966
|
C | CTTT | 75 | a0001c0001t0001g0019a0001c0001t0001g0027a0001c0001t0001g0038others(72): Show | 76 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(73): Show |
intron_variant | MODIFIER | c.746-948_746-946dup others(3): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160063966 | |||||
chr5:160064053
|
C | T | 1 | a0001c0001t0002g0304 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.746-879C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160064053 | ||||||
chr5:160064126
|
C | A | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.746-806C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160064126 | ||||||
chr5:160064501
|
C | G | 10 | a0001c0001t0002g0301a0001c0001t0002g0308a0001c0001t0002g0311others(7): Show | 10 | HG02132.hp2 NA18951.hp1 NA18962.hp2 others(7): Show |
intron_variant | MODIFIER | c.746-431C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160064501 | ||||||
chr5:160064513
|
A | G | 190 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(187): Show | 197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.746-419A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160064513 | ||||||
chr5:160064585
|
G | A | 5 | a0002c0002t0001g0248a0002c0002t0001g0249a0002c0002t0001g0250others(2): Show | 5 | HG01928.hp1 HG02723.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.746-347G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160064585 | ||||||
chr5:160064730
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.746-202G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160064730 | ||||||
chr5:160064761
|
A | G | 3 | a0001c0001t0001g0364a0001c0001t0001g0365a0001c0001t0001g0366 | 3 | HG02055.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.746-171A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160064761 | ||||||
chr5:160064828
|
A | AGATACTT others(263): Show |
1 | a0001c0001t0001g0147 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.746-88_746-87insTT others(268): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160064828 | |||||
chr5:160064828
|
A | AGATACTT others(264): Show |
1 | a0001c0001t0001g0137 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.746-88_746-87insTT others(269): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160064828 | |||||
chr5:160064828
|
A | AGATACTT others(265): Show |
1 | a0001c0001t0001g0141 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.746-88_746-87insTT others(270): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160064828 |