geneid | 54970 |
---|---|
ensemblid | ENSG00000149292.17 |
hgncid | 23700 |
symbol | TTC12 |
name | tetratricopeptide repeat domain 12 |
refseq_nuc | NM_017868.4 |
refseq_prot | NP_060338.3 |
ensembl_nuc | ENST00000529221.6 |
ensembl_prot | ENSP00000433757.1 |
mane_status | MANE Select |
chr | chr11 |
start | 113314583 |
end | 113366387 |
strand | + |
ver | v1.2 |
region | chr11:113314583-113366387 |
region5000 | chr11:113309583-113371387 |
regionname0 | TTC12_chr11_113314583_113366387 |
regionname5000 | TTC12_chr11_113309583_113371387 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 705 | 227 | 69 | 32 | 90 | 8 | 26 | 70 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0002 | 0/0 | 705 | 102 | 9 | 25 | 46 | 4 | 18 | 33 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0003 | 0/0 | 705 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0004 | 0/0 | 705 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0005 | 0/0 | 705 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0006 | 0/0 | 705 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0007 | 0/0 | 705 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0008 | 0/0 | 705 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0009 | 0/0 | 705 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0010 | 0/0 | 705 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0011 | 0/0 | 705 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0012 | 0/0 | 705 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2118 | 212 | 60 | 30 | 90 | 6 | 24 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
c0002 | 0/0 | 2118 | 93 | 5 | 25 | 44 | 4 | 15 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
c0003 | 0/0 | 2118 | 11 | 6 | 1 | 0 | 2 | 2 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
c0004 | 0/0 | 2118 | 4 | 4 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
c0005 | 0/0 | 2118 | 3 | 0 | 0 | 3 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
c0006 | 0/0 | 2118 | 3 | 2 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
c0007 | 0/0 | 2118 | 2 | 0 | 0 | 0 | 0 | 2 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
c0008 | 0/0 | 2118 | 2 | 0 | 2 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
c0009 | 0/0 | 2118 | 2 | 2 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
c0010 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
c0011 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
c0012 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
c0013 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
c0014 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
c0015 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
c0016 | 0/0 | 2118 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
c0017 | 0/0 | 2118 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
c0018 | 0/0 | 2118 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
c0019 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
c0020 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
c0021 | 0/0 | 2118 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 139 | 338 | 79 | 58 | 141 | 12 | 46 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
t0002 | 0/0 | 139 | 3 | 1 | 2 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
t0003 | 0/0 | 139 | 2 | 2 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
t0004 | 0/0 | 139 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0006 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0007 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0008 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0009 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0016 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0044 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0046 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0050 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0116 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0243 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2118 | 212 | 60 | 30 | 90 | 6 | 24 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0001c0003 | 0/0 | 2118 | 11 | 6 | 1 | 0 | 2 | 2 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0001c0006 | 0/0 | 2118 | 3 | 2 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0001c0011 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0002c0002 | 0/0 | 2118 | 93 | 5 | 25 | 44 | 4 | 15 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0002c0004 | 0/0 | 2118 | 4 | 4 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0002c0007 | 0/0 | 2118 | 2 | 0 | 0 | 0 | 0 | 2 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0002c0018 | 0/0 | 2118 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0002c0019 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0002c0020 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0003c0008 | 0/0 | 2118 | 2 | 0 | 2 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0003c0016 | 0/0 | 2118 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0004c0005 | 0/0 | 2118 | 3 | 0 | 0 | 3 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0005c0009 | 0/0 | 2118 | 2 | 2 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0006c0021 | 0/0 | 2118 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0007c0017 | 0/0 | 2118 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0008c0010 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0009c0012 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0010c0014 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0011c0013 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0012c0015 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2256 | 208 | 59 | 28 | 89 | 6 | 24 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0001c0001t0002 | 0/0 | 2256 | 3 | 1 | 2 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0001c0001t0004 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0001c0003t0001 | 0/0 | 2256 | 11 | 6 | 1 | 0 | 2 | 2 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0001c0006t0001 | 0/0 | 2256 | 3 | 2 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0001c0011t0001 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0002c0002t0001 | 0/0 | 2256 | 93 | 5 | 25 | 44 | 4 | 15 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0002c0004t0001 | 0/0 | 2256 | 4 | 4 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0002c0007t0001 | 0/0 | 2256 | 2 | 0 | 0 | 0 | 0 | 2 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0002c0018t0001 | 0/0 | 2256 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0002c0019t0001 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0002c0020t0001 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0003c0008t0001 | 0/0 | 2256 | 2 | 0 | 2 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0003c0016t0001 | 0/0 | 2256 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0004c0005t0001 | 0/0 | 2256 | 3 | 0 | 0 | 3 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0005c0009t0003 | 0/0 | 2256 | 2 | 2 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0006c0021t0001 | 0/0 | 2256 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0007c0017t0001 | 0/0 | 2256 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0008c0010t0001 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0009c0012t0001 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0010c0014t0001 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0011c0013t0001 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
a0012c0015t0001 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | copy fasta | chr11 | 113309583 | 113371387 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0007 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0050 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0116 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0243 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0003t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0003t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0003t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0006t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0006t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0001c0011t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0001 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0016 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0004t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0004t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0004t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0004t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0007t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0007t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0018t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0019t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0002c0020t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0003c0008t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0003c0016t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0004c0005t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0004c0005t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0005c0009t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0005c0009t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0006c0021t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0007c0017t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0008c0010t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0009c0012t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0010c0014t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0011c0013t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
a0012c0015t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0002 | c0002 | t0001 | g0016 | EUR | GBR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | GBR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0238 | EUR | FIN | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0195 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0041 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00642 | hp1 | a0001 | c0003 | t0001 | g0110 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0167 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0200 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0041 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0036 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0036 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0166 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0037 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0165 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0013 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01243 | hp2 | a0001 | c0006 | t0001 | g0022 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01255 | hp1 | a0003 | c0008 | t0001 | g0023 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0034 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0157 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01346 | hp1 | a0003 | c0008 | t0001 | g0023 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0159 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01516 | hp1 | a0001 | c0003 | t0001 | g0087 | EUR | IBS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01517 | hp1 | a0001 | c0003 | t0001 | g0086 | EUR | IBS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0037 | EUR | IBS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01891 | hp1 | a0001 | c0003 | t0001 | g0118 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0203 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0155 | AMR | PEL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0169 | AMR | PEL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02004 | hp2 | a0007 | c0017 | t0001 | g0006 | AMR | PEL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02027 | hp2 | a0011 | c0013 | t0001 | g0123 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02451 | hp2 | a0002 | c0004 | t0001 | g0173 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02572 | hp1 | a0005 | c0009 | t0003 | g0074 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02572 | hp2 | a0001 | c0011 | t0001 | g0058 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0196 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02647 | hp2 | a0001 | c0003 | t0001 | g0108 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0016 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0168 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0151 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0194 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02723 | hp2 | a0001 | c0003 | t0001 | g0220 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0197 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02738 | hp2 | a0001 | c0003 | t0001 | g0059 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02818 | hp2 | a0002 | c0004 | t0001 | g0176 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02896 | hp2 | a0005 | c0009 | t0003 | g0075 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03130 | hp1 | a0002 | c0004 | t0001 | g0172 | AFR | ESN | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03139 | hp2 | a0001 | c0006 | t0001 | g0201 | AFR | ESN | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | MSL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0190 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03239 | hp2 | a0003 | c0016 | t0001 | g0077 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03486 | hp2 | a0002 | c0004 | t0001 | g0174 | AFR | MSL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0034 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03491 | hp1 | a0002 | c0018 | t0001 | g0035 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0175 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03654 | hp2 | a0001 | c0003 | t0001 | g0217 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | STU | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | STU | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03710 | hp2 | a0002 | c0007 | t0001 | g0163 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | STU | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0150 | SAS | STU | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG04184 | hp2 | a0002 | c0007 | t0001 | g0164 | SAS | BEB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0187 | SAS | STU | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | STU | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0035 | SAS | STU | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG04228 | hp1 | a0006 | c0021 | t0001 | g0184 | SAS | STU | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0185 | SAS | STU | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | YRI | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | YRI | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | YRI | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | YRI | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18962 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18972 | hp1 | a0002 | c0020 | t0001 | g0183 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18974 | hp1 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18981 | hp1 | a0012 | c0015 | t0001 | g0061 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18988 | hp2 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18995 | hp1 | a0008 | c0010 | t0001 | g0145 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18997 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19009 | hp2 | a0004 | c0005 | t0001 | g0040 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19030 | hp1 | a0001 | c0006 | t0001 | g0022 | AFR | LWK | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | LWK | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | LWK | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | LWK | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19055 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19057 | hp1 | a0004 | c0005 | t0001 | g0040 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19083 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19086 | hp2 | a0004 | c0005 | t0001 | g0179 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19087 | hp1 | a0002 | c0019 | t0001 | g0248 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19240 | hp1 | a0009 | c0012 | t0001 | g0057 | AFR | YRI | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | YRI | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0198 | AFR | ASW | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0158 | EUR | TSI | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0016 | EUR | TSI | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | TSI | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | GIH | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0188 | SAS | GIH | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0207 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA20300 | hp1 | a0001 | c0003 | t0001 | g0205 | AFR | USA | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA20300 | hp2 | a0001 | c0003 | t0001 | g0109 | AFR | USA | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | LWK | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
NA21309 | hp2 | a0010 | c0014 | t0001 | g0114 | AFR | LWK | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0243 | REF | REF | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0116 | REF | REF | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:113323347
|
G | C | 1 | a0004 | 3 | NA19009.hp2 NA19057.hp1 NA19086.hp2 |
missense_variant | MODERATE | c.118G>C | p.Glu40Gln | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/22 | 169/2256 | 118/2118 | 40/705 | chr11 | 113323347 | ||
chr11:113323446
|
A | C | 5 | a0002a0004a0005others(2): Show | 109 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(106): Show |
missense_variant | MODERATE | c.217A>C | p.Met73Leu | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/22 | 268/2256 | 217/2118 | 73/705 | chr11 | 113323446 | ||
chr11:113325530
|
A | G | 1 | a0005 | 2 | HG02572.hp1 HG02896.hp2 |
missense_variant | MODERATE | c.329A>G | p.Lys110Arg | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/22 | 380/2256 | 329/2118 | 110/705 | chr11 | 113325530 | ||
chr11:113325570
|
A | C | 1 | a0006 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.369A>C | p.Glu123Asp | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/22 | 420/2256 | 369/2118 | 123/705 | chr11 | 113325570 | ||
chr11:113325584
|
G | A | 1 | a0008 | 1 | NA18995.hp1 | missense_variant | MODERATE | c.383G>A | p.Arg128His | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/22 | 434/2256 | 383/2118 | 128/705 | chr11 | 113325584 | ||
chr11:113352155
|
G | A | 1 | a0007 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.1394G>A | p.Arg465Gln | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/22 | 1445/2256 | 1394/2118 | 465/705 | chr11 | 113352155 | ||
chr11:113352163
|
A | T | 1 | a0003 | 3 | HG01255.hp1 HG01346.hp1 HG03239.hp2 |
missense_variant | MODERATE | c.1402A>T | p.Met468Leu | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/22 | 1453/2256 | 1402/2118 | 468/705 | chr11 | 113352163 | ||
chr11:113359426
|
A | G | 1 | a0012 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.1510A>G | p.Met504Val | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 17/22 | 1561/2256 | 1510/2118 | 504/705 | chr11 | 113359426 | ||
chr11:113362474
|
T | C | 1 | a0009 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.1688T>C | p.Val563Ala | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 19/22 | 1739/2256 | 1688/2118 | 563/705 | chr11 | 113362474 | ||
chr11:113363853
|
A | G | 1 | a0010 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1742A>G | p.Tyr581Cys | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 20/22 | 1793/2256 | 1742/2118 | 581/705 | chr11 | 113363853 | ||
chr11:113366253
|
G | A | 1 | a0011 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.2071G>A | p.Gly691Ser | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 22/22 | 2122/2256 | 2071/2118 | 691/705 | chr11 | 113366253 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:113323346
|
G | A | 1 | a0002c0007 | 2 | HG03710.hp2 HG04184.hp2 |
synonymous_variant | LOW | c.117G>A | p.Leu39Leu | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/22 | 168/2256 | 117/2118 | 39/705 | chr11 | 113323346 | ||
chr11:113325630
|
C | T | 1 | a0002c0020 | 1 | NA18972.hp1 | synonymous_variant | LOW | c.429C>T | p.Tyr143Tyr | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/22 | 480/2256 | 429/2118 | 143/705 | chr11 | 113325630 | ||
chr11:113339374
|
C | T | 1 | a0001c0006 | 3 | HG01243.hp2 HG03139.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.726C>T | p.Ala242Ala | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/22 | 777/2256 | 726/2118 | 242/705 | chr11 | 113339374 | ||
chr11:113344402
|
C | T | 3 | a0001c0003a0001c0006a0002c0019 | 15 | HG00642.hp1 HG01243.hp2 HG01516.hp1 others(12): Show |
synonymous_variant | LOW | c.1116C>T | p.Ser372Ser | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/22 | 1167/2256 | 1116/2118 | 372/705 | chr11 | 113344402 | ||
chr11:113352099
|
G | A | 2 | a0001c0011a0002c0004 | 5 | HG02451.hp2 HG02572.hp2 HG02818.hp2 others(2): Show |
synonymous_variant | LOW | c.1338G>A | p.Ser446Ser | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/22 | 1389/2256 | 1338/2118 | 446/705 | chr11 | 113352099 | ||
chr11:113363881
|
G | A | 1 | a0003c0016 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.1770G>A | p.Thr590Thr | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 20/22 | 1821/2256 | 1770/2118 | 590/705 | chr11 | 113363881 | ||
chr11:113364953
|
G | A | 1 | a0002c0018 | 1 | HG03491.hp1 | synonymous_variant | LOW | c.1935G>A | p.Thr645Thr | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/22 | 1986/2256 | 1935/2118 | 645/705 | chr11 | 113364953 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:113314607
|
T | A | 1 | a0001c0001t0002 | 3 | HG00738.hp1 HG01099.hp2 HG02559.hp2 |
5_prime_UTR_variant | MODIFIER | c.-27T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/22 | 1651 | chr11 | 113314607 | |||||
chr11:113314611
|
C | T | 1 | a0001c0001t0004 | 1 | NA18974.hp1 | 5_prime_UTR_variant | MODIFIER | c.-23C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/22 | 1647 | chr11 | 113314611 | |||||
chr11:113316254
|
C | T | 1 | a0005c0009t0003 | 2 | HG02572.hp1 HG02896.hp2 |
5_prime_UTR_variant | MODIFIER | c.-4C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/22 | 4 | chr11 | 113316254 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:113314683
|
G | T | 1 | a0001c0001t0001g0252 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-16+65G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113314683 | ||||||
chr11:113314745
|
C | T | 6 | a0001c0001t0001g0019a0001c0001t0001g0052a0001c0001t0001g0053others(3): Show | 10 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-16+127C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113314745 | ||||||
chr11:113314764
|
T | A | 1 | a0002c0002t0001g0054 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-16+146T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113314764 | ||||||
chr11:113314842
|
C | T | 1 | a0002c0019t0001g0248 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-16+224C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113314842 | ||||||
chr11:113314857
|
T | TGGGGCAG others(17): Show |
17 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(14): Show | 22 | HG00738.hp1 HG01099.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.-16+242_-16+265dup others(24): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 113314857 | |||||
chr11:113314857
|
T | TGGGGCAG others(41): Show |
8 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0218others(5): Show | 11 | HG01099.hp1 HG02280.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-16+265_-16+266ins others(48): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 113314857 | |||||
chr11:113314857
|
T | TGGGGCAG others(17): Show |
1 | a0001c0001t0001g0247 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-16+249_-16+250ins others(24): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 113314857 | |||||
chr11:113314869
|
C | CGCGCGGG others(17): Show |
28 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0049others(25): Show | 35 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.-16+265_-16+266ins others(24): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 113314869 | |||||
chr11:113314869
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-16+251C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113314869 | ||||||
chr11:113314873
|
C | T | 1 | a0001c0001t0001g0051 | 2 | NA18991.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-16+255C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113314873 | ||||||
chr11:113315080
|
C | T | 5 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0003t0001g0203others(2): Show | 5 | HG01891.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+462C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113315080 | ||||||
chr11:113315153
|
C | CT | 104 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(101): Show | 141 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.-16+536dupT | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 113315153 | |||||
chr11:113315223
|
ACTCGTCG others(11): Show |
A | 23 | a0002c0002t0001g0005a0002c0002t0001g0011a0002c0002t0001g0012others(20): Show | 34 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.-16+608_-16+625del others(18): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 113315223 | |||||
chr11:113315423
|
G | C | 2 | a0001c0001t0002g0043a0001c0001t0002g0206 | 3 | HG00738.hp1 HG01099.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-16+805G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113315423 | ||||||
chr11:113315594
|
A | G | 1 | a0001c0001t0002g0206 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-15-649A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113315594 | ||||||
chr11:113315650
|
A | G | 3 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0003t0001g0217 | 3 | HG03017.hp1 HG03654.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-15-593A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113315650 | ||||||
chr11:113315708
|
G | A | 1 | a0001c0001t0001g0048 | 2 | HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-15-535G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113315708 | ||||||
chr11:113315741
|
G | A | 6 | a0002c0002t0001g0036a0002c0002t0001g0037a0002c0002t0001g0165others(3): Show | 8 | HG00733.hp1 HG01081.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15-502G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113315741 | ||||||
chr11:113315750
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-15-493C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113315750 | ||||||
chr11:113316054
|
G | A | 162 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(159): Show | 217 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.-15-189G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113316054 | ||||||
chr11:113316073
|
C | T | 2 | a0005c0009t0003g0074a0005c0009t0003g0075 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-15-170C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113316073 | ||||||
chr11:113316157
|
C | T | 50 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0014others(47): Show | 72 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.-15-86C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113316157 | ||||||
chr11:113316455
|
G | C | 1 | a0002c0002t0001g0169 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.58+140G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113316455 | ||||||
chr11:113316961
|
A | G | 6 | a0001c0001t0001g0019a0001c0001t0001g0052a0001c0001t0001g0053others(3): Show | 10 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.58+646A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113316961 | ||||||
chr11:113317104
|
C | G | 1 | a0001c0001t0001g0148 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.58+789C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113317104 | ||||||
chr11:113317120
|
C | A | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG03017.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.58+805C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113317120 | ||||||
chr11:113317227
|
A | G | 50 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(47): Show | 65 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.58+912A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113317227 | ||||||
chr11:113317475
|
G | A | 140 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(137): Show | 192 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.58+1160G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113317475 | ||||||
chr11:113317536
|
C | T | 1 | a0002c0002t0001g0200 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.58+1221C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113317536 | ||||||
chr11:113317718
|
A | C | 3 | a0001c0001t0001g0050a0001c0001t0001g0245a0001c0001t0001g0246 | 4 | HG01243.hp1 HG02258.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.58+1403A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113317718 | ||||||
chr11:113317749
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.58+1434C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113317749 | ||||||
chr11:113317800
|
CT | C | 51 | a0001c0001t0001g0208a0002c0002t0001g0001a0002c0002t0001g0006others(48): Show | 73 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.58+1494delT | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 113317800 | |||||
chr11:113317810
|
A | C | 50 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0014others(47): Show | 72 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.58+1495A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113317810 | ||||||
chr11:113318003
|
T | G | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG03017.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.58+1688T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113318003 | ||||||
chr11:113318166
|
T | C | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0055others(3): Show | 8 | HG01109.hp1 HG01123.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.58+1851T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113318166 | ||||||
chr11:113318201
|
T | G | 23 | a0002c0002t0001g0005a0002c0002t0001g0011a0002c0002t0001g0012others(20): Show | 34 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.58+1886T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113318201 | ||||||
chr11:113318235
|
CAG | C | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0055others(3): Show | 8 | HG01109.hp1 HG01123.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.58+1924_58+1925del others(2): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 113318235 | |||||
chr11:113318411
|
T | C | 3 | a0001c0001t0001g0076a0003c0008t0001g0023a0003c0016t0001g0077 | 4 | HG01255.hp1 HG01346.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+2096T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113318411 | ||||||
chr11:113318515
|
C | T | 23 | a0002c0002t0001g0005a0002c0002t0001g0011a0002c0002t0001g0012others(20): Show | 34 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.58+2200C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113318515 | ||||||
chr11:113318570
|
C | T | 1 | a0002c0002t0001g0199 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.58+2255C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113318570 | ||||||
chr11:113318609
|
T | TG | 54 | a0001c0001t0002g0043a0001c0001t0002g0206a0001c0003t0001g0217others(51): Show | 77 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.58+2301dupG | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 113318609 | |||||
chr11:113318919
|
C | T | 2 | a0002c0007t0001g0163a0002c0007t0001g0164 | 2 | HG03710.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.58+2604C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113318919 | ||||||
chr11:113319025
|
A | G | 1 | a0001c0001t0001g0147 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.58+2710A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113319025 | ||||||
chr11:113319317
|
T | C | 2 | a0001c0001t0002g0043a0001c0001t0002g0206 | 3 | HG00738.hp1 HG01099.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.58+3002T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113319317 | ||||||
chr11:113319322
|
G | A | 3 | a0002c0002t0001g0038a0002c0002t0001g0170a0002c0002t0001g0171 | 4 | HG02071.hp1 NA18981.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.58+3007G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113319322 | ||||||
chr11:113319482
|
A | G | 1 | a0002c0002t0001g0207 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.58+3167A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113319482 | ||||||
chr11:113319503
|
G | A | 1 | a0002c0002t0001g0207 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.58+3188G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113319503 | ||||||
chr11:113319560
|
G | A | 58 | a0001c0001t0001g0019a0001c0001t0001g0052a0001c0001t0001g0053others(55): Show | 84 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.58+3245G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113319560 | ||||||
chr11:113319678
|
GA | G | 35 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0215others(32): Show | 47 | HG00609.hp1 HG00738.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.58+3376delA | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 113319678 | |||||
chr11:113319763
|
C | T | 1 | a0002c0002t0001g0198 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.58+3448C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113319763 | ||||||
chr11:113319802
|
C | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0055others(3): Show | 8 | HG01109.hp1 HG01123.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-3486C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113319802 | ||||||
chr11:113320153
|
C | T | 77 | a0001c0001t0001g0244a0002c0002t0001g0001a0002c0002t0001g0005others(74): Show | 110 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.59-3135C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320153 | ||||||
chr11:113320232
|
C | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0055others(3): Show | 8 | HG01109.hp1 HG01123.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-3056C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320232 | ||||||
chr11:113320233
|
G | A | 2 | a0005c0009t0003g0074a0005c0009t0003g0075 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.59-3055G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320233 | ||||||
chr11:113320246
|
A | G | 2 | a0005c0009t0003g0074a0005c0009t0003g0075 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.59-3042A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320246 | ||||||
chr11:113320248
|
G | C | 5 | a0002c0002t0001g0175a0002c0004t0001g0172a0002c0004t0001g0173others(2): Show | 5 | HG02451.hp2 HG02818.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3040G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320248 | ||||||
chr11:113320248
|
G | T | 3 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0003t0001g0217 | 3 | HG03017.hp1 HG03654.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.59-3040G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320248 | ||||||
chr11:113320330
|
A | C | 1 | a0001c0001t0001g0004 | 6 | HG00408.hp2 HG02129.hp1 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-2958A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320330 | ||||||
chr11:113320421
|
C | T | 5 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0003t0001g0203others(2): Show | 5 | HG01891.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-2867C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320421 | ||||||
chr11:113320424
|
C | A | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226 | 3 | HG02886.hp2 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.59-2864C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320424 | ||||||
chr11:113320537
|
A | C | 6 | a0001c0001t0001g0019a0001c0001t0001g0052a0001c0001t0001g0053others(3): Show | 10 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.59-2751A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320537 | ||||||
chr11:113320631
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | NA18970.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.59-2657G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320631 | ||||||
chr11:113320706
|
C | T | 49 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(46): Show | 64 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.59-2582C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320706 | ||||||
chr11:113320836
|
C | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG03017.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.59-2452C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320836 | ||||||
chr11:113320858
|
A | T | 1 | a0002c0002t0001g0197 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.59-2430A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320858 | ||||||
chr11:113320875
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.59-2413C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320875 | ||||||
chr11:113321365
|
G | T | 1 | a0008c0010t0001g0145 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.59-1923G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113321365 | ||||||
chr11:113321570
|
G | T | 10 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0215others(7): Show | 10 | HG01891.hp2 HG02572.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.59-1718G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113321570 | ||||||
chr11:113321590
|
A | G | 3 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0003t0001g0217 | 3 | HG03017.hp1 HG03654.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.59-1698A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113321590 | ||||||
chr11:113321648
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.59-1640G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113321648 | ||||||
chr11:113321684
|
G | A | 50 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0014others(47): Show | 72 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.59-1604G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113321684 | ||||||
chr11:113321702
|
A | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0250a0001c0001t0001g0251 | 5 | HG02258.hp1 HG02280.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-1586A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113321702 | ||||||
chr11:113321797
|
T | C | 1 | a0002c0002t0001g0150 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.59-1491T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113321797 | ||||||
chr11:113321799
|
C | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0242a0001c0001t0001g0243 | 6 | HG00642.hp2 HG01070.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-1489C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113321799 | ||||||
chr11:113321802
|
G | T | 140 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(137): Show | 192 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.59-1486G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113321802 | ||||||
chr11:113321859
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.59-1429A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113321859 | ||||||
chr11:113322075
|
C | T | 48 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(45): Show | 62 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.59-1213C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113322075 | ||||||
chr11:113322340
|
C | G | 134 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(131): Show | 182 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.59-948C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113322340 | ||||||
chr11:113322340
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.59-948C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113322340 | ||||||
chr11:113322484
|
C | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0209 | 3 | HG01358.hp1 NA18956.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.59-804C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113322484 | ||||||
chr11:113322484
|
C | G | 46 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(43): Show | 59 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.59-804C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113322484 | ||||||
chr11:113322595
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.59-693C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113322595 | ||||||
chr11:113322657
|
C | T | 1 | a0002c0002t0001g0168 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.59-631C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113322657 | ||||||
chr11:113322683
|
A | C | 1 | a0001c0003t0001g0205 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.59-605A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113322683 | ||||||
chr11:113322879
|
C | T | 134 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(131): Show | 182 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.59-409C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113322879 | ||||||
chr11:113322888
|
G | A | 1 | a0001c0001t0001g0024 | 2 | HG01255.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.59-400G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113322888 | ||||||
chr11:113322890
|
T | G | 1 | a0001c0001t0001g0144 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.59-398T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113322890 | ||||||
chr11:113322951
|
G | T | 1 | a0002c0002t0001g0207 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.59-337G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113322951 | ||||||
chr11:113323102
|
C | CA | 48 | a0001c0001t0001g0055a0001c0001t0001g0081a0001c0001t0001g0082others(45): Show | 63 | HG00609.hp1 HG01069.hp1 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.59-167dupA | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 113323102 | |||||
chr11:113323111
|
A | C | 1 | a0002c0002t0001g0162 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.59-177A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113323111 | ||||||
chr11:113323114
|
A | C | 1 | a0002c0002t0001g0200 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.59-174A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113323114 | ||||||
chr11:113323189
|
T | C | 1 | a0001c0001t0001g0085 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.59-99T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113323189 | ||||||
chr11:113323241
|
C | G | 21 | a0001c0001t0001g0017a0001c0001t0001g0044a0001c0001t0001g0045others(18): Show | 29 | HG00738.hp1 HG01099.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.59-47C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113323241 | ||||||
chr11:113323254
|
T | C | 1 | a0001c0001t0001g0008 | 3 | HG01074.hp2 HG03942.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.59-34T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113323254 | ||||||
chr11:113323499
|
C | A | 1 | a0002c0007t0001g0163 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.222+48C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/21 | chr11 | 113323499 | ||||||
chr11:113323510
|
G | A | 2 | a0001c0001t0001g0228a0001c0001t0001g0252 | 2 | HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.222+59G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/21 | chr11 | 113323510 | ||||||
chr11:113323597
|
AT | A | 23 | a0002c0002t0001g0005a0002c0002t0001g0011a0002c0002t0001g0012others(20): Show | 34 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.222+156delT | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr11 | 113323597 | |||||
chr11:113323640
|
C | T | 5 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0003t0001g0203others(2): Show | 5 | HG01891.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+189C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/21 | chr11 | 113323640 | ||||||
chr11:113323723
|
G | A | 2 | a0002c0002t0001g0015a0002c0002t0001g0177 | 4 | HG02015.hp1 HG02027.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.223-271G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/21 | chr11 | 113323723 | ||||||
chr11:113323726
|
T | G | 14 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0025others(11): Show | 18 | HG00140.hp2 HG01074.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.223-268T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/21 | chr11 | 113323726 | ||||||
chr11:113323739
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.223-255C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/21 | chr11 | 113323739 | ||||||
chr11:113323775
|
G | T | 1 | a0001c0001t0001g0222 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.223-219G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/21 | chr11 | 113323775 | ||||||
chr11:113323828
|
C | A | 5 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0003t0001g0203others(2): Show | 5 | HG01891.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-166C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/21 | chr11 | 113323828 | ||||||
chr11:113323932
|
A | G | 5 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0003t0001g0203others(2): Show | 5 | HG01891.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-62A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/21 | chr11 | 113323932 | ||||||
chr11:113324206
|
C | T | 8 | a0001c0001t0001g0050a0001c0001t0001g0228a0001c0001t0001g0239others(5): Show | 9 | HG01243.hp1 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.244+191C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 4/21 | chr11 | 113324206 | ||||||
chr11:113324319
|
C | A | 6 | a0001c0001t0001g0019a0001c0001t0001g0052a0001c0001t0001g0053others(3): Show | 10 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.245-286C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 4/21 | chr11 | 113324319 | ||||||
chr11:113324467
|
G | A | 3 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0003t0001g0217 | 3 | HG03017.hp1 HG03654.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.245-138G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 4/21 | chr11 | 113324467 | ||||||
chr11:113324482
|
G | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | NA18984.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.245-123G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 4/21 | chr11 | 113324482 | ||||||
chr11:113324687
|
T | G | 5 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0003t0001g0203others(2): Show | 5 | HG01891.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.322+5T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 5/21 | chr11 | 113324687 | ||||||
chr11:113324830
|
A | T | 1 | a0002c0002t0001g0196 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.322+148A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 5/21 | chr11 | 113324830 | ||||||
chr11:113324873
|
A | G | 154 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0010others(151): Show | 216 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.322+191A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 5/21 | chr11 | 113324873 | ||||||
chr11:113324889
|
A | G | 76 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(73): Show | 109 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.322+207A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 5/21 | chr11 | 113324889 | ||||||
chr11:113324974
|
G | A | 3 | a0002c0002t0001g0178a0002c0002t0001g0180a0002c0002t0001g0181 | 3 | HG00423.hp2 HG00673.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.322+292G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 5/21 | chr11 | 113324974 | ||||||
chr11:113325202
|
A | T | 2 | a0001c0001t0001g0070a0001c0006t0001g0022 | 3 | HG01243.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.323-322A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 5/21 | chr11 | 113325202 | ||||||
chr11:113325371
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.323-153T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 5/21 | chr11 | 113325371 | ||||||
chr11:113325435
|
G | A | 1 | a0003c0008t0001g0023 | 2 | HG01255.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.323-89G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 5/21 | chr11 | 113325435 | ||||||
chr11:113325509
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.323-15C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 5/21 | chr11 | 113325509 | ||||||
chr11:113325792
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.444+147A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113325792 | ||||||
chr11:113325811
|
C | G | 1 | a0001c0001t0001g0135 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.444+166C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113325811 | ||||||
chr11:113326026
|
C | T | 1 | a0002c0002t0001g0207 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.444+381C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113326026 | ||||||
chr11:113326029
|
C | CT | 4 | a0001c0001t0001g0241a0001c0011t0001g0058a0002c0002t0001g0175others(1): Show | 4 | HG02572.hp2 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+390dupT | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr11 | 113326029 | |||||
chr11:113326113
|
C | T | 13 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(10): Show | 16 | HG00558.hp2 HG00673.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.444+468C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113326113 | ||||||
chr11:113326136
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.444+491A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113326136 | ||||||
chr11:113326521
|
T | A | 171 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(168): Show | 236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.444+876T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113326521 | ||||||
chr11:113326550
|
GGAAGAGG others(11): Show |
G | 1 | a0002c0002t0001g0207 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.444+909_444+926del others(18): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr11 | 113326550 | |||||
chr11:113326598
|
TG | T | 5 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(2): Show | 5 | NA18945.hp2 NA18957.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+957delG | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr11 | 113326598 | |||||
chr11:113327350
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.444+1705C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113327350 | ||||||
chr11:113327421
|
AC | A | 80 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(77): Show | 104 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.444+1779delC | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr11 | 113327421 | |||||
chr11:113327517
|
G | T | 1 | a0001c0001t0001g0243 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.444+1872G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113327517 | ||||||
chr11:113327540
|
T | C | 1 | a0001c0001t0001g0029 | 2 | NA18960.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.444+1895T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113327540 | ||||||
chr11:113327792
|
C | G | 1 | a0001c0001t0001g0226 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.445-2128C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113327792 | ||||||
chr11:113327913
|
G | A | 1 | a0001c0006t0001g0022 | 2 | HG01243.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.445-2007G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113327913 | ||||||
chr11:113327963
|
C | G | 15 | a0001c0001t0001g0010a0001c0001t0001g0062a0001c0001t0001g0063others(12): Show | 17 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.445-1957C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113327963 | ||||||
chr11:113328177
|
G | A | 1 | a0002c0002t0001g0151 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.445-1743G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113328177 | ||||||
chr11:113328203
|
G | A | 2 | a0001c0003t0001g0059a0002c0019t0001g0248 | 2 | HG02738.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.445-1717G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113328203 | ||||||
chr11:113328210
|
G | A | 7 | a0001c0003t0001g0059a0001c0003t0001g0086a0001c0003t0001g0087others(4): Show | 8 | HG01243.hp2 HG01516.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.445-1710G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113328210 | ||||||
chr11:113328293
|
A | G | 4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0222others(1): Show | 6 | HG02622.hp1 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-1627A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113328293 | ||||||
chr11:113328302
|
A | C | 16 | a0001c0001t0001g0113a0001c0001t0001g0136a0001c0001t0001g0204others(13): Show | 16 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-1618A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113328302 | ||||||
chr11:113328424
|
C | T | 34 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0024others(31): Show | 55 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.445-1496C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113328424 | ||||||
chr11:113328504
|
A | G | 2 | a0004c0005t0001g0040a0004c0005t0001g0179 | 3 | NA19009.hp2 NA19057.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.445-1416A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113328504 | ||||||
chr11:113328551
|
C | G | 6 | a0001c0001t0001g0204a0001c0011t0001g0058a0002c0004t0001g0172others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-1369C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113328551 | ||||||
chr11:113328618
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.445-1302C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113328618 | ||||||
chr11:113328669
|
C | A | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG00733.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.445-1251C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113328669 | ||||||
chr11:113328983
|
G | A | 4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0222others(1): Show | 6 | HG02622.hp1 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-937G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113328983 | ||||||
chr11:113329142
|
T | A | 1 | a0002c0002t0001g0165 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.445-778T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113329142 | ||||||
chr11:113329281
|
C | T | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(112): Show | 146 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.445-639C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113329281 | ||||||
chr11:113329386
|
C | G | 1 | a0009c0012t0001g0057 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.445-534C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113329386 | ||||||
chr11:113329532
|
C | T | 2 | a0001c0006t0001g0022a0001c0006t0001g0201 | 3 | HG01243.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.445-388C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113329532 | ||||||
chr11:113329535
|
G | T | 1 | a0002c0002t0001g0171 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.445-385G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113329535 | ||||||
chr11:113329540
|
C | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0107a0001c0001t0002g0043 | 6 | HG00738.hp1 HG01099.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-380C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113329540 | ||||||
chr11:113329542
|
G | A | 7 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0110others(4): Show | 7 | HG00642.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-378G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113329542 | ||||||
chr11:113329582
|
C | T | 1 | a0001c0006t0001g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.445-338C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113329582 | ||||||
chr11:113329725
|
G | C | 1 | a0002c0002t0001g0005 | 5 | NA18960.hp2 NA19000.hp2 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-195G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113329725 | ||||||
chr11:113329836
|
A | G | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(96): Show | 129 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.445-84A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113329836 | ||||||
chr11:113329893
|
G | T | 1 | a0001c0001t0001g0106 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.445-27G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113329893 | ||||||
chr11:113329987
|
G | A | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(160): Show | 222 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(219): Show |
splice_region_variant&intron_variant | LOW | c.504+8G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113329987 | ||||||
chr11:113330009
|
A | G | 16 | a0001c0003t0001g0059a0001c0003t0001g0086a0001c0003t0001g0087others(13): Show | 17 | HG00642.hp1 HG01243.hp2 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.504+30A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113330009 | ||||||
chr11:113330063
|
G | T | 4 | a0001c0011t0001g0058a0002c0004t0001g0172a0002c0004t0001g0173others(1): Show | 4 | HG02451.hp2 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.504+84G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113330063 | ||||||
chr11:113330148
|
C | T | 1 | a0001c0001t0002g0206 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.504+169C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113330148 | ||||||
chr11:113330185
|
C | G | 2 | a0005c0009t0003g0074a0005c0009t0003g0075 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.504+206C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113330185 | ||||||
chr11:113330558
|
C | G | 35 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0020others(32): Show | 57 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.504+579C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113330558 | ||||||
chr11:113330615
|
C | G | 2 | a0001c0001t0001g0084a0001c0001t0001g0139 | 2 | NA18967.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.504+636C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113330615 | ||||||
chr11:113330647
|
C | T | 7 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0110others(4): Show | 7 | HG00642.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+668C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113330647 | ||||||
chr11:113330801
|
T | A | 1 | a0001c0001t0001g0249 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.504+822T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113330801 | ||||||
chr11:113330968
|
G | A | 1 | a0002c0002t0001g0194 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.504+989G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113330968 | ||||||
chr11:113331119
|
C | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(92): Show | 123 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.504+1140C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113331119 | ||||||
chr11:113331137
|
T | C | 1 | a0001c0003t0001g0217 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.504+1158T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113331137 | ||||||
chr11:113331230
|
G | A | 11 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0222others(8): Show | 14 | HG01243.hp2 HG01516.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.504+1251G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113331230 | ||||||
chr11:113331570
|
C | A | 1 | a0002c0002t0001g0034 | 2 | HG01261.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.504+1591C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113331570 | ||||||
chr11:113331689
|
A | G | 5 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0110others(2): Show | 5 | HG00642.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.504+1710A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113331689 | ||||||
chr11:113331708
|
G | C | 220 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(217): Show | 301 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(298): Show |
intron_variant | MODIFIER | c.504+1729G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113331708 | ||||||
chr11:113331966
|
T | C | 4 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0107others(1): Show | 8 | HG00738.hp1 HG01099.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.504+1987T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113331966 | ||||||
chr11:113332033
|
A | ATGCCAAT others(6056): Show |
1 | a0002c0002t0001g0170 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.504+2072_504+2073i others(6065): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr11 | 113332033 | |||||
chr11:113332301
|
C | A | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(110): Show | 144 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.504+2322C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113332301 | ||||||
chr11:113332421
|
C | T | 7 | a0001c0003t0001g0059a0001c0003t0001g0086a0001c0003t0001g0087others(4): Show | 8 | HG01243.hp2 HG01516.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.504+2442C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113332421 | ||||||
chr11:113332447
|
G | A | 1 | a0002c0002t0001g0165 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.504+2468G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113332447 | ||||||
chr11:113332526
|
C | T | 2 | a0002c0002t0001g0014a0002c0002t0001g0198 | 4 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.505-2440C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113332526 | ||||||
chr11:113332592
|
G | A | 1 | a0005c0009t0003g0074 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.505-2374G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113332592 | ||||||
chr11:113332717
|
A | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0079 | 3 | NA18970.hp1 NA19002.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.505-2249A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113332717 | ||||||
chr11:113332755
|
G | C | 2 | a0001c0006t0001g0022a0001c0006t0001g0201 | 3 | HG01243.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.505-2211G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113332755 | ||||||
chr11:113332796
|
A | G | 1 | a0001c0003t0001g0059 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.505-2170A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113332796 | ||||||
chr11:113333273
|
A | G | 2 | a0001c0003t0001g0059a0002c0019t0001g0248 | 2 | HG02738.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.505-1693A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333273 | ||||||
chr11:113333315
|
C | T | 5 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0110others(2): Show | 5 | HG00642.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.505-1651C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333315 | ||||||
chr11:113333352
|
C | A | 1 | a0012c0015t0001g0061 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.505-1614C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333352 | ||||||
chr11:113333435
|
T | A | 43 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(40): Show | 62 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.505-1531T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333435 | ||||||
chr11:113333488
|
G | A | 8 | a0001c0001t0001g0204a0001c0011t0001g0058a0002c0004t0001g0172others(5): Show | 8 | HG02451.hp2 HG02572.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.505-1478G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333488 | ||||||
chr11:113333544
|
C | T | 35 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0020others(32): Show | 57 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.505-1422C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333544 | ||||||
chr11:113333552
|
A | T | 5 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0110others(2): Show | 5 | HG00642.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.505-1414A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333552 | ||||||
chr11:113333558
|
G | A | 7 | a0001c0003t0001g0059a0001c0003t0001g0086a0001c0003t0001g0087others(4): Show | 8 | HG01243.hp2 HG01516.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.505-1408G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333558 | ||||||
chr11:113333649
|
G | C | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.505-1317G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333649 | ||||||
chr11:113333703
|
G | A | 2 | a0001c0006t0001g0022a0001c0006t0001g0201 | 3 | HG01243.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.505-1263G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333703 | ||||||
chr11:113333759
|
A | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(110): Show | 144 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.505-1207A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333759 | ||||||
chr11:113333807
|
A | T | 2 | a0001c0006t0001g0022a0001c0006t0001g0201 | 3 | HG01243.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.505-1159A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333807 | ||||||
chr11:113333840
|
C | A | 1 | a0001c0001t0001g0219 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.505-1126C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333840 | ||||||
chr11:113334028
|
G | A | 1 | a0002c0002t0001g0155 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.505-938G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113334028 | ||||||
chr11:113334074
|
A | T | 1 | a0002c0002t0001g0193 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.505-892A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113334074 | ||||||
chr11:113334130
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.505-836C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113334130 | ||||||
chr11:113334154
|
A | G | 1 | a0002c0002t0001g0197 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.505-812A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113334154 | ||||||
chr11:113334190
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.505-776A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113334190 | ||||||
chr11:113334296
|
G | A | 2 | a0001c0001t0001g0062a0002c0002t0001g0182 | 2 | NA18945.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.505-670G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113334296 | ||||||
chr11:113334313
|
C | A | 1 | a0001c0001t0001g0063 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.505-653C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113334313 | ||||||
chr11:113334452
|
G | T | 8 | a0001c0001t0001g0055a0001c0001t0001g0093a0001c0001t0001g0234others(5): Show | 8 | HG00323.hp1 HG02698.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.505-514G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113334452 | ||||||
chr11:113334456
|
ACT | A | 34 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0024others(31): Show | 55 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.505-509_505-508del others(2): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113334456 | ||||||
chr11:113334873
|
T | C | 2 | a0001c0006t0001g0022a0001c0006t0001g0201 | 3 | HG01243.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.505-93T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113334873 | ||||||
chr11:113335313
|
G | C | 2 | a0001c0001t0001g0078a0002c0020t0001g0183 | 2 | NA18972.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.576+276G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113335313 | ||||||
chr11:113335313
|
G | T | 1 | a0001c0001t0001g0132 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.576+276G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113335313 | ||||||
chr11:113335355
|
A | G | 4 | a0001c0003t0001g0059a0001c0003t0001g0086a0001c0003t0001g0087others(1): Show | 4 | HG01516.hp1 HG01517.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+318A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113335355 | ||||||
chr11:113335363
|
A | C | 34 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0024others(31): Show | 55 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.576+326A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113335363 | ||||||
chr11:113335415
|
T | C | 1 | a0001c0001t0001g0021 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.576+378T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113335415 | ||||||
chr11:113335467
|
T | C | 1 | a0001c0003t0001g0217 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.576+430T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113335467 | ||||||
chr11:113335553
|
G | A | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(156): Show | 214 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.576+516G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113335553 | ||||||
chr11:113335631
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.576+594C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113335631 | ||||||
chr11:113335742
|
A | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(103): Show | 136 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.576+705A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113335742 | ||||||
chr11:113336002
|
T | G | 7 | a0001c0003t0001g0059a0001c0003t0001g0086a0001c0003t0001g0087others(4): Show | 8 | HG01243.hp2 HG01516.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.576+965T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113336002 | ||||||
chr11:113336077
|
A | C | 34 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0024others(31): Show | 55 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.576+1040A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113336077 | ||||||
chr11:113336141
|
G | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0025 | 5 | HG01074.hp2 HG02004.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.576+1104G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113336141 | ||||||
chr11:113336145
|
T | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(92): Show | 123 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.576+1108T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113336145 | ||||||
chr11:113336357
|
T | G | 5 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0110others(2): Show | 5 | HG00642.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+1320T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113336357 | ||||||
chr11:113336362
|
G | A | 2 | a0001c0006t0001g0022a0001c0006t0001g0201 | 3 | HG01243.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.576+1325G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113336362 | ||||||
chr11:113336392
|
T | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0223a0001c0001t0001g0231 | 5 | HG02809.hp1 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.576+1355T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113336392 | ||||||
chr11:113336458
|
C | T | 1 | a0002c0002t0001g0192 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.576+1421C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113336458 | ||||||
chr11:113336854
|
C | G | 1 | a0001c0001t0001g0055 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.576+1817C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113336854 | ||||||
chr11:113336867
|
G | A | 5 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(2): Show | 5 | NA18945.hp2 NA18957.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.576+1830G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113336867 | ||||||
chr11:113336871
|
C | T | 1 | a0001c0001t0001g0021 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.576+1834C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113336871 | ||||||
chr11:113337224
|
A | C | 6 | a0001c0001t0001g0204a0001c0011t0001g0058a0002c0004t0001g0172others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.577-1550A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113337224 | ||||||
chr11:113337376
|
C | T | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(152): Show | 208 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.577-1398C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113337376 | ||||||
chr11:113337404
|
A | T | 1 | a0001c0001t0001g0055 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.577-1370A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113337404 | ||||||
chr11:113337421
|
T | C | 1 | a0002c0002t0001g0175 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.577-1353T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113337421 | ||||||
chr11:113337464
|
C | A | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(160): Show | 222 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.577-1310C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113337464 | ||||||
chr11:113337525
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.577-1249C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113337525 | ||||||
chr11:113337660
|
A | G | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(156): Show | 214 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.577-1114A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113337660 | ||||||
chr11:113337767
|
G | A | 7 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0110others(4): Show | 7 | HG00642.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.577-1007G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113337767 | ||||||
chr11:113337811
|
G | A | 80 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(77): Show | 104 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.577-963G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113337811 | ||||||
chr11:113337813
|
G | GGACCAGG others(14): Show |
2 | a0001c0003t0001g0203a0001c0003t0001g0205 | 2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.577-959_577-939dup others(21): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr11 | 113337813 | |||||
chr11:113338038
|
C | T | 2 | a0001c0006t0001g0022a0001c0006t0001g0201 | 3 | HG01243.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.577-736C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113338038 | ||||||
chr11:113338069
|
T | TTTG | 4 | a0002c0002t0001g0035a0002c0002t0001g0185a0002c0018t0001g0035others(1): Show | 4 | HG03491.hp1 HG04204.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-678_577-676dup others(3): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr11 | 113338069 | |||||
chr11:113338069
|
TTTG | T | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(148): Show | 206 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.577-678_577-676del others(3): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr11 | 113338069 | |||||
chr11:113338137
|
T | G | 1 | a0001c0001t0001g0250 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.577-637T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113338137 | ||||||
chr11:113338226
|
A | G | 1 | a0005c0009t0003g0074 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.577-548A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113338226 | ||||||
chr11:113338465
|
G | A | 1 | a0001c0003t0001g0118 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.577-309G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113338465 | ||||||
chr11:113338474
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0223 | 4 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-300A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113338474 | ||||||
chr11:113338486
|
A | G | 2 | a0001c0003t0001g0109a0001c0003t0001g0110 | 2 | HG00642.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.577-288A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113338486 | ||||||
chr11:113338706
|
C | G | 35 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0020others(32): Show | 57 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.577-68C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113338706 | ||||||
chr11:113338998
|
T | C | 1 | a0001c0001t0001g0020 | 2 | HG01109.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.637+164T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 9/21 | chr11 | 113338998 | ||||||
chr11:113339209
|
GA | G | 14 | a0001c0003t0001g0059a0001c0003t0001g0086a0001c0003t0001g0087others(11): Show | 15 | HG00642.hp1 HG01243.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.638-68delA | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 113339209 | |||||
chr11:113339639
|
G | T | 1 | a0001c0001t0001g0208 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.826+165G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113339639 | ||||||
chr11:113339712
|
C | T | 4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0222others(1): Show | 6 | HG02622.hp1 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.826+238C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113339712 | ||||||
chr11:113339736
|
T | A | 1 | a0001c0003t0001g0217 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.826+262T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113339736 | ||||||
chr11:113339868
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.826+394C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113339868 | ||||||
chr11:113339872
|
C | T | 2 | a0001c0003t0001g0086a0001c0003t0001g0087 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.826+398C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113339872 | ||||||
chr11:113339964
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.826+490G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113339964 | ||||||
chr11:113339973
|
C | T | 14 | a0001c0003t0001g0059a0001c0003t0001g0086a0001c0003t0001g0087others(11): Show | 15 | HG00642.hp1 HG01243.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.826+499C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113339973 | ||||||
chr11:113340039
|
G | A | 1 | a0001c0003t0001g0217 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.826+565G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113340039 | ||||||
chr11:113340068
|
T | A | 2 | a0002c0002t0001g0035a0002c0018t0001g0035 | 2 | HG03491.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.826+594T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113340068 | ||||||
chr11:113340268
|
G | T | 1 | a0001c0001t0001g0080 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.827-396G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113340268 | ||||||
chr11:113340390
|
G | A | 2 | a0001c0001t0001g0221a0001c0001t0001g0239 | 2 | HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.827-274G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113340390 | ||||||
chr11:113340414
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.827-250G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113340414 | ||||||
chr11:113340465
|
G | A | 2 | a0005c0009t0003g0074a0005c0009t0003g0075 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.827-199G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113340465 | ||||||
chr11:113340607
|
G | T | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(116): Show | 150 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.827-57G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113340607 | ||||||
chr11:113340648
|
T | G | 35 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0020others(32): Show | 57 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.827-16T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113340648 | ||||||
chr11:113340956
|
G | C | 1 | a0001c0001t0001g0020 | 2 | HG01109.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.896+223G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 11/21 | chr11 | 113340956 | ||||||
chr11:113341091
|
A | G | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(102): Show | 135 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.896+358A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 11/21 | chr11 | 113341091 | ||||||
chr11:113341251
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.896+518A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 11/21 | chr11 | 113341251 | ||||||
chr11:113341396
|
GATATAA | G | 1 | a0002c0002t0001g0014 | 3 | HG01069.hp2 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.897-432_897-427del others(6): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr11 | 113341396 | |||||
chr11:113341425
|
T | G | 5 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0110others(2): Show | 5 | HG00642.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.897-412T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 11/21 | chr11 | 113341425 | ||||||
chr11:113341452
|
A | G | 1 | a0001c0001t0002g0206 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.897-385A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 11/21 | chr11 | 113341452 | ||||||
chr11:113341452
|
A | T | 1 | a0001c0001t0001g0130 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.897-385A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 11/21 | chr11 | 113341452 | ||||||
chr11:113341453
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.897-384T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 11/21 | chr11 | 113341453 | ||||||
chr11:113341805
|
C | T | 2 | a0005c0009t0003g0074a0005c0009t0003g0075 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.897-32C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 11/21 | chr11 | 113341805 | ||||||
chr11:113341831
|
T | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(98): Show | 129 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
splice_region_variant&intron_variant | LOW | c.897-6T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 11/21 | chr11 | 113341831 | ||||||
chr11:113341975
|
A | C | 1 | a0001c0001t0001g0049 | 2 | HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.985+50A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113341975 | ||||||
chr11:113341980
|
C | T | 4 | a0001c0001t0001g0221a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.985+55C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113341980 | ||||||
chr11:113342042
|
G | A | 1 | a0001c0001t0001g0031 | 2 | NA18991.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.985+117G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113342042 | ||||||
chr11:113342050
|
C | T | 1 | a0001c0006t0001g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.985+125C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113342050 | ||||||
chr11:113342181
|
C | T | 1 | a0001c0001t0001g0047 | 2 | NA19054.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.985+256C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113342181 | ||||||
chr11:113342239
|
C | A | 7 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0110others(4): Show | 7 | HG00642.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.985+314C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113342239 | ||||||
chr11:113342347
|
C | G | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(102): Show | 135 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.985+422C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113342347 | ||||||
chr11:113342455
|
T | G | 7 | a0001c0003t0001g0059a0001c0003t0001g0086a0001c0003t0001g0087others(4): Show | 8 | HG01243.hp2 HG01516.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.985+530T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113342455 | ||||||
chr11:113342511
|
G | T | 14 | a0001c0003t0001g0059a0001c0003t0001g0086a0001c0003t0001g0087others(11): Show | 15 | HG00642.hp1 HG01243.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.985+586G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113342511 | ||||||
chr11:113342576
|
T | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(83): Show | 110 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.985+651T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113342576 | ||||||
chr11:113342588
|
G | T | 4 | a0001c0001t0001g0113a0001c0001t0001g0136a0001c0001t0001g0233others(1): Show | 4 | HG02630.hp1 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.985+663G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113342588 | ||||||
chr11:113342809
|
G | A | 1 | a0001c0001t0001g0252 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.985+884G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113342809 | ||||||
chr11:113342822
|
G | C | 2 | a0005c0009t0003g0074a0005c0009t0003g0075 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.985+897G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113342822 | ||||||
chr11:113342880
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.985+955G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113342880 | ||||||
chr11:113343068
|
A | G | 1 | a0001c0001t0004g0129 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.985+1143A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113343068 | ||||||
chr11:113343089
|
G | A | 2 | a0002c0002t0001g0036a0002c0002t0001g0167 | 3 | HG00733.hp1 HG01081.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.985+1164G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113343089 | ||||||
chr11:113343134
|
A | G | 5 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0110others(2): Show | 5 | HG00642.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.986-1138A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113343134 | ||||||
chr11:113343217
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0218a0001c0001t0001g0242others(3): Show | 9 | HG00642.hp2 HG01070.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.986-1055A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113343217 | ||||||
chr11:113343218
|
TGAG | T | 4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0222others(1): Show | 6 | HG02622.hp1 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.986-1052_986-1050d others(5): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 113343218 | |||||
chr11:113343256
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0138 | 9 | NA18956.hp1 NA18963.hp2 NA18978.hp2 others(6): Show |
intron_variant | MODIFIER | c.986-1016C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113343256 | ||||||
chr11:113343363
|
A | T | 1 | a0001c0001t0001g0079 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.986-909A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113343363 | ||||||
chr11:113343713
|
G | T | 5 | a0001c0003t0001g0059a0001c0003t0001g0086a0001c0003t0001g0087others(2): Show | 5 | HG01516.hp1 HG01517.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.986-559G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113343713 | ||||||
chr11:113343871
|
C | T | 1 | a0001c0003t0001g0217 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.986-401C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113343871 | ||||||
chr11:113344098
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.986-174C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113344098 | ||||||
chr11:113344110
|
C | T | 2 | a0005c0009t0003g0074a0005c0009t0003g0075 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.986-162C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113344110 | ||||||
chr11:113344658
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0223 | 4 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154+218G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113344658 | ||||||
chr11:113344696
|
G | A | 1 | a0001c0001t0001g0004 | 6 | HG00408.hp2 HG02129.hp1 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1154+256G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113344696 | ||||||
chr11:113344798
|
A | T | 1 | a0001c0001t0001g0021 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1154+358A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113344798 | ||||||
chr11:113344832
|
T | C | 1 | a0001c0001t0001g0119 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1154+392T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113344832 | ||||||
chr11:113345007
|
T | C | 5 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0110others(2): Show | 5 | HG00642.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1154+567T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113345007 | ||||||
chr11:113345201
|
G | A | 59 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(56): Show | 80 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1154+761G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113345201 | ||||||
chr11:113345239
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0002g0043 | 4 | HG00738.hp1 HG01099.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154+799C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113345239 | ||||||
chr11:113345317
|
G | C | 3 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0107 | 6 | HG01109.hp1 HG01123.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1154+877G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113345317 | ||||||
chr11:113345444
|
CTG | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(98): Show | 129 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.1154+1008_1154+100 others(6): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr11 | 113345444 | |||||
chr11:113345487
|
C | T | 1 | a0001c0006t0001g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1154+1047C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113345487 | ||||||
chr11:113345582
|
A | T | 1 | a0002c0002t0001g0191 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1154+1142A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113345582 | ||||||
chr11:113345864
|
A | G | 4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0222others(1): Show | 6 | HG02622.hp1 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1154+1424A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113345864 | ||||||
chr11:113345907
|
ACCTCGGG others(8): Show |
A | 2 | a0001c0006t0001g0022a0001c0006t0001g0201 | 3 | HG01243.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1154+1471_1154+148 others(19): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr11 | 113345907 | |||||
chr11:113345996
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1154+1556C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113345996 | ||||||
chr11:113346066
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1154+1626G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346066 | ||||||
chr11:113346084
|
G | A | 1 | a0002c0002t0001g0151 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1154+1644G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346084 | ||||||
chr11:113346171
|
C | A | 1 | a0002c0002t0001g0034 | 2 | HG01261.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1154+1731C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346171 | ||||||
chr11:113346265
|
T | C | 1 | a0001c0001t0001g0242 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1154+1825T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346265 | ||||||
chr11:113346302
|
C | G | 1 | a0001c0003t0001g0217 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1154+1862C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346302 | ||||||
chr11:113346318
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1154+1878C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346318 | ||||||
chr11:113346458
|
A | T | 1 | a0001c0003t0001g0220 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1154+2018A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346458 | ||||||
chr11:113346463
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1154+2023C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346463 | ||||||
chr11:113346601
|
C | G | 12 | a0001c0001t0001g0113a0001c0001t0001g0136a0001c0001t0001g0221others(9): Show | 12 | HG02280.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1154+2161C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346601 | ||||||
chr11:113346642
|
A | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(83): Show | 110 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.1154+2202A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346642 | ||||||
chr11:113346652
|
G | GA | 4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0222others(1): Show | 6 | HG02622.hp1 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1154+2220dupA | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr11 | 113346652 | |||||
chr11:113346747
|
T | A | 4 | a0001c0003t0001g0059a0001c0003t0001g0086a0001c0003t0001g0087others(1): Show | 4 | HG01516.hp1 HG01517.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154+2307T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346747 | ||||||
chr11:113346751
|
G | GA | 8 | a0001c0001t0001g0065a0001c0001t0001g0097a0001c0001t0001g0101others(5): Show | 8 | HG01192.hp1 HG01192.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1154+2328dupA | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr11 | 113346751 | |||||
chr11:113346751
|
GA | G | 10 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0053others(7): Show | 13 | HG00741.hp1 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1154+2328delA | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr11 | 113346751 | |||||
chr11:113346752
|
A | G | 1 | a0002c0002t0001g0190 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1154+2312A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346752 | ||||||
chr11:113346918
|
G | T | 5 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0110others(2): Show | 5 | HG00642.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1154+2478G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346918 | ||||||
chr11:113346978
|
G | T | 1 | a0001c0001t0001g0100 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1154+2538G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346978 | ||||||
chr11:113347018
|
G | C | 1 | a0002c0004t0001g0173 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1154+2578G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113347018 | ||||||
chr11:113347328
|
C | T | 36 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(33): Show | 60 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1155-2745C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113347328 | ||||||
chr11:113347867
|
C | T | 1 | a0002c0002t0001g0175 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1155-2206C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113347867 | ||||||
chr11:113348082
|
G | A | 7 | a0001c0001t0001g0093a0001c0001t0001g0234a0001c0001t0001g0235others(4): Show | 7 | HG00323.hp1 HG02698.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1155-1991G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113348082 | ||||||
chr11:113348171
|
A | T | 1 | a0002c0020t0001g0183 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1155-1902A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113348171 | ||||||
chr11:113348180
|
C | T | 3 | a0001c0001t0001g0202a0005c0009t0003g0074a0005c0009t0003g0075 | 3 | HG02572.hp1 HG02896.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1155-1893C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113348180 | ||||||
chr11:113348248
|
G | A | 1 | a0001c0003t0001g0217 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1155-1825G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113348248 | ||||||
chr11:113348288
|
A | C | 1 | a0001c0001t0001g0142 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1155-1785A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113348288 | ||||||
chr11:113348603
|
A | G | 7 | a0001c0003t0001g0059a0001c0003t0001g0086a0001c0003t0001g0087others(4): Show | 8 | HG01243.hp2 HG01516.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.1155-1470A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113348603 | ||||||
chr11:113348680
|
G | A | 14 | a0001c0003t0001g0059a0001c0003t0001g0086a0001c0003t0001g0087others(11): Show | 15 | HG00642.hp1 HG01243.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.1155-1393G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113348680 | ||||||
chr11:113348700
|
A | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0139 | 2 | NA18967.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.1155-1373A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113348700 | ||||||
chr11:113348786
|
G | A | 1 | a0001c0006t0001g0022 | 2 | HG01243.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1155-1287G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113348786 | ||||||
chr11:113348836
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1155-1237G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113348836 | ||||||
chr11:113348860
|
A | C | 6 | a0001c0001t0001g0019a0001c0001t0001g0143a0001c0001t0001g0227others(3): Show | 8 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1155-1213A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113348860 | ||||||
chr11:113349011
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1155-1062C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113349011 | ||||||
chr11:113349185
|
A | G | 2 | a0001c0001t0001g0049a0001c0001t0002g0043 | 4 | HG00738.hp1 HG01099.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1155-888A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113349185 | ||||||
chr11:113349205
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0223a0001c0001t0001g0231 | 5 | HG02809.hp1 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1155-868C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113349205 | ||||||
chr11:113349308
|
C | T | 6 | a0001c0001t0001g0050a0001c0001t0001g0228a0001c0001t0001g0240others(3): Show | 7 | HG01243.hp1 HG02258.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1155-765C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113349308 | ||||||
chr11:113349323
|
A | T | 1 | a0001c0001t0001g0049 | 2 | HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1155-750A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113349323 | ||||||
chr11:113349449
|
C | T | 1 | a0002c0002t0001g0185 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1155-624C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113349449 | ||||||
chr11:113349524
|
C | A | 2 | a0001c0003t0001g0203a0001c0003t0001g0205 | 2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1155-549C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113349524 | ||||||
chr11:113349877
|
G | A | 2 | a0001c0003t0001g0203a0001c0003t0001g0205 | 2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1155-196G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113349877 | ||||||
chr11:113350189
|
T | C | 2 | a0001c0001t0001g0092a0002c0002t0001g0012 | 4 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1247+24T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 14/21 | chr11 | 113350189 | ||||||
chr11:113350475
|
T | A | 4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0222others(1): Show | 6 | HG02622.hp1 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1247+310T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 14/21 | chr11 | 113350475 | ||||||
chr11:113350518
|
C | A | 2 | a0002c0002t0001g0039a0002c0002t0001g0193 | 3 | NA18962.hp2 NA18967.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1247+353C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 14/21 | chr11 | 113350518 | ||||||
chr11:113350620
|
G | T | 1 | a0001c0001t0001g0233 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1247+455G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 14/21 | chr11 | 113350620 | ||||||
chr11:113350847
|
G | A | 1 | a0002c0002t0001g0186 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1248-392G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 14/21 | chr11 | 113350847 | ||||||
chr11:113350884
|
A | T | 1 | a0001c0001t0001g0070 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1248-355A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 14/21 | chr11 | 113350884 | ||||||
chr11:113350918
|
A | G | 2 | a0001c0001t0001g0221a0001c0001t0001g0239 | 2 | HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1248-321A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 14/21 | chr11 | 113350918 | ||||||
chr11:113351064
|
A | G | 1 | a0002c0002t0001g0153 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1248-175A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 14/21 | chr11 | 113351064 | ||||||
chr11:113351072
|
A | G | 2 | a0001c0001t0001g0135a0002c0002t0001g0199 | 2 | HG00558.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.1248-167A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 14/21 | chr11 | 113351072 | ||||||
chr11:113351504
|
C | T | 1 | a0001c0001t0001g0025 | 2 | HG02004.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1308+205C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 15/21 | chr11 | 113351504 | ||||||
chr11:113351685
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0128others(2): Show | 12 | NA18956.hp1 NA18963.hp2 NA18972.hp2 others(9): Show |
intron_variant | MODIFIER | c.1309-385G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 15/21 | chr11 | 113351685 | ||||||
chr11:113352209
|
T | C | 3 | a0001c0001t0001g0115a0002c0002t0001g0011a0002c0002t0001g0154 | 5 | HG00609.hp1 HG01496.hp1 HG01978.hp2 others(2): Show |
splice_donor_variant&intron_variant | HIGH | c.1446+2T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113352209 | ||||||
chr11:113352262
|
G | T | 14 | a0001c0003t0001g0059a0001c0003t0001g0086a0001c0003t0001g0087others(11): Show | 15 | HG00642.hp1 HG01243.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.1446+55G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113352262 | ||||||
chr11:113352354
|
A | AT | 7 | a0001c0003t0001g0059a0001c0003t0001g0086a0001c0003t0001g0087others(4): Show | 8 | HG01243.hp2 HG01516.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.1446+148dupT | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr11 | 113352354 | |||||
chr11:113352365
|
G | T | 1 | a0001c0001t0001g0141 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1446+158G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113352365 | ||||||
chr11:113352389
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1446+182G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113352389 | ||||||
chr11:113352412
|
T | A | 7 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0110others(4): Show | 7 | HG00642.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1446+205T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113352412 | ||||||
chr11:113352520
|
G | A | 7 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0110others(4): Show | 7 | HG00642.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1446+313G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113352520 | ||||||
chr11:113352735
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1446+528A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113352735 | ||||||
chr11:113352785
|
T | A | 14 | a0001c0003t0001g0059a0001c0003t0001g0086a0001c0003t0001g0087others(11): Show | 15 | HG00642.hp1 HG01243.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.1446+578T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113352785 | ||||||
chr11:113352906
|
G | A | 2 | a0001c0001t0001g0049a0001c0001t0002g0043 | 4 | HG00738.hp1 HG01099.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1446+699G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113352906 | ||||||
chr11:113353256
|
T | C | 1 | a0002c0002t0001g0181 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1446+1049T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113353256 | ||||||
chr11:113353295
|
C | T | 33 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0024others(30): Show | 54 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1446+1088C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113353295 | ||||||
chr11:113353298
|
A | C | 1 | a0001c0003t0001g0217 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1446+1091A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113353298 | ||||||
chr11:113353328
|
T | G | 1 | a0001c0001t0001g0093 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1446+1121T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113353328 | ||||||
chr11:113353398
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1446+1191T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113353398 | ||||||
chr11:113353538
|
G | A | 6 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0053others(3): Show | 9 | HG01243.hp1 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1446+1331G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113353538 | ||||||
chr11:113353682
|
A | G | 38 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(35): Show | 62 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1446+1475A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113353682 | ||||||
chr11:113353754
|
T | C | 4 | a0001c0003t0001g0059a0001c0003t0001g0086a0001c0003t0001g0087others(1): Show | 4 | HG01516.hp1 HG01517.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1446+1547T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113353754 | ||||||
chr11:113354022
|
A | T | 1 | a0001c0001t0001g0049 | 2 | HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1446+1815A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113354022 | ||||||
chr11:113354194
|
C | G | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(116): Show | 150 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1446+1987C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113354194 | ||||||
chr11:113354393
|
C | G | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1446+2186C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113354393 | ||||||
chr11:113354422
|
C | T | 33 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0024others(30): Show | 54 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1446+2215C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113354422 | ||||||
chr11:113354495
|
A | G | 7 | a0001c0001t0001g0093a0001c0001t0001g0234a0001c0001t0001g0235others(4): Show | 7 | HG00323.hp1 HG02698.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1446+2288A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113354495 | ||||||
chr11:113354877
|
A | T | 14 | a0001c0003t0001g0059a0001c0003t0001g0086a0001c0003t0001g0087others(11): Show | 15 | HG00642.hp1 HG01243.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.1446+2670A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113354877 | ||||||
chr11:113354958
|
G | C | 1 | a0001c0001t0001g0088 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1446+2751G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113354958 | ||||||
chr11:113354991
|
TC | T | 2 | a0001c0006t0001g0022a0001c0006t0001g0201 | 3 | HG01243.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1446+2787delC | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr11 | 113354991 | |||||
chr11:113355032
|
G | A | 1 | a0001c0001t0001g0026 | 2 | NA18993.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1446+2825G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113355032 | ||||||
chr11:113355096
|
T | C | 1 | a0001c0001t0001g0252 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1446+2889T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113355096 | ||||||
chr11:113355139
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1446+2932A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113355139 | ||||||
chr11:113355276
|
T | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0223a0001c0001t0001g0231 | 5 | HG02809.hp1 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1446+3069T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113355276 | ||||||
chr11:113355484
|
G | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(102): Show | 135 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.1446+3277G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113355484 | ||||||
chr11:113355568
|
C | A | 3 | a0001c0001t0001g0221a0001c0001t0001g0225a0001c0001t0001g0239 | 3 | HG02280.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1446+3361C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113355568 | ||||||
chr11:113355682
|
G | A | 5 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0110others(2): Show | 5 | HG00642.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1446+3475G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113355682 | ||||||
chr11:113355953
|
A | T | 2 | a0001c0003t0001g0203a0001c0003t0001g0205 | 2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1447-3410A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113355953 | ||||||
chr11:113356509
|
A | G | 1 | a0002c0002t0001g0154 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1447-2854A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113356509 | ||||||
chr11:113356562
|
G | C | 4 | a0001c0003t0001g0059a0001c0003t0001g0086a0001c0003t0001g0087others(1): Show | 4 | HG01516.hp1 HG01517.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1447-2801G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113356562 | ||||||
chr11:113356647
|
ATTTCCTC others(5): Show |
A | 10 | a0001c0001t0001g0113a0001c0001t0001g0136a0001c0001t0001g0221others(7): Show | 10 | HG02280.hp2 HG02559.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1447-2713_1447-270 others(16): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr11 | 113356647 | |||||
chr11:113356657
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1447-2706C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113356657 | ||||||
chr11:113356888
|
T | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0029others(14): Show | 32 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.1447-2475T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113356888 | ||||||
chr11:113356941
|
C | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0107 | 4 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1447-2422C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113356941 | ||||||
chr11:113357001
|
G | C | 38 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(35): Show | 62 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1447-2362G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113357001 | ||||||
chr11:113357068
|
T | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(116): Show | 150 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1447-2295T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113357068 | ||||||
chr11:113357195
|
A | T | 6 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0053others(3): Show | 9 | HG01243.hp1 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1447-2168A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113357195 | ||||||
chr11:113357626
|
G | A | 2 | a0001c0006t0001g0022a0001c0006t0001g0201 | 3 | HG01243.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1447-1737G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113357626 | ||||||
chr11:113357657
|
G | C | 5 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(2): Show | 5 | NA18945.hp2 NA18957.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1447-1706G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113357657 | ||||||
chr11:113357779
|
T | C | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(116): Show | 150 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1447-1584T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113357779 | ||||||
chr11:113357824
|
C | T | 4 | a0001c0001t0001g0113a0001c0001t0001g0136a0001c0001t0001g0233others(1): Show | 4 | HG02630.hp1 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1447-1539C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113357824 | ||||||
chr11:113358136
|
A | G | 1 | a0002c0002t0001g0036 | 2 | HG01081.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1447-1227A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113358136 | ||||||
chr11:113358174
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1447-1189C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113358174 | ||||||
chr11:113358458
|
A | G | 5 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0110others(2): Show | 5 | HG00642.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1447-905A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113358458 | ||||||
chr11:113358576
|
T | G | 1 | a0001c0001t0001g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1447-787T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113358576 | ||||||
chr11:113358612
|
A | G | 1 | a0002c0002t0001g0185 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1447-751A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113358612 | ||||||
chr11:113358943
|
T | C | 48 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(45): Show | 72 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.1447-420T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113358943 | ||||||
chr11:113359200
|
C | CT | 10 | a0001c0001t0001g0017a0001c0001t0001g0223a0001c0001t0001g0231others(7): Show | 13 | HG01243.hp2 HG01516.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.1447-162dupT | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr11 | 113359200 | |||||
chr11:113359207
|
A | G | 1 | a0002c0002t0001g0199 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1447-156A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113359207 | ||||||
chr11:113359213
|
C | T | 4 | a0001c0001t0001g0148a0002c0002t0001g0150a0002c0002t0001g0158others(1): Show | 4 | HG00741.hp2 HG04115.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.1447-150C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113359213 | ||||||
chr11:113359283
|
G | A | 1 | a0002c0002t0001g0154 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1447-80G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113359283 | ||||||
chr11:113359605
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1545+144C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 17/21 | chr11 | 113359605 | ||||||
chr11:113359694
|
G | T | 1 | a0001c0001t0001g0126 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1545+233G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 17/21 | chr11 | 113359694 | ||||||
chr11:113359736
|
G | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0223a0001c0001t0001g0231 | 5 | HG02809.hp1 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546-204G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 17/21 | chr11 | 113359736 | ||||||
chr11:113359737
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1546-203C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 17/21 | chr11 | 113359737 | ||||||
chr11:113359838
|
G | A | 2 | a0001c0003t0001g0086a0001c0003t0001g0087 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1546-102G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 17/21 | chr11 | 113359838 | ||||||
chr11:113359878
|
C | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(95): Show | 125 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1546-62C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 17/21 | chr11 | 113359878 | ||||||
chr11:113360020
|
C | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0246a0001c0001t0001g0250 | 5 | HG02258.hp2 HG02280.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1614+12C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360020 | ||||||
chr11:113360051
|
C | CTTGTTTT others(3): Show |
5 | a0001c0001t0001g0017a0001c0001t0001g0223a0001c0001t0001g0231others(2): Show | 8 | HG01243.hp2 HG02809.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1614+61_1614+70dup others(10): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr11 | 113360051 | |||||
chr11:113360051
|
C | CTTGTTTT others(8): Show |
8 | a0001c0003t0001g0059a0001c0003t0001g0086a0001c0003t0001g0087others(5): Show | 14 | HG01516.hp1 HG01517.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.1614+56_1614+70dup others(15): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr11 | 113360051 | |||||
chr11:113360051
|
C | CTTGTTTT others(13): Show |
35 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0024others(32): Show | 51 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.1614+51_1614+70dup others(20): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr11 | 113360051 | |||||
chr11:113360051
|
C | CTTGTTTT others(18): Show |
2 | a0001c0001t0001g0018a0001c0001t0001g0107 | 4 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1614+46_1614+70dup others(25): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr11 | 113360051 | |||||
chr11:113360206
|
A | G | 221 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(218): Show | 303 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(300): Show |
intron_variant | MODIFIER | c.1614+198A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360206 | ||||||
chr11:113360208
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1614+200A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360208 | ||||||
chr11:113360409
|
GA | G | 9 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0049others(6): Show | 14 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1614+412delA | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr11 | 113360409 | |||||
chr11:113360454
|
G | T | 8 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0053others(5): Show | 12 | HG01243.hp1 HG01243.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1614+446G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360454 | ||||||
chr11:113360485
|
T | C | 1 | a0001c0001t0004g0129 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1614+477T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360485 | ||||||
chr11:113360569
|
A | T | 1 | a0002c0002t0001g0157 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1614+561A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360569 | ||||||
chr11:113360625
|
G | C | 8 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0053others(5): Show | 12 | HG01243.hp1 HG01243.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1614+617G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360625 | ||||||
chr11:113360628
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1614+620C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360628 | ||||||
chr11:113360668
|
CCT | C | 2 | a0001c0001t0001g0044a0001c0001t0001g0209 | 3 | HG01358.hp1 NA18956.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1614+661_1614+662d others(4): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360668 | ||||||
chr11:113360723
|
G | A | 8 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0053others(5): Show | 12 | HG01243.hp1 HG01243.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1614+715G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360723 | ||||||
chr11:113360761
|
G | A | 1 | a0001c0001t0001g0052 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1614+753G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360761 | ||||||
chr11:113360869
|
G | T | 1 | a0001c0003t0001g0217 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1614+861G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360869 | ||||||
chr11:113360879
|
G | A | 5 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0110others(2): Show | 5 | HG00642.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1614+871G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360879 | ||||||
chr11:113360892
|
C | T | 44 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(41): Show | 67 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.1614+884C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360892 | ||||||
chr11:113360896
|
C | T | 11 | a0001c0001t0001g0113a0001c0001t0001g0136a0001c0001t0001g0221others(8): Show | 12 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1614+888C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360896 | ||||||
chr11:113360969
|
G | A | 31 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0065others(28): Show | 49 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.1614+961G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360969 | ||||||
chr11:113360987
|
G | T | 1 | a0001c0001t0001g0106 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1614+979G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360987 | ||||||
chr11:113361021
|
G | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0223a0001c0001t0001g0231 | 5 | HG02809.hp1 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1614+1013G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113361021 | ||||||
chr11:113361168
|
G | A | 1 | a0001c0006t0001g0022 | 2 | HG01243.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1614+1160G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113361168 | ||||||
chr11:113361198
|
C | A | 1 | a0001c0001t0001g0224 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1614+1190C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113361198 | ||||||
chr11:113361208
|
C | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0223a0001c0001t0001g0231others(1): Show | 6 | HG02809.hp1 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1615-1193C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113361208 | ||||||
chr11:113361244
|
A | T | 11 | a0001c0001t0001g0083a0001c0001t0001g0120a0001c0001t0001g0124others(8): Show | 11 | HG00639.hp1 HG01256.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1615-1157A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113361244 | ||||||
chr11:113361348
|
A | G | 8 | a0001c0001t0001g0113a0001c0001t0001g0136a0001c0001t0001g0221others(5): Show | 8 | HG02280.hp2 HG02630.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1615-1053A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113361348 | ||||||
chr11:113361367
|
A | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0223a0001c0001t0001g0231others(1): Show | 6 | HG02809.hp1 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1615-1034A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113361367 | ||||||
chr11:113361374
|
C | T | 2 | a0001c0003t0001g0203a0001c0003t0001g0205 | 2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1615-1027C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113361374 | ||||||
chr11:113361490
|
T | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0079 | 3 | NA18970.hp1 NA19002.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1615-911T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113361490 | ||||||
chr11:113361576
|
ATC | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(94): Show | 124 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.1615-823_1615-822d others(4): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr11 | 113361576 | |||||
chr11:113361700
|
T | G | 40 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0020others(37): Show | 61 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.1615-701T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113361700 | ||||||
chr11:113361951
|
AT | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0223a0001c0001t0001g0231 | 5 | HG02809.hp1 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1615-447delT | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr11 | 113361951 | |||||
chr11:113361954
|
T | TA | 39 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0020others(36): Show | 59 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.1615-432dupA | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr11 | 113361954 | |||||
chr11:113361954
|
TA | T | 6 | a0001c0001t0001g0052a0001c0001t0001g0120a0001c0001t0001g0125others(3): Show | 7 | HG01256.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1615-432delA | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr11 | 113361954 | |||||
chr11:113361981
|
C | T | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(153): Show | 210 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.1615-420C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113361981 | ||||||
chr11:113362109
|
T | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0210 | 3 | NA18987.hp2 NA19065.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1615-292T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113362109 | ||||||
chr11:113362337
|
G | A | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(155): Show | 214 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.1615-64G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113362337 | ||||||
chr11:113362342
|
T | TAA | 2 | a0001c0001t0001g0018a0001c0001t0001g0107 | 4 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1615-57_1615-56dup others(2): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr11 | 113362342 | |||||
chr11:113362653
|
G | A | 6 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0053others(3): Show | 9 | HG01243.hp1 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1716+151G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 19/21 | chr11 | 113362653 | ||||||
chr11:113362724
|
A | G | 6 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0053others(3): Show | 9 | HG01243.hp1 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1716+222A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 19/21 | chr11 | 113362724 | ||||||
chr11:113362783
|
C | G | 1 | a0001c0001t0001g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1716+281C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 19/21 | chr11 | 113362783 | ||||||
chr11:113362822
|
T | C | 1 | a0002c0002t0001g0195 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1716+320T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 19/21 | chr11 | 113362822 | ||||||
chr11:113362842
|
A | G | 7 | a0001c0001t0001g0093a0001c0001t0001g0234a0001c0001t0001g0235others(4): Show | 7 | HG00323.hp1 HG02698.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1716+340A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 19/21 | chr11 | 113362842 | ||||||
chr11:113362898
|
C | T | 4 | a0001c0003t0001g0059a0001c0003t0001g0086a0001c0003t0001g0087others(1): Show | 4 | HG01516.hp1 HG01517.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1716+396C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 19/21 | chr11 | 113362898 | ||||||
chr11:113363004
|
T | C | 2 | a0002c0002t0001g0015a0002c0002t0001g0177 | 4 | HG02015.hp1 HG02027.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.1716+502T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 19/21 | chr11 | 113363004 | ||||||
chr11:113363171
|
C | T | 4 | a0001c0003t0001g0059a0001c0003t0001g0086a0001c0003t0001g0087others(1): Show | 4 | HG01516.hp1 HG01517.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1717-657C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 19/21 | chr11 | 113363171 | ||||||
chr11:113363572
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1717-256C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 19/21 | chr11 | 113363572 | ||||||
chr11:113363744
|
G | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(113): Show | 147 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.1717-84G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 19/21 | chr11 | 113363744 | ||||||
chr11:113363749
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(94): Show | 124 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.1717-79A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 19/21 | chr11 | 113363749 | ||||||
chr11:113363957
|
T | C | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(123): Show | 171 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.1816+30T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 20/21 | chr11 | 113363957 | ||||||
chr11:113363997
|
C | T | 8 | a0001c0001t0001g0113a0001c0001t0001g0136a0001c0001t0001g0221others(5): Show | 8 | HG02280.hp2 HG02630.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1816+70C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 20/21 | chr11 | 113363997 | ||||||
chr11:113364001
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1816+74G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 20/21 | chr11 | 113364001 | ||||||
chr11:113364053
|
A | G | 42 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(39): Show | 49 | HG00140.hp1 HG00423.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1816+126A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 20/21 | chr11 | 113364053 | ||||||
chr11:113364273
|
A | G | 1 | a0002c0002t0001g0151 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1816+346A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 20/21 | chr11 | 113364273 | ||||||
chr11:113364309
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG01346.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1816+382C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 20/21 | chr11 | 113364309 | ||||||
chr11:113364384
|
C | A | 1 | a0002c0002t0001g0169 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1817-451C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 20/21 | chr11 | 113364384 | ||||||
chr11:113364697
|
A | G | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(147): Show | 204 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.1817-138A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 20/21 | chr11 | 113364697 | ||||||
chr11:113364743
|
G | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0107others(2): Show | 9 | HG02055.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1817-92G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 20/21 | chr11 | 113364743 | ||||||
chr11:113364807
|
T | C | 1 | a0001c0006t0001g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1817-28T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 20/21 | chr11 | 113364807 | ||||||
chr11:113365142
|
A | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(110): Show | 144 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.2042+82A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113365142 | ||||||
chr11:113365189
|
C | T | 6 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0053others(3): Show | 9 | HG01243.hp1 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2042+129C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113365189 | ||||||
chr11:113365276
|
G | A | 1 | a0001c0001t0001g0020 | 2 | HG01109.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.2042+216G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113365276 | ||||||
chr11:113365294
|
G | A | 1 | a0002c0002t0001g0182 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2042+234G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113365294 | ||||||
chr11:113365365
|
C | G | 3 | a0001c0001t0001g0056a0001c0001t0001g0112a0001c0001t0001g0146 | 3 | HG03453.hp1 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2042+305C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113365365 | ||||||
chr11:113365477
|
A | G | 46 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0020others(43): Show | 70 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.2042+417A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113365477 | ||||||
chr11:113365498
|
G | A | 1 | a0001c0006t0001g0022 | 2 | HG01243.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2042+438G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113365498 | ||||||
chr11:113365594
|
T | C | 1 | a0002c0002t0001g0167 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2042+534T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113365594 | ||||||
chr11:113365613
|
C | A | 1 | a0001c0001t0001g0048 | 2 | HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.2042+553C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113365613 | ||||||
chr11:113365770
|
G | C | 42 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0020others(39): Show | 66 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.2043-455G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113365770 | ||||||
chr11:113366040
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2043-185C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113366040 | ||||||
chr11:113366109
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2043-116A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113366109 | ||||||
chr11:113366201
|
G | C | 1 | a0001c0001t0001g0128 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2043-24G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113366201 |