geneid | 7272 |
---|---|
ensemblid | ENSG00000112742.10 |
hgncid | 12401 |
symbol | TTK |
name | TTK protein kinase |
refseq_nuc | NM_003318.5 |
refseq_prot | NP_003309.2 |
ensembl_nuc | ENST00000369798.7 |
ensembl_prot | ENSP00000358813.2 |
mane_status | MANE Select |
chr | chr6 |
start | 80004649 |
end | 80042527 |
strand | + |
ver | v1.2 |
region | chr6:80004649-80042527 |
region5000 | chr6:79999649-80047527 |
regionname0 | TTK_chr6_80004649_80042527 |
regionname5000 | TTK_chr6_79999649_80047527 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 857 | 319 | 86 | 49 | 128 | 10 | 44 | 105 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0002 | 0/0 | 857 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0003 | 0/0 | 857 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0004 | 0/0 | 857 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0005 | 0/0 | 857 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0006 | 0/0 | 857 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2574 | 284 | 68 | 44 | 126 | 7 | 37 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
c0002 | 0/0 | 2574 | 16 | 0 | 5 | 2 | 3 | 6 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
c0003 | 0/0 | 2574 | 8 | 8 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
c0004 | 0/0 | 2574 | 7 | 7 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
c0005 | 0/0 | 2574 | 3 | 2 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
c0006 | 0/0 | 2574 | 3 | 0 | 3 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
c0007 | 0/0 | 2574 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
c0008 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
c0009 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
c0010 | 0/0 | 2574 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
c0011 | 0/0 | 2574 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
c0012 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 393 | 282 | 62 | 45 | 130 | 6 | 37 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
t0002 | 0/0 | 393 | 23 | 22 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
t0003 | 0/0 | 393 | 15 | 0 | 5 | 1 | 3 | 6 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
t0004 | 0/0 | 393 | 4 | 3 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
t0005 | 0/0 | 393 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
t0006 | 0/0 | 393 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
t0007 | 0/0 | 393 | 1 | 0 | 0 | 0 | 1 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
t0008 | 0/0 | 393 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 20 | 2 | 2 | 12 | 1 | 3 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0002 | 0/0 | 9 | 4 | 0 | 3 | 0 | 2 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0003 | 0/0 | 9 | 0 | 1 | 5 | 1 | 2 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0004 | 0/0 | 8 | 1 | 3 | 4 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0005 | 0/0 | 8 | 0 | 2 | 5 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0006 | 0/0 | 7 | 1 | 0 | 6 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0008 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0009 | 0/0 | 5 | 2 | 3 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0011 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0013 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0014 | 0/0 | 4 | 2 | 0 | 1 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0018 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0019 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0023 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0066 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2574 | 284 | 68 | 44 | 126 | 7 | 37 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0001c0002 | 0/0 | 2574 | 16 | 0 | 5 | 2 | 3 | 6 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0001c0003 | 0/0 | 2574 | 8 | 8 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0001c0004 | 0/0 | 2574 | 7 | 7 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0001c0005 | 0/0 | 2574 | 3 | 2 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0001c0008 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0002c0006 | 0/0 | 2574 | 3 | 0 | 3 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0003c0007 | 0/0 | 2574 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0004c0010 | 0/0 | 2574 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0004c0011 | 0/0 | 2574 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0005c0012 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0006c0009 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2966 | 258 | 45 | 42 | 126 | 6 | 37 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0001c0001t0002 | 0/0 | 2966 | 23 | 22 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0001c0001t0005 | 0/0 | 2966 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0001c0001t0007 | 0/0 | 2966 | 1 | 0 | 0 | 0 | 1 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0001c0001t0008 | 0/0 | 2966 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0001c0002t0003 | 0/0 | 2966 | 15 | 0 | 5 | 1 | 3 | 6 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0001c0002t0006 | 0/0 | 2966 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0001c0003t0001 | 0/0 | 2966 | 8 | 8 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0001c0004t0001 | 0/0 | 2966 | 7 | 7 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0001c0005t0004 | 0/0 | 2966 | 3 | 2 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0001c0008t0004 | 0/0 | 2966 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0002c0006t0001 | 0/0 | 2966 | 3 | 0 | 3 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0003c0007t0001 | 0/0 | 2966 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0004c0010t0001 | 0/0 | 2966 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0004c0011t0001 | 0/0 | 2966 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0005c0012t0001 | 0/0 | 2966 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
a0006c0009t0001 | 0/0 | 2966 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | copy fasta | chr6 | 79999649 | 80047527 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 20 | 2 | 2 | 12 | 1 | 3 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0002 | 0/0 | 9 | 4 | 0 | 3 | 0 | 2 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0003 | 0/0 | 7 | 0 | 1 | 3 | 1 | 2 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0004 | 0/0 | 8 | 1 | 3 | 4 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0005 | 0/0 | 7 | 0 | 2 | 4 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0006 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0009 | 0/0 | 5 | 2 | 3 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0014 | 0/0 | 4 | 2 | 0 | 1 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0066 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0002g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0002g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0002g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0002g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0005g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0007g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0001t0008g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0002t0003g0019 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0002t0003g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0002t0003g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0002t0003g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0002t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0002t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0002t0006g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0003t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0003t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0003t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0003t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0004t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0004t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0004t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0004t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0004t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0005t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0005t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0005t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0001c0008t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0002c0006t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0003c0007t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0003c0007t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0004c0010t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0004c0011t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0005c0012t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
a0006c0009t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | GBR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG00140 | hp2 | a0001 | c0001 | t0007 | g0101 | EUR | GBR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | FIN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG00673 | hp1 | a0001 | c0002 | t0006 | g0176 | EAS | CHS | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG00733 | hp1 | a0001 | c0002 | t0003 | g0019 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG00733 | hp2 | a0002 | c0006 | t0001 | g0020 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01069 | hp1 | a0002 | c0006 | t0001 | g0020 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01071 | hp1 | a0002 | c0006 | t0001 | g0020 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01074 | hp1 | a0001 | c0002 | t0003 | g0045 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01081 | hp1 | a0001 | c0002 | t0003 | g0177 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01106 | hp1 | a0001 | c0002 | t0003 | g0019 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01515 | hp1 | a0001 | c0002 | t0003 | g0043 | EUR | IBS | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | IBS | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01517 | hp2 | a0001 | c0002 | t0003 | g0043 | EUR | IBS | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01952 | hp2 | a0001 | c0001 | t0008 | g0112 | AMR | PEL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02129 | hp2 | a0004 | c0011 | t0001 | g0006 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02257 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02258 | hp2 | a0001 | c0004 | t0001 | g0188 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02280 | hp2 | a0005 | c0012 | t0001 | g0104 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02300 | hp2 | a0001 | c0002 | t0003 | g0172 | AMR | PEL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02451 | hp2 | a0001 | c0003 | t0001 | g0184 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02615 | hp2 | a0001 | c0004 | t0001 | g0021 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02647 | hp2 | a0001 | c0003 | t0001 | g0185 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02738 | hp1 | a0001 | c0002 | t0003 | g0044 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02809 | hp1 | a0001 | c0004 | t0001 | g0181 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02818 | hp2 | a0001 | c0004 | t0001 | g0021 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03195 | hp1 | a0001 | c0004 | t0001 | g0182 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03195 | hp2 | a0006 | c0009 | t0001 | g0179 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03209 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | MSL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | MSL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03486 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | MSL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03492 | hp2 | a0001 | c0002 | t0003 | g0019 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03516 | hp1 | a0001 | c0005 | t0004 | g0189 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03540 | hp2 | a0001 | c0004 | t0001 | g0021 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03579 | hp1 | a0001 | c0005 | t0004 | g0192 | AFR | MSL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03654 | hp2 | a0001 | c0002 | t0003 | g0178 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | STU | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | STU | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03831 | hp2 | a0001 | c0002 | t0003 | g0044 | SAS | BEB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | STU | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG04115 | hp2 | a0001 | c0002 | t0003 | g0173 | SAS | STU | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | STU | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | STU | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | STU | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG04204 | hp2 | a0001 | c0005 | t0004 | g0191 | SAS | STU | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | STU | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18522 | hp2 | a0001 | c0004 | t0001 | g0186 | AFR | YRI | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18906 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | YRI | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | YRI | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18945 | hp1 | a0003 | c0007 | t0001 | g0003 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18960 | hp2 | a0003 | c0007 | t0001 | g0005 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18983 | hp1 | a0004 | c0010 | t0001 | g0003 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19005 | hp2 | a0001 | c0002 | t0003 | g0045 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19030 | hp1 | a0001 | c0008 | t0004 | g0187 | AFR | LWK | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | YRI | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA19240 | hp2 | a0001 | c0003 | t0001 | g0183 | AFR | YRI | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA20805 | hp1 | a0001 | c0002 | t0003 | g0174 | EUR | TSI | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | TSI | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | GIH | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA20905 | hp2 | a0001 | c0002 | t0003 | g0175 | SAS | GIH | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG06807 | hp1 | a0001 | c0001 | t0005 | g0148 | AFR | USA | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | USA | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | USA | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0066 | REF | REF | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0080 | REF | REF | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:80007902
|
C | T | 1 | a0005 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.233C>T | p.Pro78Leu | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 3/22 | 300/2966 | 233/2574 | 78/857 | chr6 | 80007902 | ||
chr6:80007959
|
C | T | 1 | a0002 | 3 | HG00733.hp2 HG01069.hp1 HG01071.hp1 |
missense_variant | MODERATE | c.290C>T | p.Ala97Val | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 3/22 | 357/2966 | 290/2574 | 97/857 | chr6 | 80007959 | ||
chr6:80011736
|
A | G | 1 | a0004 | 2 | HG02129.hp2 NA18983.hp1 |
missense_variant | MODERATE | c.736A>G | p.Met246Val | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 7/22 | 803/2966 | 736/2574 | 246/857 | chr6 | 80011736 | ||
chr6:80014544
|
C | G | 1 | a0006 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.1066C>G | p.Leu356Val | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/22 | 1133/2966 | 1066/2574 | 356/857 | chr6 | 80014544 | ||
chr6:80027896
|
C | T | 1 | a0003 | 2 | NA18945.hp1 NA18960.hp2 |
missense_variant | MODERATE | c.1406C>T | p.Pro469Leu | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/22 | 1473/2966 | 1406/2574 | 469/857 | chr6 | 80027896 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:80022445
|
G | A | 1 | a0001c0004 | 7 | HG02258.hp2 HG02615.hp2 HG02809.hp1 others(4): Show |
synonymous_variant | LOW | c.1230G>A | p.Pro410Pro | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/22 | 1297/2966 | 1230/2574 | 410/857 | chr6 | 80022445 | ||
chr6:80026431
|
A | G | 1 | a0001c0003 | 8 | HG02257.hp1 HG02451.hp2 HG02647.hp2 others(5): Show |
synonymous_variant | LOW | c.1311A>G | p.Pro437Pro | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 12/22 | 1378/2966 | 1311/2574 | 437/857 | chr6 | 80026431 | ||
chr6:80031526
|
A | T | 3 | a0001c0002a0001c0005a0001c0008 | 20 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(17): Show |
synonymous_variant | LOW | c.1581A>T | p.Ile527Ile | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/22 | 1648/2966 | 1581/2574 | 527/857 | chr6 | 80031526 | ||
chr6:80035287
|
C | T | 1 | a0001c0008 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1794C>T | p.Ile598Ile | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 16/22 | 1861/2966 | 1794/2574 | 598/857 | chr6 | 80035287 | ||
chr6:80036479
|
T | C | 1 | a0001c0008 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1929T>C | p.Ile643Ile | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/22 | 1996/2966 | 1929/2574 | 643/857 | chr6 | 80036479 | ||
chr6:80036524
|
A | C | 1 | a0004c0011 | 1 | HG02129.hp2 | synonymous_variant | LOW | c.1974A>C | p.Gly658Gly | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/22 | 2041/2966 | 1974/2574 | 658/857 | chr6 | 80036524 | ||
chr6:80040255
|
A | C | 1 | a0001c0002 | 16 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(13): Show |
synonymous_variant | LOW | c.2367A>C | p.Pro789Pro | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 20/22 | 2434/2966 | 2367/2574 | 789/857 | chr6 | 80040255 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:80004671
|
T | C | 1 | a0001c0001t0002 | 23 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-45T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/22 | 1173 | chr6 | 80004671 | |||||
chr6:80004676
|
G | C | 1 | a0001c0001t0005 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-40G>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/22 | 1168 | chr6 | 80004676 | |||||
chr6:80004681
|
A | G | 1 | a0001c0001t0008 | 1 | HG01952.hp2 | 5_prime_UTR_variant | MODIFIER | c.-35A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/22 | 1163 | chr6 | 80004681 | |||||
chr6:80042225
|
G | A | 4 | a0001c0002t0003a0001c0002t0006a0001c0005t0004others(1): Show | 20 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*23G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 22/22 | 23 | chr6 | 80042225 | |||||
chr6:80042354
|
G | A | 1 | a0001c0001t0007 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*152G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 22/22 | 152 | chr6 | 80042354 | |||||
chr6:80042377
|
C | T | 2 | a0001c0002t0003a0001c0002t0006 | 16 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*175C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 22/22 | 175 | chr6 | 80042377 | |||||
chr6:80042424
|
A | T | 1 | a0001c0002t0006 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*222A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 22/22 | 222 | chr6 | 80042424 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:80004778
|
T | C | 13 | a0001c0001t0002g0012a0001c0001t0002g0015a0001c0001t0002g0016others(10): Show | 23 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.-3+65T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/21 | chr6 | 80004778 | ||||||
chr6:80004793
|
G | T | 13 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(10): Show | 27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.-3+80G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/21 | chr6 | 80004793 | ||||||
chr6:80005051
|
C | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.-3+338C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/21 | chr6 | 80005051 | ||||||
chr6:80005060
|
A | G | 1 | a0001c0001t0001g0049 | 2 | HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-3+347A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/21 | chr6 | 80005060 | ||||||
chr6:80005089
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-3+376G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/21 | chr6 | 80005089 | ||||||
chr6:80005147
|
G | T | 1 | a0001c0001t0001g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-3+434G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/21 | chr6 | 80005147 | ||||||
chr6:80005200
|
C | G | 1 | a0001c0001t0001g0106 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-3+487C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/21 | chr6 | 80005200 | ||||||
chr6:80005203
|
T | TTTG | 5 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0103others(2): Show | 7 | HG02280.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+491_-3+492insTG others(1): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 80005203 | |||||
chr6:80005446
|
G | A | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(80): Show | 125 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.-2-396G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/21 | chr6 | 80005446 | ||||||
chr6:80005475
|
C | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.-2-367C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/21 | chr6 | 80005475 | ||||||
chr6:80005550
|
T | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.-2-292T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/21 | chr6 | 80005550 | ||||||
chr6:80005556
|
AT | A | 11 | a0001c0002t0003g0019a0001c0002t0003g0043a0001c0002t0003g0044others(8): Show | 16 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-2-278delT | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 80005556 | |||||
chr6:80006038
|
A | G | 12 | a0001c0001t0002g0012a0001c0001t0002g0015a0001c0001t0002g0016others(9): Show | 22 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.139+56A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80006038 | ||||||
chr6:80006042
|
A | G | 1 | a0001c0001t0002g0057 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.139+60A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80006042 | ||||||
chr6:80006121
|
T | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.139+139T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80006121 | ||||||
chr6:80006212
|
A | C | 1 | a0001c0001t0001g0102 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.139+230A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80006212 | ||||||
chr6:80006515
|
C | A | 1 | a0002c0006t0001g0020 | 3 | HG00733.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.139+533C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80006515 | ||||||
chr6:80006612
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.139+630T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80006612 | ||||||
chr6:80006872
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.139+890G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80006872 | ||||||
chr6:80006903
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.140-906A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80006903 | ||||||
chr6:80007178
|
C | A | 13 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(10): Show | 27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.140-631C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80007178 | ||||||
chr6:80007219
|
G | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.140-590G>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80007219 | ||||||
chr6:80007487
|
G | C | 13 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(10): Show | 27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.140-322G>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80007487 | ||||||
chr6:80007499
|
C | A | 1 | a0001c0001t0001g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.140-310C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80007499 | ||||||
chr6:80007571
|
G | T | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 251 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.140-238G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80007571 | ||||||
chr6:80007614
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0169others(1): Show | 6 | HG03834.hp1 NA18945.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.140-195C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80007614 | ||||||
chr6:80007629
|
A | T | 14 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0002g0012others(11): Show | 24 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.140-180A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80007629 | ||||||
chr6:80008113
|
G | A | 1 | a0001c0002t0003g0172 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.362+82G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 3/21 | chr6 | 80008113 | ||||||
chr6:80008539
|
T | C | 2 | a0001c0001t0001g0180a0006c0009t0001g0179 | 2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.469+47T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80008539 | ||||||
chr6:80008628
|
A | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.469+136A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80008628 | ||||||
chr6:80008630
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.469+138A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80008630 | ||||||
chr6:80008796
|
G | A | 13 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(10): Show | 27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.469+304G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80008796 | ||||||
chr6:80008929
|
C | CTG | 8 | a0001c0001t0001g0032a0001c0001t0001g0098a0001c0001t0001g0110others(5): Show | 9 | HG02451.hp2 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.469+475_469+476dup others(2): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | |||||
chr6:80008929
|
C | CTGTG | 6 | a0001c0001t0001g0099a0001c0001t0001g0111a0001c0002t0003g0172others(3): Show | 8 | HG01071.hp2 HG02300.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.469+473_469+476dup others(4): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | |||||
chr6:80008929
|
C | CTGTGTG | 5 | a0001c0002t0003g0019a0001c0002t0003g0173a0001c0003t0001g0010others(2): Show | 11 | HG00733.hp1 HG01106.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.469+471_469+476dup others(6): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | |||||
chr6:80008929
|
C | CTGTGTGT others(1): Show |
10 | a0001c0001t0001g0033a0001c0001t0001g0113a0001c0001t0001g0114others(7): Show | 13 | HG00558.hp1 HG01106.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.469+469_469+476dup others(8): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | |||||
chr6:80008929
|
C | CTGTGTGT others(3): Show |
21 | a0001c0001t0001g0002a0001c0001t0001g0100a0001c0001t0001g0108others(18): Show | 30 | HG00558.hp2 HG00673.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.469+467_469+476dup others(10): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | |||||
chr6:80008929
|
C | CTGTGTGT others(5): Show |
29 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0041others(26): Show | 40 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.469+465_469+476dup others(12): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | |||||
chr6:80008929
|
C | CTGTGTGT others(7): Show |
25 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(22): Show | 51 | HG00323.hp2 HG00673.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.469+463_469+476dup others(14): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | |||||
chr6:80008929
|
C | CTGTGTGT others(9): Show |
11 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(8): Show | 15 | HG01167.hp1 HG01496.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.469+461_469+476dup others(16): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | |||||
chr6:80008929
|
C | CTGTGTGT others(11): Show |
7 | a0001c0001t0001g0042a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 8 | HG01891.hp1 HG01952.hp1 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.469+459_469+476dup others(18): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | |||||
chr6:80008929
|
C | CTGTGTGT others(13): Show |
3 | a0001c0001t0001g0040a0001c0001t0001g0166a0001c0001t0001g0167 | 4 | HG01496.hp2 HG01515.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.469+457_469+476dup others(20): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | |||||
chr6:80008929
|
CTG | C | 39 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(36): Show | 78 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.469+475_469+476del others(2): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | |||||
chr6:80008929
|
CTGTG | C | 11 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0059others(8): Show | 13 | HG01175.hp1 HG01192.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.469+473_469+476del others(4): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | |||||
chr6:80008929
|
CTGTGTG | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0082a0001c0001t0001g0106 | 3 | HG03225.hp1 NA18973.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.469+471_469+476del others(6): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | |||||
chr6:80008929
|
CTGTGTGT others(1): Show |
C | 14 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(11): Show | 28 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.469+469_469+476del others(8): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | |||||
chr6:80008929
|
CTGTGTGT others(3): Show |
C | 1 | a0001c0001t0001g0109 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.469+467_469+476del others(10): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | |||||
chr6:80008929
|
CTGTGTGT others(5): Show |
C | 1 | a0001c0001t0001g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.469+465_469+476del others(12): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | |||||
chr6:80009619
|
T | C | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(81): Show | 126 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.469+1127T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80009619 | ||||||
chr6:80009695
|
A | G | 1 | a0001c0001t0001g0032 | 2 | HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.470-1119A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80009695 | ||||||
chr6:80009746
|
T | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0058others(3): Show | 10 | HG00408.hp1 HG02132.hp1 HG03654.hp1 others(7): Show |
intron_variant | MODIFIER | c.470-1068T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80009746 | ||||||
chr6:80009773
|
C | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.470-1041C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80009773 | ||||||
chr6:80009798
|
G | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.470-1016G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80009798 | ||||||
chr6:80009831
|
A | G | 4 | a0001c0003t0001g0010a0001c0003t0001g0183a0001c0003t0001g0184others(1): Show | 8 | HG02257.hp1 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.470-983A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80009831 | ||||||
chr6:80009859
|
C | G | 1 | a0001c0002t0003g0045 | 2 | HG01074.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.470-955C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80009859 | ||||||
chr6:80010067
|
C | T | 15 | a0001c0002t0003g0019a0001c0002t0003g0043a0001c0002t0003g0044others(12): Show | 20 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.470-747C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80010067 | ||||||
chr6:80010349
|
A | G | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | NA18950.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.470-465A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80010349 | ||||||
chr6:80010506
|
C | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.470-308C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80010506 | ||||||
chr6:80010569
|
C | T | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(80): Show | 125 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.470-245C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80010569 | ||||||
chr6:80010670
|
A | G | 6 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0141others(3): Show | 8 | HG02083.hp2 NA18952.hp2 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.470-144A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80010670 | ||||||
chr6:80010770
|
G | GTA | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 215 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.470-44_470-43insTA | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80010770 | ||||||
chr6:80010771
|
C | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 215 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.470-43C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80010771 | ||||||
chr6:80010773
|
T | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 215 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.470-41T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80010773 | ||||||
chr6:80010774
|
T | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 215 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.470-40T>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80010774 | ||||||
chr6:80010785
|
A | C | 1 | a0001c0001t0001g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.470-29A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80010785 | ||||||
chr6:80010970
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.613+13G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 5/21 | chr6 | 80010970 | ||||||
chr6:80011016
|
G | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.613+59G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 5/21 | chr6 | 80011016 | ||||||
chr6:80011025
|
A | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.613+68A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 5/21 | chr6 | 80011025 | ||||||
chr6:80011056
|
G | A | 1 | a0001c0008t0004g0187 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.613+99G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 5/21 | chr6 | 80011056 | ||||||
chr6:80011163
|
A | G | 1 | a0001c0003t0001g0185 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.613+206A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 5/21 | chr6 | 80011163 | ||||||
chr6:80011188
|
AT | A | 14 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(11): Show | 28 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.614-233delT | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 80011188 | |||||
chr6:80011310
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.614-124A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 5/21 | chr6 | 80011310 | ||||||
chr6:80011315
|
T | A | 23 | a0001c0001t0001g0180a0001c0001t0002g0012a0001c0001t0002g0015others(20): Show | 39 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.614-119T>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 5/21 | chr6 | 80011315 | ||||||
chr6:80011328
|
A | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.614-106A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 5/21 | chr6 | 80011328 | ||||||
chr6:80011806
|
G | C | 12 | a0001c0001t0002g0012a0001c0001t0002g0015a0001c0001t0002g0016others(9): Show | 22 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
splice_region_variant&intron_variant | LOW | c.801+5G>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 7/21 | chr6 | 80011806 | ||||||
chr6:80011812
|
T | G | 1 | a0001c0001t0001g0022 | 3 | NA19001.hp1 NA19076.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.801+11T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 7/21 | chr6 | 80011812 | ||||||
chr6:80012015
|
C | T | 1 | a0001c0008t0004g0187 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.896+35C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 8/21 | chr6 | 80012015 | ||||||
chr6:80012138
|
T | C | 17 | a0001c0001t0001g0143a0001c0001t0001g0163a0001c0002t0003g0019others(14): Show | 22 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.896+158T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 8/21 | chr6 | 80012138 | ||||||
chr6:80012212
|
T | A | 2 | a0001c0001t0001g0100a0001c0001t0007g0101 | 2 | HG00140.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.896+232T>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 8/21 | chr6 | 80012212 | ||||||
chr6:80012290
|
C | A | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(122): Show | 190 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.896+310C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 8/21 | chr6 | 80012290 | ||||||
chr6:80012316
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.896+336C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 8/21 | chr6 | 80012316 | ||||||
chr6:80012411
|
C | A | 12 | a0001c0001t0002g0012a0001c0001t0002g0015a0001c0001t0002g0016others(9): Show | 22 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.896+431C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 8/21 | chr6 | 80012411 | ||||||
chr6:80012639
|
T | G | 1 | a0001c0001t0001g0144 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.897-640T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 8/21 | chr6 | 80012639 | ||||||
chr6:80012654
|
C | T | 14 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(11): Show | 28 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.897-625C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 8/21 | chr6 | 80012654 | ||||||
chr6:80012789
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.897-490A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 8/21 | chr6 | 80012789 | ||||||
chr6:80012836
|
G | A | 1 | a0001c0001t0001g0066 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.897-443G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 8/21 | chr6 | 80012836 | ||||||
chr6:80012909
|
T | C | 1 | a0001c0001t0001g0067 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.897-370T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 8/21 | chr6 | 80012909 | ||||||
chr6:80012912
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.897-367G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 8/21 | chr6 | 80012912 | ||||||
chr6:80013140
|
C | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.897-139C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 8/21 | chr6 | 80013140 | ||||||
chr6:80013427
|
C | T | 5 | a0001c0004t0001g0021a0001c0004t0001g0181a0001c0004t0001g0182others(2): Show | 7 | HG02258.hp2 HG02615.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.984+61C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80013427 | ||||||
chr6:80013481
|
T | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.984+115T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80013481 | ||||||
chr6:80013512
|
C | A | 15 | a0001c0002t0003g0019a0001c0002t0003g0043a0001c0002t0003g0044others(12): Show | 20 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.984+146C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80013512 | ||||||
chr6:80013573
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.984+207A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80013573 | ||||||
chr6:80013666
|
G | A | 15 | a0001c0002t0003g0019a0001c0002t0003g0043a0001c0002t0003g0044others(12): Show | 20 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.984+300G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80013666 | ||||||
chr6:80013686
|
G | A | 2 | a0001c0001t0002g0053a0001c0001t0002g0054 | 2 | HG02109.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.984+320G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80013686 | ||||||
chr6:80013763
|
G | A | 2 | a0001c0004t0001g0181a0001c0004t0001g0186 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.984+397G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80013763 | ||||||
chr6:80013880
|
T | C | 1 | a0001c0001t0001g0058 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.984+514T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80013880 | ||||||
chr6:80013915
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0007g0101 | 2 | HG00140.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.985-548G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80013915 | ||||||
chr6:80014030
|
A | G | 2 | a0001c0001t0001g0180a0006c0009t0001g0179 | 2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.985-433A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80014030 | ||||||
chr6:80014085
|
G | C | 12 | a0001c0001t0002g0012a0001c0001t0002g0015a0001c0001t0002g0016others(9): Show | 22 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.985-378G>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80014085 | ||||||
chr6:80014213
|
T | C | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070 | 3 | HG01257.hp1 HG01943.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.985-250T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80014213 | ||||||
chr6:80014439
|
T | C | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(80): Show | 125 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.985-24T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80014439 | ||||||
chr6:80014595
|
A | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1108+9A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80014595 | ||||||
chr6:80014654
|
A | C | 1 | a0001c0001t0001g0077 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1108+68A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80014654 | ||||||
chr6:80014686
|
T | C | 1 | a0001c0003t0001g0183 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1108+100T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80014686 | ||||||
chr6:80014745
|
C | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1108+159C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80014745 | ||||||
chr6:80014815
|
T | C | 1 | a0001c0001t0001g0196 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1108+229T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80014815 | ||||||
chr6:80014827
|
T | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1108+241T>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80014827 | ||||||
chr6:80014949
|
C | T | 11 | a0001c0002t0003g0019a0001c0002t0003g0043a0001c0002t0003g0044others(8): Show | 16 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1108+363C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80014949 | ||||||
chr6:80014976
|
T | C | 1 | a0001c0001t0001g0033 | 2 | HG01106.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.1108+390T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80014976 | ||||||
chr6:80015034
|
C | T | 1 | a0001c0002t0003g0045 | 2 | HG01074.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1108+448C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80015034 | ||||||
chr6:80015038
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1108+452A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80015038 | ||||||
chr6:80015141
|
A | G | 15 | a0001c0002t0003g0019a0001c0002t0003g0043a0001c0002t0003g0044others(12): Show | 20 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1108+555A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80015141 | ||||||
chr6:80015189
|
T | TGGG | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1108+604_1108+606d others(5): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 80015189 | |||||
chr6:80015256
|
A | G | 1 | a0001c0008t0004g0187 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1108+670A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80015256 | ||||||
chr6:80015283
|
G | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0071 | 4 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.1108+697G>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80015283 | ||||||
chr6:80015290
|
G | A | 1 | a0002c0006t0001g0020 | 3 | HG00733.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1108+704G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80015290 | ||||||
chr6:80015335
|
T | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1108+749T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80015335 | ||||||
chr6:80015574
|
C | A | 3 | a0001c0005t0004g0189a0001c0005t0004g0191a0001c0005t0004g0192 | 3 | HG03516.hp1 HG03579.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1108+988C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80015574 | ||||||
chr6:80015780
|
T | C | 4 | a0001c0003t0001g0010a0001c0003t0001g0183a0001c0003t0001g0184others(1): Show | 8 | HG02257.hp1 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1108+1194T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80015780 | ||||||
chr6:80015799
|
A | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0162 | 3 | HG01167.hp1 HG01496.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1108+1213A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80015799 | ||||||
chr6:80015892
|
C | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1108+1306C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80015892 | ||||||
chr6:80015942
|
C | A | 1 | a0001c0004t0001g0188 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1108+1356C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80015942 | ||||||
chr6:80016096
|
T | G | 1 | a0001c0001t0001g0109 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1108+1510T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80016096 | ||||||
chr6:80016209
|
G | C | 1 | a0001c0001t0001g0046 | 2 | HG03239.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1108+1623G>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80016209 | ||||||
chr6:80016276
|
C | G | 12 | a0001c0001t0002g0012a0001c0001t0002g0015a0001c0001t0002g0016others(9): Show | 22 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.1108+1690C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80016276 | ||||||
chr6:80016276
|
C | T | 13 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(10): Show | 27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1108+1690C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80016276 | ||||||
chr6:80016277
|
T | G | 1 | a0001c0001t0002g0051 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1108+1691T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80016277 | ||||||
chr6:80016390
|
C | T | 1 | a0001c0003t0001g0184 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1108+1804C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80016390 | ||||||
chr6:80016444
|
G | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1108+1858G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80016444 | ||||||
chr6:80016461
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1108+1875A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80016461 | ||||||
chr6:80016676
|
C | G | 1 | a0001c0001t0001g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1108+2090C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80016676 | ||||||
chr6:80016721
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1108+2135G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80016721 | ||||||
chr6:80017053
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1108+2467T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80017053 | ||||||
chr6:80017071
|
C | T | 1 | a0002c0006t0001g0020 | 3 | HG00733.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1108+2485C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80017071 | ||||||
chr6:80017107
|
A | C | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1108+2521A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80017107 | ||||||
chr6:80017313
|
T | C | 1 | a0001c0001t0002g0055 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1108+2727T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80017313 | ||||||
chr6:80017434
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1108+2848A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80017434 | ||||||
chr6:80017487
|
C | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1108+2901C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80017487 | ||||||
chr6:80017555
|
A | G | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1108+2969A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80017555 | ||||||
chr6:80017781
|
C | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1108+3195C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80017781 | ||||||
chr6:80017822
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1108+3236C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80017822 | ||||||
chr6:80018107
|
C | T | 1 | a0001c0001t0002g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1108+3521C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80018107 | ||||||
chr6:80018182
|
C | CA | 7 | a0001c0001t0001g0059a0001c0004t0001g0021a0001c0004t0001g0181others(4): Show | 11 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1108+3608dupA | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 80018182 | |||||
chr6:80018182
|
CA | C | 7 | a0001c0001t0001g0070a0001c0001t0001g0100a0001c0001t0007g0101others(4): Show | 11 | HG00140.hp2 HG01943.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1108+3608delA | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 80018182 | |||||
chr6:80018199
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1108+3613G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80018199 | ||||||
chr6:80018236
|
A | T | 1 | a0001c0008t0004g0187 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1108+3650A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80018236 | ||||||
chr6:80018239
|
T | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1108+3653T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80018239 | ||||||
chr6:80018445
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1108+3859A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80018445 | ||||||
chr6:80018461
|
CA | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(135): Show | 217 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.1109-3850delA | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 80018461 | |||||
chr6:80018578
|
C | A | 13 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(10): Show | 27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1109-3746C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80018578 | ||||||
chr6:80018621
|
C | T | 2 | a0001c0001t0001g0180a0006c0009t0001g0179 | 2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1109-3703C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80018621 | ||||||
chr6:80018626
|
CA | C | 60 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0024others(57): Show | 94 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1109-3676delA | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 80018626 | |||||
chr6:80018626
|
CAA | C | 11 | a0001c0001t0001g0083a0001c0001t0002g0051a0001c0002t0003g0019others(8): Show | 16 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1109-3677_1109-367 others(6): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 80018626 | |||||
chr6:80018648
|
A | AG | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG00741.hp1 HG02071.hp2 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.1109-3676_1109-367 others(5): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80018648 | ||||||
chr6:80018648
|
A | G | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(131): Show | 212 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1109-3676A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80018648 | ||||||
chr6:80018649
|
T | A | 1 | a0001c0001t0001g0106 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1109-3675T>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80018649 | ||||||
chr6:80018690
|
A | G | 2 | a0001c0001t0001g0153a0001c0001t0001g0159 | 2 | HG00323.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1109-3634A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80018690 | ||||||
chr6:80019074
|
A | G | 14 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(11): Show | 28 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.1109-3250A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80019074 | ||||||
chr6:80019087
|
C | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1109-3237C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80019087 | ||||||
chr6:80019217
|
A | C | 1 | a0001c0001t0001g0100 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1109-3107A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80019217 | ||||||
chr6:80020053
|
T | TACATATA others(1): Show |
139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1109-2266_1109-225 others(12): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 80020053 | |||||
chr6:80020195
|
G | T | 1 | a0001c0005t0004g0191 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1109-2129G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80020195 | ||||||
chr6:80020282
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1109-2042A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80020282 | ||||||
chr6:80020545
|
A | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1109-1779A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80020545 | ||||||
chr6:80020788
|
A | T | 1 | a0001c0001t0001g0149 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1109-1536A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80020788 | ||||||
chr6:80020852
|
A | G | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 221 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.1109-1472A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80020852 | ||||||
chr6:80021004
|
C | T | 2 | a0001c0001t0001g0180a0006c0009t0001g0179 | 2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1109-1320C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80021004 | ||||||
chr6:80021131
|
C | G | 15 | a0001c0002t0003g0019a0001c0002t0003g0043a0001c0002t0003g0044others(12): Show | 20 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1109-1193C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80021131 | ||||||
chr6:80021159
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1109-1165T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80021159 | ||||||
chr6:80021249
|
G | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 251 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.1109-1075G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80021249 | ||||||
chr6:80021297
|
A | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1109-1027A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80021297 | ||||||
chr6:80021349
|
C | T | 6 | a0001c0001t0001g0030a0001c0001t0001g0088a0001c0001t0001g0089others(3): Show | 7 | NA18954.hp2 NA18984.hp1 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1109-975C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80021349 | ||||||
chr6:80021432
|
GGCACCAC others(6): Show |
G | 4 | a0001c0003t0001g0010a0001c0003t0001g0183a0001c0003t0001g0184others(1): Show | 8 | HG02257.hp1 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1109-891_1109-879d others(15): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80021432 | ||||||
chr6:80021485
|
A | C | 3 | a0001c0001t0001g0034a0001c0001t0001g0166a0001c0001t0005g0148 | 4 | HG03130.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1109-839A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80021485 | ||||||
chr6:80021958
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 129 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.1109-366A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80021958 | ||||||
chr6:80022032
|
A | G | 13 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(10): Show | 27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1109-292A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80022032 | ||||||
chr6:80022131
|
A | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0075 | 6 | HG02129.hp1 NA18968.hp1 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.1109-193A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80022131 | ||||||
chr6:80022139
|
T | G | 1 | a0001c0001t0001g0153 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1109-185T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80022139 | ||||||
chr6:80022141
|
T | C | 4 | a0001c0001t0001g0117a0001c0001t0001g0119a0001c0001t0001g0122others(1): Show | 4 | NA18956.hp2 NA18991.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.1109-183T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80022141 | ||||||
chr6:80022294
|
G | T | 1 | a0001c0001t0001g0029 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1109-30G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80022294 | ||||||
chr6:80022524
|
C | T | 10 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(7): Show | 22 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.1257+52C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80022524 | ||||||
chr6:80022525
|
G | A | 15 | a0001c0002t0003g0019a0001c0002t0003g0043a0001c0002t0003g0044others(12): Show | 20 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1257+53G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80022525 | ||||||
chr6:80022639
|
A | G | 1 | a0001c0008t0004g0187 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1257+167A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80022639 | ||||||
chr6:80022813
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1257+341G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80022813 | ||||||
chr6:80022887
|
C | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 220 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.1257+415C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80022887 | ||||||
chr6:80022954
|
C | T | 2 | a0001c0001t0001g0180a0006c0009t0001g0179 | 2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1257+482C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80022954 | ||||||
chr6:80023036
|
C | G | 1 | a0001c0008t0004g0187 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1257+564C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80023036 | ||||||
chr6:80023055
|
A | C | 2 | a0001c0001t0001g0143a0001c0001t0001g0163 | 2 | HG03239.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1257+583A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80023055 | ||||||
chr6:80023331
|
C | T | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(122): Show | 190 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.1257+859C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80023331 | ||||||
chr6:80023365
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1257+893G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80023365 | ||||||
chr6:80023366
|
G | T | 7 | a0001c0001t0001g0180a0001c0004t0001g0021a0001c0004t0001g0181others(4): Show | 9 | HG02258.hp2 HG02615.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1257+894G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80023366 | ||||||
chr6:80023399
|
T | C | 6 | a0001c0001t0001g0079a0001c0001t0001g0161a0001c0003t0001g0010others(3): Show | 10 | HG02257.hp1 HG02451.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1257+927T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80023399 | ||||||
chr6:80023449
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1257+977C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80023449 | ||||||
chr6:80023453
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1257+981T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80023453 | ||||||
chr6:80023461
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1257+989T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80023461 | ||||||
chr6:80023465
|
C | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1257+993C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80023465 | ||||||
chr6:80023512
|
GA | G | 13 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(10): Show | 27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1257+1042delA | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 80023512 | |||||
chr6:80023535
|
G | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 175 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.1257+1063G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80023535 | ||||||
chr6:80023562
|
C | T | 3 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0092 | 4 | HG02809.hp2 HG03516.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1257+1090C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80023562 | ||||||
chr6:80024003
|
T | A | 1 | a0001c0001t0001g0110 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1257+1531T>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80024003 | ||||||
chr6:80024030
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1257+1558T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80024030 | ||||||
chr6:80024167
|
A | G | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(80): Show | 125 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.1257+1695A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80024167 | ||||||
chr6:80024192
|
G | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1257+1720G>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80024192 | ||||||
chr6:80024259
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1257+1787G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80024259 | ||||||
chr6:80024286
|
C | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0083a0001c0001t0001g0084 | 4 | HG02257.hp2 HG02572.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1257+1814C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80024286 | ||||||
chr6:80024475
|
T | C | 1 | a0001c0001t0001g0123 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1258-1903T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80024475 | ||||||
chr6:80024481
|
G | A | 1 | a0001c0002t0006g0176 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1258-1897G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80024481 | ||||||
chr6:80024860
|
G | GTCCAGAC others(10): Show |
1 | a0001c0001t0001g0109 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1258-1515_1258-149 others(21): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 80024860 | |||||
chr6:80025040
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1258-1338A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80025040 | ||||||
chr6:80025153
|
G | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1258-1225G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80025153 | ||||||
chr6:80025178
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1258-1200G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80025178 | ||||||
chr6:80025226
|
T | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | NA18942.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.1258-1152T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80025226 | ||||||
chr6:80025262
|
C | T | 1 | a0001c0001t0001g0048 | 2 | NA19006.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1258-1116C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80025262 | ||||||
chr6:80025448
|
A | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0127 | 2 | HG02132.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1258-930A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80025448 | ||||||
chr6:80025518
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1258-860T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80025518 | ||||||
chr6:80025605
|
G | T | 1 | a0001c0001t0001g0070 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1258-773G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80025605 | ||||||
chr6:80025859
|
C | CT | 7 | a0001c0001t0001g0026a0001c0001t0001g0067a0001c0001t0001g0074others(4): Show | 10 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1258-503dupT | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 80025859 | |||||
chr6:80025859
|
CT | C | 13 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(10): Show | 27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1258-503delT | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 80025859 | |||||
chr6:80025896
|
AAG | A | 5 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0103others(2): Show | 7 | HG02280.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1258-480_1258-479d others(4): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 80025896 | |||||
chr6:80025991
|
TGAG | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1258-383_1258-381d others(5): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 80025991 | |||||
chr6:80026277
|
A | G | 13 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(10): Show | 27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1258-101A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80026277 | ||||||
chr6:80027027
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0007g0101 | 2 | HG00140.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1394+513G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 12/21 | chr6 | 80027027 | ||||||
chr6:80027218
|
G | C | 1 | a0001c0001t0001g0076 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1395-667G>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 12/21 | chr6 | 80027218 | ||||||
chr6:80027270
|
A | G | 15 | a0001c0002t0003g0019a0001c0002t0003g0043a0001c0002t0003g0044others(12): Show | 20 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1395-615A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 12/21 | chr6 | 80027270 | ||||||
chr6:80027493
|
C | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1395-392C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 12/21 | chr6 | 80027493 | ||||||
chr6:80027544
|
A | G | 5 | a0001c0004t0001g0021a0001c0004t0001g0181a0001c0004t0001g0182others(2): Show | 7 | HG02258.hp2 HG02615.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1395-341A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 12/21 | chr6 | 80027544 | ||||||
chr6:80027576
|
G | A | 11 | a0001c0001t0001g0180a0001c0003t0001g0010a0001c0003t0001g0183others(8): Show | 17 | HG02257.hp1 HG02258.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1395-309G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 12/21 | chr6 | 80027576 | ||||||
chr6:80027617
|
C | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0145a0001c0001t0001g0158others(1): Show | 11 | HG00738.hp2 HG01081.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.1395-268C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 12/21 | chr6 | 80027617 | ||||||
chr6:80027805
|
A | G | 1 | a0005c0012t0001g0104 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1395-80A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 12/21 | chr6 | 80027805 | ||||||
chr6:80027865
|
A | T | 1 | a0001c0001t0001g0032 | 2 | HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1395-20A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 12/21 | chr6 | 80027865 | ||||||
chr6:80028027
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1521+16T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028027 | ||||||
chr6:80028036
|
G | T | 1 | a0001c0002t0003g0177 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1521+25G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028036 | ||||||
chr6:80028051
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1521+40C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028051 | ||||||
chr6:80028057
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1521+46G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028057 | ||||||
chr6:80028086
|
A | G | 4 | a0001c0001t0001g0024a0001c0001t0001g0195a0001c0001t0001g0198others(1): Show | 6 | HG01891.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1521+75A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028086 | ||||||
chr6:80028167
|
C | T | 4 | a0001c0003t0001g0010a0001c0003t0001g0183a0001c0003t0001g0184others(1): Show | 8 | HG02257.hp1 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1521+156C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028167 | ||||||
chr6:80028297
|
T | TTTTA | 18 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0029others(15): Show | 24 | HG02717.hp1 HG02886.hp1 HG02896.hp1 others(21): Show |
intron_variant | MODIFIER | c.1521+318_1521+321d others(6): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 80028297 | |||||
chr6:80028297
|
TTTTA | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 214 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.1521+318_1521+321d others(6): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 80028297 | |||||
chr6:80028379
|
G | A | 12 | a0001c0001t0002g0012a0001c0001t0002g0015a0001c0001t0002g0016others(9): Show | 22 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.1521+368G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028379 | ||||||
chr6:80028389
|
G | A | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1521+378G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028389 | ||||||
chr6:80028413
|
G | T | 1 | a0001c0001t0001g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1521+402G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028413 | ||||||
chr6:80028465
|
G | A | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1521+454G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028465 | ||||||
chr6:80028609
|
C | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1521+598C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028609 | ||||||
chr6:80028621
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1521+610G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028621 | ||||||
chr6:80028715
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1521+704T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028715 | ||||||
chr6:80028916
|
G | A | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 174 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.1521+905G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028916 | ||||||
chr6:80029011
|
G | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1521+1000G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80029011 | ||||||
chr6:80029111
|
A | G | 1 | a0001c0004t0001g0182 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1521+1100A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80029111 | ||||||
chr6:80029175
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1521+1164G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80029175 | ||||||
chr6:80029268
|
A | C | 1 | a0001c0008t0004g0187 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1521+1257A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80029268 | ||||||
chr6:80029449
|
C | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1521+1438C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80029449 | ||||||
chr6:80029460
|
C | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 221 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.1521+1449C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80029460 | ||||||
chr6:80029682
|
A | C | 1 | a0001c0003t0001g0185 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1521+1671A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80029682 | ||||||
chr6:80029718
|
G | T | 6 | a0001c0001t0001g0030a0001c0001t0001g0088a0001c0001t0001g0089others(3): Show | 7 | NA18954.hp2 NA18984.hp1 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1521+1707G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80029718 | ||||||
chr6:80030042
|
A | G | 5 | a0001c0004t0001g0021a0001c0004t0001g0181a0001c0004t0001g0182others(2): Show | 7 | HG02258.hp2 HG02615.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1522-1425A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030042 | ||||||
chr6:80030057
|
G | C | 13 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(10): Show | 27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1522-1410G>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030057 | ||||||
chr6:80030059
|
A | G | 13 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(10): Show | 27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1522-1408A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030059 | ||||||
chr6:80030063
|
C | G | 1 | a0001c0001t0001g0073 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1522-1404C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030063 | ||||||
chr6:80030115
|
A | T | 1 | a0001c0002t0003g0175 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1522-1352A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030115 | ||||||
chr6:80030184
|
T | G | 15 | a0001c0002t0003g0019a0001c0002t0003g0043a0001c0002t0003g0044others(12): Show | 20 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1522-1283T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030184 | ||||||
chr6:80030217
|
CT | C | 1 | a0002c0006t0001g0020 | 3 | HG00733.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1522-1245delT | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 80030217 | |||||
chr6:80030331
|
G | T | 2 | a0001c0001t0001g0100a0001c0001t0007g0101 | 2 | HG00140.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1522-1136G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030331 | ||||||
chr6:80030470
|
G | A | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(83): Show | 130 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.1522-997G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030470 | ||||||
chr6:80030484
|
A | G | 9 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(6): Show | 21 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.1522-983A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030484 | ||||||
chr6:80030535
|
C | G | 1 | a0001c0003t0001g0185 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1522-932C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030535 | ||||||
chr6:80030722
|
A | C | 5 | a0001c0001t0001g0113a0001c0001t0001g0118a0001c0001t0001g0135others(2): Show | 5 | HG01175.hp2 HG02145.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1522-745A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030722 | ||||||
chr6:80030742
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1522-725T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030742 | ||||||
chr6:80030903
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1522-564C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030903 | ||||||
chr6:80031044
|
C | CA | 14 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(11): Show | 28 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.1522-408dupA | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 80031044 | |||||
chr6:80031044
|
CA | C | 9 | a0001c0001t0001g0071a0001c0001t0001g0089a0001c0001t0001g0122others(6): Show | 11 | HG00741.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1522-408delA | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 80031044 | |||||
chr6:80031077
|
A | C | 5 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0025others(2): Show | 10 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1522-390A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80031077 | ||||||
chr6:80031361
|
T | A | 1 | a0001c0001t0001g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1522-106T>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80031361 | ||||||
chr6:80031611
|
G | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1614+52G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80031611 | ||||||
chr6:80031688
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1614+129A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80031688 | ||||||
chr6:80031701
|
C | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 215 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.1614+142C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80031701 | ||||||
chr6:80031711
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1614+152C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80031711 | ||||||
chr6:80031731
|
A | T | 11 | a0001c0001t0001g0180a0001c0003t0001g0010a0001c0003t0001g0183others(8): Show | 17 | HG02257.hp1 HG02258.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1614+172A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80031731 | ||||||
chr6:80031736
|
T | C | 1 | a0001c0001t0001g0088 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1614+177T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80031736 | ||||||
chr6:80031753
|
A | G | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(80): Show | 125 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.1614+194A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80031753 | ||||||
chr6:80031836
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1614+277G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80031836 | ||||||
chr6:80031901
|
C | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1614+342C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80031901 | ||||||
chr6:80032207
|
C | A | 1 | a0006c0009t0001g0179 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1614+648C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80032207 | ||||||
chr6:80032285
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1614+726C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80032285 | ||||||
chr6:80032384
|
A | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1614+825A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80032384 | ||||||
chr6:80032451
|
T | G | 1 | a0002c0006t0001g0020 | 3 | HG00733.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1614+892T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80032451 | ||||||
chr6:80032638
|
A | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1614+1079A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80032638 | ||||||
chr6:80032657
|
T | TA | 14 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(11): Show | 28 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.1614+1099dupA | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr6 | 80032657 | |||||
chr6:80032822
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1614+1263A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80032822 | ||||||
chr6:80032840
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1614+1281C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80032840 | ||||||
chr6:80032871
|
G | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1614+1312G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80032871 | ||||||
chr6:80032914
|
A | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1614+1355A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80032914 | ||||||
chr6:80033163
|
A | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1614+1604A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80033163 | ||||||
chr6:80033180
|
A | G | 1 | a0001c0001t0001g0064 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1614+1621A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80033180 | ||||||
chr6:80033233
|
T | C | 1 | a0001c0001t0001g0066 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1614+1674T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80033233 | ||||||
chr6:80033393
|
G | A | 1 | a0002c0006t0001g0020 | 3 | HG00733.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1615-1592G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80033393 | ||||||
chr6:80033466
|
T | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1615-1519T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80033466 | ||||||
chr6:80033488
|
A | C | 2 | a0001c0001t0001g0180a0006c0009t0001g0179 | 2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1615-1497A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80033488 | ||||||
chr6:80033571
|
A | G | 11 | a0001c0002t0003g0019a0001c0002t0003g0043a0001c0002t0003g0044others(8): Show | 16 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1615-1414A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80033571 | ||||||
chr6:80033615
|
G | A | 2 | a0001c0001t0001g0180a0006c0009t0001g0179 | 2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1615-1370G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80033615 | ||||||
chr6:80033705
|
A | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1615-1280A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80033705 | ||||||
chr6:80033739
|
C | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1615-1246C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80033739 | ||||||
chr6:80033763
|
C | CATGTGT | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(81): Show | 126 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1615-1219_1615-121 others(10): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr6 | 80033763 | |||||
chr6:80033814
|
A | G | 1 | a0001c0001t0001g0028 | 2 | HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1615-1171A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80033814 | ||||||
chr6:80033849
|
C | T | 4 | a0001c0003t0001g0010a0001c0003t0001g0183a0001c0003t0001g0184others(1): Show | 8 | HG02257.hp1 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1615-1136C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80033849 | ||||||
chr6:80033950
|
A | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1615-1035A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80033950 | ||||||
chr6:80034388
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1615-597G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80034388 | ||||||
chr6:80034399
|
C | T | 11 | a0001c0002t0003g0019a0001c0002t0003g0043a0001c0002t0003g0044others(8): Show | 16 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1615-586C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80034399 | ||||||
chr6:80034461
|
T | G | 1 | a0001c0001t0001g0023 | 3 | HG01168.hp2 HG01433.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1615-524T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80034461 | ||||||
chr6:80034553
|
G | C | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 220 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.1615-432G>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80034553 | ||||||
chr6:80034647
|
A | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1615-338A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80034647 | ||||||
chr6:80034648
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1615-337G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80034648 | ||||||
chr6:80034853
|
C | G | 1 | a0001c0001t0001g0032 | 2 | HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1615-132C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80034853 | ||||||
chr6:80034921
|
T | G | 1 | a0001c0001t0001g0141 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1615-64T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80034921 | ||||||
chr6:80035438
|
A | G | 11 | a0001c0001t0001g0180a0001c0003t0001g0010a0001c0003t0001g0183others(8): Show | 17 | HG02257.hp1 HG02258.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1924+21A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 16/21 | chr6 | 80035438 | ||||||
chr6:80035589
|
C | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1924+172C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 16/21 | chr6 | 80035589 | ||||||
chr6:80035614
|
C | G | 1 | a0001c0001t0001g0199 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1924+197C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 16/21 | chr6 | 80035614 | ||||||
chr6:80035692
|
A | C | 1 | a0001c0001t0001g0086 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1924+275A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 16/21 | chr6 | 80035692 | ||||||
chr6:80035721
|
G | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1924+304G>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 16/21 | chr6 | 80035721 | ||||||
chr6:80035795
|
G | T | 1 | a0001c0001t0001g0155 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1924+378G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 16/21 | chr6 | 80035795 | ||||||
chr6:80036262
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1925-213A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 16/21 | chr6 | 80036262 | ||||||
chr6:80036681
|
T | A | 1 | a0001c0001t0001g0106 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2049+82T>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80036681 | ||||||
chr6:80036861
|
A | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.2049+262A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80036861 | ||||||
chr6:80036872
|
C | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2049+273C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80036872 | ||||||
chr6:80036873
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2049+274G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80036873 | ||||||
chr6:80036885
|
T | A | 1 | a0001c0001t0001g0103 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2049+286T>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80036885 | ||||||
chr6:80036956
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2049+357A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80036956 | ||||||
chr6:80037258
|
A | G | 1 | a0002c0006t0001g0020 | 3 | HG00733.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2049+659A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80037258 | ||||||
chr6:80037493
|
G | A | 1 | a0001c0002t0003g0178 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2050-474G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80037493 | ||||||
chr6:80037561
|
G | A | 1 | a0001c0001t0001g0039 | 2 | NA18952.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2050-406G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80037561 | ||||||
chr6:80037636
|
G | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.2050-331G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80037636 | ||||||
chr6:80037661
|
A | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.2050-306A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80037661 | ||||||
chr6:80037716
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2050-251C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80037716 | ||||||
chr6:80037760
|
G | A | 1 | a0001c0001t0001g0035 | 2 | NA18950.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.2050-207G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80037760 | ||||||
chr6:80037792
|
A | G | 15 | a0001c0002t0003g0019a0001c0002t0003g0043a0001c0002t0003g0044others(12): Show | 20 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2050-175A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80037792 | ||||||
chr6:80037865
|
T | TATA | 5 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0103others(2): Show | 7 | HG02280.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2050-72_2050-70dup others(3): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr6 | 80037865 | |||||
chr6:80037865
|
TATA | T | 21 | a0001c0001t0001g0133a0001c0001t0001g0149a0001c0001t0002g0012others(18): Show | 34 | HG01074.hp1 HG01109.hp1 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.2050-72_2050-70del others(3): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr6 | 80037865 | |||||
chr6:80037865
|
TATAATA | T | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(105): Show | 171 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.2050-75_2050-70del others(6): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr6 | 80037865 | |||||
chr6:80037865
|
TATAATAA others(2): Show |
T | 10 | a0001c0001t0001g0125a0001c0001t0001g0151a0001c0002t0003g0019others(7): Show | 13 | HG00673.hp1 HG00733.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.2050-78_2050-70del others(9): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr6 | 80037865 | |||||
chr6:80037865
|
TATAATAA others(5): Show |
T | 6 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0058others(3): Show | 10 | HG00408.hp1 HG02132.hp1 HG03654.hp1 others(7): Show |
intron_variant | MODIFIER | c.2050-81_2050-70del others(12): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr6 | 80037865 | |||||
chr6:80037895
|
A | C | 1 | a0001c0008t0004g0187 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2050-72A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80037895 | ||||||
chr6:80037903
|
A | C | 1 | a0001c0001t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2050-64A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80037903 | ||||||
chr6:80038100
|
C | G | 2 | a0001c0001t0002g0051a0001c0001t0002g0056 | 2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2130+53C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80038100 | ||||||
chr6:80038187
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2130+140G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80038187 | ||||||
chr6:80038220
|
C | T | 9 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(6): Show | 21 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.2130+173C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80038220 | ||||||
chr6:80038317
|
G | A | 1 | a0001c0001t0001g0047 | 2 | HG01943.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.2130+270G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80038317 | ||||||
chr6:80038488
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2130+441T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80038488 | ||||||
chr6:80038525
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2130+478T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80038525 | ||||||
chr6:80038594
|
G | T | 1 | a0001c0001t0001g0062 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2130+547G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80038594 | ||||||
chr6:80038719
|
G | A | 3 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099 | 3 | NA18977.hp1 NA19003.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.2130+672G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80038719 | ||||||
chr6:80038900
|
G | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 251 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.2131-796G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80038900 | ||||||
chr6:80039062
|
A | G | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(81): Show | 126 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.2131-634A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80039062 | ||||||
chr6:80039208
|
G | A | 4 | a0001c0003t0001g0010a0001c0003t0001g0183a0001c0003t0001g0184others(1): Show | 8 | HG02257.hp1 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2131-488G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80039208 | ||||||
chr6:80039391
|
C | CAAGT | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 327 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(324): Show |
intron_variant | MODIFIER | c.2131-303_2131-302i others(6): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 80039391 | |||||
chr6:80039489
|
A | G | 15 | a0001c0002t0003g0019a0001c0002t0003g0043a0001c0002t0003g0044others(12): Show | 20 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2131-207A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80039489 | ||||||
chr6:80039673
|
G | A | 13 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(10): Show | 27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.2131-23G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80039673 | ||||||
chr6:80039958
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2307+86G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 19/21 | chr6 | 80039958 | ||||||
chr6:80040124
|
G | A | 1 | a0001c0001t0001g0066 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2308-72G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 19/21 | chr6 | 80040124 | ||||||
chr6:80040168
|
T | C | 1 | a0002c0006t0001g0020 | 3 | HG00733.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2308-28T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 19/21 | chr6 | 80040168 | ||||||
chr6:80040289
|
T | A | 4 | a0001c0005t0004g0189a0001c0005t0004g0191a0001c0005t0004g0192others(1): Show | 4 | HG03516.hp1 HG03579.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.2392+9T>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 20/21 | chr6 | 80040289 | ||||||
chr6:80040376
|
C | G | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(81): Show | 126 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.2392+96C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 20/21 | chr6 | 80040376 | ||||||
chr6:80040532
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2393-74T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 20/21 | chr6 | 80040532 | ||||||
chr6:80040573
|
C | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 212 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.2393-33C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 20/21 | chr6 | 80040573 | ||||||
chr6:80040575
|
G | T | 1 | a0002c0006t0001g0020 | 3 | HG00733.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2393-31G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 20/21 | chr6 | 80040575 | ||||||
chr6:80040745
|
A | G | 1 | a0001c0001t0001g0028 | 2 | HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2490+42A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80040745 | ||||||
chr6:80040864
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2490+161C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80040864 | ||||||
chr6:80040935
|
C | G | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 212 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.2490+232C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80040935 | ||||||
chr6:80041016
|
T | C | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 212 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.2490+313T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80041016 | ||||||
chr6:80041281
|
A | T | 1 | a0001c0004t0001g0181 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2490+578A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80041281 | ||||||
chr6:80041308
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2490+605C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80041308 | ||||||
chr6:80041413
|
T | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | NA18942.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.2491-706T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80041413 | ||||||
chr6:80041551
|
T | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0157 | 3 | NA18950.hp1 NA18975.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2491-568T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80041551 | ||||||
chr6:80041658
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2491-461G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80041658 | ||||||
chr6:80041814
|
CTTTA | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0084 | 3 | HG02257.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2491-300_2491-297d others(6): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr6 | 80041814 | |||||
chr6:80041866
|
A | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0061 | 2 | HG01175.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2491-253A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80041866 | ||||||
chr6:80041975
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2491-144A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80041975 | ||||||
chr6:80042030
|
A | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0092 | 2 | NA19057.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.2491-89A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80042030 | ||||||
chr6:80042063
|
G | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(111): Show | 173 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.2491-56G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80042063 |