geneid | 1075 |
---|---|
ensemblid | ENSG00000109861.17 |
hgncid | 2528 |
symbol | CTSC |
name | cathepsin C |
refseq_nuc | NM_001814.6 |
refseq_prot | NP_001805.4 |
ensembl_nuc | ENST00000227266.10 |
ensembl_prot | ENSP00000227266.4 |
mane_status | MANE Select |
chr | chr11 |
start | 88293592 |
end | 88337736 |
strand | - |
ver | v1.2 |
region | chr11:88293592-88337736 |
region5000 | chr11:88288592-88342736 |
regionname0 | CTSC_chr11_88293592_88337736 |
regionname5000 | CTSC_chr11_88288592_88342736 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 463 | 367 | 80 | 60 | 177 | 11 | 38 | 134 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
a0002 | 0/0 | 463 | 47 | 11 | 8 | 25 | 1 | 2 | 22 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
a0003 | 1/0 | 463 | 18 | 4 | 8 | 0 | 4 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
a0004 | 0/0 | 463 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
a0005 | 0/0 | 463 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1392 | 365 | 79 | 60 | 176 | 11 | 38 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
c0002 | 0/0 | 1392 | 47 | 11 | 8 | 25 | 1 | 2 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
c0003 | 1/0 | 1392 | 18 | 4 | 8 | 0 | 4 | 1 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
c0004 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
c0005 | 0/0 | 1392 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
c0006 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
c0007 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 479 | 412 | 89 | 67 | 201 | 13 | 40 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
t0002 | 0/0 | 479 | 15 | 4 | 7 | 0 | 3 | 1 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
t0003 | 0/0 | 479 | 3 | 0 | 2 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
t0004 | 0/0 | 479 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
t0005 | 0/0 | 578 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
t0006 | 0/0 | 479 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
t0007 | 0/0 | 479 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 15 | 1 | 7 | 6 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0002 | 0/0 | 12 | 0 | 0 | 11 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0003 | 0/0 | 12 | 0 | 1 | 10 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0005 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0006 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0008 | 1/0 | 5 | 0 | 2 | 0 | 2 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0009 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0011 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0021 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0042 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0254 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1392 | 365 | 79 | 60 | 176 | 11 | 38 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
a0001c0004 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
a0001c0006 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
a0002c0002 | 0/0 | 1392 | 47 | 11 | 8 | 25 | 1 | 2 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
a0003c0003 | 1/0 | 1392 | 18 | 4 | 8 | 0 | 4 | 1 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
a0004c0005 | 0/0 | 1392 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
a0005c0007 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1870 | 343 | 72 | 51 | 175 | 8 | 36 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
a0001c0001t0002 | 0/0 | 1870 | 15 | 4 | 7 | 0 | 3 | 1 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
a0001c0001t0003 | 0/0 | 1870 | 3 | 0 | 2 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
a0001c0001t0004 | 0/0 | 1870 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
a0001c0001t0005 | 0/0 | 1969 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
a0001c0001t0006 | 0/0 | 1870 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
a0001c0001t0007 | 0/0 | 1870 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
a0001c0004t0001 | 0/0 | 1870 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
a0001c0006t0001 | 0/0 | 1870 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
a0002c0002t0001 | 0/0 | 1870 | 47 | 11 | 8 | 25 | 1 | 2 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
a0003c0003t0001 | 1/0 | 1870 | 18 | 4 | 8 | 0 | 4 | 1 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
a0004c0005t0001 | 0/0 | 1870 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
a0005c0007t0001 | 0/0 | 1870 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | copy fasta | chr11 | 88288592 | 88342736 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 15 | 1 | 7 | 6 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0002 | 0/0 | 12 | 0 | 0 | 11 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0003 | 0/0 | 12 | 0 | 1 | 10 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0011 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0254 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0002g0006 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0006g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0001t0007g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0004t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0001c0006t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0005 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0002c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0003c0003t0001g0008 | 1/0 | 5 | 0 | 2 | 0 | 2 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0003c0003t0001g0021 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0003c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0003c0003t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0003c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0003c0003t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0003c0003t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0003c0003t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0003c0003t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0003c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0003c0003t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0003c0003t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0004c0005t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
a0005c0007t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | GBR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0102 | EUR | GBR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | GBR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0223 | EUR | FIN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0244 | EUR | FIN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | FIN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00323 | hp2 | a0003 | c0003 | t0001 | g0021 | EUR | FIN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0105 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00738 | hp1 | a0003 | c0003 | t0001 | g0008 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00741 | hp1 | a0003 | c0003 | t0001 | g0021 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0316 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01109 | hp2 | a0003 | c0003 | t0001 | g0298 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01168 | hp2 | a0003 | c0003 | t0001 | g0021 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01169 | hp1 | a0003 | c0003 | t0001 | g0171 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0314 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01192 | hp2 | a0003 | c0003 | t0001 | g0008 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01243 | hp2 | a0003 | c0003 | t0001 | g0304 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01346 | hp1 | a0003 | c0003 | t0001 | g0303 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0050 | EUR | IBS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01516 | hp2 | a0003 | c0003 | t0001 | g0008 | EUR | IBS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0006 | EUR | IBS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01517 | hp2 | a0003 | c0003 | t0001 | g0008 | EUR | IBS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0047 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0106 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0112 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0101 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0311 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | CDX | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CDX | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02257 | hp2 | a0001 | c0006 | t0001 | g0089 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0110 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0103 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02717 | hp2 | a0001 | c0001 | t0005 | g0056 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02738 | hp2 | a0004 | c0005 | t0001 | g0248 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02809 | hp1 | a0003 | c0003 | t0001 | g0299 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0312 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02895 | hp2 | a0003 | c0003 | t0001 | g0300 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02897 | hp1 | a0003 | c0003 | t0001 | g0301 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0109 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03041 | hp1 | a0003 | c0003 | t0001 | g0117 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | MSL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | MSL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | MSL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03453 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | MSL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | MSL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0315 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | STU | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | STU | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0114 | SAS | BEB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | BEB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | BEB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG04115 | hp1 | a0003 | c0003 | t0001 | g0302 | SAS | STU | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | STU | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | BEB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | STU | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | STU | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0115 | SAS | STU | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | STU | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | STU | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | STU | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | YRI | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | YRI | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | CHB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18747 | hp2 | a0001 | c0004 | t0001 | g0094 | EAS | CHB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | YRI | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | YRI | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18986 | hp1 | a0001 | c0001 | t0006 | g0172 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18993 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | LWK | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | LWK | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0293 | AFR | LWK | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19055 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19072 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA19240 | hp2 | a0001 | c0001 | t0007 | g0317 | AFR | YRI | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ASW | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ASW | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0225 | EUR | TSI | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0053 | EUR | TSI | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | TSI | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA20805 | hp2 | a0003 | c0003 | t0001 | g0297 | EUR | TSI | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0092 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03471 | hp1 | a0005 | c0007 | t0001 | g0313 | AFR | MSL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | MSL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | USA | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | USA | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | USA | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | USA | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0254 | REF | REF | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
homoSapiens_grch38 | hp1 | a0003 | c0003 | t0001 | g0008 | REF | REF | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:88294041
|
T | C | 1 | a0002 | 47 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(44): Show |
missense_variant | MODERATE | c.1357A>G | p.Ile453Val | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 7/7 | 1421/1870 | 1357/1392 | 453/463 | chr11 | 88294041 | ||
chr11:88294395
|
C | G | 1 | a0004 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.1003G>C | p.Glu335Gln | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 7/7 | 1067/1870 | 1003/1392 | 335/463 | chr11 | 88294395 | ||
chr11:88312415
|
A | G | 4 | a0001a0002a0004others(1): Show | 416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
missense_variant | MODERATE | c.458T>C | p.Ile153Thr | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/7 | 522/1870 | 458/1392 | 153/463 | chr11 | 88312415 | ||
chr11:88337611
|
G | A | 1 | a0005 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.62C>T | p.Ala21Val | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/7 | 126/1870 | 62/1392 | 21/463 | chr11 | 88337611 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:88294225
|
A | C | 1 | a0002c0002 | 47 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(44): Show |
synonymous_variant | LOW | c.1173T>G | p.Thr391Thr | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 7/7 | 1237/1870 | 1173/1392 | 391/463 | chr11 | 88294225 | ||
chr11:88296197
|
G | A | 1 | a0001c0006 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.825C>T | p.Thr275Thr | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/7 | 889/1870 | 825/1392 | 275/463 | chr11 | 88296197 | ||
chr11:88312429
|
A | G | 1 | a0001c0004 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.444T>C | p.Asn148Asn | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/7 | 508/1870 | 444/1392 | 148/463 | chr11 | 88312429 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:88293751
|
T | G | 1 | a0001c0001t0006 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*255A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 7/7 | 255 | chr11 | 88293751 | |||||
chr11:88293785
|
T | C | 1 | a0001c0001t0005 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*221A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 7/7 | 221 | chr11 | 88293785 | |||||
chr11:88293814
|
T | TAGAAAAA others(92): Show |
1 | a0001c0001t0005 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*191_*192insTTTTTT others(93): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 7/7 | 191 | chr11 | 88293814 | |||||
chr11:88337690
|
A | G | 3 | a0001c0001t0002a0001c0001t0005a0001c0001t0007 | 17 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-18T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/7 | 18 | chr11 | 88337690 | |||||
chr11:88337707
|
C | G | 1 | a0001c0001t0004 | 1 | HG01884.hp1 | 5_prime_UTR_variant | MODIFIER | c.-35G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/7 | 35 | chr11 | 88337707 | |||||
chr11:88337717
|
G | C | 1 | a0001c0001t0003 | 3 | HG01081.hp2 HG01192.hp1 HG03654.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-45C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/7 | chr11 | 88337717 | ||||||
chr11:88337726
|
G | A | 1 | a0001c0001t0007 | 1 | NA19240.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-54C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/7 | chr11 | 88337726 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:88294672
|
T | G | 4 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0281others(1): Show | 8 | NA18943.hp1 NA18944.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.890-164A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88294672 | ||||||
chr11:88294811
|
G | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | NA18612.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.890-303C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88294811 | ||||||
chr11:88295288
|
A | G | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.890-780T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88295288 | ||||||
chr11:88295291
|
A | C | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.890-783T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88295291 | ||||||
chr11:88295301
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.890-793A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88295301 | ||||||
chr11:88295325
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.889+808A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88295325 | ||||||
chr11:88295358
|
G | T | 137 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(134): Show | 182 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.889+775C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88295358 | ||||||
chr11:88295424
|
G | C | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0273 | 3 | HG01243.hp1 HG02451.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.889+709C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88295424 | ||||||
chr11:88295672
|
T | C | 195 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(192): Show | 259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.889+461A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88295672 | ||||||
chr11:88295673
|
G | A | 1 | a0005c0007t0001g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.889+460C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88295673 | ||||||
chr11:88295767
|
G | C | 2 | a0002c0002t0001g0114a0002c0002t0001g0115 | 2 | HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.889+366C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88295767 | ||||||
chr11:88295936
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.889+197A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88295936 | ||||||
chr11:88296027
|
T | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0060 | 3 | HG02818.hp2 HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.889+106A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88296027 | ||||||
chr11:88296097
|
A | C | 3 | a0001c0001t0001g0181a0001c0001t0001g0189a0001c0001t0001g0200 | 3 | HG00673.hp2 HG02027.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.889+36T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88296097 | ||||||
chr11:88296319
|
A | C | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.758-55T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88296319 | ||||||
chr11:88296417
|
T | C | 137 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(134): Show | 182 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.758-153A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88296417 | ||||||
chr11:88296449
|
T | C | 137 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(134): Show | 182 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.758-185A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88296449 | ||||||
chr11:88296725
|
T | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(107): Show | 157 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.758-461A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88296725 | ||||||
chr11:88296825
|
T | C | 41 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0019others(38): Show | 64 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.758-561A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88296825 | ||||||
chr11:88296833
|
A | G | 39 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0019others(36): Show | 61 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.758-569T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88296833 | ||||||
chr11:88296989
|
A | T | 304 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(301): Show | 415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
intron_variant | MODIFIER | c.758-725T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88296989 | ||||||
chr11:88297041
|
C | T | 1 | a0001c0001t0007g0317 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.758-777G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88297041 | ||||||
chr11:88297168
|
A | T | 1 | a0001c0001t0001g0060 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.758-904T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88297168 | ||||||
chr11:88297198
|
C | T | 2 | a0001c0001t0001g0245a0001c0001t0001g0268 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.758-934G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88297198 | ||||||
chr11:88297289
|
C | T | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(302): Show | 416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.758-1025G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88297289 | ||||||
chr11:88297305
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.758-1041T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88297305 | ||||||
chr11:88297521
|
A | G | 104 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 142 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.758-1257T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88297521 | ||||||
chr11:88297587
|
T | C | 1 | a0001c0001t0001g0076 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.758-1323A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88297587 | ||||||
chr11:88297617
|
G | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(132): Show | 206 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.758-1353C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88297617 | ||||||
chr11:88297731
|
G | C | 1 | a0001c0001t0001g0197 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.758-1467C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88297731 | ||||||
chr11:88297763
|
G | A | 99 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(96): Show | 135 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.758-1499C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88297763 | ||||||
chr11:88298044
|
G | C | 1 | a0001c0001t0001g0078 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.758-1780C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298044 | ||||||
chr11:88298050
|
T | C | 46 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(43): Show | 80 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.758-1786A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298050 | ||||||
chr11:88298060
|
G | A | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.758-1796C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298060 | ||||||
chr11:88298064
|
C | T | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 346 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(343): Show |
intron_variant | MODIFIER | c.758-1800G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298064 | ||||||
chr11:88298124
|
T | C | 2 | a0001c0001t0001g0167a0001c0001t0001g0288 | 2 | HG01993.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.758-1860A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298124 | ||||||
chr11:88298263
|
A | G | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.758-1999T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298263 | ||||||
chr11:88298413
|
A | C | 1 | a0001c0001t0001g0118 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.757+2117T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298413 | ||||||
chr11:88298462
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.757+2068G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298462 | ||||||
chr11:88298548
|
G | A | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.757+1982C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298548 | ||||||
chr11:88298595
|
T | C | 2 | a0001c0001t0001g0140a0001c0001t0001g0170 | 2 | HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.757+1935A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298595 | ||||||
chr11:88298625
|
A | G | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.757+1905T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298625 | ||||||
chr11:88298633
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.757+1897T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298633 | ||||||
chr11:88298697
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.757+1833G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298697 | ||||||
chr11:88298713
|
A | T | 1 | a0003c0003t0001g0117 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.757+1817T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298713 | ||||||
chr11:88298794
|
G | C | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.757+1736C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298794 | ||||||
chr11:88298893
|
A | C | 1 | a0001c0001t0001g0236 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.757+1637T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298893 | ||||||
chr11:88298958
|
G | A | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.757+1572C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298958 | ||||||
chr11:88299056
|
G | A | 155 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(152): Show | 201 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.757+1474C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299056 | ||||||
chr11:88299110
|
T | A | 1 | a0001c0001t0001g0188 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.757+1420A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299110 | ||||||
chr11:88299153
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.757+1377G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299153 | ||||||
chr11:88299251
|
A | G | 40 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(37): Show | 71 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.757+1279T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299251 | ||||||
chr11:88299278
|
A | G | 1 | a0002c0002t0001g0110 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.757+1252T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299278 | ||||||
chr11:88299393
|
T | G | 1 | a0001c0001t0001g0078 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.757+1137A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299393 | ||||||
chr11:88299394
|
A | T | 1 | a0001c0001t0001g0078 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.757+1136T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299394 | ||||||
chr11:88299467
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.757+1063G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299467 | ||||||
chr11:88299531
|
G | T | 1 | a0001c0001t0001g0213 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.757+999C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299531 | ||||||
chr11:88299683
|
C | T | 1 | a0001c0001t0001g0239 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.757+847G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299683 | ||||||
chr11:88299806
|
G | C | 1 | a0001c0001t0001g0167 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.757+724C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299806 | ||||||
chr11:88299901
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.757+629G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299901 | ||||||
chr11:88299966
|
G | C | 1 | a0001c0001t0001g0291 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.757+564C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299966 | ||||||
chr11:88300344
|
A | T | 72 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(69): Show | 86 | HG00280.hp1 HG00423.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.757+186T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88300344 | ||||||
chr11:88300353
|
T | C | 306 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(303): Show | 417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
intron_variant | MODIFIER | c.757+177A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88300353 | ||||||
chr11:88300431
|
C | A | 1 | a0002c0002t0001g0293 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.757+99G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88300431 | ||||||
chr11:88300440
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.757+90A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88300440 | ||||||
chr11:88300493
|
A | G | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(302): Show | 416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.757+37T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88300493 | ||||||
chr11:88300506
|
A | G | 2 | a0001c0001t0001g0175a0001c0001t0001g0207 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.757+24T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88300506 | ||||||
chr11:88300836
|
G | A | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0005g0056others(1): Show | 4 | HG02486.hp1 HG02717.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.642-191C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88300836 | ||||||
chr11:88300839
|
GTTTC | G | 53 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0018others(50): Show | 66 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.642-198_642-195del others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88300839 | ||||||
chr11:88300924
|
T | G | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.642-279A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88300924 | ||||||
chr11:88300995
|
A | G | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128 | 3 | HG01243.hp1 HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.642-350T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88300995 | ||||||
chr11:88301377
|
G | A | 1 | a0001c0001t0001g0042 | 2 | HG00140.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.642-732C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301377 | ||||||
chr11:88301461
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.642-816C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301461 | ||||||
chr11:88301712
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.642-1067G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301712 | ||||||
chr11:88301742
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.642-1097G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301742 | ||||||
chr11:88301799
|
AAC | A | 40 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(37): Show | 71 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.642-1156_642-1155d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301799 | ||||||
chr11:88301804
|
ACG | A | 10 | a0001c0001t0001g0046a0001c0001t0001g0123a0001c0001t0001g0124others(7): Show | 11 | HG01891.hp1 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.642-1161_642-1160d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301804 | ||||||
chr11:88301804
|
ACGCG | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0119a0001c0001t0001g0145others(1): Show | 5 | HG00639.hp1 HG01069.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.642-1163_642-1160d others(6): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301804 | ||||||
chr11:88301806
|
G | GCA | 4 | a0001c0001t0001g0020a0001c0001t0001g0041a0001c0001t0001g0250others(1): Show | 7 | HG01884.hp2 HG01952.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.642-1162_642-1161i others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301806 | ||||||
chr11:88301806
|
GCGCGCA | G | 49 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0018others(46): Show | 61 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.642-1167_642-1162d others(8): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301806 | ||||||
chr11:88301807
|
C | T | 2 | a0003c0003t0001g0300a0003c0003t0001g0301 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.642-1162G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301807 | ||||||
chr11:88301808
|
G | A | 7 | a0001c0001t0001g0020a0001c0001t0001g0041a0001c0001t0001g0250others(4): Show | 12 | HG01884.hp2 HG01952.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.642-1163C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301808 | ||||||
chr11:88301808
|
G | GCA | 96 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(93): Show | 127 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.642-1164_642-1163i others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301808 | ||||||
chr11:88301808
|
G | GCACA | 20 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0120others(17): Show | 23 | HG00323.hp1 HG00597.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.642-1164_642-1163i others(6): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301808 | ||||||
chr11:88301808
|
G | GCACACAC others(1): Show |
4 | a0001c0001t0001g0010a0001c0001t0001g0187a0001c0001t0001g0196others(1): Show | 7 | NA18953.hp2 NA18955.hp2 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.642-1164_642-1163i others(10): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301808 | ||||||
chr11:88301808
|
G | GCACACAC others(3): Show |
7 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0188others(4): Show | 8 | HG02602.hp2 NA18948.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.642-1164_642-1163i others(12): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301808 | ||||||
chr11:88301808
|
G | GCACACAC others(5): Show |
1 | a0001c0001t0001g0222 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.642-1164_642-1163i others(14): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301808 | ||||||
chr11:88301810
|
G | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(231): Show | 328 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.642-1165C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301810 | ||||||
chr11:88301810
|
G | GCA | 3 | a0001c0001t0001g0246a0001c0001t0001g0251a0001c0001t0001g0306 | 3 | HG00423.hp2 NA18967.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.642-1167_642-1166d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301810 | ||||||
chr11:88301835
|
C | CACAG | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.642-1191_642-1190i others(6): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301835 | ||||||
chr11:88301835
|
C | G | 46 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(43): Show | 80 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.642-1190G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301835 | ||||||
chr11:88301837
|
G | C | 59 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0018others(56): Show | 75 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.642-1192C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301837 | ||||||
chr11:88301839
|
G | C | 51 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0018others(48): Show | 64 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.642-1194C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301839 | ||||||
chr11:88301861
|
C | T | 157 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(154): Show | 203 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.642-1216G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301861 | ||||||
chr11:88302203
|
G | A | 1 | a0002c0002t0001g0293 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.642-1558C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302203 | ||||||
chr11:88302418
|
T | C | 8 | a0001c0001t0002g0006a0001c0001t0002g0049a0001c0001t0002g0050others(5): Show | 12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.642-1773A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302418 | ||||||
chr11:88302424
|
C | T | 1 | a0001c0001t0002g0053 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.642-1779G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302424 | ||||||
chr11:88302583
|
A | G | 3 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204 | 3 | HG02135.hp1 HG02165.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.642-1938T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302583 | ||||||
chr11:88302585
|
C | T | 5 | a0002c0002t0001g0097a0002c0002t0001g0098a0002c0002t0001g0099others(2): Show | 5 | NA18940.hp2 NA18968.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.642-1940G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302585 | ||||||
chr11:88302620
|
C | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(42): Show | 79 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.642-1975G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302620 | ||||||
chr11:88302625
|
CA | C | 44 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0018others(41): Show | 57 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.642-1981delT | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302625 | ||||||
chr11:88302625
|
CAA | C | 8 | a0001c0001t0001g0138a0001c0001t0001g0288a0001c0001t0002g0006others(5): Show | 12 | HG01069.hp2 HG01071.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.642-1982_642-1981d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302625 | ||||||
chr11:88302625
|
CAAA | C | 6 | a0001c0001t0001g0046a0001c0001t0002g0055a0002c0002t0001g0096others(3): Show | 7 | HG00733.hp2 HG01891.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.642-1983_642-1981d others(5): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302625 | ||||||
chr11:88302625
|
CAAAA | C | 48 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0059others(45): Show | 61 | HG00140.hp1 HG00642.hp1 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.642-1984_642-1981d others(6): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302625 | ||||||
chr11:88302625
|
CAAAAA | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 260 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.642-1985_642-1981d others(7): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302625 | ||||||
chr11:88302625
|
CAAAAAAA others(4): Show |
C | 6 | a0001c0001t0001g0034a0001c0001t0001g0132a0001c0001t0001g0231others(3): Show | 7 | HG00280.hp2 HG00323.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.642-1991_642-1981d others(13): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302625 | ||||||
chr11:88302816
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.642-2171A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302816 | ||||||
chr11:88302914
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.642-2269G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302914 | ||||||
chr11:88302929
|
T | C | 1 | a0001c0001t0001g0253 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.642-2284A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302929 | ||||||
chr11:88303041
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.642-2396T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303041 | ||||||
chr11:88303326
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.642-2681G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303326 | ||||||
chr11:88303329
|
C | T | 1 | a0001c0001t0001g0046 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.642-2684G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303329 | ||||||
chr11:88303333
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.642-2688G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303333 | ||||||
chr11:88303352
|
T | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(42): Show | 79 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.642-2707A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303352 | ||||||
chr11:88303388
|
G | C | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(150): Show | 199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.642-2743C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303388 | ||||||
chr11:88303421
|
C | T | 78 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(75): Show | 110 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.642-2776G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303421 | ||||||
chr11:88303641
|
T | G | 31 | a0001c0001t0001g0122a0002c0002t0001g0005a0002c0002t0001g0016others(28): Show | 42 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.642-2996A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303641 | ||||||
chr11:88303671
|
T | C | 203 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(200): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.642-3026A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303671 | ||||||
chr11:88303903
|
C | T | 1 | a0001c0001t0001g0046 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.642-3258G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303903 | ||||||
chr11:88303914
|
C | CAG | 1 | a0001c0001t0001g0020 | 3 | HG03130.hp1 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.642-3271_642-3270d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303914 | ||||||
chr11:88303962
|
G | A | 4 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 4 | HG02647.hp2 HG02896.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-3317C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303962 | ||||||
chr11:88303980
|
G | A | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.642-3335C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303980 | ||||||
chr11:88304054
|
G | C | 2 | a0001c0001t0001g0261a0001c0001t0001g0263 | 2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.642-3409C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88304054 | ||||||
chr11:88304296
|
G | A | 1 | a0002c0002t0001g0312 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.642-3651C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88304296 | ||||||
chr11:88304400
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.642-3755G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88304400 | ||||||
chr11:88304733
|
C | A | 5 | a0001c0001t0001g0131a0001c0001t0001g0134a0001c0001t0001g0135others(2): Show | 5 | HG02922.hp2 HG03130.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.642-4088G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88304733 | ||||||
chr11:88304747
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.642-4102C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88304747 | ||||||
chr11:88304833
|
C | A | 8 | a0001c0001t0002g0006a0001c0001t0002g0049a0001c0001t0002g0050others(5): Show | 12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.642-4188G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88304833 | ||||||
chr11:88305054
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0169 | 2 | HG01358.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.641+4109G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305054 | ||||||
chr11:88305059
|
C | G | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.641+4104G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305059 | ||||||
chr11:88305095
|
C | CA | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(191): Show | 263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.641+4067dupT | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305095 | ||||||
chr11:88305095
|
C | CAA | 49 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0019others(46): Show | 75 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.641+4066_641+4067d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305095 | ||||||
chr11:88305141
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.641+4022T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305141 | ||||||
chr11:88305476
|
C | G | 5 | a0001c0001t0001g0020a0001c0001t0001g0041a0001c0001t0001g0257others(2): Show | 8 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.641+3687G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305476 | ||||||
chr11:88305583
|
C | T | 155 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(152): Show | 201 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.641+3580G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305583 | ||||||
chr11:88305608
|
A | G | 8 | a0001c0001t0002g0006a0001c0001t0002g0049a0001c0001t0002g0050others(5): Show | 12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.641+3555T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305608 | ||||||
chr11:88305621
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.641+3542G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305621 | ||||||
chr11:88305655
|
A | T | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(244): Show | 344 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(341): Show |
intron_variant | MODIFIER | c.641+3508T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305655 | ||||||
chr11:88305871
|
C | G | 1 | a0001c0001t0001g0060 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.641+3292G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305871 | ||||||
chr11:88305874
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.641+3289C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305874 | ||||||
chr11:88305882
|
A | G | 1 | a0001c0001t0007g0317 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.641+3281T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305882 | ||||||
chr11:88305895
|
G | T | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.641+3268C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305895 | ||||||
chr11:88305980
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.641+3183C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305980 | ||||||
chr11:88306012
|
G | C | 1 | a0001c0001t0001g0254 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.641+3151C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306012 | ||||||
chr11:88306121
|
T | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(244): Show | 344 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(341): Show |
intron_variant | MODIFIER | c.641+3042A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306121 | ||||||
chr11:88306156
|
C | A | 31 | a0001c0001t0001g0122a0002c0002t0001g0005a0002c0002t0001g0016others(28): Show | 42 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.641+3007G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306156 | ||||||
chr11:88306197
|
T | C | 1 | a0001c0001t0001g0042 | 2 | HG00140.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.641+2966A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306197 | ||||||
chr11:88306276
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.641+2887A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306276 | ||||||
chr11:88306314
|
G | T | 1 | a0001c0001t0003g0315 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.641+2849C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306314 | ||||||
chr11:88306404
|
C | T | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.641+2759G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306404 | ||||||
chr11:88306429
|
C | A | 1 | a0001c0001t0002g0051 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.641+2734G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306429 | ||||||
chr11:88306503
|
G | C | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(150): Show | 199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.641+2660C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306503 | ||||||
chr11:88306519
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.641+2644G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306519 | ||||||
chr11:88306522
|
C | G | 2 | a0001c0001t0001g0071a0001c0001t0001g0073 | 2 | HG03491.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.641+2641G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306522 | ||||||
chr11:88306577
|
T | C | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(302): Show | 416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.641+2586A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306577 | ||||||
chr11:88306669
|
A | T | 1 | a0001c0001t0001g0046 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.641+2494T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306669 | ||||||
chr11:88306936
|
AC | A | 7 | a0001c0001t0001g0181a0001c0001t0001g0189a0001c0001t0001g0190others(4): Show | 7 | HG00423.hp1 HG00609.hp2 HG00673.hp2 others(4): Show |
intron_variant | MODIFIER | c.641+2226delG | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306936 | ||||||
chr11:88306977
|
C | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(42): Show | 79 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.641+2186G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306977 | ||||||
chr11:88307028
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.641+2135G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307028 | ||||||
chr11:88307158
|
G | A | 48 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0018others(45): Show | 61 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.641+2005C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307158 | ||||||
chr11:88307173
|
T | C | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.641+1990A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307173 | ||||||
chr11:88307175
|
TTC | T | 31 | a0001c0001t0001g0122a0002c0002t0001g0005a0002c0002t0001g0016others(28): Show | 42 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.641+1986_641+1987d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307175 | ||||||
chr11:88307230
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.641+1933A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307230 | ||||||
chr11:88307255
|
C | A | 1 | a0002c0002t0001g0107 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.641+1908G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307255 | ||||||
chr11:88307331
|
C | T | 31 | a0001c0001t0001g0122a0002c0002t0001g0005a0002c0002t0001g0016others(28): Show | 42 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.641+1832G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307331 | ||||||
chr11:88307357
|
A | G | 8 | a0001c0001t0002g0006a0001c0001t0002g0049a0001c0001t0002g0050others(5): Show | 12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.641+1806T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307357 | ||||||
chr11:88307407
|
T | C | 2 | a0001c0001t0003g0314a0001c0001t0003g0316 | 2 | HG01081.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.641+1756A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307407 | ||||||
chr11:88307489
|
C | A | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.641+1674G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307489 | ||||||
chr11:88307556
|
C | CT | 47 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0018others(44): Show | 60 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.641+1606dupA | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307556 | ||||||
chr11:88307556
|
C | CTT | 12 | a0001c0001t0001g0139a0001c0001t0001g0146a0001c0001t0001g0147others(9): Show | 14 | HG00733.hp1 HG01192.hp1 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.641+1605_641+1606d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307556 | ||||||
chr11:88307556
|
CT | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(219): Show | 313 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.641+1606delA | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307556 | ||||||
chr11:88307845
|
C | T | 4 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 4 | HG02647.hp2 HG02896.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.641+1318G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307845 | ||||||
chr11:88307908
|
T | C | 1 | a0003c0003t0001g0303 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.641+1255A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307908 | ||||||
chr11:88307929
|
G | A | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.641+1234C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307929 | ||||||
chr11:88307965
|
T | G | 54 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0018others(51): Show | 68 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.641+1198A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307965 | ||||||
chr11:88307992
|
G | C | 2 | a0001c0001t0001g0179a0001c0001t0001g0182 | 2 | NA18612.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.641+1171C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307992 | ||||||
chr11:88308035
|
A | T | 2 | a0001c0001t0005g0056a0001c0001t0007g0317 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.641+1128T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88308035 | ||||||
chr11:88308084
|
G | A | 2 | a0001c0001t0005g0056a0001c0001t0007g0317 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.641+1079C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88308084 | ||||||
chr11:88308347
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.641+816C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88308347 | ||||||
chr11:88308433
|
G | A | 31 | a0001c0001t0001g0122a0002c0002t0001g0005a0002c0002t0001g0016others(28): Show | 42 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.641+730C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88308433 | ||||||
chr11:88308472
|
A | ATTATT | 31 | a0001c0001t0001g0122a0002c0002t0001g0005a0002c0002t0001g0016others(28): Show | 42 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.641+686_641+690dup others(5): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88308472 | ||||||
chr11:88308472
|
ATTATT | A | 158 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(155): Show | 206 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.641+686_641+690del others(5): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88308472 | ||||||
chr11:88308545
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.641+618G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88308545 | ||||||
chr11:88308568
|
A | G | 31 | a0001c0001t0001g0122a0002c0002t0001g0005a0002c0002t0001g0016others(28): Show | 42 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.641+595T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88308568 | ||||||
chr11:88308769
|
C | T | 36 | a0001c0001t0001g0060a0001c0001t0001g0122a0001c0001t0002g0048others(33): Show | 49 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.641+394G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88308769 | ||||||
chr11:88308810
|
C | A | 34 | a0001c0001t0001g0122a0002c0002t0001g0005a0002c0002t0001g0016others(31): Show | 47 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.641+353G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88308810 | ||||||
chr11:88309102
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0169 | 2 | HG01358.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.641+61C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88309102 | ||||||
chr11:88309129
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.641+34T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88309129 | ||||||
chr11:88309406
|
G | C | 1 | a0001c0001t0001g0283 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.486-88C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309406 | ||||||
chr11:88309461
|
A | G | 1 | a0001c0001t0001g0182 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.486-143T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309461 | ||||||
chr11:88309606
|
A | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0288 | 2 | HG01993.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.486-288T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309606 | ||||||
chr11:88309680
|
T | C | 39 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(36): Show | 69 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.486-362A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309680 | ||||||
chr11:88309774
|
T | C | 1 | a0001c0001t0001g0230 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.486-456A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309774 | ||||||
chr11:88309809
|
TGC | T | 19 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0043others(16): Show | 26 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.486-493_486-492del others(2): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309809 | ||||||
chr11:88309810
|
GCGCGCAC others(3): Show |
G | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.486-502_486-493del others(10): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309810 | ||||||
chr11:88309812
|
G | GCA | 12 | a0001c0001t0001g0044a0001c0001t0001g0133a0001c0001t0001g0183others(9): Show | 13 | HG02486.hp1 HG02572.hp2 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.486-495_486-494ins others(2): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309812 | ||||||
chr11:88309812
|
G | GCACA | 8 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0194others(5): Show | 8 | HG02602.hp1 HG02698.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.486-495_486-494ins others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309812 | ||||||
chr11:88309812
|
GCGCA | G | 63 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0019others(60): Show | 88 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.486-498_486-495del others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309812 | ||||||
chr11:88309812
|
GCGCACA | G | 28 | a0001c0001t0001g0177a0001c0001t0001g0227a0001c0001t0001g0273others(25): Show | 39 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.486-500_486-495del others(6): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309812 | ||||||
chr11:88309812
|
GCGCACAC others(1): Show |
G | 4 | a0002c0002t0001g0095a0002c0002t0001g0097a0002c0002t0001g0098others(1): Show | 4 | NA18940.hp2 NA18968.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-502_486-495del others(8): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309812 | ||||||
chr11:88309812
|
GCGCACAC others(5): Show |
G | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.486-506_486-495del others(12): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309812 | ||||||
chr11:88309814
|
G | A | 81 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(78): Show | 100 | HG00280.hp1 HG00544.hp1 HG00673.hp2 others(97): Show |
intron_variant | MODIFIER | c.486-496C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309814 | ||||||
chr11:88309814
|
G | GCA | 3 | a0001c0001t0001g0031a0001c0001t0001g0158a0003c0003t0001g0299 | 4 | HG00597.hp1 HG02809.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-498_486-497dup others(2): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309814 | ||||||
chr11:88309814
|
GCA | G | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0139others(3): Show | 6 | HG01243.hp1 HG02451.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.486-498_486-497del others(2): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309814 | ||||||
chr11:88309814
|
GCACA | G | 9 | a0001c0001t0001g0014a0001c0001t0001g0078a0001c0001t0001g0084others(6): Show | 12 | HG01074.hp2 HG01978.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.486-500_486-497del others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309814 | ||||||
chr11:88309814
|
GCACACA | G | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(35): Show | 69 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.486-502_486-497del others(6): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309814 | ||||||
chr11:88309818
|
A | G | 4 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0005g0056others(1): Show | 4 | HG01243.hp1 HG02451.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-500T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309818 | ||||||
chr11:88309824
|
A | G | 1 | a0001c0001t0002g0048 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.486-506T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309824 | ||||||
chr11:88310048
|
A | T | 1 | a0001c0001t0001g0046 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.486-730T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310048 | ||||||
chr11:88310180
|
C | CT | 177 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(174): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.486-863dupA | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310180 | ||||||
chr11:88310180
|
C | CTT | 6 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(3): Show | 6 | HG02074.hp2 HG02148.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.486-864_486-863dup others(2): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310180 | ||||||
chr11:88310180
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.486-862G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310180 | ||||||
chr11:88310180
|
CT | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(86): Show | 136 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.486-863delA | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310180 | ||||||
chr11:88310180
|
CTT | C | 9 | a0001c0001t0001g0062a0001c0001t0001g0090a0001c0001t0001g0138others(6): Show | 9 | HG01255.hp1 HG01975.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.486-864_486-863del others(2): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310180 | ||||||
chr11:88310340
|
T | C | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.486-1022A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310340 | ||||||
chr11:88310449
|
ACTAT | A | 8 | a0001c0001t0002g0006a0001c0001t0002g0049a0001c0001t0002g0050others(5): Show | 12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.486-1135_486-1132d others(6): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310449 | ||||||
chr11:88310453
|
T | C | 44 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(41): Show | 78 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.486-1135A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310453 | ||||||
chr11:88310512
|
T | A | 1 | a0001c0001t0001g0034 | 2 | HG03688.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.486-1194A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310512 | ||||||
chr11:88310556
|
T | C | 57 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0018others(54): Show | 70 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.486-1238A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310556 | ||||||
chr11:88310557
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.486-1239C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310557 | ||||||
chr11:88310579
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.486-1261C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310579 | ||||||
chr11:88310704
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.486-1386A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310704 | ||||||
chr11:88310727
|
TATC | T | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.486-1412_486-1410d others(5): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310727 | ||||||
chr11:88310898
|
G | GCT | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(302): Show | 416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.485+1488_485+1489d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310898 | ||||||
chr11:88310913
|
T | C | 8 | a0001c0001t0002g0006a0001c0001t0002g0049a0001c0001t0002g0050others(5): Show | 12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.485+1475A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310913 | ||||||
chr11:88311183
|
A | T | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+1205T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88311183 | ||||||
chr11:88311276
|
C | A | 56 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0018others(53): Show | 70 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.485+1112G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88311276 | ||||||
chr11:88311336
|
G | C | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+1052C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88311336 | ||||||
chr11:88311378
|
T | A | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+1010A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88311378 | ||||||
chr11:88311418
|
C | A | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+970G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88311418 | ||||||
chr11:88311445
|
C | T | 1 | a0001c0001t0001g0046 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.485+943G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88311445 | ||||||
chr11:88311598
|
T | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0289a0001c0001t0001g0290 | 6 | HG01074.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+790A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88311598 | ||||||
chr11:88311720
|
T | A | 8 | a0001c0001t0002g0006a0001c0001t0002g0049a0001c0001t0002g0050others(5): Show | 12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.485+668A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88311720 | ||||||
chr11:88311853
|
C | T | 4 | a0001c0001t0001g0018a0001c0001t0001g0151a0001c0001t0001g0166others(1): Show | 6 | HG00408.hp1 NA18945.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+535G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88311853 | ||||||
chr11:88311925
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0170 | 2 | HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.485+463G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88311925 | ||||||
chr11:88311957
|
C | T | 44 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(41): Show | 78 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.485+431G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88311957 | ||||||
chr11:88312096
|
T | G | 49 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0018others(46): Show | 62 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.485+292A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88312096 | ||||||
chr11:88312108
|
A | C | 51 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0018others(48): Show | 64 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.485+280T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88312108 | ||||||
chr11:88312116
|
T | A | 1 | a0001c0001t0001g0075 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.485+272A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88312116 | ||||||
chr11:88312268
|
C | T | 1 | a0002c0002t0001g0293 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.485+120G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88312268 | ||||||
chr11:88312647
|
C | CT | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(302): Show | 416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.319-94dupA | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88312647 | ||||||
chr11:88312726
|
T | C | 2 | a0001c0001t0005g0056a0001c0001t0007g0317 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.319-172A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88312726 | ||||||
chr11:88312911
|
T | C | 6 | a0001c0001t0001g0020a0001c0001t0001g0041a0001c0001t0001g0257others(3): Show | 9 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.319-357A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88312911 | ||||||
chr11:88312980
|
G | T | 303 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(300): Show | 414 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(411): Show |
intron_variant | MODIFIER | c.319-426C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88312980 | ||||||
chr11:88313060
|
A | C | 5 | a0001c0001t0001g0129a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG02109.hp1 HG02886.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.319-506T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313060 | ||||||
chr11:88313071
|
T | C | 2 | a0001c0001t0001g0226a0001c0001t0001g0277 | 2 | HG03239.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.319-517A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313071 | ||||||
chr11:88313108
|
T | C | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(302): Show | 416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.319-554A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313108 | ||||||
chr11:88313109
|
G | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(42): Show | 79 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.319-555C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313109 | ||||||
chr11:88313222
|
A | C | 10 | a0001c0001t0001g0010a0001c0001t0001g0185a0001c0001t0001g0186others(7): Show | 13 | HG02602.hp2 NA18948.hp2 NA18953.hp2 others(10): Show |
intron_variant | MODIFIER | c.319-668T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313222 | ||||||
chr11:88313226
|
C | T | 32 | a0001c0001t0001g0122a0001c0001t0001g0126a0002c0002t0001g0005others(29): Show | 43 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.319-672G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313226 | ||||||
chr11:88313333
|
G | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0174a0001c0001t0001g0180others(3): Show | 12 | HG02027.hp2 HG02080.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.319-779C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313333 | ||||||
chr11:88313471
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.319-917T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313471 | ||||||
chr11:88313567
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.319-1013G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313567 | ||||||
chr11:88313706
|
C | A | 1 | a0001c0001t0001g0197 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.319-1152G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313706 | ||||||
chr11:88313799
|
G | GA | 5 | a0001c0001t0001g0079a0002c0002t0001g0022a0002c0002t0001g0096others(2): Show | 7 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.319-1246dupT | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313799 | ||||||
chr11:88313960
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.319-1406G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313960 | ||||||
chr11:88313962
|
T | A | 2 | a0002c0002t0001g0108a0002c0002t0001g0113 | 2 | NA19057.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.319-1408A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313962 | ||||||
chr11:88314021
|
G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(100): Show | 153 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.319-1467C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88314021 | ||||||
chr11:88314119
|
G | C | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.319-1565C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88314119 | ||||||
chr11:88314198
|
C | T | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-1644G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88314198 | ||||||
chr11:88314556
|
C | T | 1 | a0001c0001t0002g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.319-2002G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88314556 | ||||||
chr11:88314573
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.319-2019C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88314573 | ||||||
chr11:88314604
|
T | C | 2 | a0001c0001t0001g0060a0001c0001t0002g0048 | 2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.319-2050A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88314604 | ||||||
chr11:88314718
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.319-2164C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88314718 | ||||||
chr11:88314738
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.319-2184C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88314738 | ||||||
chr11:88314954
|
C | CA | 3 | a0001c0001t0001g0009a0001c0001t0001g0160a0001c0001t0001g0161 | 6 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.319-2401dupT | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88314954 | ||||||
chr11:88314959
|
A | G | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-2405T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88314959 | ||||||
chr11:88314961
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.319-2407G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88314961 | ||||||
chr11:88315088
|
T | C | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-2534A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88315088 | ||||||
chr11:88315105
|
T | C | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-2551A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88315105 | ||||||
chr11:88315117
|
T | C | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.319-2563A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88315117 | ||||||
chr11:88315168
|
G | C | 158 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(155): Show | 204 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.319-2614C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88315168 | ||||||
chr11:88315365
|
T | A | 1 | a0001c0001t0001g0220 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.319-2811A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88315365 | ||||||
chr11:88315594
|
T | A | 8 | a0001c0001t0002g0006a0001c0001t0002g0049a0001c0001t0002g0050others(5): Show | 12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.319-3040A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88315594 | ||||||
chr11:88315606
|
AAAT | A | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-3055_319-3053d others(5): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88315606 | ||||||
chr11:88315773
|
CAG | C | 154 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(151): Show | 200 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.319-3221_319-3220d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88315773 | ||||||
chr11:88315805
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.319-3251C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88315805 | ||||||
chr11:88315821
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.319-3267A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88315821 | ||||||
chr11:88315966
|
G | C | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-3412C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88315966 | ||||||
chr11:88316025
|
G | T | 1 | a0001c0001t0001g0197 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.319-3471C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316025 | ||||||
chr11:88316375
|
G | A | 154 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(151): Show | 200 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.319-3821C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316375 | ||||||
chr11:88316446
|
G | A | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.319-3892C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316446 | ||||||
chr11:88316475
|
C | CTAAA | 43 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(40): Show | 77 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.319-3925_319-3922d others(6): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316475 | ||||||
chr11:88316475
|
C | CTAAATAA others(1): Show |
7 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0118others(4): Show | 7 | HG02280.hp2 HG02647.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.319-3929_319-3922d others(10): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316475 | ||||||
chr11:88316475
|
C | CTAAATAA others(5): Show |
144 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(141): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.319-3933_319-3922d others(14): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316475 | ||||||
chr11:88316475
|
C | CTAAATAA others(9): Show |
70 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(67): Show | 89 | HG00280.hp1 HG00323.hp1 HG00673.hp2 others(86): Show |
intron_variant | MODIFIER | c.319-3937_319-3922d others(18): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316475 | ||||||
chr11:88316475
|
C | CTAAATAA others(13): Show |
21 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0179others(18): Show | 21 | HG00609.hp2 HG01261.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.319-3941_319-3922d others(22): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316475 | ||||||
chr11:88316475
|
C | CTAAATAA others(17): Show |
1 | a0001c0001t0002g0058 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.319-3945_319-3922d others(26): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316475 | ||||||
chr11:88316500
|
T | TAAATAAA others(5): Show |
8 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0062others(5): Show | 10 | HG00639.hp1 HG01069.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.319-3947_319-3946i others(14): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316500 | ||||||
chr11:88316501
|
A | AAATAAAT others(17): Show |
1 | a0001c0001t0001g0144 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.319-3948_319-3947i others(26): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316501 | ||||||
chr11:88316548
|
T | C | 4 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0207others(1): Show | 4 | HG02602.hp1 HG03017.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.319-3994A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316548 | ||||||
chr11:88316584
|
C | A | 1 | a0001c0001t0001g0170 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.319-4030G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316584 | ||||||
chr11:88316610
|
CAT | C | 158 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(155): Show | 204 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.319-4058_319-4057d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316610 | ||||||
chr11:88316655
|
C | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0088 | 3 | HG00735.hp1 HG02683.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.319-4101G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316655 | ||||||
chr11:88316656
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.319-4102A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316656 | ||||||
chr11:88316680
|
C | T | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-4126G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316680 | ||||||
chr11:88316728
|
T | C | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.319-4174A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316728 | ||||||
chr11:88316812
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.319-4258T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316812 | ||||||
chr11:88316814
|
A | C | 4 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 4 | HG02647.hp2 HG02896.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-4260T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316814 | ||||||
chr11:88316849
|
A | C | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-4295T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316849 | ||||||
chr11:88316885
|
T | C | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-4331A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316885 | ||||||
chr11:88316891
|
T | A | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-4337A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316891 | ||||||
chr11:88317029
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0184 | 2 | HG02080.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.319-4475G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317029 | ||||||
chr11:88317087
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.319-4533G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317087 | ||||||
chr11:88317116
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.319-4562C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317116 | ||||||
chr11:88317141
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.319-4587T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317141 | ||||||
chr11:88317210
|
G | A | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-4656C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317210 | ||||||
chr11:88317246
|
C | G | 2 | a0003c0003t0001g0300a0003c0003t0001g0301 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.319-4692G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317246 | ||||||
chr11:88317434
|
T | TTAGTCTT others(1): Show |
3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-4881_319-4880i others(10): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317434 | ||||||
chr11:88317599
|
G | T | 1 | a0001c0001t0001g0046 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.319-5045C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317599 | ||||||
chr11:88317623
|
G | A | 1 | a0003c0003t0001g0117 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.319-5069C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317623 | ||||||
chr11:88317665
|
T | C | 10 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(7): Show | 21 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.319-5111A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317665 | ||||||
chr11:88317671
|
G | A | 1 | a0002c0002t0001g0293 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.319-5117C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317671 | ||||||
chr11:88317697
|
G | A | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-5143C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317697 | ||||||
chr11:88317712
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.319-5158A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317712 | ||||||
chr11:88317864
|
A | G | 2 | a0003c0003t0001g0021a0003c0003t0001g0171 | 4 | HG00323.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-5310T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317864 | ||||||
chr11:88318125
|
T | A | 32 | a0001c0001t0001g0122a0001c0001t0001g0126a0002c0002t0001g0005others(29): Show | 43 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.319-5571A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318125 | ||||||
chr11:88318298
|
C | T | 1 | a0001c0001t0001g0221 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.319-5744G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318298 | ||||||
chr11:88318340
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.319-5786G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318340 | ||||||
chr11:88318437
|
T | C | 1 | a0001c0001t0006g0172 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.319-5883A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318437 | ||||||
chr11:88318563
|
C | T | 1 | a0002c0002t0001g0293 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.319-6009G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318563 | ||||||
chr11:88318622
|
T | C | 1 | a0002c0002t0001g0096 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.319-6068A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318622 | ||||||
chr11:88318631
|
C | G | 81 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(78): Show | 113 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.319-6077G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318631 | ||||||
chr11:88318708
|
G | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(130): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.319-6154C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318708 | ||||||
chr11:88318716
|
A | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(134): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.319-6162T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318716 | ||||||
chr11:88318751
|
C | T | 1 | a0002c0002t0001g0293 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.319-6197G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318751 | ||||||
chr11:88318769
|
A | G | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-6215T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318769 | ||||||
chr11:88318797
|
T | A | 1 | a0002c0002t0001g0091 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.319-6243A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318797 | ||||||
chr11:88318862
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.319-6308A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318862 | ||||||
chr11:88318904
|
G | A | 50 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0018others(47): Show | 63 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.319-6350C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318904 | ||||||
chr11:88318971
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.319-6417A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318971 | ||||||
chr11:88319075
|
C | T | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(35): Show | 69 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.319-6521G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88319075 | ||||||
chr11:88319210
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.319-6656T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88319210 | ||||||
chr11:88319318
|
T | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(35): Show | 69 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.319-6764A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88319318 | ||||||
chr11:88319350
|
T | C | 5 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0209others(2): Show | 5 | HG01346.hp2 HG01934.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-6796A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88319350 | ||||||
chr11:88319465
|
C | G | 2 | a0002c0002t0001g0102a0002c0002t0001g0105 | 2 | HG00140.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.319-6911G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88319465 | ||||||
chr11:88319672
|
A | G | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.319-7118T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88319672 | ||||||
chr11:88320003
|
T | C | 2 | a0001c0001t0001g0060a0001c0001t0002g0048 | 2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.319-7449A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88320003 | ||||||
chr11:88320742
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.319-8188G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88320742 | ||||||
chr11:88320811
|
T | C | 269 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(266): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.319-8257A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88320811 | ||||||
chr11:88320823
|
C | T | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-8269G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88320823 | ||||||
chr11:88320888
|
G | C | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-8334C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88320888 | ||||||
chr11:88320924
|
C | T | 2 | a0002c0002t0001g0114a0002c0002t0001g0115 | 2 | HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.319-8370G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88320924 | ||||||
chr11:88321178
|
G | C | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(286): Show | 394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.319-8624C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321178 | ||||||
chr11:88321178
|
G | T | 1 | a0001c0001t0001g0144 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.319-8624C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321178 | ||||||
chr11:88321284
|
T | C | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.319-8730A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321284 | ||||||
chr11:88321403
|
G | A | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(35): Show | 69 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.319-8849C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321403 | ||||||
chr11:88321439
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG02523.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.319-8885G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321439 | ||||||
chr11:88321550
|
G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0137 | 3 | NA19063.hp2 NA19088.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.319-8996C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321550 | ||||||
chr11:88321602
|
G | A | 1 | a0001c0001t0006g0172 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.319-9048C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321602 | ||||||
chr11:88321643
|
T | C | 1 | a0002c0002t0001g0293 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.319-9089A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321643 | ||||||
chr11:88321744
|
C | T | 1 | a0002c0002t0001g0103 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.319-9190G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321744 | ||||||
chr11:88321768
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.319-9214T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321768 | ||||||
chr11:88321842
|
T | C | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-9288A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321842 | ||||||
chr11:88321852
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.319-9298T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321852 | ||||||
chr11:88321894
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0289a0001c0001t0001g0290 | 6 | HG01074.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.319-9340C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321894 | ||||||
chr11:88321921
|
C | T | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(302): Show | 416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.319-9367G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321921 | ||||||
chr11:88322002
|
G | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(93): Show | 143 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.319-9448C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322002 | ||||||
chr11:88322032
|
A | T | 1 | a0001c0001t0001g0067 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.319-9478T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322032 | ||||||
chr11:88322123
|
T | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(38): Show | 75 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.319-9569A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322123 | ||||||
chr11:88322161
|
G | C | 1 | a0001c0001t0001g0287 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.319-9607C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322161 | ||||||
chr11:88322199
|
C | T | 1 | a0001c0001t0006g0172 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.319-9645G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322199 | ||||||
chr11:88322367
|
T | C | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.319-9813A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322367 | ||||||
chr11:88322490
|
T | G | 1 | a0001c0001t0001g0165 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.319-9936A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322490 | ||||||
chr11:88322525
|
G | A | 8 | a0001c0001t0002g0006a0001c0001t0002g0049a0001c0001t0002g0050others(5): Show | 12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.319-9971C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322525 | ||||||
chr11:88322605
|
G | A | 1 | a0002c0002t0001g0104 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.319-10051C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322605 | ||||||
chr11:88322606
|
A | T | 1 | a0002c0002t0001g0104 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.319-10052T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322606 | ||||||
chr11:88322621
|
A | T | 290 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(287): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.319-10067T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322621 | ||||||
chr11:88322626
|
A | G | 290 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(287): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.319-10072T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322626 | ||||||
chr11:88322962
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.319-10408T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322962 | ||||||
chr11:88323007
|
C | T | 3 | a0001c0001t0001g0066a0001c0001t0001g0179a0001c0001t0001g0182 | 3 | NA18612.hp1 NA18944.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.319-10453G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88323007 | ||||||
chr11:88323108
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.319-10554C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88323108 | ||||||
chr11:88323121
|
C | T | 1 | a0002c0002t0001g0103 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.319-10567G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88323121 | ||||||
chr11:88323228
|
T | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.319-10674A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88323228 | ||||||
chr11:88323415
|
GC | G | 32 | a0001c0001t0001g0122a0001c0001t0001g0126a0002c0002t0001g0005others(29): Show | 43 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.319-10862delG | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88323415 | ||||||
chr11:88323461
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.319-10907C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88323461 | ||||||
chr11:88323614
|
T | C | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-11060A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88323614 | ||||||
chr11:88323696
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.319-11142T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88323696 | ||||||
chr11:88323698
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.319-11144C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88323698 | ||||||
chr11:88323774
|
G | A | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(296): Show | 410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.318+11163C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88323774 | ||||||
chr11:88323790
|
C | T | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | NA19066.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.318+11147G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88323790 | ||||||
chr11:88324021
|
C | A | 2 | a0001c0001t0005g0056a0001c0001t0007g0317 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.318+10916G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88324021 | ||||||
chr11:88324087
|
C | G | 157 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(154): Show | 203 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.318+10850G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88324087 | ||||||
chr11:88324326
|
T | C | 1 | a0001c0001t0001g0025 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.318+10611A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88324326 | ||||||
chr11:88324552
|
G | GA | 157 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(154): Show | 203 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.318+10384dupT | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88324552 | ||||||
chr11:88324633
|
C | T | 1 | a0001c0001t0001g0239 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.318+10304G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88324633 | ||||||
chr11:88324714
|
G | A | 3 | a0002c0002t0001g0016a0002c0002t0001g0109a0002c0002t0001g0110 | 5 | HG02258.hp2 HG02809.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.318+10223C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88324714 | ||||||
chr11:88324988
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.318+9949C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88324988 | ||||||
chr11:88325088
|
AAAG | A | 81 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(78): Show | 112 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.318+9846_318+9848d others(5): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88325088 | ||||||
chr11:88325177
|
T | C | 1 | a0002c0002t0001g0293 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.318+9760A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88325177 | ||||||
chr11:88325262
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.318+9675A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88325262 | ||||||
chr11:88325635
|
A | T | 1 | a0001c0001t0001g0059 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.318+9302T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88325635 | ||||||
chr11:88325756
|
G | C | 1 | a0001c0001t0001g0133 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.318+9181C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88325756 | ||||||
chr11:88325921
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.318+9016A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88325921 | ||||||
chr11:88326122
|
G | C | 1 | a0001c0001t0001g0212 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.318+8815C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326122 | ||||||
chr11:88326326
|
C | G | 1 | a0001c0001t0001g0181 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.318+8611G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326326 | ||||||
chr11:88326367
|
GCT | G | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.318+8568_318+8569d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326367 | ||||||
chr11:88326487
|
T | C | 1 | a0001c0001t0001g0263 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.318+8450A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326487 | ||||||
chr11:88326515
|
G | A | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(284): Show | 392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.318+8422C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326515 | ||||||
chr11:88326519
|
C | A | 1 | a0001c0001t0001g0144 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.318+8418G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326519 | ||||||
chr11:88326525
|
G | C | 1 | a0001c0001t0001g0213 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.318+8412C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326525 | ||||||
chr11:88326526
|
T | TA | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(130): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.318+8410dupT | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326526 | ||||||
chr11:88326526
|
T | TAA | 151 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(148): Show | 197 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.318+8409_318+8410d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326526 | ||||||
chr11:88326571
|
T | C | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(285): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.318+8366A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326571 | ||||||
chr11:88326572
|
A | T | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(285): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.318+8365T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326572 | ||||||
chr11:88326576
|
T | C | 1 | a0001c0001t0001g0264 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.318+8361A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326576 | ||||||
chr11:88326648
|
T | A | 1 | a0001c0001t0001g0214 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.318+8289A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326648 | ||||||
chr11:88326706
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.318+8231C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326706 | ||||||
chr11:88326713
|
T | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(285): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.318+8224A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326713 | ||||||
chr11:88326714
|
T | C | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(285): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.318+8223A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326714 | ||||||
chr11:88326726
|
C | T | 2 | a0001c0001t0005g0056a0001c0001t0007g0317 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.318+8211G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326726 | ||||||
chr11:88326760
|
C | A | 1 | a0003c0003t0001g0117 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.318+8177G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326760 | ||||||
chr11:88326968
|
G | A | 32 | a0001c0001t0001g0122a0001c0001t0001g0126a0002c0002t0001g0005others(29): Show | 43 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.318+7969C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326968 | ||||||
chr11:88326969
|
T | G | 4 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 4 | HG02647.hp2 HG02896.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+7968A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326969 | ||||||
chr11:88327032
|
C | T | 157 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(154): Show | 203 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.318+7905G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88327032 | ||||||
chr11:88327331
|
T | C | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.318+7606A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88327331 | ||||||
chr11:88327401
|
A | AGAATATT others(22): Show |
2 | a0001c0001t0001g0123a0001c0001t0001g0125 | 2 | HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.318+7507_318+7535d others(31): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88327401 | ||||||
chr11:88327458
|
C | T | 1 | a0002c0002t0001g0102 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.318+7479G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88327458 | ||||||
chr11:88327475
|
A | G | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.318+7462T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88327475 | ||||||
chr11:88327526
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0002g0048 | 2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.318+7411G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88327526 | ||||||
chr11:88327569
|
C | T | 154 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(151): Show | 200 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.318+7368G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88327569 | ||||||
chr11:88327674
|
C | A | 5 | a0001c0001t0001g0215a0001c0001t0001g0306a0001c0001t0001g0307others(2): Show | 5 | HG02698.hp1 NA18975.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.318+7263G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88327674 | ||||||
chr11:88327678
|
C | T | 4 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0005g0056others(1): Show | 4 | HG01243.hp1 HG02451.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+7259G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88327678 | ||||||
chr11:88327845
|
G | A | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.318+7092C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88327845 | ||||||
chr11:88327930
|
T | C | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.318+7007A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88327930 | ||||||
chr11:88328113
|
C | T | 1 | a0001c0001t0001g0023 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.318+6824G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88328113 | ||||||
chr11:88328237
|
A | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(95): Show | 146 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.318+6700T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88328237 | ||||||
chr11:88328488
|
A | G | 8 | a0001c0001t0002g0006a0001c0001t0002g0049a0001c0001t0002g0050others(5): Show | 12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.318+6449T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88328488 | ||||||
chr11:88328502
|
T | C | 5 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0232others(2): Show | 9 | HG00544.hp1 NA18943.hp1 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.318+6435A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88328502 | ||||||
chr11:88328524
|
C | T | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.318+6413G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88328524 | ||||||
chr11:88328693
|
T | C | 1 | a0001c0001t0001g0046 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.318+6244A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88328693 | ||||||
chr11:88328721
|
G | A | 31 | a0001c0001t0001g0122a0002c0002t0001g0005a0002c0002t0001g0016others(28): Show | 42 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.318+6216C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88328721 | ||||||
chr11:88328741
|
C | T | 12 | a0001c0001t0001g0177a0001c0001t0001g0227a0001c0001t0002g0006others(9): Show | 16 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.318+6196G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88328741 | ||||||
chr11:88328831
|
T | G | 5 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0217others(2): Show | 7 | HG01496.hp1 HG01943.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.318+6106A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88328831 | ||||||
chr11:88329112
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.318+5825G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329112 | ||||||
chr11:88329180
|
T | TAGA | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(285): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.318+5756_318+5757i others(5): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329180 | ||||||
chr11:88329253
|
G | A | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128 | 3 | HG01243.hp1 HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.318+5684C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329253 | ||||||
chr11:88329256
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0280 | 2 | HG01099.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.318+5681G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329256 | ||||||
chr11:88329327
|
C | G | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(93): Show | 144 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.318+5610G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329327 | ||||||
chr11:88329343
|
G | A | 1 | a0001c0001t0001g0042 | 2 | HG00140.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.318+5594C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329343 | ||||||
chr11:88329411
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0288 | 2 | HG01993.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.318+5526C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329411 | ||||||
chr11:88329455
|
C | CA | 8 | a0001c0001t0002g0006a0001c0001t0002g0049a0001c0001t0002g0050others(5): Show | 12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.318+5481dupT | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329455 | ||||||
chr11:88329455
|
C | CAAA | 6 | a0001c0001t0001g0177a0001c0001t0001g0227a0001c0001t0002g0048others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.318+5479_318+5481d others(5): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329455 | ||||||
chr11:88329455
|
CAA | C | 31 | a0001c0001t0001g0122a0001c0001t0001g0126a0002c0002t0001g0005others(28): Show | 44 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.318+5480_318+5481d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329455 | ||||||
chr11:88329455
|
CAAA | C | 13 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0127others(10): Show | 13 | HG00423.hp1 HG00621.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.318+5479_318+5481d others(5): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329455 | ||||||
chr11:88329455
|
CAAAA | C | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(191): Show | 253 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.318+5478_318+5481d others(6): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329455 | ||||||
chr11:88329455
|
CAAAAA | C | 44 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(41): Show | 76 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.318+5477_318+5481d others(7): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329455 | ||||||
chr11:88329455
|
CAAAAAAA others(4): Show |
C | 1 | a0003c0003t0001g0297 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.318+5471_318+5481d others(13): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329455 | ||||||
chr11:88329455
|
CAAAAAAA others(11): Show |
C | 3 | a0001c0001t0001g0014a0001c0001t0001g0289a0001c0001t0001g0290 | 6 | HG01074.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.318+5464_318+5481d others(20): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329455 | ||||||
chr11:88329489
|
T | C | 1 | a0001c0001t0002g0048 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.318+5448A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329489 | ||||||
chr11:88329716
|
T | TTG | 4 | a0001c0001t0001g0177a0001c0001t0001g0227a0001c0001t0002g0057others(1): Show | 4 | HG02965.hp2 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.318+5219_318+5220d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329716 | ||||||
chr11:88329771
|
G | A | 5 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0217others(2): Show | 7 | HG01496.hp1 HG01943.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.318+5166C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329771 | ||||||
chr11:88329815
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.318+5122G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329815 | ||||||
chr11:88329878
|
T | C | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(285): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.318+5059A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329878 | ||||||
chr11:88329899
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.318+5038C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329899 | ||||||
chr11:88330057
|
G | C | 1 | a0001c0001t0001g0046 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.318+4880C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330057 | ||||||
chr11:88330173
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.318+4764A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330173 | ||||||
chr11:88330264
|
C | A | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.318+4673G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330264 | ||||||
chr11:88330425
|
T | A | 1 | a0001c0001t0001g0221 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.318+4512A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330425 | ||||||
chr11:88330468
|
C | A | 2 | a0002c0002t0001g0114a0002c0002t0001g0115 | 2 | HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.318+4469G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330468 | ||||||
chr11:88330537
|
C | G | 1 | a0001c0001t0001g0179 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.318+4400G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330537 | ||||||
chr11:88330573
|
G | T | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.318+4364C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330573 | ||||||
chr11:88330591
|
G | A | 1 | a0001c0001t0001g0222 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.318+4346C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330591 | ||||||
chr11:88330597
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.318+4340G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330597 | ||||||
chr11:88330755
|
G | A | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.318+4182C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330755 | ||||||
chr11:88330776
|
C | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(92): Show | 142 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.318+4161G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330776 | ||||||
chr11:88330780
|
A | G | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.318+4157T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330780 | ||||||
chr11:88330795
|
C | T | 12 | a0001c0001t0001g0177a0001c0001t0001g0227a0001c0001t0002g0006others(9): Show | 16 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.318+4142G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330795 | ||||||
chr11:88330831
|
G | A | 1 | a0001c0001t0001g0031 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.318+4106C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330831 | ||||||
chr11:88330834
|
T | G | 1 | a0001c0001t0001g0222 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.318+4103A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330834 | ||||||
chr11:88330858
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.318+4079A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330858 | ||||||
chr11:88330922
|
G | A | 1 | a0002c0002t0001g0017 | 3 | NA18953.hp1 NA19006.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.318+4015C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330922 | ||||||
chr11:88330924
|
T | C | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.318+4013A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330924 | ||||||
chr11:88330973
|
G | C | 1 | a0001c0001t0001g0269 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.318+3964C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330973 | ||||||
chr11:88331063
|
C | T | 12 | a0001c0001t0001g0177a0001c0001t0001g0227a0001c0001t0002g0006others(9): Show | 16 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.318+3874G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331063 | ||||||
chr11:88331219
|
C | G | 1 | a0001c0001t0001g0236 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.318+3718G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331219 | ||||||
chr11:88331280
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.318+3657A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331280 | ||||||
chr11:88331307
|
C | T | 4 | a0002c0002t0001g0097a0002c0002t0001g0098a0002c0002t0001g0099others(1): Show | 4 | NA18940.hp2 NA18968.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.318+3630G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331307 | ||||||
chr11:88331433
|
G | C | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.318+3504C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331433 | ||||||
chr11:88331438
|
G | A | 2 | a0001c0001t0005g0056a0001c0001t0007g0317 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.318+3499C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331438 | ||||||
chr11:88331466
|
T | C | 5 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272others(2): Show | 5 | HG02717.hp1 HG02723.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.318+3471A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331466 | ||||||
chr11:88331518
|
G | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(92): Show | 142 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.318+3419C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331518 | ||||||
chr11:88331582
|
A | G | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.318+3355T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331582 | ||||||
chr11:88331652
|
A | G | 1 | a0001c0001t0002g0049 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.318+3285T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331652 | ||||||
chr11:88331742
|
T | G | 1 | a0001c0001t0001g0121 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.318+3195A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331742 | ||||||
chr11:88331814
|
A | C | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(302): Show | 416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.318+3123T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331814 | ||||||
chr11:88331962
|
C | A | 4 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(1): Show | 4 | HG00741.hp2 HG01099.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.318+2975G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331962 | ||||||
chr11:88331997
|
C | T | 1 | a0002c0002t0001g0293 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.318+2940G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331997 | ||||||
chr11:88332135
|
C | T | 1 | a0003c0003t0001g0117 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.318+2802G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88332135 | ||||||
chr11:88332150
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.318+2787T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88332150 | ||||||
chr11:88332259
|
T | C | 154 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(151): Show | 200 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.318+2678A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88332259 | ||||||
chr11:88332326
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.318+2611A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88332326 | ||||||
chr11:88332416
|
T | C | 1 | a0002c0002t0001g0116 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.318+2521A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88332416 | ||||||
chr11:88332990
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0289a0001c0001t0001g0290 | 6 | HG01074.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.318+1947C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88332990 | ||||||
chr11:88333086
|
C | T | 3 | a0003c0003t0001g0297a0003c0003t0001g0298a0003c0003t0001g0299 | 3 | HG01109.hp2 HG02809.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.318+1851G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88333086 | ||||||
chr11:88333210
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.318+1727G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88333210 | ||||||
chr11:88333276
|
A | G | 1 | a0002c0002t0001g0293 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.318+1661T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88333276 | ||||||
chr11:88333320
|
T | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(38): Show | 75 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.318+1617A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88333320 | ||||||
chr11:88333471
|
G | C | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.318+1466C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88333471 | ||||||
chr11:88333546
|
A | C | 12 | a0001c0001t0001g0177a0001c0001t0001g0227a0001c0001t0002g0006others(9): Show | 16 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.318+1391T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88333546 | ||||||
chr11:88333569
|
G | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(93): Show | 144 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.318+1368C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88333569 | ||||||
chr11:88333669
|
T | G | 1 | a0001c0001t0001g0043 | 2 | NA18950.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.318+1268A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88333669 | ||||||
chr11:88333685
|
G | T | 1 | a0001c0001t0001g0178 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.318+1252C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88333685 | ||||||
chr11:88333701
|
CA | C | 154 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(151): Show | 200 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.318+1235delT | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88333701 | ||||||
chr11:88333763
|
G | A | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.318+1174C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88333763 | ||||||
chr11:88333887
|
C | CT | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(35): Show | 69 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.318+1049dupA | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88333887 | ||||||
chr11:88334008
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.318+929T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334008 | ||||||
chr11:88334068
|
T | G | 4 | a0001c0001t0001g0034a0001c0001t0001g0229a0001c0001t0001g0230others(1): Show | 5 | HG03017.hp1 HG03654.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.318+869A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334068 | ||||||
chr11:88334168
|
T | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0281others(1): Show | 8 | NA18943.hp1 NA18944.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.318+769A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334168 | ||||||
chr11:88334179
|
G | A | 4 | a0001c0001t0001g0087a0001c0001t0001g0123a0001c0001t0001g0124others(1): Show | 4 | HG02015.hp2 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+758C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334179 | ||||||
chr11:88334226
|
T | C | 83 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(80): Show | 115 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.318+711A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334226 | ||||||
chr11:88334323
|
A | G | 2 | a0001c0001t0001g0060a0001c0001t0002g0048 | 2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.318+614T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334323 | ||||||
chr11:88334347
|
T | C | 20 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0042others(17): Show | 27 | HG00140.hp2 HG00544.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.318+590A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334347 | ||||||
chr11:88334484
|
A | C | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(156): Show | 206 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.318+453T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334484 | ||||||
chr11:88334586
|
C | G | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(285): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.318+351G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334586 | ||||||
chr11:88334596
|
T | C | 154 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(151): Show | 200 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.318+341A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334596 | ||||||
chr11:88334658
|
G | T | 306 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(303): Show | 417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
intron_variant | MODIFIER | c.318+279C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334658 | ||||||
chr11:88334681
|
C | T | 31 | a0001c0001t0001g0122a0002c0002t0001g0005a0002c0002t0001g0016others(28): Show | 42 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.318+256G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334681 | ||||||
chr11:88334830
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 4 | NA18964.hp2 NA18974.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+107G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334830 | ||||||
chr11:88334836
|
T | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(285): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.318+101A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334836 | ||||||
chr11:88334884
|
G | T | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(285): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.318+53C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334884 | ||||||
chr11:88335088
|
GA | G | 33 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0001g0232others(30): Show | 44 | HG00140.hp1 HG00544.hp1 HG00642.hp1 others(41): Show |
splice_region_variant&intron_variant | LOW | c.173-7delT | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335088 | ||||||
chr11:88335136
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.173-54C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335136 | ||||||
chr11:88335161
|
T | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(285): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.173-79A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335161 | ||||||
chr11:88335199
|
GCA | G | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.173-119_173-118del others(2): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335199 | ||||||
chr11:88335293
|
T | C | 8 | a0001c0001t0002g0006a0001c0001t0002g0049a0001c0001t0002g0050others(5): Show | 12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.173-211A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335293 | ||||||
chr11:88335375
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.173-293C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335375 | ||||||
chr11:88335428
|
G | T | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(285): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.173-346C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335428 | ||||||
chr11:88335585
|
A | G | 4 | a0001c0001t0001g0177a0001c0001t0001g0227a0001c0001t0002g0057others(1): Show | 4 | HG02965.hp2 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.173-503T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335585 | ||||||
chr11:88335597
|
C | T | 52 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0018others(49): Show | 66 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.173-515G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335597 | ||||||
chr11:88335677
|
C | G | 4 | a0001c0001t0001g0034a0001c0001t0001g0229a0001c0001t0001g0230others(1): Show | 5 | HG03017.hp1 HG03654.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.173-595G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335677 | ||||||
chr11:88335678
|
T | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(38): Show | 75 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.173-596A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335678 | ||||||
chr11:88335833
|
C | T | 31 | a0001c0001t0001g0122a0002c0002t0001g0005a0002c0002t0001g0016others(28): Show | 42 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.173-751G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335833 | ||||||
chr11:88335837
|
G | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(92): Show | 142 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.173-755C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335837 | ||||||
chr11:88335948
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.173-866C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335948 | ||||||
chr11:88336014
|
T | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(35): Show | 69 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.173-932A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336014 | ||||||
chr11:88336077
|
A | G | 3 | a0002c0002t0001g0026a0002c0002t0001g0095a0002c0002t0001g0096 | 4 | NA18966.hp1 NA19003.hp1 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.173-995T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336077 | ||||||
chr11:88336082
|
G | C | 1 | a0001c0001t0001g0292 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.173-1000C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336082 | ||||||
chr11:88336145
|
A | G | 71 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(68): Show | 85 | HG00280.hp1 HG00423.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.173-1063T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336145 | ||||||
chr11:88336155
|
G | T | 290 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(287): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.173-1073C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336155 | ||||||
chr11:88336237
|
TTA | T | 4 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(1): Show | 4 | HG00741.hp2 HG01099.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.173-1157_173-1156d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336237 | ||||||
chr11:88336238
|
TAA | T | 277 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(274): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.173-1158_173-1157d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336238 | ||||||
chr11:88336238
|
TAAA | T | 6 | a0001c0001t0001g0119a0001c0001t0001g0173a0001c0001t0001g0174others(3): Show | 6 | HG02015.hp1 HG02083.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.173-1159_173-1157d others(5): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336238 | ||||||
chr11:88336289
|
C | T | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(302): Show | 416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.173-1207G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336289 | ||||||
chr11:88336306
|
C | G | 8 | a0001c0001t0002g0006a0001c0001t0002g0049a0001c0001t0002g0050others(5): Show | 12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.172+1195G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336306 | ||||||
chr11:88336307
|
G | A | 1 | a0002c0002t0001g0293 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.172+1194C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336307 | ||||||
chr11:88336395
|
C | A | 4 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(1): Show | 4 | HG00741.hp2 HG01099.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.172+1106G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336395 | ||||||
chr11:88336419
|
ATCCTAGC others(3): Show |
A | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.172+1072_172+1081d others(12): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336419 | ||||||
chr11:88336438
|
C | T | 306 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(303): Show | 417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
intron_variant | MODIFIER | c.172+1063G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336438 | ||||||
chr11:88336539
|
C | CA | 8 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0305others(5): Show | 8 | HG02257.hp2 HG04199.hp1 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.172+961dupT | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336539 | ||||||
chr11:88336539
|
CA | C | 97 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0018others(94): Show | 122 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.172+961delT | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336539 | ||||||
chr11:88336554
|
A | G | 1 | a0002c0002t0001g0092 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.172+947T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336554 | ||||||
chr11:88336557
|
A | T | 1 | a0001c0001t0001g0061 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.172+944T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336557 | ||||||
chr11:88336643
|
T | G | 1 | a0001c0001t0001g0310 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.172+858A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336643 | ||||||
chr11:88336703
|
G | T | 1 | a0001c0001t0001g0118 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.172+798C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336703 | ||||||
chr11:88336733
|
A | G | 1 | a0002c0002t0001g0091 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.172+768T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336733 | ||||||
chr11:88336921
|
T | C | 4 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0005g0056others(1): Show | 4 | HG02717.hp2 HG03195.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.172+580A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336921 | ||||||
chr11:88336942
|
A | T | 8 | a0001c0001t0002g0006a0001c0001t0002g0049a0001c0001t0002g0050others(5): Show | 12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.172+559T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336942 | ||||||
chr11:88336995
|
G | A | 3 | a0002c0002t0001g0022a0002c0002t0001g0311a0002c0002t0001g0312 | 5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.172+506C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336995 | ||||||
chr11:88337042
|
G | GA | 48 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(45): Show | 82 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.172+458dupT | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88337042 | ||||||
chr11:88337066
|
C | G | 1 | a0003c0003t0001g0117 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.172+435G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88337066 | ||||||
chr11:88337167
|
C | T | 31 | a0001c0001t0001g0093a0001c0004t0001g0094a0002c0002t0001g0005others(28): Show | 42 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.172+334G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88337167 | ||||||
chr11:88337244
|
G | A | 1 | a0001c0001t0001g0046 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.172+257C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88337244 | ||||||
chr11:88337395
|
C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(48): Show | 85 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.172+106G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88337395 |