geneid | 1509 |
---|---|
ensemblid | ENSG00000117984.15 |
hgncid | 2529 |
symbol | CTSD |
name | cathepsin D |
refseq_nuc | NM_001909.5 |
refseq_prot | NP_001900.1 |
ensembl_nuc | ENST00000236671.7 |
ensembl_prot | ENSP00000236671.2 |
mane_status | MANE Select |
chr | chr11 |
start | 1752755 |
end | 1763927 |
strand | - |
ver | v1.2 |
region | chr11:1752755-1763927 |
region5000 | chr11:1747755-1768927 |
regionname0 | CTSD_chr11_1752755_1763927 |
regionname5000 | CTSD_chr11_1747755_1768927 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 412 | 367 | 89 | 64 | 157 | 14 | 41 | 117 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0002 | 0/0 | 412 | 17 | 3 | 8 | 1 | 0 | 5 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0003 | 0/0 | 412 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0004 | 0/0 | 412 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1239 | 338 | 82 | 61 | 139 | 14 | 40 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
c0002 | 0/0 | 1239 | 18 | 0 | 0 | 18 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
c0003 | 0/0 | 1239 | 17 | 3 | 8 | 1 | 0 | 5 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
c0004 | 0/0 | 1239 | 7 | 6 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
c0005 | 0/0 | 1239 | 2 | 1 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
c0006 | 0/0 | 1239 | 2 | 0 | 2 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
c0007 | 0/0 | 1239 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
c0008 | 0/0 | 1239 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 817 | 306 | 73 | 51 | 133 | 12 | 36 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
t0002 | 0/1 | 817 | 45 | 10 | 12 | 15 | 1 | 6 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
t0003 | 0/0 | 817 | 10 | 2 | 5 | 1 | 1 | 1 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
t0004 | 0/0 | 817 | 5 | 5 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
t0005 | 0/0 | 815 | 4 | 0 | 3 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
t0006 | 0/0 | 817 | 4 | 0 | 0 | 4 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
t0007 | 0/0 | 817 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
t0008 | 0/0 | 817 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
t0009 | 0/0 | 817 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
t0010 | 0/0 | 817 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
t0011 | 0/0 | 817 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
t0012 | 0/0 | 817 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
t0013 | 0/0 | 817 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
t0014 | 0/0 | 817 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
t0015 | 0/0 | 817 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
t0016 | 0/0 | 817 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
t0017 | 0/0 | 817 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 26 | 0 | 8 | 15 | 0 | 3 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0002 | 0/0 | 26 | 1 | 1 | 13 | 4 | 7 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0003 | 0/0 | 15 | 8 | 3 | 1 | 0 | 3 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0004 | 0/0 | 11 | 0 | 5 | 3 | 0 | 3 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0005 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0006 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0007 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0009 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0010 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0011 | 0/0 | 5 | 1 | 2 | 1 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0014 | 0/0 | 5 | 0 | 1 | 0 | 3 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0015 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0016 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0019 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0020 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0025 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0026 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0028 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0031 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0033 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0034 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0045 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0046 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0058 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0059 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0060 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0129 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1239 | 338 | 82 | 61 | 139 | 14 | 40 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0001c0002 | 0/0 | 1239 | 18 | 0 | 0 | 18 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0001c0004 | 0/0 | 1239 | 7 | 6 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0001c0005 | 0/0 | 1239 | 2 | 1 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0001c0006 | 0/0 | 1239 | 2 | 0 | 2 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0002c0003 | 0/0 | 1239 | 17 | 3 | 8 | 1 | 0 | 5 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0003c0008 | 0/0 | 1239 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0004c0007 | 0/0 | 1239 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2055 | 286 | 73 | 49 | 115 | 12 | 36 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0001c0001t0002 | 0/1 | 2055 | 23 | 2 | 3 | 14 | 1 | 2 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0001c0001t0003 | 0/0 | 2055 | 8 | 0 | 5 | 1 | 1 | 1 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0001c0001t0004 | 0/0 | 2055 | 5 | 5 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0001c0001t0005 | 0/0 | 2053 | 4 | 0 | 3 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0001c0001t0006 | 0/0 | 2055 | 4 | 0 | 0 | 4 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0001c0001t0007 | 0/0 | 2055 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0001c0001t0008 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0001c0001t0009 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0001c0001t0011 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0001c0001t0012 | 0/0 | 2055 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0001c0001t0013 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0001c0001t0015 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0001c0002t0001 | 0/0 | 2055 | 16 | 0 | 0 | 16 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0001c0002t0010 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0001c0002t0016 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0001c0004t0002 | 0/0 | 2055 | 7 | 6 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0001c0005t0002 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0001c0005t0014 | 0/0 | 2055 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0001c0006t0001 | 0/0 | 2055 | 2 | 0 | 2 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0002c0003t0002 | 0/0 | 2055 | 14 | 1 | 8 | 1 | 0 | 4 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0002c0003t0003 | 0/0 | 2055 | 2 | 2 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0002c0003t0017 | 0/0 | 2055 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0003c0008t0001 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
a0004c0007t0001 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | copy fasta | chr11 | 1747755 | 1768927 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 26 | 0 | 8 | 15 | 0 | 3 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0002 | 0/0 | 26 | 1 | 1 | 13 | 4 | 7 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0003 | 0/0 | 15 | 8 | 3 | 1 | 0 | 3 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0004 | 0/0 | 11 | 0 | 5 | 3 | 0 | 3 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0006 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0007 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0010 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0014 | 0/0 | 5 | 0 | 1 | 0 | 3 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0015 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0025 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0028 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0034 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0059 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0129 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0002g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0002g0019 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0002g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0002g0045 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0002g0060 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0002g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0003g0016 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0004g0031 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0005g0026 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0005g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0006g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0006g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0007g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0007g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0008g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0009g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0011g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0012g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0013g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0001t0015g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0002t0001g0005 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0002t0001g0033 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0002t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0002t0010g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0002t0016g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0004t0002g0009 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0004t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0005t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0005t0014g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0001c0006t0001g0058 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0002c0003t0002g0011 | 0/0 | 5 | 1 | 2 | 1 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0002c0003t0002g0020 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0002c0003t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0002c0003t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0002c0003t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0002c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0002c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0002c0003t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0002c0003t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0002c0003t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0002c0003t0017g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0003c0008t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
a0004c0007t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0118 | EUR | FIN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0060 | EUR | FIN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | FIN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00408 | hp2 | a0001 | c0002 | t0010 | g0167 | EAS | CHS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | CHS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00609 | hp2 | a0001 | c0001 | t0013 | g0140 | EAS | CHS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00733 | hp2 | a0001 | c0001 | t0012 | g0098 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0074 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG00741 | hp2 | a0002 | c0003 | t0002 | g0020 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01070 | hp2 | a0002 | c0003 | t0002 | g0011 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01071 | hp1 | a0002 | c0003 | t0002 | g0011 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01074 | hp1 | a0001 | c0001 | t0005 | g0117 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01074 | hp2 | a0001 | c0001 | t0005 | g0026 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01081 | hp1 | a0002 | c0003 | t0002 | g0020 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01168 | hp2 | a0001 | c0006 | t0001 | g0058 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01169 | hp2 | a0001 | c0006 | t0001 | g0058 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01175 | hp2 | a0002 | c0003 | t0002 | g0067 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01261 | hp1 | a0002 | c0003 | t0002 | g0065 | AMR | CLM | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01346 | hp2 | a0001 | c0004 | t0002 | g0009 | AMR | CLM | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01361 | hp1 | a0002 | c0003 | t0002 | g0070 | AMR | CLM | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | CLM | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01433 | hp1 | a0002 | c0003 | t0002 | g0066 | AMR | CLM | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | IBS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | IBS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02027 | hp1 | a0002 | c0003 | t0002 | g0011 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02083 | hp2 | a0003 | c0008 | t0001 | g0165 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02132 | hp1 | a0001 | c0001 | t0008 | g0095 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CDX | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02273 | hp1 | a0001 | c0001 | t0005 | g0026 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02280 | hp1 | a0002 | c0003 | t0003 | g0071 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02683 | hp1 | a0001 | c0001 | t0005 | g0026 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02683 | hp2 | a0002 | c0003 | t0002 | g0020 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02809 | hp2 | a0001 | c0004 | t0002 | g0009 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02886 | hp2 | a0001 | c0004 | t0002 | g0009 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02965 | hp1 | a0001 | c0005 | t0002 | g0063 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02970 | hp1 | a0001 | c0004 | t0002 | g0187 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02976 | hp2 | a0002 | c0003 | t0003 | g0072 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03041 | hp1 | a0001 | c0004 | t0002 | g0009 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0162 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03239 | hp1 | a0001 | c0005 | t0014 | g0186 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0163 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0124 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03516 | hp1 | a0001 | c0004 | t0002 | g0009 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | STU | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03704 | hp1 | a0002 | c0003 | t0017 | g0193 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | BEB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03927 | hp1 | a0002 | c0003 | t0002 | g0069 | SAS | BEB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03942 | hp2 | a0002 | c0003 | t0002 | g0011 | SAS | BEB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | BEB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | STU | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0086 | SAS | STU | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG04204 | hp2 | a0002 | c0003 | t0002 | g0068 | SAS | STU | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | STU | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | YRI | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18747 | hp1 | a0001 | c0002 | t0016 | g0192 | EAS | CHB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | YRI | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18950 | hp1 | a0001 | c0001 | t0006 | g0102 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18953 | hp1 | a0004 | c0007 | t0001 | g0061 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18967 | hp2 | a0001 | c0001 | t0015 | g0191 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18977 | hp2 | a0001 | c0001 | t0006 | g0022 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18978 | hp2 | a0001 | c0001 | t0007 | g0103 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18983 | hp2 | a0001 | c0001 | t0006 | g0022 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19005 | hp2 | a0001 | c0001 | t0006 | g0022 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19043 | hp2 | a0001 | c0001 | t0011 | g0126 | AFR | LWK | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19084 | hp2 | a0001 | c0001 | t0007 | g0096 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA20129 | hp1 | a0001 | c0001 | t0009 | g0064 | AFR | ASW | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ASW | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | TSI | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | TSI | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | GIH | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02559 | hp1 | a0001 | c0004 | t0002 | g0009 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | USA | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
HG06807 | hp2 | a0002 | c0003 | t0002 | g0011 | AFR | USA | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | USA | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | USA | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | LWK | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | LWK | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0089 | REF | REF | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0129 | REF | REF | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:1754040
|
C | T | 1 | a0003 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.926G>A | p.Arg309His | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 7/9 | 994/2055 | 926/1239 | 309/412 | chr11 | 1754040 | ||
chr11:1761364
|
G | A | 1 | a0002 | 17 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
missense_variant | MODERATE | c.173C>T | p.Ala58Val | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/9 | 241/2055 | 173/1239 | 58/412 | chr11 | 1761364 | ||
chr11:1763846
|
C | G | 1 | a0004 | 1 | NA18953.hp1 | missense_variant | MODERATE | c.14G>C | p.Ser5Thr | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/9 | 82/2055 | 14/1239 | 5/412 | chr11 | 1763846 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:1753527
|
G | T | 1 | a0001c0006 | 2 | HG01168.hp2 HG01169.hp2 |
synonymous_variant | LOW | c.1215C>A | p.Gly405Gly | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 1283/2055 | 1215/1239 | 405/412 | chr11 | 1753527 | ||
chr11:1754015
|
G | A | 1 | a0001c0002 | 18 | HG00408.hp2 HG02056.hp1 HG02135.hp1 others(15): Show |
synonymous_variant | LOW | c.951C>T | p.Ala317Ala | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 7/9 | 1019/2055 | 951/1239 | 317/412 | chr11 | 1754015 | ||
chr11:1758975
|
A | G | 3 | a0001c0004a0001c0005a0002c0003 | 26 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(23): Show |
synonymous_variant | LOW | c.465T>C | p.Thr155Thr | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/9 | 533/2055 | 465/1239 | 155/412 | chr11 | 1758975 | ||
chr11:1759637
|
G | A | 1 | a0002c0003 | 17 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
splice_region_variant&synonymous_variant | LOW | c.231C>T | p.Ala77Ala | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 3/9 | 299/2055 | 231/1239 | 77/412 | chr11 | 1759637 | ||
chr11:1761348
|
G | A | 1 | a0001c0004 | 7 | HG01346.hp2 HG02559.hp1 HG02809.hp2 others(4): Show |
synonymous_variant | LOW | c.189C>T | p.Thr63Thr | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/9 | 257/2055 | 189/1239 | 63/412 | chr11 | 1761348 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:1752849
|
G | A | 1 | a0001c0001t0006 | 4 | NA18950.hp1 NA18977.hp2 NA18983.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*654C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 654 | chr11 | 1752849 | |||||
chr11:1752906
|
T | G | 8 | a0001c0001t0002a0001c0001t0012a0001c0001t0013others(5): Show | 49 | HG00323.hp1 HG00609.hp2 HG00733.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*597A>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 597 | chr11 | 1752906 | |||||
chr11:1753100
|
G | A | 1 | a0001c0001t0007 | 2 | NA18978.hp2 NA19084.hp2 |
3_prime_UTR_variant | MODIFIER | c.*403C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 403 | chr11 | 1753100 | |||||
chr11:1753203
|
C | T | 1 | a0001c0001t0004 | 5 | HG02257.hp2 HG02258.hp2 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*300G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 300 | chr11 | 1753203 | |||||
chr11:1753209
|
C | G | 1 | a0001c0001t0011 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*294G>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 294 | chr11 | 1753209 | |||||
chr11:1753227
|
G | A | 1 | a0001c0001t0013 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*276C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 276 | chr11 | 1753227 | |||||
chr11:1753290
|
GGA | G | 1 | a0001c0001t0005 | 4 | HG01074.hp1 HG01074.hp2 HG02273.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*211_*212delTC | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 211 | chr11 | 1753290 | |||||
chr11:1753293
|
G | C | 1 | a0001c0005t0014 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*210C>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 210 | chr11 | 1753293 | |||||
chr11:1753359
|
C | T | 1 | a0001c0002t0010 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*144G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 144 | chr11 | 1753359 | |||||
chr11:1753436
|
T | C | 9 | a0001c0001t0002a0001c0001t0003a0001c0001t0013others(6): Show | 58 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*67A>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 67 | chr11 | 1753436 | |||||
chr11:1753484
|
C | T | 1 | a0001c0001t0009 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*19G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 19 | chr11 | 1753484 | |||||
chr11:1753492
|
C | T | 1 | a0001c0001t0008 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 11 | chr11 | 1753492 | |||||
chr11:1763862
|
C | A | 1 | a0001c0001t0015 | 1 | NA18967.hp2 | 5_prime_UTR_variant | MODIFIER | c.-3G>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/9 | 3 | chr11 | 1763862 | |||||
chr11:1763891
|
G | A | 1 | a0001c0002t0016 | 1 | NA18747.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-32C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/9 | chr11 | 1763891 | ||||||
chr11:1763912
|
G | A | 1 | a0002c0003t0017 | 1 | HG03704.hp1 | 5_prime_UTR_variant | MODIFIER | c.-53C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/9 | 53 | chr11 | 1763912 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:1753677
|
C | T | 1 | a0001c0001t0002g0060 | 2 | HG00323.hp1 HG01069.hp2 |
splice_region_variant&intron_variant | LOW | c.1072-7G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 8/8 | chr11 | 1753677 | ||||||
chr11:1753704
|
A | G | 15 | a0001c0001t0002g0060a0001c0004t0002g0009a0001c0004t0002g0187others(12): Show | 27 | HG00323.hp1 HG00741.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1072-34T>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 8/8 | chr11 | 1753704 | ||||||
chr11:1753711
|
C | G | 1 | a0001c0001t0001g0052 | 2 | NA18949.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1072-41G>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 8/8 | chr11 | 1753711 | ||||||
chr11:1753714
|
G | GC | 14 | a0001c0001t0001g0079a0001c0001t0001g0097a0001c0001t0001g0101others(11): Show | 14 | HG00558.hp2 HG01109.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.1072-45dupG | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 8/8 | chr11 | 1753714 | ||||||
chr11:1753796
|
C | T | 1 | a0001c0001t0002g0116 | 1 | HG01993.hp2 | splice_region_variant&intron_variant | LOW | c.1071+7G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 8/8 | chr11 | 1753796 | ||||||
chr11:1754155
|
C | T | 12 | a0001c0001t0001g0170a0001c0001t0002g0060a0001c0001t0005g0117others(9): Show | 19 | HG00323.hp1 HG00741.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.828-17G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754155 | ||||||
chr11:1754212
|
A | C | 1 | a0001c0001t0001g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.828-74T>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754212 | ||||||
chr11:1754348
|
T | TGAGGGGC others(64): Show |
1 | a0001c0001t0001g0057 | 2 | NA18949.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.828-281_828-211dup others(71): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754348 | ||||||
chr11:1754348
|
T | TGAGGGGC others(161): Show |
1 | a0001c0001t0001g0111 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.828-211_828-210ins others(168): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754348 | ||||||
chr11:1754348
|
T | TGAGGGGC others(74): Show |
1 | a0001c0001t0001g0149 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.828-211_828-210ins others(81): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754348 | ||||||
chr11:1754348
|
T | TGAGGGGC others(91): Show |
18 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0054others(15): Show | 34 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.828-211_828-210ins others(98): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754348 | ||||||
chr11:1754348
|
T | TGAGGGGC others(162): Show |
1 | a0001c0001t0001g0188 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.828-211_828-210ins others(169): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754348 | ||||||
chr11:1754358
|
G | GGAGGGAT others(20): Show |
3 | a0001c0001t0001g0059a0001c0001t0002g0089a0001c0001t0002g0116 | 4 | HG01993.hp2 HG02300.hp2 NA20905.hp2 others(1): Show |
intron_variant | MODIFIER | c.828-247_828-221dup others(27): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754358 | ||||||
chr11:1754358
|
G | GGAGGGAT others(47): Show |
1 | a0001c0001t0001g0176 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.828-221_828-220ins others(54): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754358 | ||||||
chr11:1754358
|
GGAGGGAT others(20): Show |
G | 1 | a0001c0001t0003g0124 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.828-247_828-221del others(27): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754358 | ||||||
chr11:1754380
|
G | C | 1 | a0001c0001t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.828-242C>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754380 | ||||||
chr11:1754382
|
C | CATGGAGG others(78): Show |
1 | a0001c0001t0002g0138 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.828-245_828-244ins others(85): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754382 | ||||||
chr11:1754385
|
A | G | 1 | a0001c0001t0002g0138 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.828-247T>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754385 | ||||||
chr11:1754396
|
G | GGGGATGG others(11): Show |
1 | a0002c0003t0002g0065 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.828-259_828-258ins others(18): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754396 | ||||||
chr11:1754405
|
G | GGGGCATA others(126): Show |
1 | a0001c0001t0001g0047 | 2 | HG02071.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.828-268_828-267ins others(133): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754405 | ||||||
chr11:1754405
|
G | GGGGCATA others(251): Show |
4 | a0001c0001t0001g0008a0001c0001t0001g0151a0001c0001t0001g0166others(1): Show | 9 | HG02129.hp2 HG02165.hp2 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.828-268_828-267ins others(258): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754405 | ||||||
chr11:1754410
|
T | TG | 5 | a0001c0001t0001g0008a0001c0001t0001g0047a0001c0001t0001g0151others(2): Show | 11 | HG02071.hp2 HG02129.hp2 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.828-273dupC | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754410 | ||||||
chr11:1754412
|
AAGGGATG others(19): Show |
A | 2 | a0001c0001t0001g0125a0001c0001t0001g0128 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.828-300_828-275del others(26): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754412 | ||||||
chr11:1754426
|
C | CATGGAGG others(335): Show |
1 | a0002c0003t0002g0067 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.828-289_828-288ins others(342): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754426 | ||||||
chr11:1754431
|
A | AGGGATGG others(137): Show |
1 | a0001c0001t0001g0105 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.828-294_828-293ins others(144): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754431 | ||||||
chr11:1754441
|
G | GGATGGAG others(146): Show |
1 | a0001c0001t0007g0103 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.828-304_828-303ins others(153): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754441 | ||||||
chr11:1754481
|
G | GAGAGTCA others(138): Show |
1 | a0001c0001t0001g0082 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.828-344_828-343ins others(145): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754481 | ||||||
chr11:1754490
|
A | AGAGGGAT others(9): Show |
1 | a0001c0001t0001g0123 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.828-368_828-353dup others(16): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754490 | ||||||
chr11:1754490
|
A | AGAGGGAT others(17): Show |
1 | a0001c0001t0001g0173 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.828-376_828-353dup others(24): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754490 | ||||||
chr11:1754492
|
A | AGGGATGT others(26): Show |
2 | a0001c0001t0001g0023a0001c0001t0001g0122 | 4 | HG03654.hp2 NA18962.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.827+381_828-355dup others(33): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754492 | ||||||
chr11:1754499
|
T | A | 1 | a0001c0001t0001g0099 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.828-361A>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754499 | ||||||
chr11:1754499
|
T | TGGGGATG others(18): Show |
3 | a0001c0001t0001g0043a0001c0001t0001g0151a0001c0001t0011g0126 | 4 | HG01943.hp2 NA18522.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.827+382_828-362dup others(25): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754499 | ||||||
chr11:1754499
|
T | TGGGGATG others(77): Show |
1 | a0001c0001t0002g0089 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.828-362_828-361ins others(84): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754499 | ||||||
chr11:1754499
|
T | TGGGGATG others(172): Show |
1 | a0001c0001t0001g0110 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.828-362_828-361ins others(179): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754499 | ||||||
chr11:1754499
|
T | TGGGGATG others(626): Show |
1 | a0001c0001t0001g0177 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.828-362_828-361ins others(633): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754499 | ||||||
chr11:1754500
|
G | GGGGATGG others(347): Show |
1 | a0001c0001t0001g0146 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.828-363_828-362ins others(354): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754500 | ||||||
chr11:1754507
|
G | T | 1 | a0001c0005t0014g0186 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.828-369C>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754507 | ||||||
chr11:1754508
|
A | AGGGATGG others(18): Show |
3 | a0001c0001t0001g0121a0001c0001t0001g0131a0001c0001t0009g0064 | 3 | HG01884.hp1 HG02572.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.828-371_828-370ins others(25): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754508 | ||||||
chr11:1754508
|
A | AGGGATGG others(122): Show |
1 | a0001c0001t0001g0042 | 2 | HG01109.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.828-371_828-370ins others(129): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754508 | ||||||
chr11:1754508
|
A | G | 1 | a0001c0005t0014g0186 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.828-370T>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754508 | ||||||
chr11:1754516
|
A | AGGGATGG others(122): Show |
1 | a0001c0001t0001g0077 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.828-379_828-378ins others(129): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754516 | ||||||
chr11:1754524
|
AG | A | 8 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0083others(5): Show | 15 | HG00323.hp2 HG01106.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.827+381delC | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754524 | ||||||
chr11:1754525
|
G | GGGATGGA others(17): Show |
1 | a0001c0001t0001g0027 | 3 | HG01891.hp2 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.827+380_827+381ins others(24): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | ||||||
chr11:1754525
|
G | GGGATGGA others(148): Show |
2 | a0001c0001t0002g0018a0001c0001t0002g0139 | 5 | HG02135.hp2 NA18952.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.827+380_827+381ins others(155): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | ||||||
chr11:1754525
|
G | GGGATGGA others(224): Show |
1 | a0001c0001t0001g0046 | 2 | HG00741.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.827+380_827+381ins others(231): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | ||||||
chr11:1754525
|
G | GGGGATGG others(26): Show |
1 | a0001c0001t0001g0178 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.827+348_827+380dup others(33): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | ||||||
chr11:1754525
|
G | GGGGATGG others(232): Show |
1 | a0001c0001t0001g0161 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.827+380_827+381ins others(239): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | ||||||
chr11:1754525
|
G | GGGGATGT others(9): Show |
3 | a0001c0001t0001g0100a0001c0001t0001g0127a0001c0001t0003g0118 | 3 | HG00280.hp2 HG00642.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.827+380_827+381ins others(16): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | ||||||
chr11:1754525
|
G | GGGGATGT others(17): Show |
44 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(41): Show | 126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.827+380_827+381ins others(24): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | ||||||
chr11:1754525
|
G | GGGGATGT others(25): Show |
1 | a0001c0001t0002g0138 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.827+380_827+381ins others(32): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | ||||||
chr11:1754525
|
G | GGGGATGT others(33): Show |
1 | a0001c0001t0001g0108 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.827+380_827+381ins others(40): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | ||||||
chr11:1754525
|
G | GGGGATGT others(34): Show |
3 | a0001c0001t0001g0035a0001c0001t0001g0079a0001c0001t0001g0084 | 4 | NA18612.hp1 NA18997.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.827+380_827+381ins others(41): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | ||||||
chr11:1754525
|
G | GGGGATGT others(59): Show |
1 | a0001c0001t0001g0012 | 5 | NA18612.hp2 NA18945.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.827+380_827+381ins others(66): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | ||||||
chr11:1754525
|
G | GGGGATGT others(141): Show |
1 | a0001c0001t0001g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.827+380_827+381ins others(148): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | ||||||
chr11:1754525
|
G | GGGGATGT others(137): Show |
1 | a0001c0001t0001g0036 | 2 | NA19079.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.827+380_827+381ins others(144): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | ||||||
chr11:1754525
|
G | GGGGATGT others(190): Show |
1 | a0001c0001t0001g0157 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.827+380_827+381ins others(197): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | ||||||
chr11:1754525
|
G | GGGGATGT others(145): Show |
1 | a0001c0001t0001g0087 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.827+380_827+381ins others(152): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | ||||||
chr11:1754525
|
G | GGGGATGT others(178): Show |
1 | a0002c0003t0002g0020 | 3 | HG00741.hp2 HG01081.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.827+380_827+381ins others(185): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | ||||||
chr11:1754525
|
G | GGGGATGT others(121): Show |
2 | a0001c0001t0001g0015a0001c0001t0001g0190 | 5 | HG01496.hp1 HG04199.hp1 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.827+380_827+381ins others(128): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | ||||||
chr11:1754525
|
G | GGGGATGT others(303): Show |
1 | a0001c0001t0001g0081 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.827+380_827+381ins others(310): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | ||||||
chr11:1754525
|
G | GGGGATGT others(67): Show |
1 | a0001c0001t0001g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.827+380_827+381ins others(74): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | ||||||
chr11:1754525
|
G | GGGGATGT others(50): Show |
1 | a0001c0001t0001g0184 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.827+380_827+381ins others(57): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | ||||||
chr11:1754525
|
G | GGGGATGT others(92): Show |
1 | a0001c0001t0001g0090 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.827+380_827+381ins others(99): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | ||||||
chr11:1754525
|
G | GGGGATGT others(51): Show |
1 | a0001c0001t0001g0183 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.827+380_827+381ins others(58): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | ||||||
chr11:1754525
|
G | GGGGATGT others(52): Show |
1 | a0001c0001t0001g0182 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.827+380_827+381ins others(59): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | ||||||
chr11:1754525
|
GGGGATGG others(1): Show |
G | 5 | a0001c0001t0001g0107a0001c0001t0002g0045a0001c0002t0001g0033others(2): Show | 8 | HG02056.hp1 HG02074.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.827+373_827+380del others(8): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | ||||||
chr11:1754532
|
G | T | 6 | a0001c0001t0001g0024a0001c0001t0001g0039a0001c0001t0001g0111others(3): Show | 10 | HG01243.hp1 HG03490.hp1 HG03492.hp2 others(7): Show |
intron_variant | MODIFIER | c.827+374C>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754532 | ||||||
chr11:1754533
|
A | AG | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(72): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.827+372dupC | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | ||||||
chr11:1754533
|
A | AGGGATGG others(10): Show |
2 | a0001c0001t0001g0100a0001c0001t0001g0144 | 2 | HG02886.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.827+356_827+372dup others(17): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | ||||||
chr11:1754533
|
A | AGGGATGG others(85): Show |
4 | a0001c0001t0001g0007a0001c0001t0001g0085a0001c0001t0001g0132others(1): Show | 9 | HG00408.hp1 HG01346.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.827+372_827+373ins others(92): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | ||||||
chr11:1754533
|
A | AGGGATGG others(129): Show |
1 | a0002c0003t0002g0065 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.827+372_827+373ins others(136): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | ||||||
chr11:1754533
|
A | AGGGATGG others(104): Show |
1 | a0002c0003t0002g0068 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.827+372_827+373ins others(111): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | ||||||
chr11:1754533
|
A | AGGGATGG others(88): Show |
1 | a0001c0001t0004g0162 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.827+372_827+373ins others(95): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | ||||||
chr11:1754533
|
A | AGGGATGG others(122): Show |
1 | a0001c0001t0001g0153 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.827+372_827+373ins others(129): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | ||||||
chr11:1754533
|
A | AGGGATGG others(35): Show |
1 | a0001c0001t0001g0149 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.827+372_827+373ins others(42): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | ||||||
chr11:1754533
|
A | AGGGATGG others(138): Show |
1 | a0001c0001t0012g0098 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.827+372_827+373ins others(145): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | ||||||
chr11:1754533
|
A | AGGGATGG others(134): Show |
1 | a0001c0001t0001g0180 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.827+372_827+373ins others(141): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | ||||||
chr11:1754533
|
A | AGGGATGG others(139): Show |
1 | a0002c0003t0003g0071 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.827+372_827+373ins others(146): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | ||||||
chr11:1754533
|
A | AGGGATGG others(146): Show |
5 | a0001c0001t0002g0060a0002c0003t0002g0011a0002c0003t0002g0066others(2): Show | 10 | HG00323.hp1 HG01069.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.827+372_827+373ins others(153): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | ||||||
chr11:1754533
|
A | AGGGATGG others(114): Show |
1 | a0001c0001t0003g0078 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.827+372_827+373ins others(121): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | ||||||
chr11:1754533
|
A | AGGGATGG others(225): Show |
1 | a0001c0001t0001g0158 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.827+372_827+373ins others(232): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | ||||||
chr11:1754533
|
A | AGGGATGG others(130): Show |
4 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0119others(1): Show | 6 | HG02109.hp1 HG02630.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.827+372_827+373ins others(137): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | ||||||
chr11:1754533
|
A | AGGGATGG others(138): Show |
1 | a0001c0001t0001g0160 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.827+372_827+373ins others(145): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | ||||||
chr11:1754533
|
A | AGGGATGG others(155): Show |
1 | a0001c0001t0001g0143 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.827+372_827+373ins others(162): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | ||||||
chr11:1754533
|
A | AGGGATGG others(336): Show |
1 | a0001c0001t0001g0159 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.827+372_827+373ins others(343): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | ||||||
chr11:1754533
|
A | G | 6 | a0001c0001t0001g0024a0001c0001t0001g0039a0001c0001t0001g0111others(3): Show | 10 | HG01243.hp1 HG03490.hp1 HG03492.hp2 others(7): Show |
intron_variant | MODIFIER | c.827+373T>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | ||||||
chr11:1754541
|
A | AGGGATGG others(2): Show |
3 | a0001c0001t0001g0062a0001c0001t0001g0172a0001c0001t0001g0179 | 3 | NA18953.hp2 NA18954.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.827+356_827+364dup others(9): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754541 | ||||||
chr11:1754544
|
GATGGAGG others(18): Show |
G | 1 | a0001c0005t0002g0063 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.827+337_827+361del others(25): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754544 | ||||||
chr11:1754549
|
A | AGGGGATG others(27): Show |
1 | a0001c0001t0001g0171 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.827+356_827+357ins others(34): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754549 | ||||||
chr11:1754550
|
G | GGGATGGA others(153): Show |
1 | a0002c0003t0017g0193 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.827+355_827+356ins others(160): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754550 | ||||||
chr11:1754550
|
G | GGGGATGG others(18): Show |
1 | a0001c0001t0001g0154 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.827+355_827+356ins others(25): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754550 | ||||||
chr11:1754552
|
G | GATGGAGG others(18): Show |
1 | a0001c0002t0001g0053 | 2 | NA18947.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.827+353_827+354ins others(25): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754552 | ||||||
chr11:1754552
|
G | GATGGAGG others(35): Show |
2 | a0001c0001t0001g0024a0001c0001t0001g0111 | 4 | NA19011.hp1 NA19082.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.827+353_827+354ins others(42): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754552 | ||||||
chr11:1754559
|
GGGATGGA others(29): Show |
G | 1 | a0001c0001t0001g0164 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.827+311_827+346del others(36): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754559 | ||||||
chr11:1754561
|
G | A | 1 | a0001c0005t0014g0186 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.827+345C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754561 | ||||||
chr11:1754561
|
G | GATGGAGG others(34): Show |
1 | a0001c0001t0001g0044 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.827+344_827+345ins others(41): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754561 | ||||||
chr11:1754561
|
G | GATGGAGG others(118): Show |
1 | a0001c0004t0002g0009 | 6 | HG01346.hp2 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.827+344_827+345ins others(125): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754561 | ||||||
chr11:1754561
|
G | GATGGAGG others(176): Show |
1 | a0001c0004t0002g0187 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.827+344_827+345ins others(183): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754561 | ||||||
chr11:1754597
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.827+309C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754597 | ||||||
chr11:1754602
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.827+304T>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754602 | ||||||
chr11:1754603
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.827+303C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754603 | ||||||
chr11:1754612
|
GGGGATGG others(10): Show |
G | 2 | a0001c0001t0001g0038a0004c0007t0001g0061 | 3 | HG00438.hp2 NA18953.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.827+277_827+293del others(17): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754612 | ||||||
chr11:1754621
|
G | C | 1 | a0001c0005t0014g0186 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.827+285C>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754621 | ||||||
chr11:1754638
|
C | T | 1 | a0001c0001t0002g0135 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.827+268G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754638 | ||||||
chr11:1754736
|
TGGAGGGG others(3): Show |
T | 1 | a0001c0001t0001g0152 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.827+160_827+169del others(10): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754736 | ||||||
chr11:1754794
|
TC | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 385 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(382): Show |
intron_variant | MODIFIER | c.827+111delG | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754794 | ||||||
chr11:1754855
|
C | T | 1 | a0001c0001t0005g0117 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.827+51G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754855 | ||||||
chr11:1754858
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.827+48G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754858 | ||||||
chr11:1754859
|
G | A | 1 | a0002c0003t0002g0070 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.827+47C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754859 | ||||||
chr11:1754859
|
G | GC | 6 | a0001c0001t0001g0104a0001c0001t0001g0112a0001c0001t0001g0147others(3): Show | 6 | HG03098.hp2 HG03654.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.827+46dupG | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754859 | ||||||
chr11:1754865
|
G | A | 13 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0130others(10): Show | 17 | HG02109.hp1 HG02257.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.827+41C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754865 | ||||||
chr11:1754882
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.827+24C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754882 | ||||||
chr11:1755049
|
T | A | 1 | a0001c0001t0002g0029 | 3 | NA18983.hp1 NA19011.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.705-21A>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1755049 | ||||||
chr11:1755102
|
G | A | 27 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0023others(24): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.705-74C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1755102 | ||||||
chr11:1755417
|
G | C | 31 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0017others(28): Show | 58 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.705-389C>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1755417 | ||||||
chr11:1755510
|
G | A | 10 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0077others(7): Show | 14 | HG00558.hp1 HG01496.hp1 HG03927.hp2 others(11): Show |
intron_variant | MODIFIER | c.705-482C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1755510 | ||||||
chr11:1755609
|
T | G | 1 | a0001c0005t0002g0063 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.705-581A>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1755609 | ||||||
chr11:1755703
|
C | T | 1 | a0001c0001t0001g0025 | 3 | HG00639.hp2 HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.705-675G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1755703 | ||||||
chr11:1755715
|
C | A | 1 | a0001c0005t0014g0186 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.705-687G>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1755715 | ||||||
chr11:1755806
|
T | C | 3 | a0001c0001t0001g0113a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG00438.hp1 HG04184.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.705-778A>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1755806 | ||||||
chr11:1755807
|
T | C | 12 | a0001c0005t0014g0186a0002c0003t0002g0011a0002c0003t0002g0020others(9): Show | 18 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.705-779A>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1755807 | ||||||
chr11:1755890
|
C | T | 1 | a0003c0008t0001g0165 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.705-862G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1755890 | ||||||
chr11:1755978
|
G | A | 12 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0156others(9): Show | 16 | HG02109.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.705-950C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1755978 | ||||||
chr11:1756082
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.705-1054A>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756082 | ||||||
chr11:1756109
|
C | CGTGTGCC others(25): Show |
1 | a0001c0001t0001g0156 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.705-1113_705-1082d others(34): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756109 | ||||||
chr11:1756124
|
C | G | 2 | a0002c0003t0003g0071a0002c0003t0003g0072 | 2 | HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.705-1096G>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756124 | ||||||
chr11:1756139
|
G | GCTGTGTG others(26): Show |
1 | a0001c0001t0001g0134 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.705-1144_705-1112d others(35): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756139 | ||||||
chr11:1756196
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.704+1128C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756196 | ||||||
chr11:1756277
|
G | A | 1 | a0001c0001t0001g0040 | 2 | NA18981.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.704+1047C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756277 | ||||||
chr11:1756285
|
C | T | 2 | a0001c0004t0002g0009a0001c0004t0002g0187 | 7 | HG01346.hp2 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.704+1039G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756285 | ||||||
chr11:1756587
|
G | A | 30 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0034others(27): Show | 54 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.704+737C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756587 | ||||||
chr11:1756636
|
T | C | 82 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(79): Show | 140 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(137): Show |
intron_variant | MODIFIER | c.704+688A>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756636 | ||||||
chr11:1756728
|
A | T | 2 | a0001c0005t0002g0063a0001c0005t0014g0186 | 2 | HG02965.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.704+596T>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756728 | ||||||
chr11:1756739
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.704+585G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756739 | ||||||
chr11:1756740
|
G | A | 1 | a0001c0005t0014g0186 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.704+584C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756740 | ||||||
chr11:1756745
|
C | T | 2 | a0002c0003t0002g0066a0002c0003t0002g0067 | 2 | HG01175.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.704+579G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756745 | ||||||
chr11:1756807
|
G | C | 1 | a0001c0005t0014g0186 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.704+517C>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756807 | ||||||
chr11:1756861
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.704+463G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756861 | ||||||
chr11:1756874
|
G | A | 11 | a0002c0003t0002g0011a0002c0003t0002g0020a0002c0003t0002g0065others(8): Show | 17 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.704+450C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756874 | ||||||
chr11:1756917
|
C | A | 2 | a0001c0004t0002g0009a0001c0004t0002g0187 | 7 | HG01346.hp2 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.704+407G>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756917 | ||||||
chr11:1756946
|
G | A | 11 | a0002c0003t0002g0011a0002c0003t0002g0020a0002c0003t0002g0065others(8): Show | 17 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.704+378C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756946 | ||||||
chr11:1757056
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.704+268G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1757056 | ||||||
chr11:1757091
|
C | T | 42 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(39): Show | 74 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.704+233G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1757091 | ||||||
chr11:1757141
|
C | T | 3 | a0001c0004t0002g0009a0001c0004t0002g0187a0001c0005t0002g0063 | 8 | HG01346.hp2 HG02559.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.704+183G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1757141 | ||||||
chr11:1757244
|
A | G | 1 | a0001c0001t0001g0170 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.704+80T>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1757244 | ||||||
chr11:1757266
|
C | T | 11 | a0002c0003t0002g0011a0002c0003t0002g0020a0002c0003t0002g0065others(8): Show | 17 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.704+58G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1757266 | ||||||
chr11:1757583
|
C | A | 1 | a0001c0001t0009g0064 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.472-27G>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1757583 | ||||||
chr11:1757589
|
A | G | 1 | a0001c0001t0002g0116 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.472-33T>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1757589 | ||||||
chr11:1757655
|
C | T | 15 | a0001c0004t0002g0009a0001c0004t0002g0187a0001c0005t0002g0063others(12): Show | 26 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.472-99G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1757655 | ||||||
chr11:1757717
|
C | A | 12 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0051others(9): Show | 20 | HG02055.hp1 HG02258.hp1 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.472-161G>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1757717 | ||||||
chr11:1757755
|
G | A | 11 | a0002c0003t0002g0011a0002c0003t0002g0020a0002c0003t0002g0065others(8): Show | 17 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.472-199C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1757755 | ||||||
chr11:1757783
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.472-227C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1757783 | ||||||
chr11:1757802
|
A | C | 1 | a0001c0005t0014g0186 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.472-246T>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1757802 | ||||||
chr11:1757893
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.472-337C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1757893 | ||||||
chr11:1757908
|
C | T | 65 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(62): Show | 155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.472-352G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1757908 | ||||||
chr11:1757975
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.472-419G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1757975 | ||||||
chr11:1758025
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.472-469G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1758025 | ||||||
chr11:1758038
|
C | T | 1 | a0001c0001t0001g0049 | 2 | HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.472-482G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1758038 | ||||||
chr11:1758344
|
C | T | 1 | a0001c0005t0014g0186 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.471+625G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1758344 | ||||||
chr11:1758420
|
A | T | 1 | a0001c0001t0002g0089 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.471+549T>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1758420 | ||||||
chr11:1758503
|
G | C | 1 | a0001c0001t0001g0141 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.471+466C>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1758503 | ||||||
chr11:1758534
|
C | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0143a0001c0001t0001g0144others(3): Show | 12 | HG02258.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.471+435G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1758534 | ||||||
chr11:1758538
|
C | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0046a0001c0001t0001g0142 | 8 | HG00140.hp1 HG00741.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.471+431G>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1758538 | ||||||
chr11:1758572
|
T | A | 3 | a0001c0001t0004g0031a0001c0001t0004g0162a0001c0001t0004g0163 | 5 | HG02257.hp2 HG02258.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+397A>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1758572 | ||||||
chr11:1758588
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.471+381G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1758588 | ||||||
chr11:1758702
|
G | A | 1 | a0001c0005t0014g0186 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.471+267C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1758702 | ||||||
chr11:1758831
|
C | T | 1 | a0001c0001t0001g0034 | 3 | HG02622.hp2 HG02735.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.471+138G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1758831 | ||||||
chr11:1759104
|
G | A | 12 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0156others(9): Show | 16 | HG02109.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.353-17C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 3/8 | chr11 | 1759104 | ||||||
chr11:1759464
|
G | A | 1 | a0001c0001t0001g0030 | 3 | HG02818.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.352+52C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 3/8 | chr11 | 1759464 | ||||||
chr11:1759468
|
T | C | 2 | a0001c0001t0003g0074a0001c0005t0014g0186 | 2 | HG00738.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.352+48A>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 3/8 | chr11 | 1759468 | ||||||
chr11:1759474
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0087 | 4 | HG00733.hp1 HG00738.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.352+42T>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 3/8 | chr11 | 1759474 | ||||||
chr11:1759725
|
C | CAAGCCCT others(1): Show |
15 | a0001c0004t0002g0009a0001c0004t0002g0187a0001c0005t0002g0063others(12): Show | 26 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.229-87_229-86insCA others(6): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1759725 | ||||||
chr11:1759785
|
C | A | 1 | a0001c0005t0014g0186 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.229-146G>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1759785 | ||||||
chr11:1759908
|
G | C | 1 | a0001c0005t0002g0063 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.229-269C>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1759908 | ||||||
chr11:1760253
|
G | A | 1 | a0001c0001t0001g0051 | 2 | HG02647.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.229-614C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1760253 | ||||||
chr11:1760330
|
C | T | 2 | a0001c0001t0001g0190a0001c0001t0002g0086 | 2 | HG04199.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.229-691G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1760330 | ||||||
chr11:1760530
|
AG | A | 3 | a0001c0004t0002g0009a0001c0004t0002g0187a0001c0005t0014g0186 | 8 | HG01346.hp2 HG02559.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.228+778delC | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1760530 | ||||||
chr11:1760534
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.228+775C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1760534 | ||||||
chr11:1760560
|
T | C | 69 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(66): Show | 116 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.228+749A>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1760560 | ||||||
chr11:1760578
|
T | C | 11 | a0002c0003t0002g0011a0002c0003t0002g0020a0002c0003t0002g0065others(8): Show | 17 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.228+731A>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1760578 | ||||||
chr11:1760651
|
T | C | 1 | a0001c0001t0001g0084 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.228+658A>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1760651 | ||||||
chr11:1761066
|
G | A | 1 | a0001c0001t0001g0052 | 2 | NA18949.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.228+243C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1761066 | ||||||
chr11:1761176
|
G | C | 15 | a0001c0004t0002g0009a0001c0004t0002g0187a0001c0005t0002g0063others(12): Show | 26 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.228+133C>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1761176 | ||||||
chr11:1761213
|
G | A | 2 | a0002c0003t0003g0071a0002c0003t0003g0072 | 2 | HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.228+96C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1761213 | ||||||
chr11:1761278
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.228+31C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1761278 | ||||||
chr11:1761521
|
A | G | 1 | a0001c0005t0002g0063 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.69-53T>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1761521 | ||||||
chr11:1761523
|
G | T | 1 | a0002c0003t0002g0065 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.69-55C>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1761523 | ||||||
chr11:1761531
|
T | C | 14 | a0001c0004t0002g0009a0001c0004t0002g0187a0001c0005t0014g0186others(11): Show | 25 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.69-63A>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1761531 | ||||||
chr11:1761649
|
C | A | 1 | a0001c0001t0001g0055 | 2 | NA18940.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.69-181G>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1761649 | ||||||
chr11:1761701
|
G | A | 1 | a0003c0008t0001g0165 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.69-233C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1761701 | ||||||
chr11:1761714
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.69-246C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1761714 | ||||||
chr11:1761745
|
C | T | 2 | a0001c0004t0002g0009a0001c0004t0002g0187 | 7 | HG01346.hp2 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.69-277G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1761745 | ||||||
chr11:1761822
|
T | G | 1 | a0001c0001t0001g0183 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.69-354A>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1761822 | ||||||
chr11:1761869
|
G | A | 9 | a0001c0001t0001g0032a0001c0001t0001g0168a0001c0002t0001g0005others(6): Show | 21 | HG00408.hp2 HG02040.hp1 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.69-401C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1761869 | ||||||
chr11:1761959
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.69-491G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1761959 | ||||||
chr11:1762030
|
C | G | 2 | a0001c0001t0003g0074a0001c0005t0014g0186 | 2 | HG00738.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.69-562G>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762030 | ||||||
chr11:1762048
|
C | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0077others(8): Show | 15 | HG00558.hp1 HG01496.hp1 HG03927.hp2 others(12): Show |
intron_variant | MODIFIER | c.69-580G>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762048 | ||||||
chr11:1762186
|
G | C | 1 | a0001c0001t0001g0170 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.69-718C>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762186 | ||||||
chr11:1762208
|
C | G | 2 | a0001c0001t0001g0076a0001c0001t0015g0191 | 2 | HG02132.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.69-740G>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762208 | ||||||
chr11:1762298
|
C | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 4 | NA18940.hp1 NA18986.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.69-830G>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762298 | ||||||
chr11:1762420
|
A | AGGAAGCT others(7): Show |
1 | a0001c0002t0001g0075 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.69-966_69-953dupCC others(12): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762420 | ||||||
chr11:1762422
|
G | A | 1 | a0001c0005t0002g0063 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.69-954C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762422 | ||||||
chr11:1762527
|
A | G | 15 | a0001c0001t0003g0074a0001c0004t0002g0009a0001c0004t0002g0187others(12): Show | 26 | HG00738.hp2 HG00741.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.69-1059T>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762527 | ||||||
chr11:1762529
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.69-1061G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762529 | ||||||
chr11:1762562
|
G | A | 22 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0054others(19): Show | 40 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.69-1094C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762562 | ||||||
chr11:1762565
|
C | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG02523.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.69-1097G>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762565 | ||||||
chr11:1762566
|
T | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG02523.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.69-1098A>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762566 | ||||||
chr11:1762858
|
G | C | 2 | a0001c0004t0002g0009a0001c0004t0002g0187 | 7 | HG01346.hp2 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.68+934C>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762858 | ||||||
chr11:1762903
|
G | A | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0002g0060 | 4 | HG00323.hp1 HG01069.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+889C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762903 | ||||||
chr11:1763070
|
A | G | 15 | a0001c0004t0002g0009a0001c0004t0002g0187a0001c0005t0002g0063others(12): Show | 26 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.68+722T>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1763070 | ||||||
chr11:1763207
|
C | G | 1 | a0001c0001t0009g0064 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.68+585G>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1763207 | ||||||
chr11:1763217
|
G | A | 3 | a0001c0004t0002g0009a0001c0004t0002g0187a0001c0005t0014g0186 | 8 | HG01346.hp2 HG02559.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.68+575C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1763217 | ||||||
chr11:1763354
|
A | G | 1 | a0001c0001t0001g0010 | 5 | HG01934.hp2 HG01975.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.68+438T>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1763354 | ||||||
chr11:1763364
|
G | C | 1 | a0001c0005t0002g0063 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.68+428C>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1763364 | ||||||
chr11:1763541
|
C | G | 1 | a0001c0005t0002g0063 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.68+251G>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1763541 | ||||||
chr11:1763646
|
C | CGCGCAGG others(3): Show |
1 | a0001c0001t0001g0062 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.68+136_68+145dupCG others(8): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1763646 | ||||||
chr11:1763709
|
G | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | NA18952.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.68+83C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1763709 | ||||||
chr11:1763735
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.68+57C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1763735 |