geneid | 1520 |
---|---|
ensemblid | ENSG00000163131.12 |
hgncid | 2545 |
symbol | CTSS |
name | cathepsin S |
refseq_nuc | NM_004079.5 |
refseq_prot | NP_004070.3 |
ensembl_nuc | ENST00000368985.8 |
ensembl_prot | ENSP00000357981.3 |
mane_status | MANE Select |
chr | chr1 |
start | 150730188 |
end | 150765778 |
strand | - |
ver | v1.2 |
region | chr1:150730188-150765778 |
region5000 | chr1:150725188-150770778 |
regionname0 | CTSS_chr1_150730188_150765778 |
regionname5000 | CTSS_chr1_150725188_150770778 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 331 | 228 | 61 | 29 | 105 | 10 | 22 | 81 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
a0002 | 0/1 | 331 | 110 | 21 | 18 | 51 | 5 | 14 | 41 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
a0003 | 0/0 | 331 | 6 | 0 | 3 | 0 | 1 | 2 | 0 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 996 | 228 | 61 | 29 | 105 | 10 | 22 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
c0002 | 0/1 | 996 | 110 | 21 | 18 | 51 | 5 | 14 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
c0003 | 0/0 | 996 | 6 | 0 | 3 | 0 | 1 | 2 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2940 | 135 | 8 | 29 | 73 | 8 | 17 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
t0002 | 0/1 | 2933 | 94 | 7 | 17 | 50 | 5 | 14 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
t0003 | 1/0 | 2940 | 90 | 51 | 3 | 29 | 3 | 3 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
t0004 | 0/0 | 2937 | 6 | 6 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
t0005 | 0/0 | 2931 | 6 | 6 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
t0006 | 0/0 | 2940 | 2 | 0 | 0 | 0 | 0 | 2 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
t0007 | 0/0 | 2933 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
t0008 | 0/0 | 2940 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
t0009 | 0/0 | 2933 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
t0010 | 0/0 | 2933 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
t0011 | 0/0 | 2940 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
t0012 | 0/0 | 2940 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
t0013 | 0/0 | 2940 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
t0014 | 0/0 | 2940 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
t0015 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
t0016 | 0/0 | 2940 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
t0017 | 0/0 | 2940 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0002 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0005 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0006 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0007 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0008 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0009 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0010 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0232 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 996 | 228 | 61 | 29 | 105 | 10 | 22 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
a0002c0002 | 0/1 | 996 | 110 | 21 | 18 | 51 | 5 | 14 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
a0003c0003 | 0/0 | 996 | 6 | 0 | 3 | 0 | 1 | 2 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3935 | 131 | 8 | 26 | 73 | 7 | 17 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
a0001c0001t0003 | 1/0 | 3935 | 89 | 50 | 3 | 29 | 3 | 3 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
a0001c0001t0008 | 0/0 | 3935 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
a0001c0001t0011 | 0/0 | 3935 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
a0001c0001t0012 | 0/0 | 3935 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
a0001c0001t0013 | 0/0 | 3935 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
a0001c0001t0014 | 0/0 | 3935 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
a0001c0001t0015 | 0/0 | 3926 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
a0001c0001t0016 | 0/0 | 3935 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
a0001c0001t0017 | 0/0 | 3935 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
a0002c0002t0002 | 0/1 | 3928 | 94 | 7 | 17 | 50 | 5 | 14 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
a0002c0002t0003 | 0/0 | 3935 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
a0002c0002t0004 | 0/0 | 3932 | 6 | 6 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
a0002c0002t0005 | 0/0 | 3926 | 6 | 6 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
a0002c0002t0007 | 0/0 | 3928 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
a0002c0002t0009 | 0/0 | 3928 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
a0002c0002t0010 | 0/0 | 3928 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
a0003c0003t0001 | 0/0 | 3935 | 4 | 0 | 3 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
a0003c0003t0006 | 0/0 | 3935 | 2 | 0 | 0 | 0 | 0 | 2 | CTSS_chr1_150725188_150770778 | CTSS | copy fasta | chr1 | 150725188 | 150770778 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0232 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0008g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0011g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0012g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0013g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0014g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0015g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0016g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0001c0001t0017g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0002 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0005 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0006 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0008 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0009g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0002c0002t0010g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0003c0003t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0003c0003t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0003c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
a0003c0003t0006g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0176 | EUR | GBR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0250 | EUR | GBR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00140 | hp2 | a0002 | c0002 | t0002 | g0008 | EUR | GBR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00280 | hp1 | a0003 | c0003 | t0001 | g0111 | EUR | FIN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | FIN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00323 | hp1 | a0002 | c0002 | t0002 | g0068 | EUR | FIN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0175 | EUR | FIN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0069 | EAS | CHS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | CHS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00558 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00597 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | CHS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | CHS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | CHS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00735 | hp2 | a0002 | c0002 | t0002 | g0108 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00738 | hp2 | a0002 | c0002 | t0002 | g0057 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01069 | hp2 | a0002 | c0002 | t0002 | g0051 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01074 | hp2 | a0002 | c0002 | t0002 | g0066 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01109 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0241 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01243 | hp2 | a0003 | c0003 | t0001 | g0023 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01255 | hp1 | a0003 | c0003 | t0001 | g0023 | AMR | CLM | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0080 | AMR | CLM | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01257 | hp2 | a0003 | c0003 | t0001 | g0110 | AMR | CLM | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0021 | AMR | CLM | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0048 | AMR | CLM | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01358 | hp2 | a0002 | c0002 | t0002 | g0107 | AMR | CLM | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0269 | AMR | CLM | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0249 | EUR | IBS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01517 | hp2 | a0002 | c0002 | t0002 | g0021 | EUR | IBS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01884 | hp1 | a0002 | c0002 | t0007 | g0078 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01891 | hp1 | a0002 | c0002 | t0002 | g0074 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0242 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01928 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0075 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01943 | hp2 | a0002 | c0002 | t0009 | g0061 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01978 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0109 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0248 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02015 | hp2 | a0002 | c0002 | t0002 | g0064 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02027 | hp2 | a0002 | c0002 | t0002 | g0055 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0236 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02083 | hp2 | a0001 | c0001 | t0008 | g0103 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0102 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0278 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0239 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0052 | EAS | CDX | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0224 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02258 | hp1 | a0002 | c0002 | t0005 | g0059 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02258 | hp2 | a0002 | c0002 | t0002 | g0006 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02273 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0219 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0234 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02293 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0093 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0240 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0271 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0231 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0227 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0220 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02647 | hp2 | a0002 | c0002 | t0005 | g0062 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0259 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02698 | hp2 | a0002 | c0002 | t0002 | g0047 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02735 | hp2 | a0002 | c0002 | t0002 | g0097 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02738 | hp1 | a0002 | c0002 | t0002 | g0044 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0228 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02809 | hp2 | a0002 | c0002 | t0002 | g0073 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0243 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0229 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02886 | hp2 | a0002 | c0002 | t0005 | g0090 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02895 | hp1 | a0002 | c0002 | t0005 | g0049 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02896 | hp1 | a0002 | c0002 | t0004 | g0038 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0274 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02897 | hp1 | a0002 | c0002 | t0005 | g0082 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02897 | hp2 | a0002 | c0002 | t0004 | g0037 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0237 | AFR | ESN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02965 | hp2 | a0002 | c0002 | t0004 | g0036 | AFR | ESN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02970 | hp1 | a0002 | c0002 | t0004 | g0039 | AFR | ESN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | ESN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02976 | hp1 | a0002 | c0002 | t0004 | g0045 | AFR | ESN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0245 | AFR | ESN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0225 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03041 | hp2 | a0002 | c0002 | t0002 | g0053 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0034 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03130 | hp1 | a0002 | c0002 | t0003 | g0272 | AFR | ESN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | ESN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03139 | hp1 | a0002 | c0002 | t0002 | g0072 | AFR | ESN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ESN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03209 | hp1 | a0001 | c0001 | t0014 | g0280 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03209 | hp2 | a0002 | c0002 | t0004 | g0041 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0233 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03239 | hp1 | a0001 | c0001 | t0016 | g0214 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03239 | hp2 | a0002 | c0002 | t0002 | g0042 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0238 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0246 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0275 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0056 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03490 | hp2 | a0003 | c0003 | t0006 | g0022 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0086 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03492 | hp2 | a0003 | c0003 | t0006 | g0022 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0230 | AFR | ESN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0223 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0217 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03579 | hp2 | a0002 | c0002 | t0002 | g0016 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03710 | hp1 | a0002 | c0002 | t0002 | g0098 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0101 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03831 | hp1 | a0002 | c0002 | t0002 | g0019 | SAS | BEB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03834 | hp1 | a0001 | c0001 | t0011 | g0182 | SAS | BEB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03942 | hp2 | a0002 | c0002 | t0002 | g0040 | SAS | BEB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | STU | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG04115 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | STU | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0253 | SAS | BEB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | STU | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG04199 | hp2 | a0002 | c0002 | t0002 | g0043 | SAS | STU | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0092 | SAS | STU | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | STU | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | STU | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0260 | SAS | STU | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0222 | AFR | YRI | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18522 | hp2 | a0002 | c0002 | t0005 | g0083 | AFR | YRI | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18612 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | CHB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18612 | hp2 | a0002 | c0002 | t0010 | g0087 | EAS | CHB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0264 | EAS | CHB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | YRI | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18906 | hp2 | a0002 | c0002 | t0002 | g0016 | AFR | YRI | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18939 | hp2 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18948 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18951 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18954 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18961 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18962 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18963 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18965 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18966 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18968 | hp1 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18970 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18972 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18972 | hp2 | a0001 | c0001 | t0013 | g0251 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18974 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18978 | hp2 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18982 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18982 | hp2 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18984 | hp1 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18986 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18989 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18995 | hp1 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19001 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19005 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19006 | hp1 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19009 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19010 | hp2 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0215 | AFR | LWK | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | LWK | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19043 | hp1 | a0001 | c0001 | t0017 | g0279 | AFR | LWK | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0276 | AFR | LWK | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19054 | hp1 | a0001 | c0001 | t0012 | g0187 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19057 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19058 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19062 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19063 | hp1 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19064 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19065 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19070 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19078 | hp1 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19079 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19085 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0218 | AFR | YRI | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0095 | EUR | TSI | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0252 | EUR | TSI | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | TSI | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA20805 | hp2 | a0002 | c0002 | t0002 | g0067 | EUR | TSI | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | GIH | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | GIH | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0221 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0270 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0235 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | USA | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
HG06807 | hp2 | a0001 | c0001 | t0015 | g0273 | AFR | USA | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0277 | AFR | LWK | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0065 | REF | REF | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0232 | REF | REF | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:150755063
|
G | A | 1 | a0002 | 110 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
missense_variant | MODERATE | c.337C>T | p.Arg113Trp | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/8 | 419/3936 | 337/996 | 113/331 | chr1 | 150755063 | ||
chr1:150764744
|
A | G | 1 | a0003 | 6 | HG00280.hp1 HG01243.hp2 HG01255.hp1 others(3): Show |
missense_variant | MODERATE | c.20T>C | p.Val7Ala | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/8 | 102/3936 | 20/996 | 7/331 | chr1 | 150764744 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:150730241
|
G | C | 8 | a0001c0001t0015a0001c0001t0016a0002c0002t0002others(5): Show | 111 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*2805C>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 2805 | chr1 | 150730241 | |||||
chr1:150730293
|
A | G | 1 | a0003c0003t0006 | 2 | HG03490.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2753T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 2753 | chr1 | 150730293 | |||||
chr1:150730558
|
CAGA | C | 7 | a0001c0001t0015a0002c0002t0002a0002c0002t0004others(4): Show | 110 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*2485_*2487delTCT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 2485 | chr1 | 150730558 | |||||
chr1:150730815
|
T | C | 1 | a0001c0001t0016 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2231A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 2231 | chr1 | 150730815 | |||||
chr1:150730880
|
T | C | 1 | a0001c0001t0014 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2166A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 2166 | chr1 | 150730880 | |||||
chr1:150730890
|
TAACA | T | 6 | a0001c0001t0015a0002c0002t0002a0002c0002t0005others(3): Show | 104 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2152_*2155delTGTT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 2152 | chr1 | 150730890 | |||||
chr1:150730920
|
CTG | C | 2 | a0001c0001t0015a0002c0002t0005 | 7 | HG02258.hp1 HG02647.hp2 HG02886.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2124_*2125delCA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 2124 | chr1 | 150730920 | |||||
chr1:150731008
|
A | G | 1 | a0001c0001t0013 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2038T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 2038 | chr1 | 150731008 | |||||
chr1:150731722
|
T | G | 1 | a0002c0002t0009 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1324A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 1324 | chr1 | 150731722 | |||||
chr1:150731739
|
T | C | 1 | a0001c0001t0016 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1307A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 1307 | chr1 | 150731739 | |||||
chr1:150731882
|
A | C | 1 | a0001c0001t0011 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1164T>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 1164 | chr1 | 150731882 | |||||
chr1:150732205
|
G | A | 1 | a0001c0001t0012 | 1 | NA19054.hp1 | 3_prime_UTR_variant | MODIFIER | c.*841C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 841 | chr1 | 150732205 | |||||
chr1:150732378
|
G | A | 1 | a0001c0001t0017 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*668C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 668 | chr1 | 150732378 | |||||
chr1:150732380
|
T | C | 1 | a0002c0002t0010 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*666A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 666 | chr1 | 150732380 | |||||
chr1:150732604
|
A | G | 1 | a0002c0002t0007 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*442T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 442 | chr1 | 150732604 | |||||
chr1:150765721
|
C | T | 5 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(2): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
5_prime_UTR_variant | MODIFIER | c.-25G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/8 | 958 | chr1 | 150765721 | |||||
chr1:150765724
|
A | G | 7 | a0001c0001t0008a0002c0002t0002a0002c0002t0004others(4): Show | 110 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
5_prime_UTR_variant | MODIFIER | c.-28T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/8 | 961 | chr1 | 150765724 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:150733180
|
C | T | 1 | a0001c0001t0016g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.897-35G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150733180 | ||||||
chr1:150733279
|
G | A | 87 | a0001c0001t0015g0273a0001c0001t0016g0214a0002c0002t0002g0002others(84): Show | 111 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.897-134C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150733279 | ||||||
chr1:150733306
|
A | G | 1 | a0001c0001t0001g0146 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.897-161T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150733306 | ||||||
chr1:150733403
|
C | A | 1 | a0001c0001t0001g0185 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.897-258G>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150733403 | ||||||
chr1:150733911
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.897-766C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150733911 | ||||||
chr1:150734188
|
C | T | 1 | a0002c0002t0002g0073 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.897-1043G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150734188 | ||||||
chr1:150734265
|
G | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.897-1120C>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150734265 | ||||||
chr1:150734318
|
C | T | 28 | a0001c0001t0003g0001a0001c0001t0003g0014a0001c0001t0003g0032others(25): Show | 38 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.897-1173G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150734318 | ||||||
chr1:150734905
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.897-1760A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150734905 | ||||||
chr1:150735096
|
G | T | 1 | a0001c0001t0016g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.897-1951C>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150735096 | ||||||
chr1:150735120
|
G | A | 86 | a0001c0001t0015g0273a0002c0002t0002g0002a0002c0002t0002g0004others(83): Show | 110 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.897-1975C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150735120 | ||||||
chr1:150735160
|
A | T | 86 | a0001c0001t0015g0273a0002c0002t0002g0002a0002c0002t0002g0004others(83): Show | 110 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.897-2015T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150735160 | ||||||
chr1:150735187
|
T | C | 1 | a0001c0001t0001g0011 | 3 | HG00423.hp2 NA18988.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.897-2042A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150735187 | ||||||
chr1:150735209
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | NA18979.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.897-2064C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150735209 | ||||||
chr1:150735307
|
T | C | 1 | a0001c0001t0016g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.897-2162A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150735307 | ||||||
chr1:150735516
|
C | T | 80 | a0001c0001t0015g0273a0002c0002t0002g0002a0002c0002t0002g0004others(77): Show | 104 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.897-2371G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150735516 | ||||||
chr1:150735590
|
T | C | 1 | a0001c0001t0001g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.897-2445A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150735590 | ||||||
chr1:150735623
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.897-2478C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150735623 | ||||||
chr1:150735686
|
T | C | 1 | a0002c0002t0002g0056 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.897-2541A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150735686 | ||||||
chr1:150735755
|
A | AT | 14 | a0001c0001t0001g0145a0001c0001t0001g0158a0001c0001t0001g0184others(11): Show | 15 | HG01261.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.897-2611dupA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150735755 | ||||||
chr1:150735755
|
AT | A | 86 | a0001c0001t0001g0113a0001c0001t0001g0212a0001c0001t0003g0264others(83): Show | 110 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.897-2611delA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150735755 | ||||||
chr1:150736161
|
G | A | 1 | a0002c0002t0002g0040 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.897-3016C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150736161 | ||||||
chr1:150736320
|
G | C | 1 | a0001c0001t0003g0255 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.897-3175C>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150736320 | ||||||
chr1:150736585
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.897-3440A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150736585 | ||||||
chr1:150736653
|
T | A | 86 | a0001c0001t0015g0273a0002c0002t0002g0002a0002c0002t0002g0004others(83): Show | 110 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.897-3508A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150736653 | ||||||
chr1:150736772
|
T | TA | 23 | a0001c0001t0001g0149a0001c0001t0001g0176a0001c0001t0003g0013others(20): Show | 25 | HG00099.hp1 HG01109.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.897-3628dupT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150736772 | ||||||
chr1:150736836
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.897-3691G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150736836 | ||||||
chr1:150737175
|
T | G | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | HG00099.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.897-4030A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150737175 | ||||||
chr1:150737191
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | NA18979.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.897-4046G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150737191 | ||||||
chr1:150737247
|
C | T | 117 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(114): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.897-4102G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150737247 | ||||||
chr1:150737309
|
C | G | 86 | a0001c0001t0015g0273a0002c0002t0002g0002a0002c0002t0002g0004others(83): Show | 110 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.897-4164G>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150737309 | ||||||
chr1:150737354
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.897-4209C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150737354 | ||||||
chr1:150737406
|
C | T | 4 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0240others(1): Show | 4 | HG01891.hp2 HG02145.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.897-4261G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150737406 | ||||||
chr1:150737433
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0197 | 3 | NA18999.hp1 NA19009.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.897-4288C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150737433 | ||||||
chr1:150737791
|
T | G | 1 | a0001c0001t0001g0148 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.897-4646A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150737791 | ||||||
chr1:150737810
|
A | G | 1 | a0001c0001t0016g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.897-4665T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150737810 | ||||||
chr1:150737871
|
G | A | 1 | a0001c0001t0003g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.897-4726C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150737871 | ||||||
chr1:150737984
|
G | T | 5 | a0002c0002t0002g0004a0002c0002t0002g0058a0002c0002t0002g0094others(2): Show | 9 | NA18950.hp2 NA18952.hp2 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.897-4839C>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150737984 | ||||||
chr1:150738490
|
A | AT | 15 | a0001c0001t0001g0028a0001c0001t0001g0134a0001c0001t0001g0149others(12): Show | 17 | HG01109.hp2 HG01346.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.897-5346dupA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150738490 | ||||||
chr1:150738556
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.897-5411C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150738556 | ||||||
chr1:150738598
|
C | A | 1 | a0001c0001t0003g0278 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.897-5453G>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150738598 | ||||||
chr1:150738624
|
C | G | 1 | a0001c0001t0003g0278 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.897-5479G>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150738624 | ||||||
chr1:150738681
|
G | A | 11 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0269others(8): Show | 13 | HG01433.hp2 HG02109.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.897-5536C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150738681 | ||||||
chr1:150739081
|
T | C | 1 | a0001c0001t0016g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.897-5936A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150739081 | ||||||
chr1:150739281
|
C | G | 1 | a0002c0002t0002g0077 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.897-6136G>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150739281 | ||||||
chr1:150739328
|
A | T | 1 | a0001c0001t0001g0199 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.897-6183T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150739328 | ||||||
chr1:150739420
|
A | T | 87 | a0001c0001t0015g0273a0001c0001t0016g0214a0002c0002t0002g0002others(84): Show | 111 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.897-6275T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150739420 | ||||||
chr1:150739537
|
T | G | 1 | a0001c0001t0001g0129 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.897-6392A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150739537 | ||||||
chr1:150739662
|
TCAA | T | 262 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(259): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.897-6520_897-6518d others(5): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150739662 | ||||||
chr1:150739722
|
G | GA | 86 | a0001c0001t0015g0273a0001c0001t0016g0214a0002c0002t0002g0002others(83): Show | 110 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.897-6578dupT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150739722 | ||||||
chr1:150739896
|
GTTC | G | 86 | a0001c0001t0015g0273a0002c0002t0002g0002a0002c0002t0002g0004others(83): Show | 110 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.897-6754_897-6752d others(5): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150739896 | ||||||
chr1:150740450
|
G | A | 86 | a0001c0001t0015g0273a0002c0002t0002g0002a0002c0002t0002g0004others(83): Show | 110 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.897-7305C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150740450 | ||||||
chr1:150740515
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.896+7262G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150740515 | ||||||
chr1:150740592
|
C | T | 1 | a0001c0001t0003g0220 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.896+7185G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150740592 | ||||||
chr1:150740594
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | NA18979.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.896+7183C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150740594 | ||||||
chr1:150740618
|
T | G | 4 | a0002c0002t0002g0065a0002c0002t0002g0066a0002c0002t0002g0067others(1): Show | 4 | HG00323.hp1 HG01074.hp2 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.896+7159A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150740618 | ||||||
chr1:150741009
|
A | C | 1 | a0001c0001t0003g0224 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.896+6768T>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150741009 | ||||||
chr1:150741536
|
A | G | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | NA19006.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.896+6241T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150741536 | ||||||
chr1:150741884
|
AG | A | 116 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(113): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.896+5892delC | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150741884 | ||||||
chr1:150741886
|
G | C | 1 | a0002c0002t0002g0068 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.896+5891C>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150741886 | ||||||
chr1:150741887
|
G | C | 12 | a0001c0001t0003g0215a0001c0001t0003g0217a0001c0001t0003g0218others(9): Show | 12 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.896+5890C>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150741887 | ||||||
chr1:150741891
|
G | C | 1 | a0001c0001t0016g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.896+5886C>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150741891 | ||||||
chr1:150742102
|
C | G | 1 | a0001c0001t0001g0136 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.896+5675G>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150742102 | ||||||
chr1:150742175
|
TGAACCTT others(7): Show |
T | 117 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(114): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.896+5588_896+5601d others(16): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150742175 | ||||||
chr1:150742189
|
A | G | 145 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(142): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.896+5588T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150742189 | ||||||
chr1:150742682
|
T | C | 11 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0269others(8): Show | 13 | HG01433.hp2 HG02109.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.896+5095A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150742682 | ||||||
chr1:150742756
|
A | G | 11 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0269others(8): Show | 13 | HG01433.hp2 HG02109.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.896+5021T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150742756 | ||||||
chr1:150742918
|
T | C | 4 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0240others(1): Show | 4 | HG01891.hp2 HG02145.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+4859A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150742918 | ||||||
chr1:150742937
|
G | T | 1 | a0002c0002t0002g0094 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.896+4840C>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150742937 | ||||||
chr1:150742976
|
G | A | 3 | a0002c0002t0002g0017a0002c0002t0002g0071a0002c0002t0002g0079 | 4 | NA18963.hp2 NA18965.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+4801C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150742976 | ||||||
chr1:150743109
|
T | A | 1 | a0002c0002t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.896+4668A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743109 | ||||||
chr1:150743192
|
G | T | 1 | a0001c0001t0016g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.896+4585C>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743192 | ||||||
chr1:150743306
|
G | A | 100 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0269others(97): Show | 126 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.896+4471C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743306 | ||||||
chr1:150743366
|
C | CAACAGTC others(28): Show |
1 | a0002c0002t0002g0076 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.896+4376_896+4410d others(37): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743366 | ||||||
chr1:150743496
|
GAT | G | 162 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(159): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.896+4279_896+4280d others(4): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743496 | ||||||
chr1:150743496
|
GATAT | G | 92 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0240others(89): Show | 116 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.896+4277_896+4280d others(6): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743496 | ||||||
chr1:150743546
|
T | G | 6 | a0001c0001t0001g0025a0001c0001t0001g0144a0001c0001t0001g0164others(3): Show | 7 | HG00741.hp2 HG01981.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.896+4231A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743546 | ||||||
chr1:150743561
|
G | GTATGTAT others(24): Show |
5 | a0002c0002t0002g0016a0002c0002t0002g0055a0002c0002t0002g0067others(2): Show | 6 | HG00323.hp1 HG02027.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.896+4185_896+4215d others(33): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743561 | ||||||
chr1:150743561
|
G | GTATGTAT others(55): Show |
2 | a0001c0001t0003g0278a0002c0002t0002g0092 | 2 | HG02145.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.896+4154_896+4215d others(64): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743561 | ||||||
chr1:150743561
|
GTATGTAT others(24): Show |
G | 2 | a0001c0001t0001g0025a0001c0001t0001g0196 | 2 | HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.896+4185_896+4215d others(33): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743561 | ||||||
chr1:150743561
|
GTATGTAT others(55): Show |
G | 2 | a0001c0001t0001g0003a0001c0001t0001g0138 | 2 | NA18954.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.896+4154_896+4215d others(64): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743561 | ||||||
chr1:150743569
|
A | G | 1 | a0001c0001t0003g0260 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.896+4208T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743569 | ||||||
chr1:150743606
|
T | TATACATA others(102): Show |
1 | a0001c0001t0016g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.896+4170_896+4171i others(111): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743606 | ||||||
chr1:150743610
|
T | A | 2 | a0002c0002t0004g0037a0002c0002t0004g0038 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.896+4167A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743610 | ||||||
chr1:150743611
|
T | A | 2 | a0001c0001t0003g0244a0001c0001t0016g0214 | 2 | HG01884.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.896+4166A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743611 | ||||||
chr1:150743612
|
A | ATATAT | 63 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(60): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.896+4160_896+4164d others(7): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743612 | ||||||
chr1:150743612
|
A | ATATATTA others(134): Show |
1 | a0002c0002t0002g0076 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.896+4164_896+4165i others(143): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743612 | ||||||
chr1:150743612
|
A | T | 2 | a0001c0001t0003g0244a0001c0001t0016g0214 | 2 | HG01884.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.896+4165T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743612 | ||||||
chr1:150743612
|
ATATATGT others(60): Show |
A | 1 | a0001c0001t0001g0144 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.896+4098_896+4164d others(69): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743612 | ||||||
chr1:150743636
|
ATATAT | A | 28 | a0001c0001t0003g0001a0001c0001t0003g0014a0001c0001t0003g0032others(25): Show | 38 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.896+4136_896+4140d others(7): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743636 | ||||||
chr1:150743642
|
T | A | 1 | a0001c0001t0016g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.896+4135A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743642 | ||||||
chr1:150743643
|
A | ATATAT | 126 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(123): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.896+4129_896+4133d others(7): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743643 | ||||||
chr1:150743643
|
A | ATATATGT others(60): Show |
2 | a0002c0002t0002g0093a0002c0002t0004g0036 | 2 | HG02602.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.896+4133_896+4134i others(69): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743643 | ||||||
chr1:150743643
|
A | ATATATGT others(235): Show |
1 | a0001c0001t0003g0227 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.896+4133_896+4134i others(244): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743643 | ||||||
chr1:150743643
|
A | ATATATGT others(132): Show |
2 | a0001c0001t0003g0220a0001c0001t0003g0221 | 2 | HG02109.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.896+4133_896+4134i others(141): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743643 | ||||||
chr1:150743643
|
A | ATATATGT others(168): Show |
1 | a0002c0002t0004g0039 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.896+4133_896+4134i others(177): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743643 | ||||||
chr1:150743643
|
A | ATATATGT others(132): Show |
1 | a0001c0001t0003g0246 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.896+4133_896+4134i others(141): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743643 | ||||||
chr1:150743649
|
G | A | 1 | a0001c0001t0016g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.896+4128C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743649 | ||||||
chr1:150743674
|
ATATAT | A | 8 | a0001c0001t0003g0276a0001c0001t0017g0279a0002c0002t0002g0065others(5): Show | 8 | HG00408.hp2 HG01074.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.896+4098_896+4102d others(7): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743674 | ||||||
chr1:150743675
|
T | C | 2 | a0002c0002t0004g0037a0002c0002t0004g0038 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.896+4102A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743675 | ||||||
chr1:150743679
|
T | TGTATATT others(19): Show |
1 | a0002c0002t0002g0056 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.896+4097_896+4098i others(28): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743679 | ||||||
chr1:150743710
|
ATATAT | A | 5 | a0001c0001t0001g0026a0001c0001t0017g0279a0002c0002t0002g0046others(2): Show | 6 | HG00621.hp1 HG01074.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.896+4062_896+4066d others(7): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743710 | ||||||
chr1:150743744
|
T | TTATATAT others(132): Show |
2 | a0001c0001t0003g0239a0001c0001t0003g0240 | 2 | HG02145.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.896+3894_896+4032d others(141): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743744 | ||||||
chr1:150743796
|
T | C | 1 | a0002c0002t0002g0057 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.896+3981A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743796 | ||||||
chr1:150743852
|
T | TTATATAT others(24): Show |
1 | a0002c0002t0002g0075 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.896+3894_896+3924d others(33): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743852 | ||||||
chr1:150743887
|
A | ACATATAA others(423): Show |
1 | a0001c0001t0003g0243 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.896+3889_896+3890i others(432): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743887 | ||||||
chr1:150743888
|
T | TATTATAT others(167): Show |
1 | a0001c0001t0003g0238 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.896+3888_896+3889i others(176): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743888 | ||||||
chr1:150743948
|
A | T | 1 | a0001c0001t0001g0205 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.896+3829T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743948 | ||||||
chr1:150743959
|
A | ATTATATA others(28): Show |
4 | a0002c0002t0002g0008a0002c0002t0002g0044a0002c0002t0002g0107others(1): Show | 6 | HG00140.hp2 HG00735.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.896+3783_896+3817d others(37): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743959 | ||||||
chr1:150743959
|
A | ATTATATA others(63): Show |
1 | a0002c0002t0002g0095 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.896+3817_896+3818i others(72): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743959 | ||||||
chr1:150743994
|
T | G | 3 | a0001c0001t0001g0025a0001c0001t0001g0168a0001c0001t0001g0197 | 3 | HG01981.hp1 HG04204.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.896+3783A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743994 | ||||||
chr1:150743994
|
TA | T | 3 | a0001c0001t0003g0034a0001c0001t0003g0244a0001c0001t0003g0269 | 4 | HG01433.hp2 HG01884.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+3782delT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743994 | ||||||
chr1:150744030
|
T | G | 8 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0164others(5): Show | 10 | HG00741.hp2 HG03017.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.896+3747A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744030 | ||||||
chr1:150744030
|
TA | T | 12 | a0001c0001t0003g0035a0001c0001t0003g0270a0001c0001t0003g0271others(9): Show | 14 | HG01346.hp2 HG01517.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.896+3746delT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744030 | ||||||
chr1:150744031
|
ATTATATA others(28): Show |
A | 3 | a0001c0001t0001g0135a0001c0001t0001g0168a0001c0001t0001g0184 | 3 | HG01346.hp1 HG01981.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.896+3711_896+3745d others(37): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744031 | ||||||
chr1:150744031
|
ATTATATA others(252): Show |
A | 1 | a0001c0001t0003g0236 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.896+3487_896+3745d others(2): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744031 | ||||||
chr1:150744057
|
TACATAAT others(77): Show |
T | 1 | a0001c0001t0001g0134 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.896+3636_896+3719d others(86): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744057 | ||||||
chr1:150744063
|
ATATT | A | 3 | a0002c0002t0002g0019a0002c0002t0002g0056a0002c0002t0002g0057 | 4 | HG00738.hp2 HG01978.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+3710_896+3713d others(6): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744063 | ||||||
chr1:150744065
|
A | AG | 16 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0129others(13): Show | 17 | HG00558.hp2 HG00738.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.896+3711_896+3712i others(3): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744065 | ||||||
chr1:150744066
|
T | A | 16 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0129others(13): Show | 17 | HG00558.hp2 HG00738.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.896+3711A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744066 | ||||||
chr1:150744066
|
T | TA | 223 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(220): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.896+3710_896+3711i others(3): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744066 | ||||||
chr1:150744066
|
T | TATTATAT others(138): Show |
1 | a0001c0001t0001g0121 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.896+3710_896+3711i others(147): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744066 | ||||||
chr1:150744066
|
TTTATATA others(76): Show |
T | 5 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0130others(2): Show | 10 | HG01243.hp2 HG01255.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.896+3628_896+3710d others(85): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744066 | ||||||
chr1:150744082
|
A | G | 1 | a0002c0002t0002g0075 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.896+3695T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744082 | ||||||
chr1:150744092
|
TACATAAT others(42): Show |
T | 1 | a0001c0001t0003g0035 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.896+3636_896+3684d others(51): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744092 | ||||||
chr1:150744101
|
T | G | 26 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0121others(23): Show | 29 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(26): Show |
intron_variant | MODIFIER | c.896+3676A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744101 | ||||||
chr1:150744101
|
TA | T | 9 | a0001c0001t0001g0136a0001c0001t0003g0244a0001c0001t0003g0270others(6): Show | 9 | HG01884.hp2 HG01928.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.896+3675delT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744101 | ||||||
chr1:150744102
|
ATTATATA others(41): Show |
A | 9 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0024others(6): Show | 15 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.896+3627_896+3674d others(50): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744102 | ||||||
chr1:150744102
|
ATTATATA others(76): Show |
A | 2 | a0001c0001t0003g0034a0001c0001t0003g0269 | 3 | HG01433.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.896+3592_896+3674d others(85): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744102 | ||||||
chr1:150744113
|
T | C | 1 | a0001c0001t0003g0237 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.896+3664A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744113 | ||||||
chr1:150744118
|
A | G | 3 | a0002c0002t0002g0005a0002c0002t0002g0109a0002c0002t0009g0061 | 6 | HG01255.hp2 HG01928.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.896+3659T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744118 | ||||||
chr1:150744128
|
TACATAAT others(6): Show |
T | 16 | a0001c0001t0001g0128a0001c0001t0001g0132a0001c0001t0001g0135others(13): Show | 17 | HG00642.hp1 HG01167.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.896+3636_896+3648d others(15): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744128 | ||||||
chr1:150744134
|
A | ATAGATTA others(16): Show |
2 | a0001c0001t0001g0121a0001c0001t0001g0194 | 2 | NA18947.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(25): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATAGATTA others(52): Show |
2 | a0001c0001t0001g0150a0001c0001t0001g0152 | 2 | HG02602.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(61): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATAGATTA others(88): Show |
3 | a0001c0001t0001g0126a0001c0001t0001g0155a0001c0001t0001g0202 | 3 | HG00408.hp1 HG02027.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(97): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATAGATTA others(124): Show |
3 | a0001c0001t0001g0156a0001c0001t0001g0161a0001c0001t0001g0166 | 3 | HG01192.hp1 HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(133): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATAGATTA others(88): Show |
7 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0124others(4): Show | 9 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(97): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATAGATTA others(52): Show |
2 | a0001c0001t0001g0158a0001c0001t0001g0212 | 2 | HG00558.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(61): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATAGATTA others(124): Show |
3 | a0001c0001t0001g0149a0001c0001t0001g0160a0001c0001t0001g0203 | 3 | HG01109.hp2 HG01433.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(133): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATAGATTA others(88): Show |
1 | a0001c0001t0001g0191 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(97): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(16): Show |
34 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0143others(31): Show | 38 | HG00408.hp2 HG00735.hp2 HG01358.hp1 others(35): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(25): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(88): Show |
1 | a0001c0001t0001g0125 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(97): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(196): Show |
1 | a0001c0001t0001g0159 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(205): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(158): Show |
1 | a0001c0001t0001g0147 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(167): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(88): Show |
8 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0157others(5): Show | 8 | HG00280.hp2 HG00438.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(97): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(159): Show |
2 | a0001c0001t0001g0113a0001c0001t0001g0148 | 2 | NA18953.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(168): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(124): Show |
4 | a0001c0001t0001g0112a0001c0001t0001g0127a0001c0001t0001g0151others(1): Show | 4 | HG00735.hp1 HG02165.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(133): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(225): Show |
1 | a0001c0001t0003g0266 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(234): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(52): Show |
22 | a0001c0001t0001g0120a0001c0001t0001g0192a0002c0002t0002g0002others(19): Show | 33 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(61): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(124): Show |
1 | a0001c0001t0001g0122 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(133): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(160): Show |
1 | a0001c0001t0001g0201 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(169): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(88): Show |
4 | a0001c0001t0001g0177a0001c0001t0001g0178a0002c0002t0002g0006others(1): Show | 6 | HG01074.hp1 HG02258.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(97): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(155): Show |
1 | a0001c0001t0001g0118 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(164): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(124): Show |
3 | a0001c0001t0001g0179a0002c0002t0002g0067a0002c0002t0005g0062 | 3 | HG00423.hp1 HG02647.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(133): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(160): Show |
10 | a0001c0001t0001g0011a0001c0001t0001g0116a0001c0001t0001g0119others(7): Show | 12 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(9): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(169): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(196): Show |
8 | a0001c0001t0001g0010a0001c0001t0001g0141a0001c0001t0001g0142others(5): Show | 10 | HG03017.hp1 HG03942.hp1 NA18951.hp2 others(7): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(205): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(232): Show |
4 | a0001c0001t0001g0114a0001c0001t0001g0172a0001c0001t0001g0180others(1): Show | 4 | HG02004.hp2 HG02735.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(241): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(268): Show |
1 | a0001c0001t0001g0171 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(277): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(267): Show |
2 | a0001c0001t0001g0210a0002c0002t0002g0065 | 2 | HG02080.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(276): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(302): Show |
1 | a0001c0001t0013g0251 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(311): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(302): Show |
2 | a0001c0001t0003g0265a0001c0001t0003g0268 | 2 | NA18947.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(311): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(195): Show |
4 | a0001c0001t0001g0115a0001c0001t0001g0208a0002c0002t0005g0049others(1): Show | 4 | HG02818.hp1 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(204): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(267): Show |
1 | a0002c0002t0002g0073 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(276): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(266): Show |
1 | a0001c0001t0003g0213 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(275): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(301): Show |
2 | a0001c0001t0003g0014a0001c0001t0003g0257 | 4 | HG00438.hp2 NA18970.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(310): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(230): Show |
1 | a0001c0001t0001g0207 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(239): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(159): Show |
3 | a0001c0001t0001g0117a0002c0002t0002g0068a0002c0002t0005g0082 | 3 | HG00323.hp1 HG02055.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(168): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(265): Show |
13 | a0001c0001t0003g0001a0001c0001t0003g0032a0001c0001t0003g0033others(10): Show | 21 | HG00621.hp2 HG01515.hp2 HG02004.hp1 others(18): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(274): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(442): Show |
1 | a0001c0001t0003g0228 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(451): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(336): Show |
4 | a0001c0001t0003g0013a0001c0001t0003g0216a0001c0001t0003g0225others(1): Show | 6 | HG02622.hp1 HG02895.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(345): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(300): Show |
2 | a0001c0001t0003g0256a0001c0001t0003g0262 | 2 | HG02132.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(309): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(1262): Show |
1 | a0001c0001t0003g0247 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(1271): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(159): Show |
4 | a0001c0001t0003g0242a0002c0002t0002g0072a0002c0002t0002g0074others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(168): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(194): Show |
1 | a0001c0001t0003g0237 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(203): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(229): Show |
2 | a0001c0001t0003g0241a0001c0001t0003g0250 | 2 | HG00140.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(238): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(585): Show |
1 | a0001c0001t0003g0245 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(594): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(264): Show |
1 | a0001c0001t0003g0267 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(273): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(87): Show |
3 | a0001c0001t0003g0223a0001c0001t0003g0230a0002c0002t0002g0080 | 3 | HG01257.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(96): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(123): Show |
1 | a0002c0002t0002g0104 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(132): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(158): Show |
4 | a0001c0001t0003g0215a0001c0001t0003g0218a0001c0001t0003g0219others(1): Show | 4 | HG02280.hp1 HG02630.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(167): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(479): Show |
1 | a0001c0001t0003g0029 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(488): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(193): Show |
1 | a0001c0001t0003g0252 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(202): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(122): Show |
1 | a0001c0001t0003g0224 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(131): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(478): Show |
1 | a0001c0001t0003g0233 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(487): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(51): Show |
5 | a0002c0002t0002g0019a0002c0002t0002g0056a0002c0002t0002g0057others(2): Show | 6 | HG00738.hp2 HG01074.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(60): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(87): Show |
3 | a0002c0002t0002g0004a0002c0002t0002g0058a0002c0002t0002g0084 | 7 | NA18950.hp2 NA18954.hp1 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(96): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(123): Show |
1 | a0002c0002t0002g0094 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(132): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(122): Show |
2 | a0001c0001t0003g0217a0001c0001t0003g0222 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(131): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(443): Show |
1 | a0001c0001t0003g0030 | 2 | HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(452): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(372): Show |
1 | a0001c0001t0003g0235 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(381): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(157): Show |
1 | a0001c0001t0003g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(166): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATATTA others(369): Show |
1 | a0001c0001t0003g0260 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(378): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATTTAT others(15): Show |
2 | a0001c0001t0003g0220a0001c0001t0003g0221 | 2 | HG02109.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(24): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATTTAT others(51): Show |
4 | a0002c0002t0002g0042a0002c0002t0002g0043a0002c0002t0002g0046others(1): Show | 4 | HG00621.hp1 HG03239.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(60): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATTTAT others(336): Show |
2 | a0001c0001t0003g0031a0001c0001t0003g0234 | 3 | HG02280.hp2 HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(345): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATTTAT others(230): Show |
1 | a0002c0002t0002g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(239): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATTTAT others(120): Show |
1 | a0001c0001t0003g0243 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(129): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATTTAT others(406): Show |
1 | a0001c0001t0003g0246 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(415): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744134
|
A | ATATTTAT others(121): Show |
1 | a0001c0001t0003g0227 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(130): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | ||||||
chr1:150744136
|
ATGTACAC others(5): Show |
A | 2 | a0001c0001t0001g0164a0001c0001t0001g0168 | 2 | HG00741.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.896+3629_896+3640d others(14): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744136 | ||||||
chr1:150744136
|
ATGTACAC others(40): Show |
A | 1 | a0001c0001t0001g0190 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.896+3594_896+3640d others(49): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744136 | ||||||
chr1:150744137
|
TGTACACA others(5): Show |
T | 28 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0131others(25): Show | 32 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.896+3628_896+3639d others(14): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744137 | ||||||
chr1:150744141
|
C | T | 215 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(212): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.896+3636G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744141 | ||||||
chr1:150744149
|
A | G | 2 | a0001c0001t0001g0164a0001c0001t0001g0168 | 2 | HG00741.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.896+3628T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744149 | ||||||
chr1:150744150
|
T | A | 35 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0028others(32): Show | 45 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.896+3627A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744150 | ||||||
chr1:150744150
|
T | TA | 77 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0112others(74): Show | 86 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.896+3626_896+3627i others(3): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744150 | ||||||
chr1:150744184
|
A | AG | 7 | a0001c0001t0001g0028a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 8 | HG00558.hp2 HG00741.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.896+3592_896+3593i others(3): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744184 | ||||||
chr1:150744184
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.896+3593T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744184 | ||||||
chr1:150744185
|
T | A | 8 | a0001c0001t0001g0028a0001c0001t0001g0163a0001c0001t0001g0164others(5): Show | 9 | HG00558.hp2 HG00741.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.896+3592A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744185 | ||||||
chr1:150744185
|
T | TA | 73 | a0001c0001t0001g0126a0001c0001t0001g0150a0001c0001t0001g0152others(70): Show | 97 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.896+3591_896+3592i others(3): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744185 | ||||||
chr1:150744185
|
T | TATTATAT others(101): Show |
2 | a0002c0002t0002g0050a0002c0002t0002g0101 | 2 | HG03710.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.896+3591_896+3592i others(110): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744185 | ||||||
chr1:150744199
|
G | GTATATTA others(29): Show |
1 | a0001c0001t0003g0242 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.896+3577_896+3578i others(38): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744199 | ||||||
chr1:150744220
|
T | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0190 | 2 | HG01981.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.896+3557A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744220 | ||||||
chr1:150744220
|
T | TA | 65 | a0001c0001t0001g0028a0001c0001t0001g0163a0001c0001t0001g0164others(62): Show | 82 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.896+3556_896+3557i others(3): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744220 | ||||||
chr1:150744220
|
T | TATTATAT others(56): Show |
1 | a0001c0001t0016g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.896+3556_896+3557i others(65): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744220 | ||||||
chr1:150744220
|
T | TTTATATA others(65): Show |
3 | a0002c0002t0002g0006a0002c0002t0002g0016a0002c0002t0002g0071 | 4 | HG03579.hp2 NA18906.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+3556_896+3557i others(74): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744220 | ||||||
chr1:150744220
|
T | TTTATATA others(101): Show |
1 | a0002c0002t0005g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.896+3556_896+3557i others(110): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744220 | ||||||
chr1:150744223
|
ATATAT | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0144 | 3 | HG03017.hp2 HG04184.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.896+3549_896+3553d others(7): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744223 | ||||||
chr1:150744255
|
T | TA | 24 | a0001c0001t0001g0028a0001c0001t0001g0163a0001c0001t0001g0190others(21): Show | 26 | HG00558.hp2 HG01074.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.896+3521_896+3522i others(3): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744255 | ||||||
chr1:150744290
|
T | TA | 18 | a0001c0001t0001g0136a0001c0001t0003g0034a0001c0001t0003g0035others(15): Show | 20 | HG00735.hp2 HG01433.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.896+3486_896+3487i others(3): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744290 | ||||||
chr1:150744290
|
TTTATATA others(29): Show |
T | 3 | a0001c0001t0001g0164a0001c0001t0001g0168a0001c0001t0001g0196 | 3 | HG00741.hp2 HG01981.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.896+3451_896+3486d others(38): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744290 | ||||||
chr1:150744325
|
T | TTTATATA others(27): Show |
1 | a0001c0001t0001g0179 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.896+3451_896+3452i others(36): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744325 | ||||||
chr1:150744325
|
TA | T | 146 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(143): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.896+3451delT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744325 | ||||||
chr1:150744326
|
A | T | 1 | a0001c0001t0001g0179 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.896+3451T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744326 | ||||||
chr1:150744361
|
T | TTTATATA others(27): Show |
1 | a0001c0001t0001g0119 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.896+3415_896+3416i others(36): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744361 | ||||||
chr1:150744361
|
TA | T | 18 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0185others(15): Show | 19 | HG00735.hp2 HG01074.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.896+3415delT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744361 | ||||||
chr1:150744361
|
TATTATAT others(30): Show |
T | 3 | a0001c0001t0001g0128a0001c0001t0001g0134a0001c0001t0001g0184 | 3 | HG01167.hp1 HG02293.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.896+3379_896+3415d others(39): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744361 | ||||||
chr1:150744362
|
A | ATTATATA others(28): Show |
1 | a0001c0001t0003g0278 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.896+3380_896+3414d others(37): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744362 | ||||||
chr1:150744362
|
A | ATTATATA others(64): Show |
1 | a0001c0001t0003g0225 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.896+3344_896+3414d others(73): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744362 | ||||||
chr1:150744362
|
A | ATTATATA others(775): Show |
1 | a0001c0001t0003g0249 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.896+3414_896+3415i others(784): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744362 | ||||||
chr1:150744362
|
A | T | 1 | a0001c0001t0001g0119 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.896+3415T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744362 | ||||||
chr1:150744397
|
T | TTTATATA others(27): Show |
12 | a0002c0002t0002g0002a0002c0002t0002g0015a0002c0002t0002g0017others(9): Show | 14 | HG01069.hp2 HG02015.hp2 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.896+3379_896+3380i others(36): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744397 | ||||||
chr1:150744397
|
TA | T | 119 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(116): Show | 156 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.896+3379delT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744397 | ||||||
chr1:150744398
|
A | ATTATATA others(23): Show |
1 | a0002c0002t0002g0074 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.896+3378_896+3379i others(32): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744398 | ||||||
chr1:150744398
|
A | T | 12 | a0002c0002t0002g0002a0002c0002t0002g0015a0002c0002t0002g0017others(9): Show | 14 | HG01069.hp2 HG02015.hp2 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.896+3379T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744398 | ||||||
chr1:150744406
|
T | TTATATGT others(130): Show |
1 | a0002c0002t0002g0108 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.896+3370_896+3371i others(139): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744406 | ||||||
chr1:150744430
|
A | T | 1 | a0001c0001t0016g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.896+3347T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744430 | ||||||
chr1:150744430
|
ATATT | A | 5 | a0001c0001t0015g0273a0002c0002t0002g0021a0002c0002t0002g0066others(2): Show | 6 | HG01074.hp2 HG01346.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.896+3343_896+3346d others(6): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744430 | ||||||
chr1:150744433
|
T | TA | 15 | a0001c0001t0001g0119a0001c0001t0001g0135a0001c0001t0001g0136others(12): Show | 16 | HG01346.hp1 HG01515.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.896+3343_896+3344i others(3): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744433 | ||||||
chr1:150744433
|
T | TATATTAT others(201): Show |
1 | a0001c0001t0016g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.896+3343_896+3344i others(210): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744433 | ||||||
chr1:150744433
|
T | TTTATATA others(29): Show |
1 | a0001c0001t0001g0141 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.896+3308_896+3343d others(38): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744433 | ||||||
chr1:150744433
|
TTTATATA others(29): Show |
T | 7 | a0001c0001t0003g0034a0001c0001t0003g0269a0001c0001t0003g0271others(4): Show | 8 | HG01433.hp2 HG02622.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.896+3308_896+3343d others(38): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744433 | ||||||
chr1:150744440
|
A | T | 5 | a0001c0001t0015g0273a0002c0002t0002g0021a0002c0002t0002g0066others(2): Show | 6 | HG01074.hp2 HG01346.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.896+3337T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744440 | ||||||
chr1:150744441
|
T | A | 5 | a0001c0001t0015g0273a0002c0002t0002g0021a0002c0002t0002g0066others(2): Show | 6 | HG01074.hp2 HG01346.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.896+3336A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744441 | ||||||
chr1:150744441
|
T | TTATATGT others(15): Show |
1 | a0002c0002t0002g0108 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.896+3335_896+3336i others(24): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744441 | ||||||
chr1:150744447
|
G | T | 1 | a0001c0001t0003g0215 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.896+3330C>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744447 | ||||||
chr1:150744468
|
T | TTTATATA others(94): Show |
35 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(32): Show | 47 | HG00558.hp1 HG00597.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.896+3308_896+3309i others(103): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744468 | ||||||
chr1:150744468
|
T | TTTATATA others(99): Show |
3 | a0002c0002t0004g0037a0002c0002t0004g0041a0002c0002t0004g0045 | 3 | HG02897.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.896+3308_896+3309i others(108): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744468 | ||||||
chr1:150744468
|
T | TTTATATA others(93): Show |
1 | a0002c0002t0002g0063 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.896+3308_896+3309i others(102): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744468 | ||||||
chr1:150744468
|
T | TTTATATA others(129): Show |
16 | a0002c0002t0002g0004a0002c0002t0002g0008a0002c0002t0002g0042others(13): Show | 22 | HG00140.hp2 HG01109.hp1 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.896+3308_896+3309i others(138): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744468 | ||||||
chr1:150744468
|
TA | T | 20 | a0001c0001t0003g0035a0001c0001t0003g0233a0001c0001t0003g0249others(17): Show | 22 | HG00323.hp1 HG00408.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.896+3308delT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744468 | ||||||
chr1:150744469
|
A | ATTATATA others(28): Show |
3 | a0001c0001t0001g0167a0002c0002t0002g0072a0002c0002t0002g0073 | 3 | HG00438.hp1 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.896+3273_896+3307d others(37): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744469 | ||||||
chr1:150744469
|
A | ATTATATA others(59): Show |
16 | a0002c0002t0002g0002a0002c0002t0002g0015a0002c0002t0002g0017others(13): Show | 18 | HG01069.hp2 HG02015.hp2 HG02273.hp1 others(15): Show |
intron_variant | MODIFIER | c.896+3307_896+3308i others(68): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744469 | ||||||
chr1:150744469
|
A | ATTATATA others(64): Show |
1 | a0002c0002t0004g0038 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.896+3237_896+3307d others(73): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744469 | ||||||
chr1:150744469
|
A | ATTATATA others(95): Show |
1 | a0002c0002t0005g0090 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.896+3307_896+3308i others(104): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744469 | ||||||
chr1:150744469
|
A | T | 55 | a0002c0002t0002g0002a0002c0002t0002g0004a0002c0002t0002g0005others(52): Show | 73 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.896+3308T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744469 | ||||||
chr1:150744477
|
T | TTA | 5 | a0001c0001t0001g0119a0001c0001t0001g0136a0001c0001t0001g0165others(2): Show | 5 | HG00280.hp2 HG01192.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.896+3298_896+3299d others(4): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744477 | ||||||
chr1:150744477
|
T | TTATATGT others(55): Show |
1 | a0002c0002t0002g0068 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.896+3299_896+3300i others(64): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744477 | ||||||
chr1:150744504
|
T | TATTATAT others(58): Show |
1 | a0001c0001t0003g0278 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.896+3272_896+3273i others(67): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744504 | ||||||
chr1:150744504
|
TA | T | 53 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0028others(50): Show | 57 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.896+3272delT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744504 | ||||||
chr1:150744505
|
A | ATTATATA others(23): Show |
1 | a0002c0002t0002g0071 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.896+3271_896+3272i others(32): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744505 | ||||||
chr1:150744505
|
A | ATTATATA others(94): Show |
3 | a0002c0002t0002g0055a0002c0002t0002g0069a0002c0002t0002g0070 | 3 | HG00408.hp2 HG02027.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.896+3271_896+3272i others(103): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744505 | ||||||
chr1:150744513
|
T | TTA | 4 | a0001c0001t0001g0119a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG00438.hp1 HG01346.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+3262_896+3263d others(4): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744513 | ||||||
chr1:150744513
|
TTATATGT others(31): Show |
T | 1 | a0001c0001t0001g0189 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.896+3226_896+3263d others(40): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744513 | ||||||
chr1:150744528
|
G | A | 1 | a0001c0001t0003g0035 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.896+3249C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744528 | ||||||
chr1:150744537
|
A | G | 1 | a0001c0001t0016g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.896+3240T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744537 | ||||||
chr1:150744542
|
T | A | 1 | a0001c0001t0003g0224 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.896+3235A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744542 | ||||||
chr1:150744550
|
T | C | 1 | a0001c0001t0017g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.896+3227A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744550 | ||||||
chr1:150744575
|
ATATAT | A | 26 | a0001c0001t0003g0001a0001c0001t0003g0014a0001c0001t0003g0032others(23): Show | 36 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.896+3197_896+3201d others(7): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744575 | ||||||
chr1:150744580
|
T | TATTATAT others(21): Show |
1 | a0001c0001t0003g0248 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.896+3196_896+3197i others(30): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744580 | ||||||
chr1:150744580
|
T | TTATATAT others(26): Show |
1 | a0001c0001t0003g0249 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.896+3196_896+3197i others(35): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744580 | ||||||
chr1:150744604
|
G | A | 27 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0114others(24): Show | 31 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.896+3173C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744604 | ||||||
chr1:150744604
|
G | GTATACAT others(31): Show |
1 | a0001c0001t0001g0118 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.896+3172_896+3173i others(40): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744604 | ||||||
chr1:150744624
|
T | TATA | 87 | a0001c0001t0015g0273a0001c0001t0016g0214a0002c0002t0002g0002others(84): Show | 111 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.896+3150_896+3152d others(5): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744624 | ||||||
chr1:150744633
|
G | GATTATGT others(24): Show |
3 | a0001c0001t0001g0156a0001c0001t0001g0202a0001c0001t0016g0214 | 3 | HG02738.hp2 HG03239.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.896+3113_896+3143d others(33): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744633 | ||||||
chr1:150744670
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.896+3107C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744670 | ||||||
chr1:150744676
|
A | T | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.896+3101T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744676 | ||||||
chr1:150744848
|
T | G | 6 | a0001c0001t0003g0013a0001c0001t0003g0216a0001c0001t0003g0225others(3): Show | 8 | HG02622.hp1 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.896+2929A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744848 | ||||||
chr1:150744938
|
A | T | 1 | a0001c0001t0001g0026 | 2 | NA18978.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.896+2839T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744938 | ||||||
chr1:150744999
|
A | T | 5 | a0001c0001t0003g0013a0001c0001t0003g0216a0001c0001t0003g0225others(2): Show | 7 | HG02622.hp1 HG02630.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.896+2778T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744999 | ||||||
chr1:150745075
|
C | T | 1 | a0001c0001t0016g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.896+2702G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150745075 | ||||||
chr1:150745367
|
A | G | 4 | a0002c0002t0002g0065a0002c0002t0002g0066a0002c0002t0002g0067others(1): Show | 4 | HG00323.hp1 HG01074.hp2 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.896+2410T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150745367 | ||||||
chr1:150745703
|
G | A | 12 | a0001c0001t0003g0215a0001c0001t0003g0217a0001c0001t0003g0218others(9): Show | 12 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.896+2074C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150745703 | ||||||
chr1:150745710
|
G | A | 1 | a0001c0001t0017g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.896+2067C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150745710 | ||||||
chr1:150745887
|
T | G | 1 | a0001c0001t0001g0169 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.896+1890A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150745887 | ||||||
chr1:150745913
|
A | G | 1 | a0001c0001t0016g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.896+1864T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150745913 | ||||||
chr1:150745994
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.896+1783A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150745994 | ||||||
chr1:150746126
|
T | G | 24 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0012others(21): Show | 36 | HG00280.hp1 HG00642.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.896+1651A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150746126 | ||||||
chr1:150746146
|
G | A | 3 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0240 | 3 | HG02145.hp2 HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.896+1631C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150746146 | ||||||
chr1:150746477
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.896+1300G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150746477 | ||||||
chr1:150747063
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.896+714T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150747063 | ||||||
chr1:150747423
|
T | C | 1 | a0001c0001t0014g0280 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.896+354A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150747423 | ||||||
chr1:150747458
|
G | T | 1 | a0001c0001t0001g0200 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.896+319C>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150747458 | ||||||
chr1:150747723
|
T | C | 1 | a0001c0001t0003g0278 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.896+54A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150747723 | ||||||
chr1:150747902
|
A | G | 1 | a0001c0001t0003g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.794-23T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150747902 | ||||||
chr1:150748036
|
A | G | 1 | a0001c0001t0001g0131 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.794-157T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150748036 | ||||||
chr1:150748087
|
C | T | 1 | a0001c0001t0003g0242 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.794-208G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150748087 | ||||||
chr1:150748147
|
G | A | 31 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0114others(28): Show | 35 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.794-268C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150748147 | ||||||
chr1:150748677
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.794-798C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150748677 | ||||||
chr1:150748699
|
G | T | 86 | a0001c0001t0015g0273a0002c0002t0002g0002a0002c0002t0002g0004others(83): Show | 110 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.794-820C>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150748699 | ||||||
chr1:150748711
|
C | T | 3 | a0001c0001t0001g0112a0001c0001t0001g0127a0001c0001t0012g0187 | 3 | HG02165.hp1 NA18998.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.794-832G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150748711 | ||||||
chr1:150748977
|
A | G | 1 | a0001c0001t0003g0278 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.793+1029T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150748977 | ||||||
chr1:150749085
|
A | G | 1 | a0001c0001t0014g0280 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.793+921T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150749085 | ||||||
chr1:150749257
|
C | A | 1 | a0001c0001t0003g0236 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.793+749G>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150749257 | ||||||
chr1:150749424
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0197 | 3 | NA18999.hp1 NA19009.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.793+582G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150749424 | ||||||
chr1:150749524
|
G | A | 5 | a0002c0002t0002g0020a0002c0002t0002g0063a0002c0002t0002g0084others(2): Show | 6 | NA18944.hp1 NA18962.hp2 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.793+482C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150749524 | ||||||
chr1:150749550
|
TCGCCTCA others(8): Show |
T | 1 | a0001c0001t0017g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.793+441_793+455del others(15): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150749550 | ||||||
chr1:150749592
|
G | T | 1 | a0001c0001t0016g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.793+414C>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150749592 | ||||||
chr1:150749597
|
A | G | 2 | a0001c0001t0003g0247a0001c0001t0003g0249 | 2 | HG01515.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.793+409T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150749597 | ||||||
chr1:150749606
|
T | C | 1 | a0001c0001t0003g0242 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.793+400A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150749606 | ||||||
chr1:150750368
|
A | G | 88 | a0001c0001t0003g0254a0001c0001t0003g0255a0001c0001t0015g0273others(85): Show | 112 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.628-197T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 5/7 | chr1 | 150750368 | ||||||
chr1:150750587
|
G | A | 1 | a0001c0001t0003g0278 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.628-416C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 5/7 | chr1 | 150750587 | ||||||
chr1:150750723
|
A | G | 1 | a0002c0002t0002g0015 | 2 | NA18966.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.628-552T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 5/7 | chr1 | 150750723 | ||||||
chr1:150750894
|
G | A | 1 | a0001c0001t0003g0278 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.628-723C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 5/7 | chr1 | 150750894 | ||||||
chr1:150750901
|
C | G | 3 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151 | 3 | HG00735.hp1 HG01109.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.628-730G>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 5/7 | chr1 | 150750901 | ||||||
chr1:150751175
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.627+606C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 5/7 | chr1 | 150751175 | ||||||
chr1:150751271
|
T | C | 89 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0003g0278others(86): Show | 113 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.627+510A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 5/7 | chr1 | 150751271 | ||||||
chr1:150751291
|
G | A | 1 | a0002c0002t0005g0090 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.627+490C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 5/7 | chr1 | 150751291 | ||||||
chr1:150751382
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0180 | 2 | HG02004.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.627+399C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 5/7 | chr1 | 150751382 | ||||||
chr1:150751390
|
G | A | 1 | a0002c0002t0002g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.627+391C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 5/7 | chr1 | 150751390 | ||||||
chr1:150751406
|
C | T | 1 | a0001c0001t0003g0224 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.627+375G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 5/7 | chr1 | 150751406 | ||||||
chr1:150751523
|
T | C | 279 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(276): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.627+258A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 5/7 | chr1 | 150751523 | ||||||
chr1:150751772
|
A | T | 1 | a0002c0002t0004g0045 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.627+9T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 5/7 | chr1 | 150751772 | ||||||
chr1:150752055
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.400-47C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150752055 | ||||||
chr1:150752163
|
G | A | 1 | a0001c0001t0017g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.400-155C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150752163 | ||||||
chr1:150752382
|
C | T | 1 | a0002c0002t0002g0107 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.400-374G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150752382 | ||||||
chr1:150752567
|
C | T | 1 | a0002c0002t0002g0100 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.400-559G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150752567 | ||||||
chr1:150752712
|
C | T | 1 | a0001c0001t0003g0278 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.400-704G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150752712 | ||||||
chr1:150752859
|
G | T | 86 | a0001c0001t0016g0214a0002c0002t0002g0002a0002c0002t0002g0004others(83): Show | 110 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.400-851C>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150752859 | ||||||
chr1:150752860
|
T | G | 1 | a0002c0002t0002g0021 | 2 | HG01346.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.400-852A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150752860 | ||||||
chr1:150752925
|
C | A | 33 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0012others(30): Show | 48 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.400-917G>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150752925 | ||||||
chr1:150753191
|
T | G | 1 | a0002c0002t0002g0105 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.400-1183A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150753191 | ||||||
chr1:150753262
|
A | G | 1 | a0001c0001t0016g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.400-1254T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150753262 | ||||||
chr1:150753480
|
A | G | 1 | a0001c0001t0003g0269 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.400-1472T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150753480 | ||||||
chr1:150753573
|
C | T | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG00735.hp1 HG00741.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.399+1428G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150753573 | ||||||
chr1:150753683
|
C | A | 1 | a0001c0001t0001g0186 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.399+1318G>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150753683 | ||||||
chr1:150753762
|
C | T | 85 | a0002c0002t0002g0002a0002c0002t0002g0004a0002c0002t0002g0005others(82): Show | 109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.399+1239G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150753762 | ||||||
chr1:150753940
|
C | CAAACA | 82 | a0002c0002t0002g0002a0002c0002t0002g0004a0002c0002t0002g0005others(79): Show | 106 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.399+1056_399+1060d others(7): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150753940 | ||||||
chr1:150753940
|
C | CAAACAAA others(3): Show |
3 | a0002c0002t0002g0086a0002c0002t0002g0088a0002c0002t0010g0087 | 3 | HG03492.hp1 NA18612.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.399+1051_399+1060d others(12): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150753940 | ||||||
chr1:150754111
|
C | CT | 26 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0117others(23): Show | 26 | HG01891.hp2 HG01978.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.399+889dupA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150754111 | ||||||
chr1:150754111
|
CT | C | 108 | a0001c0001t0001g0028a0001c0001t0001g0186a0001c0001t0001g0197others(105): Show | 143 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.399+889delA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150754111 | ||||||
chr1:150754128
|
T | C | 2 | a0002c0002t0002g0089a0002c0002t0002g0091 | 2 | NA18960.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.399+873A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150754128 | ||||||
chr1:150754136
|
C | T | 1 | a0001c0001t0003g0217 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.399+865G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150754136 | ||||||
chr1:150754261
|
C | G | 1 | a0002c0002t0005g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.399+740G>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150754261 | ||||||
chr1:150754395
|
T | C | 1 | a0001c0001t0012g0187 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.399+606A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150754395 | ||||||
chr1:150754430
|
C | CT | 85 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0003g0261others(82): Show | 109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.399+570dupA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150754430 | ||||||
chr1:150754435
|
T | A | 9 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0269others(6): Show | 11 | HG01433.hp2 HG02109.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.399+566A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150754435 | ||||||
chr1:150754561
|
G | A | 1 | a0001c0001t0016g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.399+440C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150754561 | ||||||
chr1:150754853
|
C | T | 85 | a0002c0002t0002g0002a0002c0002t0002g0004a0002c0002t0002g0005others(82): Show | 109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.399+148G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150754853 | ||||||
chr1:150754918
|
G | A | 28 | a0001c0001t0003g0001a0001c0001t0003g0014a0001c0001t0003g0032others(25): Show | 38 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.399+83C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150754918 | ||||||
chr1:150755511
|
G | A | 20 | a0001c0001t0003g0013a0001c0001t0003g0215a0001c0001t0003g0216others(17): Show | 22 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.250-361C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150755511 | ||||||
chr1:150755556
|
A | G | 85 | a0002c0002t0002g0002a0002c0002t0002g0004a0002c0002t0002g0005others(82): Show | 109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.250-406T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150755556 | ||||||
chr1:150755672
|
G | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | NA18977.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.250-522C>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150755672 | ||||||
chr1:150756152
|
C | T | 6 | a0002c0002t0004g0036a0002c0002t0004g0037a0002c0002t0004g0038others(3): Show | 6 | HG02896.hp1 HG02897.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.250-1002G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150756152 | ||||||
chr1:150756200
|
T | C | 86 | a0001c0001t0016g0214a0002c0002t0002g0002a0002c0002t0002g0004others(83): Show | 110 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.250-1050A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150756200 | ||||||
chr1:150756290
|
G | A | 3 | a0002c0002t0002g0047a0002c0002t0002g0092a0002c0002t0002g0093 | 3 | HG02602.hp1 HG02698.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.250-1140C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150756290 | ||||||
chr1:150756543
|
T | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG04199.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.249+1315A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150756543 | ||||||
chr1:150756558
|
C | T | 1 | a0001c0001t0001g0024 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.249+1300G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150756558 | ||||||
chr1:150756708
|
C | CT | 70 | a0001c0001t0001g0117a0001c0001t0001g0144a0001c0001t0003g0248others(67): Show | 88 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.249+1149dupA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150756708 | ||||||
chr1:150756708
|
CT | C | 10 | a0001c0001t0001g0119a0001c0001t0001g0137a0001c0001t0001g0138others(7): Show | 11 | HG00558.hp2 HG02273.hp2 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.249+1149delA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150756708 | ||||||
chr1:150756712
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.249+1146A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150756712 | ||||||
chr1:150756738
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.249+1120G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150756738 | ||||||
chr1:150756871
|
C | T | 2 | a0001c0001t0003g0278a0001c0001t0017g0279 | 2 | HG02145.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.249+987G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150756871 | ||||||
chr1:150757317
|
G | A | 117 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(114): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.249+541C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150757317 | ||||||
chr1:150757507
|
G | A | 86 | a0001c0001t0016g0214a0002c0002t0002g0002a0002c0002t0002g0004others(83): Show | 110 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.249+351C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150757507 | ||||||
chr1:150757621
|
T | C | 1 | a0002c0002t0002g0099 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.249+237A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150757621 | ||||||
chr1:150757657
|
G | A | 1 | a0002c0002t0004g0036 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.249+201C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150757657 | ||||||
chr1:150757708
|
C | A | 86 | a0001c0001t0016g0214a0002c0002t0002g0002a0002c0002t0002g0004others(83): Show | 110 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.249+150G>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150757708 | ||||||
chr1:150757785
|
T | C | 1 | a0001c0001t0003g0260 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.249+73A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150757785 | ||||||
chr1:150757803
|
A | G | 86 | a0001c0001t0008g0103a0002c0002t0002g0002a0002c0002t0002g0004others(83): Show | 110 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.249+55T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150757803 | ||||||
chr1:150758053
|
A | AT | 10 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0142others(7): Show | 10 | HG01891.hp2 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.127-74dupA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150758053 | ||||||
chr1:150758350
|
A | C | 1 | a0001c0001t0001g0129 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.127-370T>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150758350 | ||||||
chr1:150758484
|
ATAT | A | 12 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0269others(9): Show | 14 | HG01433.hp2 HG02109.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.127-507_127-505del others(3): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150758484 | ||||||
chr1:150758634
|
G | C | 1 | a0002c0002t0002g0100 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.127-654C>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150758634 | ||||||
chr1:150758849
|
A | AT | 8 | a0001c0001t0001g0120a0001c0001t0001g0140a0001c0001t0001g0141others(5): Show | 8 | HG00738.hp2 HG02071.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-870dupA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150758849 | ||||||
chr1:150758894
|
G | A | 1 | a0001c0001t0017g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.127-914C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150758894 | ||||||
chr1:150758942
|
G | T | 1 | a0001c0001t0001g0206 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.127-962C>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150758942 | ||||||
chr1:150758983
|
G | A | 1 | a0002c0002t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.127-1003C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150758983 | ||||||
chr1:150759035
|
A | AT | 3 | a0001c0001t0003g0271a0001c0001t0015g0273a0002c0002t0003g0272 | 3 | HG02622.hp2 HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.127-1056dupA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150759035 | ||||||
chr1:150759037
|
TA | T | 85 | a0001c0001t0008g0103a0001c0001t0017g0279a0002c0002t0002g0002others(82): Show | 109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.127-1058delT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150759037 | ||||||
chr1:150759038
|
A | T | 36 | a0001c0001t0003g0013a0001c0001t0003g0034a0001c0001t0003g0035others(33): Show | 40 | HG00140.hp1 HG00735.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.127-1058T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150759038 | ||||||
chr1:150759041
|
T | A | 1 | a0001c0001t0001g0112 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.127-1061A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150759041 | ||||||
chr1:150759129
|
C | G | 13 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0130others(10): Show | 21 | HG00642.hp1 HG01071.hp1 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.127-1149G>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150759129 | ||||||
chr1:150759142
|
T | C | 86 | a0001c0001t0008g0103a0002c0002t0002g0002a0002c0002t0002g0004others(83): Show | 110 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.127-1162A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150759142 | ||||||
chr1:150759538
|
G | A | 1 | a0001c0001t0003g0268 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.127-1558C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150759538 | ||||||
chr1:150759597
|
A | G | 1 | a0001c0001t0003g0216 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.127-1617T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150759597 | ||||||
chr1:150759686
|
C | A | 1 | a0001c0001t0001g0129 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.127-1706G>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150759686 | ||||||
chr1:150759695
|
T | C | 13 | a0001c0001t0003g0001a0001c0001t0003g0014a0001c0001t0003g0032others(10): Show | 23 | HG00438.hp2 HG00621.hp2 HG02071.hp2 others(20): Show |
intron_variant | MODIFIER | c.127-1715A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150759695 | ||||||
chr1:150759811
|
C | A | 9 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0269others(6): Show | 11 | HG01433.hp2 HG02109.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-1831G>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150759811 | ||||||
chr1:150759822
|
G | C | 1 | a0001c0001t0016g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.127-1842C>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150759822 | ||||||
chr1:150760226
|
A | T | 1 | a0002c0002t0002g0054 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.127-2246T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150760226 | ||||||
chr1:150760241
|
A | C | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | NA19006.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.127-2261T>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150760241 | ||||||
chr1:150760249
|
C | T | 1 | a0002c0002t0002g0053 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.127-2269G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150760249 | ||||||
chr1:150760455
|
G | A | 1 | a0002c0002t0004g0045 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.127-2475C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150760455 | ||||||
chr1:150760507
|
G | A | 1 | a0001c0001t0017g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.127-2527C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150760507 | ||||||
chr1:150760569
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.127-2589C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150760569 | ||||||
chr1:150760880
|
C | CA | 17 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(14): Show | 19 | HG01433.hp2 HG02109.hp2 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.127-2901dupT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150760880 | ||||||
chr1:150760880
|
CA | C | 8 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0003g0216others(5): Show | 8 | HG01069.hp2 HG01167.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.127-2901delT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150760880 | ||||||
chr1:150760911
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.127-2931G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150760911 | ||||||
chr1:150760912
|
G | A | 1 | a0001c0001t0008g0103 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.127-2932C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150760912 | ||||||
chr1:150760940
|
G | A | 20 | a0001c0001t0003g0013a0001c0001t0003g0215a0001c0001t0003g0216others(17): Show | 22 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-2960C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150760940 | ||||||
chr1:150761048
|
G | A | 12 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0269others(9): Show | 14 | HG01433.hp2 HG02109.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.127-3068C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761048 | ||||||
chr1:150761101
|
C | T | 6 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(3): Show | 6 | HG00597.hp1 HG02027.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-3121G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761101 | ||||||
chr1:150761136
|
G | A | 1 | a0001c0001t0016g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.127-3156C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761136 | ||||||
chr1:150761173
|
C | G | 1 | a0001c0001t0001g0120 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.127-3193G>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761173 | ||||||
chr1:150761178
|
CA | C | 158 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(155): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.127-3199delT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761178 | ||||||
chr1:150761178
|
CAA | C | 92 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0003g0238others(89): Show | 116 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.127-3200_127-3199d others(4): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761178 | ||||||
chr1:150761266
|
A | G | 1 | a0001c0001t0003g0215 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.127-3286T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761266 | ||||||
chr1:150761329
|
GGAAAACA others(31): Show |
G | 1 | a0001c0001t0001g0198 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.126+3271_126+3308d others(40): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761329 | ||||||
chr1:150761561
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.126+3077C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761561 | ||||||
chr1:150761603
|
T | C | 28 | a0001c0001t0003g0001a0001c0001t0003g0014a0001c0001t0003g0032others(25): Show | 38 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.126+3035A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761603 | ||||||
chr1:150761735
|
A | G | 1 | a0001c0001t0003g0242 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.126+2903T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761735 | ||||||
chr1:150761739
|
CAAGAAAA others(8): Show |
C | 116 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(113): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.126+2884_126+2898d others(17): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761739 | ||||||
chr1:150761850
|
C | T | 1 | a0001c0001t0003g0270 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.126+2788G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761850 | ||||||
chr1:150761855
|
G | A | 1 | a0001c0001t0016g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.126+2783C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761855 | ||||||
chr1:150761960
|
A | G | 86 | a0001c0001t0008g0103a0002c0002t0002g0002a0002c0002t0002g0004others(83): Show | 110 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.126+2678T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761960 | ||||||
chr1:150762118
|
A | C | 1 | a0002c0002t0002g0050 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.126+2520T>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150762118 | ||||||
chr1:150762179
|
G | A | 86 | a0001c0001t0008g0103a0002c0002t0002g0002a0002c0002t0002g0004others(83): Show | 110 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.126+2459C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150762179 | ||||||
chr1:150762316
|
A | G | 1 | a0001c0001t0003g0278 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.126+2322T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150762316 | ||||||
chr1:150762373
|
G | GT | 5 | a0001c0001t0001g0202a0001c0001t0003g0241a0002c0002t0002g0048others(2): Show | 5 | HG01243.hp1 HG01358.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+2264dupA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150762373 | ||||||
chr1:150762901
|
C | G | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG02055.hp2 HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.126+1737G>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150762901 | ||||||
chr1:150762938
|
C | T | 3 | a0001c0001t0001g0114a0001c0001t0003g0034a0001c0001t0003g0269 | 4 | HG01433.hp2 HG02004.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+1700G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150762938 | ||||||
chr1:150763029
|
G | C | 1 | a0001c0001t0016g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.126+1609C>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150763029 | ||||||
chr1:150763104
|
TA | T | 90 | a0001c0001t0001g0113a0001c0001t0003g0238a0001c0001t0003g0239others(87): Show | 114 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.126+1533delT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150763104 | ||||||
chr1:150763350
|
A | T | 1 | a0002c0002t0002g0047 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.126+1288T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150763350 | ||||||
chr1:150763852
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.126+786G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150763852 | ||||||
chr1:150763886
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.126+752C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150763886 | ||||||
chr1:150764324
|
G | A | 20 | a0001c0001t0003g0013a0001c0001t0003g0215a0001c0001t0003g0216others(17): Show | 22 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+314C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150764324 | ||||||
chr1:150764331
|
C | T | 20 | a0001c0001t0003g0013a0001c0001t0003g0215a0001c0001t0003g0216others(17): Show | 22 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+307G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150764331 | ||||||
chr1:150764411
|
T | C | 1 | a0002c0002t0002g0106 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.126+227A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150764411 | ||||||
chr1:150764768
|
T | A | 1 | a0001c0001t0001g0201 | 1 | NA18971.hp2 | splice_region_variant&intron_variant | LOW | c.-1-4A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150764768 | ||||||
chr1:150764889
|
A | C | 1 | a0001c0001t0003g0278 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-1-125T>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150764889 | ||||||
chr1:150765089
|
T | TTCTC | 82 | a0001c0001t0008g0103a0001c0001t0016g0214a0002c0002t0002g0002others(79): Show | 106 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.-1-329_-1-326dupGA others(2): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150765089 | ||||||
chr1:150765101
|
C | CA | 6 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0003g0236others(3): Show | 6 | HG01433.hp1 HG02055.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-338dupT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150765101 | ||||||
chr1:150765101
|
C | CTCTCA | 3 | a0002c0002t0002g0107a0002c0002t0002g0108a0002c0002t0002g0109 | 3 | HG00735.hp2 HG01358.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.-1-338_-1-337insTG others(3): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150765101 | ||||||
chr1:150765102
|
A | C | 2 | a0002c0002t0002g0046a0002c0002t0004g0036 | 2 | HG02965.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.-1-338T>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150765102 | ||||||
chr1:150765210
|
A | G | 2 | a0002c0002t0004g0037a0002c0002t0004g0038 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-1-446T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150765210 | ||||||
chr1:150765269
|
G | C | 1 | a0001c0001t0014g0280 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-2+429C>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150765269 | ||||||
chr1:150765287
|
GT | G | 45 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(42): Show | 55 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.-2+410delA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150765287 | ||||||
chr1:150765300
|
T | C | 76 | a0001c0001t0008g0103a0002c0002t0002g0002a0002c0002t0002g0004others(73): Show | 100 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.-2+398A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150765300 | ||||||
chr1:150765300
|
T | TC | 24 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0269others(21): Show | 26 | HG01433.hp2 HG02109.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.-2+397_-2+398insG | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150765300 | ||||||
chr1:150765619
|
A | G | 1 | a0001c0001t0016g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-2+79T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150765619 | ||||||
chr1:150765696
|
A | ACGTGATA others(29): Show |
1 | a0001c0001t0003g0213 | 1 | NA18953.hp2 | splice_donor_variant&intron_variant | HIGH | c.-36_-2+1dupACTCTTA others(29): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150765696 |