geneid | 837 |
---|---|
ensemblid | ENSG00000196954.14 |
hgncid | 1505 |
symbol | CASP4 |
name | caspase 4 |
refseq_nuc | NM_001225.4 |
refseq_prot | NP_001216.1 |
ensembl_nuc | ENST00000444739.7 |
ensembl_prot | ENSP00000388566.2 |
mane_status | MANE Select |
chr | chr11 |
start | 104942866 |
end | 104968574 |
strand | - |
ver | v1.2 |
region | chr11:104942866-104968574 |
region5000 | chr11:104937866-104973574 |
regionname0 | CASP4_chr11_104942866_104968574 |
regionname5000 | CASP4_chr11_104937866_104973574 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 377 | 340 | 81 | 66 | 137 | 12 | 42 | 111 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0002 | 0/0 | 377 | 11 | 6 | 5 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0003 | 0/0 | 377 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0004 | 0/0 | 377 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0005 | 0/0 | 377 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1134 | 305 | 60 | 62 | 135 | 11 | 36 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
c0002 | 1/0 | 1134 | 20 | 18 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
c0003 | 0/0 | 1134 | 13 | 1 | 3 | 2 | 1 | 6 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
c0004 | 0/0 | 1134 | 9 | 6 | 3 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
c0005 | 0/0 | 1134 | 5 | 4 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
c0006 | 0/0 | 1134 | 2 | 0 | 2 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
c0007 | 0/0 | 1134 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
c0008 | 0/0 | 1134 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
c0009 | 0/0 | 1134 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
c0010 | 0/0 | 1134 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 163 | 323 | 72 | 65 | 137 | 11 | 36 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
t0002 | 0/0 | 163 | 19 | 8 | 3 | 1 | 1 | 6 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
t0003 | 0/0 | 163 | 9 | 6 | 3 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
t0004 | 0/0 | 163 | 3 | 3 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
t0005 | 0/0 | 163 | 3 | 2 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
t0006 | 0/0 | 163 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 28 | 0 | 7 | 17 | 2 | 2 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0002 | 0/0 | 21 | 1 | 5 | 11 | 1 | 3 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0005 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0006 | 0/0 | 6 | 0 | 2 | 2 | 1 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0008 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0009 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0012 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0013 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0015 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0016 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0020 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0023 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0024 | 1/0 | 3 | 1 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1134 | 305 | 60 | 62 | 135 | 11 | 36 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0001c0002 | 1/0 | 1134 | 20 | 18 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0001c0003 | 0/0 | 1134 | 13 | 1 | 3 | 2 | 1 | 6 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0001c0009 | 0/0 | 1134 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0001c0010 | 0/0 | 1134 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0002c0004 | 0/0 | 1134 | 9 | 6 | 3 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0002c0006 | 0/0 | 1134 | 2 | 0 | 2 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0003c0005 | 0/0 | 1134 | 5 | 4 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0004c0007 | 0/0 | 1134 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0005c0008 | 0/0 | 1134 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1296 | 292 | 48 | 61 | 135 | 11 | 36 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0001c0001t0002 | 0/0 | 1296 | 6 | 6 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0001c0001t0003 | 0/0 | 1296 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0001c0001t0004 | 0/0 | 1296 | 3 | 3 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0001c0001t0005 | 0/0 | 1296 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0001c0001t0006 | 0/0 | 1296 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0001c0002t0001 | 1/0 | 1296 | 19 | 17 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0001c0002t0002 | 0/0 | 1296 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0001c0003t0001 | 0/0 | 1296 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0001c0003t0002 | 0/0 | 1296 | 12 | 1 | 3 | 1 | 1 | 6 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0001c0009t0001 | 0/0 | 1296 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0001c0010t0001 | 0/0 | 1296 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0002c0004t0003 | 0/0 | 1296 | 7 | 4 | 3 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0002c0004t0005 | 0/0 | 1296 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0002c0006t0001 | 0/0 | 1296 | 2 | 0 | 2 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0003c0005t0001 | 0/0 | 1296 | 5 | 4 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0004c0007t0001 | 0/0 | 1296 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
a0005c0008t0001 | 0/0 | 1296 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | copy fasta | chr11 | 104937866 | 104973574 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 28 | 0 | 7 | 17 | 2 | 2 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0002 | 0/0 | 21 | 1 | 5 | 11 | 1 | 3 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0005 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0006 | 0/0 | 6 | 0 | 2 | 2 | 1 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0008 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0015 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0016 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0004g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0005g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0001t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0002t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0002t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0002t0001g0024 | 1/0 | 3 | 1 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0002t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0003t0002g0009 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0003t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0003t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0003t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0003t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0003t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0003t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0003t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0009t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0001c0010t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0002c0004t0003g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0002c0004t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0002c0004t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0002c0004t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0002c0004t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0002c0004t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0002c0004t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0002c0004t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0002c0006t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0003c0005t0001g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0003c0005t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0004c0007t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
a0005c0008t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | GBR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | FIN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | FIN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00323 | hp2 | a0001 | c0003 | t0002 | g0209 | EUR | FIN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00639 | hp2 | a0001 | c0003 | t0002 | g0009 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00738 | hp2 | a0002 | c0006 | t0001 | g0029 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01070 | hp2 | a0001 | c0001 | t0005 | g0202 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01099 | hp1 | a0002 | c0006 | t0001 | g0029 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01106 | hp1 | a0002 | c0004 | t0003 | g0030 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01106 | hp2 | a0001 | c0003 | t0002 | g0009 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01109 | hp1 | a0002 | c0004 | t0003 | g0056 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01175 | hp1 | a0002 | c0004 | t0003 | g0030 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01243 | hp2 | a0003 | c0005 | t0001 | g0010 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01496 | hp2 | a0001 | c0003 | t0002 | g0009 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0135 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02055 | hp2 | a0003 | c0005 | t0001 | g0010 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02132 | hp2 | a0001 | c0003 | t0002 | g0212 | EAS | KHV | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02165 | hp1 | a0001 | c0003 | t0001 | g0087 | EAS | CDX | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CDX | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0192 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0045 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0166 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02615 | hp1 | a0005 | c0008 | t0001 | g0142 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02622 | hp1 | a0002 | c0004 | t0003 | g0053 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0132 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0045 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0193 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0131 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02809 | hp1 | a0002 | c0004 | t0003 | g0058 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02809 | hp2 | a0001 | c0002 | t0002 | g0214 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02818 | hp2 | a0003 | c0005 | t0001 | g0010 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02922 | hp1 | a0003 | c0005 | t0001 | g0062 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02965 | hp2 | a0002 | c0004 | t0003 | g0057 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03017 | hp2 | a0001 | c0003 | t0002 | g0210 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | MSL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03195 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0165 | AFR | MSL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03225 | hp2 | a0002 | c0004 | t0005 | g0207 | AFR | MSL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03453 | hp2 | a0002 | c0004 | t0005 | g0213 | AFR | MSL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0216 | AFR | MSL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0198 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0191 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03540 | hp2 | a0001 | c0009 | t0001 | g0067 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | MSL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | STU | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | STU | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG04115 | hp1 | a0001 | c0003 | t0002 | g0009 | SAS | STU | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | STU | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | STU | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG04204 | hp2 | a0001 | c0003 | t0002 | g0009 | SAS | STU | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG04228 | hp1 | a0001 | c0003 | t0002 | g0208 | SAS | STU | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG04228 | hp2 | a0001 | c0003 | t0002 | g0211 | SAS | STU | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | YRI | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | YRI | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | YRI | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19085 | hp1 | a0004 | c0007 | t0001 | g0107 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0189 | AFR | YRI | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | YRI | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA20129 | hp2 | a0001 | c0003 | t0002 | g0206 | AFR | ASW | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | TSI | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | GIH | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA20905 | hp2 | a0001 | c0003 | t0002 | g0205 | SAS | GIH | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02559 | hp1 | a0002 | c0004 | t0003 | g0059 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | USA | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | USA | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA21309 | hp1 | a0003 | c0005 | t0001 | g0010 | AFR | LWK | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
NA21309 | hp2 | a0001 | c0010 | t0001 | g0047 | AFR | LWK | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0071 | REF | REF | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0024 | REF | REF | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:104947132
|
C | T | 1 | a0005 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.986G>A | p.Cys329Tyr | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/9 | 1035/1296 | 986/1134 | 329/377 | chr11 | 104947132 | ||
chr11:104948606
|
C | A | 1 | a0003 | 5 | HG01243.hp2 HG02055.hp2 HG02818.hp2 others(2): Show |
missense_variant | MODERATE | c.852G>T | p.Glu284Asp | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 6/9 | 901/1296 | 852/1134 | 284/377 | chr11 | 104948606 | ||
chr11:104948670
|
C | T | 1 | a0004 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.788G>A | p.Arg263His | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 6/9 | 837/1296 | 788/1134 | 263/377 | chr11 | 104948670 | ||
chr11:104954870
|
C | T | 1 | a0002 | 11 | HG00738.hp2 HG01099.hp1 HG01106.hp1 others(8): Show |
missense_variant | MODERATE | c.139G>A | p.Asp47Asn | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/9 | 188/1296 | 139/1134 | 47/377 | chr11 | 104954870 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:104948600
|
T | C | 8 | a0001c0001a0001c0003a0001c0009others(5): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
synonymous_variant | LOW | c.858A>G | p.Leu286Leu | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 6/9 | 907/1296 | 858/1134 | 286/377 | chr11 | 104948600 | ||
chr11:104949706
|
T | G | 1 | a0001c0009 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.618A>C | p.Val206Val | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/9 | 667/1296 | 618/1134 | 206/377 | chr11 | 104949706 | ||
chr11:104954871
|
G | A | 1 | a0001c0010 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.138C>T | p.Tyr46Tyr | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/9 | 187/1296 | 138/1134 | 46/377 | chr11 | 104954871 | ||
chr11:104954922
|
C | T | 1 | a0001c0003 | 13 | HG00323.hp2 HG00639.hp2 HG01106.hp2 others(10): Show |
synonymous_variant | LOW | c.87G>A | p.Leu29Leu | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/9 | 136/1296 | 87/1134 | 29/377 | chr11 | 104954922 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:104942869
|
G | A | 4 | a0001c0001t0003a0001c0001t0005a0002c0004t0003others(1): Show | 12 | HG01070.hp2 HG01106.hp1 HG01109.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*110C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 9/9 | 1884 | chr11 | 104942869 | |||||
chr11:104968537
|
T | A | 1 | a0001c0001t0004 | 3 | HG02451.hp2 HG02630.hp1 HG03516.hp2 |
5_prime_UTR_variant | MODIFIER | c.-12A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/9 | 12 | chr11 | 104968537 | |||||
chr11:104968573
|
G | A | 1 | a0001c0001t0006 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-48C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/9 | 48 | chr11 | 104968573 | |||||
chr11:104968573
|
G | C | 5 | a0001c0001t0002a0001c0001t0005a0001c0002t0002others(2): Show | 22 | HG00323.hp2 HG00639.hp2 HG01070.hp2 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-48C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/9 | 48 | chr11 | 104968573 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:104943004
|
G | A | 1 | a0001c0001t0001g0031 | 2 | HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.*6-31C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943004 | ||||||
chr11:104943055
|
C | G | 1 | a0001c0001t0001g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.*6-82G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943055 | ||||||
chr11:104943160
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.*6-187G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943160 | ||||||
chr11:104943247
|
G | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG00099.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.*6-274C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943247 | ||||||
chr11:104943303
|
G | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0027others(3): Show | 14 | HG00621.hp2 HG02486.hp1 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.*6-330C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943303 | ||||||
chr11:104943480
|
G | C | 1 | a0001c0001t0001g0180 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.*6-507C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943480 | ||||||
chr11:104943559
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.*6-586A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943559 | ||||||
chr11:104943574
|
C | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(188): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.*6-601G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943574 | ||||||
chr11:104943686
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.*6-713C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943686 | ||||||
chr11:104943748
|
A | G | 10 | a0001c0001t0003g0078a0001c0001t0005g0202a0002c0004t0003g0030others(7): Show | 11 | HG01070.hp2 HG01106.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.*6-775T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943748 | ||||||
chr11:104943796
|
T | C | 2 | a0001c0001t0001g0069a0001c0001t0001g0077 | 2 | HG01099.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.*6-823A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943796 | ||||||
chr11:104943811
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0101 | 2 | HG01256.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.*6-838T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943811 | ||||||
chr11:104943836
|
C | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0095 | 3 | HG02165.hp2 NA19062.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.*6-863G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943836 | ||||||
chr11:104943989
|
C | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.*5+759G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943989 | ||||||
chr11:104944005
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0002g0204 | 2 | HG02895.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.*5+743G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944005 | ||||||
chr11:104944344
|
G | GTCTCTC | 4 | a0002c0004t0003g0030a0002c0004t0003g0053a0002c0004t0003g0056others(1): Show | 5 | HG01106.hp1 HG01109.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.*5+398_*5+403dupGA others(4): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944344 | ||||||
chr11:104944344
|
GTC | G | 38 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(35): Show | 63 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.*5+402_*5+403delGA | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944344 | ||||||
chr11:104944358
|
CTCTCTCT others(7): Show |
C | 1 | a0001c0001t0001g0114 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.*5+376_*5+389delCA others(12): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944358 | ||||||
chr11:104944366
|
C | CTG | 32 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0026others(29): Show | 48 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.*5+381_*5+382insCA | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944366 | ||||||
chr11:104944366
|
C | CTGTG | 5 | a0001c0001t0001g0048a0001c0001t0001g0109a0001c0001t0002g0204others(2): Show | 5 | HG00673.hp2 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.*5+381_*5+382insCA others(2): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944366 | ||||||
chr11:104944366
|
C | G | 1 | a0001c0002t0001g0189 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.*5+382G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944366 | ||||||
chr11:104944368
|
C | CTCTCTCT others(11): Show |
1 | a0001c0001t0003g0063 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.*5+379_*5+380insCA others(16): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944368 | ||||||
chr11:104944368
|
C | CTCTCTCT others(1): Show |
5 | a0001c0001t0003g0078a0001c0001t0005g0202a0002c0004t0003g0057others(2): Show | 5 | HG01070.hp2 HG01891.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.*5+379_*5+380insCA others(6): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944368 | ||||||
chr11:104944368
|
C | CTCTG | 3 | a0001c0002t0001g0165a0001c0002t0001g0191a0001c0002t0001g0192 | 3 | HG02258.hp2 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.*5+379_*5+380insCA others(2): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944368 | ||||||
chr11:104944368
|
C | CTG | 3 | a0001c0002t0001g0131a0001c0002t0001g0132a0002c0006t0001g0029 | 4 | HG00738.hp2 HG01099.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.*5+378_*5+379dupCA | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944368 | ||||||
chr11:104944368
|
C | CTGTG | 3 | a0001c0002t0001g0014a0001c0002t0001g0017a0001c0002t0001g0135 | 8 | HG01884.hp1 HG02055.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.*5+376_*5+379dupCA others(2): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944368 | ||||||
chr11:104944368
|
C | G | 41 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0026others(38): Show | 57 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.*5+380G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944368 | ||||||
chr11:104944368
|
CTG | C | 11 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0054others(8): Show | 13 | HG01433.hp2 HG01891.hp2 HG03704.hp1 others(10): Show |
intron_variant | MODIFIER | c.*5+378_*5+379delCA | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944368 | ||||||
chr11:104944368
|
CTGTG | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.*5+376_*5+379delCA others(2): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944368 | ||||||
chr11:104944370
|
G | C | 2 | a0001c0001t0001g0039a0001c0001t0001g0168 | 3 | HG02647.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.*5+378C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944370 | ||||||
chr11:104944372
|
G | C | 3 | a0001c0001t0001g0040a0001c0001t0001g0102a0001c0001t0001g0194 | 4 | NA18982.hp1 NA19005.hp2 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.*5+376C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944372 | ||||||
chr11:104944374
|
G | C | 6 | a0001c0001t0001g0060a0001c0001t0001g0103a0001c0001t0001g0106others(3): Show | 6 | HG01993.hp2 HG02572.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.*5+374C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944374 | ||||||
chr11:104944444
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.*5+304T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944444 | ||||||
chr11:104944518
|
C | A | 37 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0026others(34): Show | 53 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.*5+230G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944518 | ||||||
chr11:104944618
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0038 | 4 | HG01891.hp2 HG03239.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.*5+130G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944618 | ||||||
chr11:104944621
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.*5+127G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944621 | ||||||
chr11:104944645
|
A | G | 5 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0134others(2): Show | 11 | HG00408.hp2 NA18941.hp2 NA18975.hp1 others(8): Show |
intron_variant | MODIFIER | c.*5+103T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944645 | ||||||
chr11:104944968
|
C | A | 1 | a0001c0001t0001g0044 | 2 | HG00733.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1036-117G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104944968 | ||||||
chr11:104945041
|
T | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1036-190A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945041 | ||||||
chr11:104945056
|
T | G | 1 | a0001c0001t0001g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1036-205A>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945056 | ||||||
chr11:104945072
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1036-221T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945072 | ||||||
chr11:104945209
|
A | T | 1 | a0001c0001t0001g0038 | 2 | HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1036-358T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945209 | ||||||
chr11:104945252
|
C | CTT | 10 | a0001c0001t0003g0063a0001c0001t0003g0078a0001c0001t0005g0202others(7): Show | 11 | HG01070.hp2 HG01106.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1036-403_1036-402d others(4): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945252 | ||||||
chr11:104945252
|
CTTT | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1036-404_1036-402d others(5): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945252 | ||||||
chr11:104945252
|
CTTTT | C | 9 | a0001c0001t0001g0039a0001c0001t0001g0079a0001c0001t0001g0096others(6): Show | 10 | HG01169.hp1 HG01256.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1036-405_1036-402d others(6): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945252 | ||||||
chr11:104945293
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1036-442G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945293 | ||||||
chr11:104945309
|
A | G | 10 | a0001c0001t0003g0078a0001c0001t0005g0202a0002c0004t0003g0030others(7): Show | 11 | HG01070.hp2 HG01106.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1036-458T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945309 | ||||||
chr11:104945546
|
G | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(188): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.1036-695C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945546 | ||||||
chr11:104945595
|
T | G | 1 | a0001c0001t0002g0215 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1036-744A>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945595 | ||||||
chr11:104945599
|
A | G | 1 | a0001c0001t0001g0031 | 2 | HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1036-748T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945599 | ||||||
chr11:104945634
|
C | T | 1 | a0001c0001t0001g0034 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1036-783G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945634 | ||||||
chr11:104945647
|
G | T | 1 | a0001c0002t0001g0191 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1036-796C>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945647 | ||||||
chr11:104945798
|
T | G | 1 | a0001c0001t0001g0104 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1036-947A>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945798 | ||||||
chr11:104945832
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1036-981A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945832 | ||||||
chr11:104945851
|
C | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(211): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1036-1000G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945851 | ||||||
chr11:104945926
|
A | C | 1 | a0001c0001t0001g0157 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1036-1075T>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945926 | ||||||
chr11:104945932
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1036-1081G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945932 | ||||||
chr11:104945956
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG02451.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1036-1105G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945956 | ||||||
chr11:104945994
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1035+1089T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945994 | ||||||
chr11:104946040
|
T | G | 1 | a0001c0001t0001g0144 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1035+1043A>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104946040 | ||||||
chr11:104946190
|
T | C | 41 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0026others(38): Show | 58 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.1035+893A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104946190 | ||||||
chr11:104946530
|
T | C | 10 | a0001c0001t0003g0078a0001c0001t0005g0202a0002c0004t0003g0030others(7): Show | 11 | HG01070.hp2 HG01106.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1035+553A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104946530 | ||||||
chr11:104946696
|
C | G | 1 | a0001c0001t0003g0063 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1035+387G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104946696 | ||||||
chr11:104946710
|
C | A | 1 | a0001c0001t0001g0177 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1035+373G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104946710 | ||||||
chr11:104946754
|
C | T | 1 | a0001c0001t0001g0031 | 2 | HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1035+329G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104946754 | ||||||
chr11:104946771
|
C | T | 37 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(34): Show | 62 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1035+312G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104946771 | ||||||
chr11:104947566
|
A | G | 38 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(35): Show | 63 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.926-374T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 6/8 | chr11 | 104947566 | ||||||
chr11:104947584
|
A | C | 1 | a0001c0001t0001g0054 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.926-392T>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 6/8 | chr11 | 104947584 | ||||||
chr11:104947643
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0038 | 4 | HG01891.hp2 HG03239.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-451T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 6/8 | chr11 | 104947643 | ||||||
chr11:104947734
|
G | A | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(211): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.926-542C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 6/8 | chr11 | 104947734 | ||||||
chr11:104947863
|
C | A | 3 | a0001c0001t0001g0167a0001c0001t0002g0199a0001c0001t0002g0200 | 3 | HG02965.hp1 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.925+670G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 6/8 | chr11 | 104947863 | ||||||
chr11:104948103
|
T | C | 1 | a0002c0004t0003g0056 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.925+430A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 6/8 | chr11 | 104948103 | ||||||
chr11:104948195
|
G | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(188): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.925+338C>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 6/8 | chr11 | 104948195 | ||||||
chr11:104948300
|
A | G | 1 | a0001c0001t0001g0188 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.925+233T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 6/8 | chr11 | 104948300 | ||||||
chr11:104948389
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.925+144C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 6/8 | chr11 | 104948389 | ||||||
chr11:104948708
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.782-32C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104948708 | ||||||
chr11:104948798
|
A | T | 1 | a0004c0007t0001g0107 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.782-122T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104948798 | ||||||
chr11:104948815
|
G | GAAACAGA others(1): Show |
182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.782-140_782-139ins others(8): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104948815 | ||||||
chr11:104948815
|
G | GAAACAGA others(3): Show |
8 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0064others(5): Show | 20 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.782-140_782-139ins others(10): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104948815 | ||||||
chr11:104948817
|
G | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(187): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.782-141C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104948817 | ||||||
chr11:104948817
|
G | GACACAC | 11 | a0001c0002t0001g0014a0001c0002t0001g0131a0001c0002t0001g0132others(8): Show | 15 | HG00738.hp2 HG01099.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.782-142_782-141ins others(6): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104948817 | ||||||
chr11:104948817
|
G | GACACACA others(1): Show |
1 | a0001c0002t0001g0017 | 3 | HG03098.hp1 HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.782-142_782-141ins others(8): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104948817 | ||||||
chr11:104948819
|
G | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(211): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.782-143C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104948819 | ||||||
chr11:104948837
|
C | CACACA | 7 | a0001c0001t0003g0078a0001c0001t0005g0202a0002c0004t0003g0053others(4): Show | 7 | HG01070.hp2 HG01109.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.782-162_782-161ins others(5): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104948837 | ||||||
chr11:104948862
|
T | C | 41 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0026others(38): Show | 58 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.782-186A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104948862 | ||||||
chr11:104948988
|
A | T | 1 | a0001c0001t0003g0063 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.782-312T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104948988 | ||||||
chr11:104949039
|
C | G | 1 | a0001c0001t0003g0063 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.782-363G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104949039 | ||||||
chr11:104949210
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.781+333G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104949210 | ||||||
chr11:104949298
|
G | C | 1 | a0001c0001t0001g0185 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.781+245C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104949298 | ||||||
chr11:104949320
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.781+223G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104949320 | ||||||
chr11:104949330
|
TTACTGTG others(2): Show |
T | 9 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0035others(6): Show | 20 | HG00609.hp1 HG00609.hp2 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.781+204_781+212del others(9): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104949330 | ||||||
chr11:104949436
|
A | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(188): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.781+107T>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104949436 | ||||||
chr11:104949481
|
C | G | 1 | a0001c0001t0001g0150 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.781+62G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104949481 | ||||||
chr11:104950026
|
A | G | 3 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0197 | 3 | HG00741.hp1 HG01346.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.547-249T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950026 | ||||||
chr11:104950158
|
A | G | 1 | a0001c0001t0001g0038 | 2 | HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.547-381T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950158 | ||||||
chr11:104950219
|
CTT | C | 12 | a0001c0002t0001g0014a0001c0002t0001g0017a0001c0002t0001g0131others(9): Show | 18 | HG00738.hp2 HG01099.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.547-444_547-443del others(2): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950219 | ||||||
chr11:104950232
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.547-455C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950232 | ||||||
chr11:104950481
|
T | C | 2 | a0003c0005t0001g0010a0003c0005t0001g0062 | 5 | HG01243.hp2 HG02055.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.546+444A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950481 | ||||||
chr11:104950545
|
C | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(61): Show | 117 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.546+380G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950545 | ||||||
chr11:104950647
|
T | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(188): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.546+278A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950647 | ||||||
chr11:104950649
|
C | T | 1 | a0001c0001t0001g0031 | 2 | HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.546+276G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950649 | ||||||
chr11:104950797
|
T | TACAC | 6 | a0001c0001t0001g0100a0001c0001t0001g0176a0001c0001t0001g0177others(3): Show | 6 | HG02132.hp2 HG03017.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.546+124_546+127dup others(4): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950797 | ||||||
chr11:104950797
|
T | TACACAC | 59 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(56): Show | 105 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.546+122_546+127dup others(6): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950797 | ||||||
chr11:104950797
|
T | TACACACA others(1): Show |
78 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(75): Show | 145 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.546+120_546+127dup others(8): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950797 | ||||||
chr11:104950797
|
T | TACACACA others(3): Show |
14 | a0001c0001t0001g0071a0001c0001t0001g0081a0001c0001t0001g0091others(11): Show | 14 | HG02027.hp1 HG02698.hp2 HG02738.hp1 others(11): Show |
intron_variant | MODIFIER | c.546+118_546+127dup others(10): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950797 | ||||||
chr11:104950797
|
T | TACACACA others(5): Show |
23 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(20): Show | 41 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.546+116_546+127dup others(12): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950797 | ||||||
chr11:104950797
|
T | TACACACA others(7): Show |
4 | a0001c0001t0001g0039a0001c0001t0001g0082a0001c0001t0001g0128others(1): Show | 5 | HG00558.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.546+114_546+127dup others(14): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950797 | ||||||
chr11:104950797
|
T | TACACACA others(9): Show |
1 | a0001c0001t0001g0089 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.546+112_546+127dup others(16): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950797 | ||||||
chr11:104950797
|
TAC | T | 18 | a0001c0001t0003g0078a0001c0001t0005g0202a0001c0002t0001g0014others(15): Show | 24 | HG01070.hp2 HG01106.hp1 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.546+126_546+127del others(2): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950797 | ||||||
chr11:104950797
|
TACAC | T | 3 | a0001c0002t0001g0131a0001c0002t0001g0132a0002c0006t0001g0029 | 4 | HG00738.hp2 HG01099.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+124_546+127del others(4): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950797 | ||||||
chr11:104950801
|
C | A | 1 | a0001c0001t0001g0159 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.546+124G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950801 | ||||||
chr11:104950823
|
C | CACACACA others(6): Show |
1 | a0001c0001t0001g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.546+101_546+102ins others(13): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950823 | ||||||
chr11:104950907
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.546+18G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950907 | ||||||
chr11:104950908
|
G | A | 1 | a0001c0001t0001g0033 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.546+17C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950908 | ||||||
chr11:104951305
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(186): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.373-207T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 3/8 | chr11 | 104951305 | ||||||
chr11:104951316
|
GCCTTTTC others(5): Show |
G | 3 | a0001c0001t0001g0167a0001c0001t0002g0199a0001c0001t0002g0200 | 3 | HG02965.hp1 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.373-230_373-219del others(12): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 3/8 | chr11 | 104951316 | ||||||
chr11:104951425
|
T | C | 3 | a0001c0002t0001g0131a0001c0002t0001g0132a0002c0006t0001g0029 | 4 | HG00738.hp2 HG01099.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-327A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 3/8 | chr11 | 104951425 | ||||||
chr11:104951450
|
C | T | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(149): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.373-352G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 3/8 | chr11 | 104951450 | ||||||
chr11:104951451
|
G | A | 9 | a0001c0001t0003g0078a0001c0001t0005g0202a0002c0004t0003g0030others(6): Show | 10 | HG01070.hp2 HG01106.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.373-353C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 3/8 | chr11 | 104951451 | ||||||
chr11:104951511
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.372+385A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 3/8 | chr11 | 104951511 | ||||||
chr11:104952074
|
C | T | 1 | a0002c0006t0001g0029 | 2 | HG00738.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.263-69G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952074 | ||||||
chr11:104952175
|
G | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0027others(3): Show | 14 | HG00621.hp2 HG02486.hp1 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.263-170C>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952175 | ||||||
chr11:104952264
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.263-259G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952264 | ||||||
chr11:104952273
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.263-268A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952273 | ||||||
chr11:104952580
|
CAAAATCC others(49): Show |
C | 1 | a0001c0001t0001g0050 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.263-631_263-576del others(56): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952580 | ||||||
chr11:104952641
|
A | T | 1 | a0001c0001t0001g0050 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.263-636T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952641 | ||||||
chr11:104952658
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0171a0001c0001t0001g0174 | 5 | HG01175.hp2 HG01934.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.263-653G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952658 | ||||||
chr11:104952693
|
T | TTTTTTTT others(48): Show |
1 | a0001c0001t0001g0050 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.263-689_263-688ins others(55): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952693 | ||||||
chr11:104952746
|
A | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0027others(6): Show | 18 | HG00621.hp2 HG01891.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.263-741T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952746 | ||||||
chr11:104952790
|
C | G | 6 | a0001c0001t0001g0091a0001c0001t0001g0097a0001c0001t0001g0098others(3): Show | 6 | HG01192.hp2 HG01261.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.263-785G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952790 | ||||||
chr11:104952886
|
A | T | 1 | a0001c0009t0001g0067 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.263-881T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952886 | ||||||
chr11:104952940
|
G | A | 3 | a0001c0001t0001g0046a0001c0001t0001g0061a0001c0002t0001g0017 | 5 | HG03098.hp1 HG03130.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.263-935C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952940 | ||||||
chr11:104952976
|
A | G | 1 | a0001c0001t0003g0063 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.263-971T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952976 | ||||||
chr11:104953070
|
T | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0061a0001c0002t0001g0017 | 5 | HG03098.hp1 HG03130.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.263-1065A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104953070 | ||||||
chr11:104953110
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.263-1105G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104953110 | ||||||
chr11:104953469
|
A | G | 6 | a0001c0001t0001g0038a0001c0001t0002g0199a0001c0001t0002g0200others(3): Show | 7 | HG01070.hp2 HG01891.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.262+1278T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104953469 | ||||||
chr11:104953578
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.262+1169A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104953578 | ||||||
chr11:104953646
|
C | G | 1 | a0001c0001t0001g0167 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.262+1101G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104953646 | ||||||
chr11:104953653
|
G | C | 3 | a0001c0001t0001g0039a0001c0001t0001g0167a0001c0001t0001g0168 | 4 | HG02647.hp1 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.262+1094C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104953653 | ||||||
chr11:104953676
|
T | A | 3 | a0001c0001t0001g0038a0001c0001t0002g0199a0001c0001t0002g0200 | 4 | HG01891.hp2 HG02965.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.262+1071A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104953676 | ||||||
chr11:104953753
|
T | A | 1 | a0001c0001t0001g0110 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.262+994A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104953753 | ||||||
chr11:104953755
|
C | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0002t0002g0214 | 3 | HG02451.hp1 HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.262+992G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104953755 | ||||||
chr11:104953758
|
G | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0002t0002g0214 | 3 | HG02451.hp1 HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.262+989C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104953758 | ||||||
chr11:104953792
|
A | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0130 | 3 | NA18953.hp2 NA18982.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.262+955T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104953792 | ||||||
chr11:104953896
|
T | A | 2 | a0001c0002t0001g0165a0001c0002t0001g0166 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.262+851A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104953896 | ||||||
chr11:104954120
|
G | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(151): Show | 249 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.262+627C>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104954120 | ||||||
chr11:104954139
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.262+608C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104954139 | ||||||
chr11:104954200
|
T | C | 1 | a0001c0001t0001g0190 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.262+547A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104954200 | ||||||
chr11:104954396
|
T | C | 1 | a0001c0001t0003g0078 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.262+351A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104954396 | ||||||
chr11:104954465
|
A | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(101): Show | 177 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.262+282T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104954465 | ||||||
chr11:104954482
|
T | G | 3 | a0001c0001t0001g0028a0001c0001t0001g0048a0001c0001t0001g0055 | 4 | HG02280.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.262+265A>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104954482 | ||||||
chr11:104954521
|
A | G | 3 | a0001c0001t0001g0039a0001c0001t0001g0167a0001c0001t0001g0168 | 4 | HG02647.hp1 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.262+226T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104954521 | ||||||
chr11:104954742
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG03579.hp1 | splice_region_variant&intron_variant | LOW | c.262+5G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104954742 | ||||||
chr11:104955164
|
C | G | 3 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0005g0202 | 3 | HG01070.hp2 HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.8-163G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104955164 | ||||||
chr11:104955247
|
A | G | 6 | a0001c0001t0001g0038a0001c0001t0002g0199a0001c0001t0002g0200others(3): Show | 7 | HG01070.hp2 HG01891.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-246T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104955247 | ||||||
chr11:104955348
|
C | G | 44 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0025others(41): Show | 65 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.8-347G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104955348 | ||||||
chr11:104955379
|
C | G | 2 | a0001c0001t0001g0156a0001c0001t0001g0160 | 2 | NA18966.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.8-378G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104955379 | ||||||
chr11:104955565
|
ATAAAT | A | 104 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(101): Show | 177 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.8-569_8-565delATTT others(1): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104955565 | ||||||
chr11:104955877
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.8-876T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104955877 | ||||||
chr11:104955897
|
G | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 263 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.8-896C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104955897 | ||||||
chr11:104955999
|
C | T | 10 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0137others(7): Show | 13 | HG02056.hp2 HG03490.hp1 NA18963.hp1 others(10): Show |
intron_variant | MODIFIER | c.8-998G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104955999 | ||||||
chr11:104956102
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.8-1101A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104956102 | ||||||
chr11:104956229
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.8-1228C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104956229 | ||||||
chr11:104956431
|
C | T | 1 | a0001c0002t0001g0131 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.8-1430G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104956431 | ||||||
chr11:104956454
|
T | C | 5 | a0001c0001t0001g0005a0001c0001t0001g0064a0001c0001t0001g0161others(2): Show | 14 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.8-1453A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104956454 | ||||||
chr11:104956490
|
T | A | 3 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193 | 3 | HG02258.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.8-1489A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104956490 | ||||||
chr11:104956815
|
G | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0002t0002g0214 | 3 | HG02451.hp1 HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.8-1814C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104956815 | ||||||
chr11:104956855
|
T | C | 3 | a0001c0001t0001g0038a0001c0001t0002g0199a0001c0001t0002g0200 | 4 | HG01891.hp2 HG02965.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-1854A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104956855 | ||||||
chr11:104956985
|
C | A | 1 | a0001c0001t0001g0151 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.8-1984G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104956985 | ||||||
chr11:104957116
|
G | T | 1 | a0001c0001t0001g0038 | 2 | HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.8-2115C>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957116 | ||||||
chr11:104957148
|
C | T | 3 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0096 | 3 | HG00621.hp1 HG02165.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.8-2147G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957148 | ||||||
chr11:104957176
|
T | C | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG02451.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.8-2175A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957176 | ||||||
chr11:104957177
|
C | A | 1 | a0001c0001t0001g0074 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.8-2176G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957177 | ||||||
chr11:104957242
|
G | GTAGTGTT others(30): Show |
1 | a0001c0001t0001g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-2278_8-2242dupTT others(35): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957242 | ||||||
chr11:104957334
|
G | A | 24 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0028others(21): Show | 39 | HG01243.hp2 HG01433.hp2 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.8-2333C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957334 | ||||||
chr11:104957369
|
A | C | 33 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0025others(30): Show | 52 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.8-2368T>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957369 | ||||||
chr11:104957380
|
G | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(56): Show | 110 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.8-2379C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957380 | ||||||
chr11:104957452
|
G | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0060a0001c0001t0001g0066others(14): Show | 22 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.8-2451C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957452 | ||||||
chr11:104957472
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.8-2471A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957472 | ||||||
chr11:104957518
|
GCTATAAT others(7): Show |
G | 4 | a0001c0001t0001g0031a0001c0001t0001g0046a0001c0001t0001g0061others(1): Show | 7 | HG03098.hp1 HG03130.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-2531_8-2518delTG others(12): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957518 | ||||||
chr11:104957579
|
A | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(104): Show | 180 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.8-2578T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957579 | ||||||
chr11:104957804
|
C | CA | 3 | a0001c0001t0001g0122a0001c0001t0001g0149a0001c0001t0001g0150 | 3 | HG02027.hp1 HG04184.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.8-2804dupT | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957804 | ||||||
chr11:104957806
|
C | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(144): Show | 241 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.8-2805G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957806 | ||||||
chr11:104957857
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0064a0001c0001t0001g0161others(2): Show | 14 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.8-2856C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957857 | ||||||
chr11:104957906
|
A | G | 8 | a0002c0004t0003g0030a0002c0004t0003g0053a0002c0004t0003g0056others(5): Show | 10 | HG00738.hp2 HG01099.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.8-2905T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957906 | ||||||
chr11:104958010
|
T | C | 28 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0031others(25): Show | 45 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.8-3009A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958010 | ||||||
chr11:104958044
|
A | G | 3 | a0001c0001t0001g0028a0001c0001t0001g0048a0001c0001t0001g0055 | 4 | HG02280.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-3043T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958044 | ||||||
chr11:104958128
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.8-3127T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958128 | ||||||
chr11:104958226
|
G | A | 145 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.8-3225C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958226 | ||||||
chr11:104958435
|
A | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 225 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.8-3434T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958435 | ||||||
chr11:104958698
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.8-3697G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958698 | ||||||
chr11:104958757
|
T | A | 1 | a0001c0001t0001g0031 | 2 | HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.8-3756A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958757 | ||||||
chr11:104958822
|
G | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0002t0002g0214 | 3 | HG02451.hp1 HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.8-3821C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958822 | ||||||
chr11:104958833
|
C | T | 24 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0060others(21): Show | 38 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.8-3832G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958833 | ||||||
chr11:104958842
|
T | A | 1 | a0001c0010t0001g0047 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.8-3841A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958842 | ||||||
chr11:104958911
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.8-3910T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958911 | ||||||
chr11:104958960
|
C | CA | 10 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0043others(7): Show | 16 | HG00423.hp1 HG00609.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.8-3960dupT | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958960 | ||||||
chr11:104958960
|
C | CAA | 8 | a0001c0003t0001g0087a0001c0003t0002g0009a0001c0003t0002g0205others(5): Show | 13 | HG00639.hp2 HG00738.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.8-3961_8-3960dupTT | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958960 | ||||||
chr11:104958960
|
CA | C | 11 | a0001c0001t0001g0038a0001c0001t0001g0052a0001c0001t0001g0055others(8): Show | 12 | HG01070.hp2 HG01169.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.8-3960delT | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958960 | ||||||
chr11:104958960
|
CAA | C | 16 | a0001c0001t0001g0019a0001c0001t0001g0051a0001c0001t0001g0089others(13): Show | 18 | HG01952.hp2 HG02055.hp1 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.8-3961_8-3960delTT | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958960 | ||||||
chr11:104958960
|
CAAA | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(75): Show | 148 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.8-3962_8-3960delTT others(1): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958960 | ||||||
chr11:104958960
|
CAAAA | C | 29 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0026others(26): Show | 46 | HG00140.hp2 HG00735.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.8-3963_8-3960delTT others(2): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958960 | ||||||
chr11:104958960
|
CAAAAAAA | C | 6 | a0002c0004t0003g0030a0002c0004t0003g0053a0002c0004t0003g0057others(3): Show | 7 | HG01106.hp1 HG01175.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-3966_8-3960delTT others(5): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958960 | ||||||
chr11:104958960
|
CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0039a0001c0001t0001g0167a0001c0001t0001g0168 | 4 | HG02647.hp1 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-3969_8-3960delTT others(8): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958960 | ||||||
chr11:104958984
|
A | G | 2 | a0001c0001t0002g0199a0001c0001t0002g0200 | 2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.8-3983T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958984 | ||||||
chr11:104959193
|
T | C | 33 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0038others(30): Show | 42 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.8-4192A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959193 | ||||||
chr11:104959259
|
T | A | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-4258A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959259 | ||||||
chr11:104959316
|
A | T | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-4315T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959316 | ||||||
chr11:104959324
|
A | T | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-4323T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959324 | ||||||
chr11:104959329
|
A | T | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-4328T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959329 | ||||||
chr11:104959333
|
CAGGCACC others(22): Show |
C | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-4361_8-4333delAT others(27): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959333 | ||||||
chr11:104959365
|
C | A | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-4364G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959365 | ||||||
chr11:104959366
|
A | T | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-4365T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959366 | ||||||
chr11:104959367
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-4366G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959367 | ||||||
chr11:104959368
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-4367A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959368 | ||||||
chr11:104959370
|
A | T | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-4369T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959370 | ||||||
chr11:104959372
|
A | T | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-4371T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959372 | ||||||
chr11:104959382
|
T | C | 28 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0031others(25): Show | 45 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.8-4381A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959382 | ||||||
chr11:104959414
|
G | A | 30 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(27): Show | 40 | HG01081.hp2 HG01243.hp1 HG02027.hp1 others(37): Show |
intron_variant | MODIFIER | c.8-4413C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959414 | ||||||
chr11:104959532
|
A | C | 3 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0005g0202 | 3 | HG01070.hp2 HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.8-4531T>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959532 | ||||||
chr11:104959542
|
T | G | 3 | a0001c0001t0001g0038a0001c0001t0002g0199a0001c0001t0002g0200 | 4 | HG01891.hp2 HG02965.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-4541A>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959542 | ||||||
chr11:104959734
|
A | T | 2 | a0003c0005t0001g0010a0003c0005t0001g0062 | 5 | HG01243.hp2 HG02055.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.8-4733T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959734 | ||||||
chr11:104959800
|
T | A | 28 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0031others(25): Show | 45 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.8-4799A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959800 | ||||||
chr11:104959827
|
G | A | 7 | a0002c0004t0003g0030a0002c0004t0003g0053a0002c0004t0003g0056others(4): Show | 8 | HG01106.hp1 HG01109.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.8-4826C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959827 | ||||||
chr11:104959864
|
C | A | 3 | a0001c0001t0001g0038a0001c0001t0002g0199a0001c0001t0002g0200 | 4 | HG01891.hp2 HG02965.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-4863G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959864 | ||||||
chr11:104959886
|
C | G | 1 | a0001c0001t0001g0090 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.8-4885G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959886 | ||||||
chr11:104959947
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.8-4946G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959947 | ||||||
chr11:104959948
|
G | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0002t0002g0214 | 3 | HG02451.hp1 HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.8-4947C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959948 | ||||||
chr11:104959980
|
G | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0064a0001c0001t0001g0083others(4): Show | 16 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.8-4979C>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959980 | ||||||
chr11:104960074
|
C | T | 1 | a0001c0001t0001g0170 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.8-5073G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960074 | ||||||
chr11:104960088
|
C | A | 1 | a0001c0001t0001g0031 | 2 | HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.8-5087G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960088 | ||||||
chr11:104960111
|
G | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 246 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.8-5110C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960111 | ||||||
chr11:104960115
|
A | G | 17 | a0001c0001t0001g0006a0001c0001t0001g0060a0001c0001t0001g0066others(14): Show | 22 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.8-5114T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960115 | ||||||
chr11:104960168
|
T | C | 1 | a0001c0001t0001g0061 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.8-5167A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960168 | ||||||
chr11:104960332
|
T | C | 4 | a0001c0001t0001g0031a0001c0001t0001g0046a0001c0001t0001g0061others(1): Show | 7 | HG03098.hp1 HG03130.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-5331A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960332 | ||||||
chr11:104960412
|
C | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0027others(5): Show | 16 | HG00621.hp2 HG02145.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.8-5411G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960412 | ||||||
chr11:104960445
|
AT | A | 7 | a0002c0004t0003g0030a0002c0004t0003g0053a0002c0004t0003g0056others(4): Show | 8 | HG01106.hp1 HG01109.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.8-5445delA | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960445 | ||||||
chr11:104960623
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.8-5622G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960623 | ||||||
chr11:104960626
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.8-5625G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960626 | ||||||
chr11:104960775
|
T | A | 1 | a0001c0001t0001g0125 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.8-5774A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960775 | ||||||
chr11:104960807
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0089a0001c0001t0001g0128others(1): Show | 11 | HG00558.hp2 HG00609.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.8-5806G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960807 | ||||||
chr11:104960808
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0089a0001c0001t0001g0128others(1): Show | 11 | HG00558.hp2 HG00609.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.8-5807G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960808 | ||||||
chr11:104960811
|
C | A | 1 | a0001c0001t0001g0152 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.8-5810G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960811 | ||||||
chr11:104960863
|
A | G | 1 | a0001c0003t0002g0208 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.8-5862T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960863 | ||||||
chr11:104960946
|
C | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0002t0002g0214 | 3 | HG02451.hp1 HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.8-5945G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960946 | ||||||
chr11:104961115
|
T | C | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG02451.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.8-6114A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961115 | ||||||
chr11:104961127
|
G | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 245 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.8-6126C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961127 | ||||||
chr11:104961205
|
C | T | 1 | a0001c0001t0006g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.8-6204G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961205 | ||||||
chr11:104961214
|
T | A | 3 | a0001c0001t0001g0038a0001c0001t0002g0199a0001c0001t0002g0200 | 4 | HG01891.hp2 HG02965.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-6213A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961214 | ||||||
chr11:104961276
|
A | G | 5 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0048others(2): Show | 7 | HG01433.hp2 HG02280.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-6275T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961276 | ||||||
chr11:104961336
|
C | A | 1 | a0001c0001t0001g0153 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.8-6335G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961336 | ||||||
chr11:104961384
|
GTGTC | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0027others(3): Show | 14 | HG00621.hp2 HG02486.hp1 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.8-6387_8-6384delGA others(2): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961384 | ||||||
chr11:104961400
|
C | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0054 | 3 | HG01433.hp2 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.8-6399G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961400 | ||||||
chr11:104961465
|
CTTGTCTG others(2): Show |
C | 3 | a0001c0001t0001g0005a0001c0001t0001g0064a0001c0001t0001g0161 | 9 | HG02109.hp1 HG02280.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.8-6473_8-6465delTA others(7): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961465 | ||||||
chr11:104961475
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0064a0001c0001t0001g0161 | 9 | HG02109.hp1 HG02280.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.8-6474C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961475 | ||||||
chr11:104961524
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.8-6523T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961524 | ||||||
chr11:104961531
|
G | T | 1 | a0001c0001t0001g0033 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.8-6530C>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961531 | ||||||
chr11:104961620
|
C | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 246 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.8-6619G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961620 | ||||||
chr11:104961738
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.8-6737A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961738 | ||||||
chr11:104961950
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.7+6569G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961950 | ||||||
chr11:104961985
|
C | T | 1 | a0002c0006t0001g0029 | 2 | HG00738.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.7+6534G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961985 | ||||||
chr11:104962164
|
T | C | 14 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0162others(11): Show | 18 | HG00323.hp2 HG00639.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.7+6355A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104962164 | ||||||
chr11:104962417
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG01256.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.7+6102C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104962417 | ||||||
chr11:104962436
|
C | T | 1 | a0001c0002t0002g0214 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.7+6083G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104962436 | ||||||
chr11:104962597
|
A | G | 5 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0048others(2): Show | 7 | HG01433.hp2 HG02280.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.7+5922T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104962597 | ||||||
chr11:104962848
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.7+5671G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104962848 | ||||||
chr11:104962849
|
A | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 263 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.7+5670T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104962849 | ||||||
chr11:104963012
|
G | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(92): Show | 160 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.7+5507C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963012 | ||||||
chr11:104963047
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0055 | 3 | HG02280.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.7+5472G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963047 | ||||||
chr11:104963117
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7+5402C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963117 | ||||||
chr11:104963127
|
C | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0027others(6): Show | 17 | HG00621.hp2 HG02145.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.7+5392G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963127 | ||||||
chr11:104963288
|
A | G | 39 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(36): Show | 55 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.7+5231T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963288 | ||||||
chr11:104963355
|
C | A | 2 | a0001c0001t0001g0046a0001c0002t0001g0017 | 4 | HG03098.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+5164G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963355 | ||||||
chr11:104963389
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7+5130G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963389 | ||||||
chr11:104963490
|
C | A | 9 | a0001c0003t0002g0009a0001c0003t0002g0205a0001c0003t0002g0206others(6): Show | 13 | HG00323.hp2 HG00639.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.7+5029G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963490 | ||||||
chr11:104963570
|
C | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0064a0001c0001t0001g0065others(5): Show | 17 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.7+4949G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963570 | ||||||
chr11:104963616
|
C | T | 35 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(32): Show | 51 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.7+4903G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963616 | ||||||
chr11:104963638
|
A | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0027others(3): Show | 14 | HG00621.hp2 HG02486.hp1 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.7+4881T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963638 | ||||||
chr11:104963653
|
T | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(93): Show | 161 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.7+4866A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963653 | ||||||
chr11:104963662
|
C | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0064a0001c0001t0001g0065others(5): Show | 17 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.7+4857G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963662 | ||||||
chr11:104963696
|
C | T | 4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0167others(1): Show | 6 | HG01891.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+4823G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963696 | ||||||
chr11:104964053
|
T | C | 14 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(11): Show | 24 | HG00621.hp2 HG01433.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.7+4466A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104964053 | ||||||
chr11:104964070
|
TATA | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0027others(3): Show | 14 | HG00621.hp2 HG02486.hp1 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.7+4446_7+4448delTA others(1): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104964070 | ||||||
chr11:104964080
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.7+4439T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104964080 | ||||||
chr11:104964189
|
G | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(35): Show | 53 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.7+4330C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104964189 | ||||||
chr11:104964222
|
A | C | 8 | a0001c0001t0001g0005a0001c0001t0001g0064a0001c0001t0001g0065others(5): Show | 17 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.7+4297T>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104964222 | ||||||
chr11:104964237
|
C | A | 2 | a0001c0001t0002g0199a0001c0001t0002g0200 | 2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.7+4282G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104964237 | ||||||
chr11:104964336
|
C | T | 33 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(30): Show | 48 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.7+4183G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104964336 | ||||||
chr11:104964405
|
A | C | 12 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(9): Show | 21 | HG00621.hp2 HG01433.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.7+4114T>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104964405 | ||||||
chr11:104964524
|
A | C | 7 | a0001c0001t0002g0201a0002c0004t0003g0030a0002c0004t0003g0056others(4): Show | 9 | HG00738.hp2 HG01099.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.7+3995T>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104964524 | ||||||
chr11:104964572
|
T | C | 1 | a0001c0001t0001g0044 | 2 | HG00733.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.7+3947A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104964572 | ||||||
chr11:104964952
|
G | T | 12 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(9): Show | 21 | HG00621.hp2 HG01433.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.7+3567C>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104964952 | ||||||
chr11:104965128
|
T | G | 1 | a0001c0001t0001g0197 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.7+3391A>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104965128 | ||||||
chr11:104965166
|
C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(48): Show | 89 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.7+3353G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104965166 | ||||||
chr11:104965373
|
C | G | 1 | a0001c0001t0001g0086 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.7+3146G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104965373 | ||||||
chr11:104965467
|
T | G | 17 | a0001c0001t0001g0162a0001c0001t0002g0199a0001c0001t0002g0200others(14): Show | 21 | HG00323.hp2 HG00639.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.7+3052A>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104965467 | ||||||
chr11:104965527
|
G | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0002t0002g0214 | 3 | HG02451.hp1 HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.7+2992C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104965527 | ||||||
chr11:104965536
|
A | G | 4 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0005g0202others(1): Show | 4 | HG01070.hp2 HG02886.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+2983T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104965536 | ||||||
chr11:104965551
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.7+2968G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104965551 | ||||||
chr11:104965640
|
G | T | 2 | a0001c0002t0001g0165a0001c0002t0001g0166 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.7+2879C>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104965640 | ||||||
chr11:104965721
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.7+2798G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104965721 | ||||||
chr11:104965737
|
A | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0048others(1): Show | 6 | HG02280.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+2782T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104965737 | ||||||
chr11:104965785
|
A | G | 40 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(37): Show | 56 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.7+2734T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104965785 | ||||||
chr11:104966072
|
G | C | 3 | a0001c0001t0001g0031a0001c0001t0001g0046a0001c0002t0001g0017 | 6 | HG03098.hp1 HG03130.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.7+2447C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966072 | ||||||
chr11:104966101
|
C | A | 1 | a0001c0001t0001g0027 | 2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.7+2418G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966101 | ||||||
chr11:104966110
|
G | A | 8 | a0001c0003t0002g0009a0001c0003t0002g0205a0001c0003t0002g0206others(5): Show | 12 | HG00323.hp2 HG00639.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.7+2409C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966110 | ||||||
chr11:104966140
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0164 | 4 | HG01109.hp2 HG01123.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+2379G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966140 | ||||||
chr11:104966271
|
A | C | 1 | a0001c0010t0001g0047 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.7+2248T>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966271 | ||||||
chr11:104966307
|
T | A | 1 | a0001c0002t0002g0214 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.7+2212A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966307 | ||||||
chr11:104966315
|
C | CCGAT | 38 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(35): Show | 54 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.7+2203_7+2204insAT others(2): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966315 | ||||||
chr11:104966430
|
C | G | 39 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(36): Show | 55 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.7+2089G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966430 | ||||||
chr11:104966517
|
G | A | 3 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0005g0202 | 3 | HG01070.hp2 HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.7+2002C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966517 | ||||||
chr11:104966588
|
A | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(35): Show | 54 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.7+1931T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966588 | ||||||
chr11:104966597
|
G | T | 26 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0060others(23): Show | 40 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.7+1922C>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966597 | ||||||
chr11:104966630
|
A | C | 1 | a0001c0001t0001g0032 | 2 | HG03831.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.7+1889T>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966630 | ||||||
chr11:104966660
|
C | T | 14 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(11): Show | 24 | HG00621.hp2 HG01433.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.7+1859G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966660 | ||||||
chr11:104966821
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.7+1698G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966821 | ||||||
chr11:104966867
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.7+1652G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966867 | ||||||
chr11:104966982
|
T | C | 1 | a0002c0004t0005g0213 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.7+1537A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966982 | ||||||
chr11:104967253
|
C | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG00099.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.7+1266G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967253 | ||||||
chr11:104967303
|
C | T | 3 | a0001c0001t0001g0020a0001c0003t0002g0205a0001c0003t0002g0206 | 5 | HG00099.hp1 HG00140.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+1216G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967303 | ||||||
chr11:104967450
|
G | A | 1 | a0001c0002t0002g0214 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.7+1069C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967450 | ||||||
chr11:104967488
|
G | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 262 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.7+1031C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967488 | ||||||
chr11:104967496
|
G | C | 3 | a0002c0004t0003g0057a0002c0004t0003g0058a0002c0004t0003g0059 | 3 | HG02559.hp1 HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.7+1023C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967496 | ||||||
chr11:104967502
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7+1017C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967502 | ||||||
chr11:104967536
|
A | G | 1 | a0001c0001t0002g0199 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.7+983T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967536 | ||||||
chr11:104967547
|
T | A | 1 | a0002c0004t0005g0213 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.7+972A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967547 | ||||||
chr11:104967580
|
T | A | 1 | a0001c0002t0002g0214 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.7+939A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967580 | ||||||
chr11:104967623
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.7+896G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967623 | ||||||
chr11:104967627
|
A | G | 6 | a0002c0004t0003g0030a0002c0004t0003g0056a0002c0004t0003g0057others(3): Show | 8 | HG00738.hp2 HG01099.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.7+892T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967627 | ||||||
chr11:104967744
|
C | T | 64 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(61): Show | 97 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.7+775G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967744 | ||||||
chr11:104967842
|
A | G | 4 | a0001c0001t0002g0201a0001c0001t0002g0203a0001c0001t0002g0204others(1): Show | 4 | HG01070.hp2 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+677T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967842 | ||||||
chr11:104967843
|
C | T | 14 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(11): Show | 24 | HG00621.hp2 HG01433.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.7+676G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967843 | ||||||
chr11:104967883
|
TTCTGTGT others(36): Show |
T | 1 | a0001c0001t0001g0162 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.7+593_7+635delCCAT others(39): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967883 | ||||||
chr11:104967996
|
G | A | 6 | a0001c0001t0001g0037a0001c0001t0001g0156a0001c0001t0001g0157others(3): Show | 7 | HG03490.hp1 NA18966.hp1 NA18993.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+523C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967996 | ||||||
chr11:104968026
|
A | G | 1 | a0002c0006t0001g0029 | 2 | HG00738.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.7+493T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104968026 | ||||||
chr11:104968112
|
C | T | 2 | a0001c0001t0002g0199a0001c0001t0002g0200 | 2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.7+407G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104968112 | ||||||
chr11:104968153
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0055 | 3 | HG02280.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.7+366G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104968153 | ||||||
chr11:104968210
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.7+309C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104968210 | ||||||
chr11:104968211
|
C | A | 1 | a0001c0001t0001g0161 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.7+308G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104968211 | ||||||
chr11:104968227
|
G | T | 12 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(9): Show | 21 | HG00621.hp2 HG01433.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.7+292C>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104968227 | ||||||
chr11:104968391
|
A | C | 2 | a0001c0001t0002g0199a0001c0001t0002g0200 | 2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.7+128T>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104968391 | ||||||
chr11:104968423
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T | C | 2 | a0001c0001t0001g0046a0001c0002t0001g0017 | 4 | HG03098.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+96A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104968423 | ||||||
chr11:104968426
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C | G | 2 | a0001c0001t0001g0046a0001c0002t0001g0017 | 4 | HG03098.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+93G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104968426 | ||||||
chr11:104968495
|
A | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 263 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.7+24T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104968495 |