geneid | 26511 |
---|---|
ensemblid | ENSG00000109220.11 |
hgncid | 1935 |
symbol | CHIC2 |
name | cysteine rich hydrophobic domain 2 |
refseq_nuc | NM_012110.4 |
refseq_prot | NP_036242.1 |
ensembl_nuc | ENST00000263921.8 |
ensembl_prot | ENSP00000263921.3 |
mane_status | MANE Select |
chr | chr4 |
start | 54009789 |
end | 54064605 |
strand | - |
ver | v1.2 |
region | chr4:54009789-54064605 |
region5000 | chr4:54004789-54069605 |
regionname0 | CHIC2_chr4_54009789_54064605 |
regionname5000 | CHIC2_chr4_54004789_54069605 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 165 | 244 | 84 | 42 | 70 | 16 | 30 | 50 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 612 | 146 | 54 | 22 | 48 | 8 | 13 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
t0002 | 0/0 | 611 | 68 | 8 | 17 | 21 | 7 | 15 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
t0003 | 0/0 | 614 | 10 | 6 | 3 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
t0004 | 1/0 | 612 | 5 | 4 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
t0005 | 0/0 | 613 | 5 | 4 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
t0006 | 0/0 | 613 | 4 | 4 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
t0007 | 0/0 | 611 | 2 | 2 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
t0008 | 0/0 | 611 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
t0009 | 0/0 | 613 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
t0010 | 0/0 | 611 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
t0011 | 0/0 | 612 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0002 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0004 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0010 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0014 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0081 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 498 | 240 | 80 | 42 | 70 | 16 | 30 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
a0001c0002 | 0/0 | 498 | 4 | 4 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1109 | 143 | 51 | 22 | 48 | 8 | 13 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
a0001c0001t0002 | 0/0 | 1108 | 68 | 8 | 17 | 21 | 7 | 15 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
a0001c0001t0003 | 0/0 | 1111 | 10 | 6 | 3 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
a0001c0001t0004 | 1/0 | 1109 | 5 | 4 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
a0001c0001t0005 | 0/0 | 1110 | 4 | 3 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
a0001c0001t0006 | 0/0 | 1110 | 4 | 4 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
a0001c0001t0007 | 0/0 | 1108 | 2 | 2 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
a0001c0001t0008 | 0/0 | 1108 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
a0001c0001t0009 | 0/0 | 1110 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
a0001c0001t0010 | 0/0 | 1108 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
a0001c0001t0011 | 0/0 | 1109 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
a0001c0002t0001 | 0/0 | 1109 | 3 | 3 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
a0001c0002t0005 | 0/0 | 1110 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | copy fasta | chr4 | 54004789 | 54069605 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0001 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0010 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0014 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0004g0081 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0007g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0007g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0008g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0009g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0010g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0011g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0002t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0011 | EUR | GBR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0196 | EUR | GBR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0056 | EUR | GBR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0055 | EUR | GBR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | FIN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | FIN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00323 | hp1 | a0001 | c0001 | t0011 | g0096 | EUR | FIN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0011 | EUR | FIN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | CHS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0121 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | CLM | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | CLM | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | CLM | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | CLM | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | CLM | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0177 | EUR | IBS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0140 | AMR | PEL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | KHV | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0215 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CDX | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CDX | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0085 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0136 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0089 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0077 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02723 | hp2 | a0001 | c0001 | t0006 | g0023 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02818 | hp1 | a0001 | c0001 | t0007 | g0219 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02818 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02965 | hp2 | a0001 | c0002 | t0005 | g0214 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | MSL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03195 | hp1 | a0001 | c0001 | t0007 | g0218 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03195 | hp2 | a0001 | c0001 | t0008 | g0019 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0216 | AFR | MSL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | MSL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0086 | AFR | MSL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03516 | hp1 | a0001 | c0001 | t0009 | g0117 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0145 | SAS | STU | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | STU | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | BEB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0144 | SAS | BEB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0143 | SAS | BEB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0048 | SAS | BEB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG04184 | hp1 | a0001 | c0001 | t0005 | g0120 | SAS | BEB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | STU | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0068 | SAS | STU | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | STU | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0124 | SAS | STU | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | STU | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | YRI | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | CHB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0155 | AFR | LWK | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0152 | AFR | LWK | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | LWK | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19065 | hp2 | a0001 | c0001 | t0010 | g0049 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | YRI | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | ASW | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | ASW | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0046 | EUR | TSI | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0112 | EUR | TSI | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | TSI | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0079 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0217 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | USA | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | USA | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | USA | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | USA | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | LWK | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | LWK | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0197 | REF | REF | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0081 | REF | REF | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:54064249
|
G | A | 1 | a0001c0002 | 4 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
synonymous_variant | LOW | c.52C>T | p.Leu18Leu | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/6 | 357/1109 | 52/498 | 18/165 | chr4 | 54064249 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:54009875
|
T | C | 1 | a0001c0001t0010 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*220A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 6/6 | 220 | chr4 | 54009875 | |||||
chr4:54009924
|
A | C | 1 | a0001c0001t0011 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*171T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 6/6 | 171 | chr4 | 54009924 | |||||
chr4:54009951
|
A | AT | 1 | a0001c0001t0006 | 4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*143dupA | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 6/6 | 143 | chr4 | 54009951 | |||||
chr4:54009954
|
T | TA | 3 | a0001c0001t0005a0001c0001t0009a0001c0002t0005 | 6 | HG02647.hp1 HG02647.hp2 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*140dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 6/6 | 140 | chr4 | 54009954 | |||||
chr4:54009954
|
T | TAA | 1 | a0001c0001t0003 | 10 | HG00642.hp2 HG01167.hp1 HG01243.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*139_*140dupTT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 6/6 | 140 | chr4 | 54009954 | |||||
chr4:54009964
|
AC | A | 4 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(1): Show | 72 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*130delG | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 6/6 | 130 | chr4 | 54009964 | |||||
chr4:54009965
|
C | A | 7 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(4): Show | 166 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*130G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 6/6 | 130 | chr4 | 54009965 | |||||
chr4:54064347
|
T | C | 1 | a0001c0001t0007 | 2 | HG02818.hp1 HG03195.hp1 |
5_prime_UTR_variant | MODIFIER | c.-47A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/6 | 47 | chr4 | 54064347 | |||||
chr4:54064527
|
C | T | 1 | a0001c0001t0008 | 1 | HG03195.hp2 | 5_prime_UTR_variant | MODIFIER | c.-227G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/6 | 227 | chr4 | 54064527 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:54010848
|
C | T | 22 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(19): Show | 24 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.448-703G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54010848 | ||||||
chr4:54010856
|
C | T | 10 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(7): Show | 10 | HG00642.hp2 HG01167.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.448-711G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54010856 | ||||||
chr4:54010954
|
A | T | 1 | a0001c0001t0002g0134 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.448-809T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54010954 | ||||||
chr4:54011189
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.448-1044A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54011189 | ||||||
chr4:54011201
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.448-1056C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54011201 | ||||||
chr4:54011274
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.448-1129A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54011274 | ||||||
chr4:54011841
|
T | A | 1 | a0001c0001t0001g0206 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.448-1696A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54011841 | ||||||
chr4:54012050
|
C | CA | 4 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+1786dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54012050 | ||||||
chr4:54012123
|
A | T | 109 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(106): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.447+1714T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54012123 | ||||||
chr4:54012183
|
C | T | 6 | a0001c0001t0002g0011a0001c0001t0002g0046a0001c0001t0002g0056others(3): Show | 7 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(4): Show |
intron_variant | MODIFIER | c.447+1654G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54012183 | ||||||
chr4:54012195
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.447+1642A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54012195 | ||||||
chr4:54012294
|
G | T | 1 | a0001c0001t0009g0117 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.447+1543C>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54012294 | ||||||
chr4:54012665
|
G | C | 66 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(63): Show | 77 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.447+1172C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54012665 | ||||||
chr4:54012732
|
T | C | 4 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+1105A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54012732 | ||||||
chr4:54012745
|
C | A | 95 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(92): Show | 110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.447+1092G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54012745 | ||||||
chr4:54012998
|
T | C | 1 | a0001c0001t0008g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.447+839A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54012998 | ||||||
chr4:54013011
|
T | C | 2 | a0001c0001t0001g0176a0001c0001t0001g0213 | 2 | HG01258.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.447+826A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54013011 | ||||||
chr4:54013126
|
T | C | 1 | a0001c0001t0005g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.447+711A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54013126 | ||||||
chr4:54013149
|
A | T | 1 | a0001c0001t0002g0033 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.447+688T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54013149 | ||||||
chr4:54013450
|
G | C | 8 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0149others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.447+387C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54013450 | ||||||
chr4:54013521
|
G | A | 2 | a0001c0001t0003g0121a0001c0001t0003g0123 | 2 | HG00642.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.447+316C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54013521 | ||||||
chr4:54013674
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.447+163G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54013674 | ||||||
chr4:54014238
|
T | C | 2 | a0001c0001t0002g0060a0001c0001t0002g0062 | 2 | HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.331-119A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54014238 | ||||||
chr4:54014450
|
C | T | 22 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(19): Show | 24 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.331-331G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54014450 | ||||||
chr4:54014539
|
T | C | 3 | a0001c0001t0002g0008a0001c0001t0002g0048a0001c0001t0002g0067 | 4 | HG02683.hp1 HG02735.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-420A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54014539 | ||||||
chr4:54015192
|
A | G | 2 | a0001c0001t0003g0121a0001c0001t0003g0123 | 2 | HG00642.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.331-1073T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54015192 | ||||||
chr4:54015259
|
G | A | 1 | a0001c0001t0002g0144 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.331-1140C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54015259 | ||||||
chr4:54015363
|
C | A | 1 | a0001c0001t0001g0212 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.331-1244G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54015363 | ||||||
chr4:54016084
|
A | G | 1 | a0001c0001t0008g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.331-1965T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54016084 | ||||||
chr4:54016123
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.331-2004C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54016123 | ||||||
chr4:54016173
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.331-2054A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54016173 | ||||||
chr4:54016289
|
TATA | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(5): Show | 9 | HG02258.hp2 HG02622.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.331-2173_331-2171d others(5): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54016289 | ||||||
chr4:54016358
|
T | C | 4 | a0001c0002t0001g0215a0001c0002t0001g0216a0001c0002t0001g0217others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-2239A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54016358 | ||||||
chr4:54016530
|
T | G | 59 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0008others(56): Show | 70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.331-2411A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54016530 | ||||||
chr4:54016594
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.331-2475G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54016594 | ||||||
chr4:54016909
|
GA | G | 33 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0075others(30): Show | 37 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.331-2791delT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54016909 | ||||||
chr4:54017082
|
T | C | 1 | a0001c0001t0002g0135 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.331-2963A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54017082 | ||||||
chr4:54017177
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.331-3058T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54017177 | ||||||
chr4:54017205
|
C | CAAATCTA others(28): Show |
3 | a0001c0002t0001g0215a0001c0002t0001g0216a0001c0002t0001g0217 | 3 | HG02145.hp2 HG02559.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.331-3121_331-3087d others(37): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54017205 | ||||||
chr4:54017213
|
A | C | 1 | a0001c0001t0005g0120 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.331-3094T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54017213 | ||||||
chr4:54017234
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.331-3115C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54017234 | ||||||
chr4:54017566
|
G | A | 5 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0149others(2): Show | 5 | HG02109.hp2 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.331-3447C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54017566 | ||||||
chr4:54018040
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.331-3921C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54018040 | ||||||
chr4:54018112
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.331-3993G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54018112 | ||||||
chr4:54018292
|
C | G | 1 | a0001c0001t0001g0080 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.331-4173G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54018292 | ||||||
chr4:54018575
|
G | T | 2 | a0001c0001t0002g0136a0001c0001t0002g0141 | 2 | HG02602.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.331-4456C>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54018575 | ||||||
chr4:54018727
|
T | A | 1 | a0001c0001t0001g0177 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.331-4608A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54018727 | ||||||
chr4:54018813
|
G | C | 10 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(7): Show | 10 | HG00642.hp2 HG01167.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.331-4694C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54018813 | ||||||
chr4:54018911
|
G | A | 1 | a0001c0001t0001g0016 | 2 | HG02809.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.331-4792C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54018911 | ||||||
chr4:54019244
|
C | CA | 59 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0008others(56): Show | 70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.331-5126dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54019244 | ||||||
chr4:54019424
|
C | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0070others(3): Show | 8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.331-5305G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54019424 | ||||||
chr4:54019424
|
C | G | 5 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0149others(2): Show | 5 | HG02109.hp2 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.331-5305G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54019424 | ||||||
chr4:54019572
|
T | A | 8 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(5): Show | 9 | HG02258.hp2 HG02622.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.331-5453A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54019572 | ||||||
chr4:54019676
|
T | G | 2 | a0001c0001t0002g0134a0001c0001t0002g0139 | 2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.331-5557A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54019676 | ||||||
chr4:54019777
|
G | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0070others(3): Show | 8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.331-5658C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54019777 | ||||||
chr4:54019787
|
G | C | 1 | a0001c0001t0001g0177 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.331-5668C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54019787 | ||||||
chr4:54019796
|
G | C | 4 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-5677C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54019796 | ||||||
chr4:54019895
|
T | TA | 93 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(90): Show | 108 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.331-5777dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54019895 | ||||||
chr4:54020031
|
G | A | 2 | a0001c0001t0003g0044a0001c0001t0003g0045 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.331-5912C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54020031 | ||||||
chr4:54020105
|
C | A | 6 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(3): Show | 6 | HG01243.hp1 HG02055.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.331-5986G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54020105 | ||||||
chr4:54020356
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.331-6237G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54020356 | ||||||
chr4:54020429
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.331-6310G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54020429 | ||||||
chr4:54020437
|
C | T | 1 | a0001c0001t0003g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.331-6318G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54020437 | ||||||
chr4:54020621
|
G | T | 1 | a0001c0001t0005g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.331-6502C>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54020621 | ||||||
chr4:54020651
|
G | A | 2 | a0001c0001t0002g0133a0001c0001t0002g0140 | 2 | HG00642.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.331-6532C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54020651 | ||||||
chr4:54020658
|
C | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0070others(3): Show | 8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.331-6539G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54020658 | ||||||
chr4:54020829
|
A | C | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.331-6710T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54020829 | ||||||
chr4:54020867
|
A | T | 89 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(86): Show | 104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.331-6748T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54020867 | ||||||
chr4:54021081
|
CTTCTCCC others(3): Show |
C | 2 | a0001c0001t0003g0122a0001c0001t0003g0124 | 2 | HG02109.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.331-6972_331-6963d others(12): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54021081 | ||||||
chr4:54021129
|
C | A | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0207 | 3 | NA18950.hp1 NA18956.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.331-7010G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54021129 | ||||||
chr4:54021193
|
C | G | 1 | a0001c0001t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.331-7074G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54021193 | ||||||
chr4:54021753
|
G | A | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(15): Show | 20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.331-7634C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54021753 | ||||||
chr4:54022114
|
C | A | 59 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0008others(56): Show | 70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.331-7995G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022114 | ||||||
chr4:54022137
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.331-8018A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022137 | ||||||
chr4:54022192
|
C | T | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(15): Show | 20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.331-8073G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022192 | ||||||
chr4:54022271
|
G | A | 1 | a0001c0001t0002g0143 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.331-8152C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022271 | ||||||
chr4:54022281
|
C | T | 1 | a0001c0001t0011g0096 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.331-8162G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022281 | ||||||
chr4:54022325
|
C | T | 22 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(19): Show | 24 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.331-8206G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022325 | ||||||
chr4:54022640
|
T | C | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.331-8521A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022640 | ||||||
chr4:54022686
|
C | A | 2 | a0001c0001t0002g0118a0001c0001t0002g0125 | 2 | HG01255.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.331-8567G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022686 | ||||||
chr4:54022699
|
G | C | 1 | a0001c0001t0002g0055 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.331-8580C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022699 | ||||||
chr4:54022702
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.331-8583G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022702 | ||||||
chr4:54022787
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.331-8668C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022787 | ||||||
chr4:54022849
|
C | G | 8 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(5): Show | 9 | HG02258.hp2 HG02622.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.331-8730G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022849 | ||||||
chr4:54022939
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.331-8820C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022939 | ||||||
chr4:54022973
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.331-8854C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022973 | ||||||
chr4:54023102
|
T | TA | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0070others(3): Show | 8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.331-8984dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023102 | ||||||
chr4:54023121
|
T | C | 4 | a0001c0002t0001g0215a0001c0002t0001g0216a0001c0002t0001g0217others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-9002A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023121 | ||||||
chr4:54023129
|
C | T | 6 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0149others(3): Show | 6 | HG02109.hp2 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.331-9010G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023129 | ||||||
chr4:54023193
|
G | A | 8 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(5): Show | 8 | HG02145.hp2 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.331-9074C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023193 | ||||||
chr4:54023212
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0148 | 5 | HG02717.hp2 HG02723.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.331-9093C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023212 | ||||||
chr4:54023217
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.331-9098C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023217 | ||||||
chr4:54023288
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.331-9169C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023288 | ||||||
chr4:54023305
|
G | A | 1 | a0001c0001t0005g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.331-9186C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023305 | ||||||
chr4:54023416
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0111a0001c0001t0001g0211 | 5 | NA18747.hp2 NA18960.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.331-9297A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023416 | ||||||
chr4:54023426
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.331-9307C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023426 | ||||||
chr4:54023453
|
G | A | 109 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(106): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.331-9334C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023453 | ||||||
chr4:54023540
|
G | A | 1 | a0001c0001t0002g0068 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.331-9421C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023540 | ||||||
chr4:54023568
|
T | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0038 | 4 | HG02622.hp1 HG02809.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-9449A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023568 | ||||||
chr4:54023650
|
C | A | 1 | a0001c0001t0001g0213 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.331-9531G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023650 | ||||||
chr4:54023719
|
C | A | 1 | a0001c0001t0001g0069 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.331-9600G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023719 | ||||||
chr4:54023845
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.331-9726G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023845 | ||||||
chr4:54023876
|
C | T | 218 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(215): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.331-9757G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023876 | ||||||
chr4:54023985
|
G | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0148 | 5 | HG02717.hp2 HG02723.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.331-9866C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023985 | ||||||
chr4:54024001
|
G | A | 1 | a0001c0001t0003g0045 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.331-9882C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54024001 | ||||||
chr4:54024049
|
G | A | 1 | a0001c0001t0002g0099 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.331-9930C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54024049 | ||||||
chr4:54024065
|
C | T | 4 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-9946G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54024065 | ||||||
chr4:54024222
|
T | A | 4 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-10103A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54024222 | ||||||
chr4:54024437
|
T | TA | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0005g0152 | 3 | HG02257.hp1 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.331-10319dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54024437 | ||||||
chr4:54024568
|
G | A | 4 | a0001c0002t0001g0215a0001c0002t0001g0216a0001c0002t0001g0217others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-10449C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54024568 | ||||||
chr4:54024639
|
G | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(15): Show | 20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.331-10520C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54024639 | ||||||
chr4:54024887
|
A | C | 1 | a0001c0001t0001g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.331-10768T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54024887 | ||||||
chr4:54025018
|
A | G | 1 | a0001c0001t0006g0023 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.331-10899T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54025018 | ||||||
chr4:54025072
|
A | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0070others(3): Show | 8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.331-10953T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54025072 | ||||||
chr4:54025766
|
G | A | 2 | a0001c0001t0003g0044a0001c0001t0003g0045 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.331-11647C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54025766 | ||||||
chr4:54025854
|
C | CA | 15 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0002g0126others(12): Show | 15 | HG00639.hp1 HG00642.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.331-11736dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54025854 | ||||||
chr4:54025854
|
C | CAA | 54 | a0001c0001t0001g0107a0001c0001t0002g0001a0001c0001t0002g0005others(51): Show | 65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.331-11737_331-1173 others(6): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54025854 | ||||||
chr4:54025854
|
CA | C | 6 | a0001c0001t0001g0021a0001c0001t0001g0157a0001c0001t0006g0022others(3): Show | 6 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.331-11736delT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54025854 | ||||||
chr4:54025923
|
G | A | 1 | a0001c0001t0002g0137 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.331-11804C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54025923 | ||||||
chr4:54026034
|
T | C | 3 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072 | 3 | HG02615.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.331-11915A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54026034 | ||||||
chr4:54026040
|
C | A | 1 | a0001c0001t0002g0065 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.331-11921G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54026040 | ||||||
chr4:54026229
|
C | A | 1 | a0001c0001t0002g0132 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.331-12110G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54026229 | ||||||
chr4:54026230
|
A | C | 1 | a0001c0001t0002g0132 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.331-12111T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54026230 | ||||||
chr4:54026232
|
T | A | 1 | a0001c0001t0002g0132 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.331-12113A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54026232 | ||||||
chr4:54026452
|
G | GGGGTTGC others(9): Show |
1 | a0001c0001t0001g0083 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.331-12334_331-1233 others(20): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54026452 | ||||||
chr4:54026456
|
G | T | 1 | a0001c0001t0001g0083 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.331-12337C>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54026456 | ||||||
chr4:54026457
|
T | G | 1 | a0001c0001t0001g0083 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.331-12338A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54026457 | ||||||
chr4:54026856
|
T | C | 8 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0149others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.331-12737A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54026856 | ||||||
chr4:54026974
|
A | C | 1 | a0001c0001t0001g0193 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.331-12855T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54026974 | ||||||
chr4:54027112
|
A | G | 95 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(92): Show | 110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.331-12993T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54027112 | ||||||
chr4:54027167
|
A | C | 1 | a0001c0001t0001g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.331-13048T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54027167 | ||||||
chr4:54027218
|
A | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0072 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.331-13099T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54027218 | ||||||
chr4:54027448
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.331-13329C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54027448 | ||||||
chr4:54027655
|
A | G | 8 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0149others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.331-13536T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54027655 | ||||||
chr4:54027764
|
A | G | 1 | a0001c0001t0007g0218 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.331-13645T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54027764 | ||||||
chr4:54028079
|
T | C | 1 | a0001c0001t0004g0086 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.331-13960A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54028079 | ||||||
chr4:54028146
|
T | C | 4 | a0001c0002t0001g0215a0001c0002t0001g0216a0001c0002t0001g0217others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-14027A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54028146 | ||||||
chr4:54028531
|
A | C | 109 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(106): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.331-14412T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54028531 | ||||||
chr4:54028737
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.331-14618A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54028737 | ||||||
chr4:54028830
|
A | G | 6 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(3): Show | 6 | HG02647.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.331-14711T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54028830 | ||||||
chr4:54028855
|
C | T | 59 | a0001c0001t0001g0156a0001c0001t0002g0001a0001c0001t0002g0005others(56): Show | 70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.331-14736G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54028855 | ||||||
chr4:54028967
|
C | A | 1 | a0001c0001t0001g0187 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.331-14848G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54028967 | ||||||
chr4:54029049
|
G | A | 1 | a0001c0001t0007g0218 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.331-14930C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54029049 | ||||||
chr4:54029113
|
C | G | 2 | a0001c0001t0003g0122a0001c0001t0003g0124 | 2 | HG02109.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.331-14994G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54029113 | ||||||
chr4:54029126
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.331-15007T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54029126 | ||||||
chr4:54029135
|
A | C | 1 | a0001c0001t0001g0112 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.331-15016T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54029135 | ||||||
chr4:54029202
|
T | C | 23 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(20): Show | 25 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.331-15083A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54029202 | ||||||
chr4:54029305
|
G | A | 1 | a0001c0001t0002g0130 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.331-15186C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54029305 | ||||||
chr4:54029340
|
G | A | 2 | a0001c0001t0003g0121a0001c0001t0003g0123 | 2 | HG00642.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.331-15221C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54029340 | ||||||
chr4:54029478
|
T | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(15): Show | 20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.331-15359A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54029478 | ||||||
chr4:54029598
|
A | C | 1 | a0001c0002t0005g0214 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.331-15479T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54029598 | ||||||
chr4:54029635
|
T | A | 19 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(16): Show | 21 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.331-15516A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54029635 | ||||||
chr4:54029647
|
A | G | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(15): Show | 20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.331-15528T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54029647 | ||||||
chr4:54030214
|
T | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG03704.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.331-16095A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030214 | ||||||
chr4:54030305
|
C | T | 1 | a0001c0001t0002g0132 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.331-16186G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030305 | ||||||
chr4:54030460
|
C | A | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(15): Show | 20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.331-16341G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030460 | ||||||
chr4:54030467
|
G | A | 1 | a0001c0001t0002g0145 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.331-16348C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030467 | ||||||
chr4:54030523
|
GA | G | 21 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(18): Show | 22 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.331-16405delT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030523 | ||||||
chr4:54030523
|
GAA | G | 71 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0016others(68): Show | 85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.331-16406_331-1640 others(6): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030523 | ||||||
chr4:54030533
|
A | T | 1 | a0001c0001t0003g0044 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.331-16414T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030533 | ||||||
chr4:54030535
|
A | T | 74 | a0001c0001t0001g0015a0001c0001t0001g0070a0001c0001t0001g0071others(71): Show | 86 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.331-16416T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030535 | ||||||
chr4:54030537
|
A | T | 97 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0070others(94): Show | 110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.331-16418T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030537 | ||||||
chr4:54030539
|
T | A | 2 | a0001c0001t0001g0110a0001c0001t0002g0082 | 2 | HG01255.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.331-16420A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030539 | ||||||
chr4:54030561
|
C | CACACACA others(3): Show |
109 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(106): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.331-16443_331-1644 others(14): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030561 | ||||||
chr4:54030618
|
A | G | 1 | a0001c0001t0002g0001 | 4 | HG00733.hp1 HG01070.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-16499T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030618 | ||||||
chr4:54030637
|
T | C | 1 | a0001c0001t0009g0117 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.331-16518A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030637 | ||||||
chr4:54030643
|
T | C | 6 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(3): Show | 6 | HG01243.hp1 HG02055.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.331-16524A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030643 | ||||||
chr4:54030666
|
A | AT | 14 | a0001c0001t0001g0101a0001c0001t0001g0146a0001c0001t0001g0147others(11): Show | 14 | HG00597.hp1 HG00597.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.331-16548dupA | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030666 | ||||||
chr4:54030666
|
AT | A | 17 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(14): Show | 18 | HG00099.hp2 HG00642.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.331-16548delA | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030666 | ||||||
chr4:54030731
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.331-16612C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030731 | ||||||
chr4:54030757
|
T | A | 1 | a0001c0001t0001g0016 | 2 | HG02809.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.331-16638A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030757 | ||||||
chr4:54030878
|
A | AT | 5 | a0001c0001t0002g0128a0001c0001t0002g0137a0001c0001t0002g0143others(2): Show | 5 | HG02257.hp2 HG03098.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.331-16760dupA | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030878 | ||||||
chr4:54030878
|
AT | A | 4 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0148others(1): Show | 6 | HG02717.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.331-16760delA | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030878 | ||||||
chr4:54030898
|
C | T | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(15): Show | 20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.331-16779G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030898 | ||||||
chr4:54030952
|
C | T | 58 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0008others(55): Show | 69 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.331-16833G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030952 | ||||||
chr4:54031178
|
G | GA | 95 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(92): Show | 110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.331-17060dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54031178 | ||||||
chr4:54031220
|
C | A | 1 | a0001c0001t0001g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.331-17101G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54031220 | ||||||
chr4:54031344
|
A | G | 1 | a0001c0001t0005g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.331-17225T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54031344 | ||||||
chr4:54031347
|
T | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0111a0001c0001t0001g0211 | 5 | NA18747.hp2 NA18960.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.331-17228A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54031347 | ||||||
chr4:54031611
|
C | CT | 57 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(54): Show | 58 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.330+17343dupA | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54031611 | ||||||
chr4:54031611
|
CT | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0002g0116others(1): Show | 5 | HG02809.hp1 HG02896.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.330+17343delA | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54031611 | ||||||
chr4:54031641
|
CAG | C | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0070others(3): Show | 8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+17312_330+1731 others(6): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54031641 | ||||||
chr4:54031676
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.330+17279C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54031676 | ||||||
chr4:54031902
|
G | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0070others(3): Show | 8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+17053C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54031902 | ||||||
chr4:54031916
|
A | G | 109 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(106): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.330+17039T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54031916 | ||||||
chr4:54032260
|
T | TCCCTCC | 4 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+16689_330+1669 others(10): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032260 | ||||||
chr4:54032286
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.330+16669A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032286 | ||||||
chr4:54032330
|
G | C | 1 | a0001c0001t0002g0145 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.330+16625C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032330 | ||||||
chr4:54032380
|
C | CG | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0070others(3): Show | 8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+16574_330+1657 others(5): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032380 | ||||||
chr4:54032381
|
T | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0070others(3): Show | 8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+16574A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032381 | ||||||
chr4:54032382
|
C | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0070others(3): Show | 8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+16573G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032382 | ||||||
chr4:54032383
|
A | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0070others(3): Show | 8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+16572T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032383 | ||||||
chr4:54032389
|
C | A | 4 | a0001c0002t0001g0215a0001c0002t0001g0216a0001c0002t0001g0217others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+16566G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032389 | ||||||
chr4:54032415
|
G | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0070others(3): Show | 8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+16540C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032415 | ||||||
chr4:54032471
|
T | G | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(15): Show | 20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.330+16484A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032471 | ||||||
chr4:54032555
|
T | C | 95 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(92): Show | 110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.330+16400A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032555 | ||||||
chr4:54032607
|
A | G | 2 | a0001c0001t0002g0009a0001c0001t0010g0049 | 3 | NA18966.hp2 NA19065.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.330+16348T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032607 | ||||||
chr4:54032643
|
AATTAC | A | 4 | a0001c0002t0001g0215a0001c0002t0001g0216a0001c0002t0001g0217others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+16307_330+1631 others(9): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032643 | ||||||
chr4:54032715
|
C | A | 1 | a0001c0001t0005g0120 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.330+16240G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032715 | ||||||
chr4:54032804
|
C | T | 95 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(92): Show | 110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.330+16151G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032804 | ||||||
chr4:54032848
|
C | T | 3 | a0001c0001t0001g0142a0001c0001t0002g0134a0001c0001t0002g0139 | 3 | HG00639.hp1 HG01109.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.330+16107G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032848 | ||||||
chr4:54033059
|
G | A | 6 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0149others(3): Show | 6 | HG02109.hp2 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.330+15896C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54033059 | ||||||
chr4:54033162
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.330+15793A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54033162 | ||||||
chr4:54033512
|
G | A | 1 | a0001c0001t0001g0038 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.330+15443C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54033512 | ||||||
chr4:54033637
|
TAG | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0186a0001c0001t0001g0187 | 4 | HG00741.hp2 HG01346.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+15316_330+1531 others(6): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54033637 | ||||||
chr4:54033697
|
A | C | 1 | a0001c0001t0001g0158 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.330+15258T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54033697 | ||||||
chr4:54033722
|
A | T | 1 | a0001c0001t0005g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.330+15233T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54033722 | ||||||
chr4:54034046
|
C | T | 1 | a0001c0001t0002g0033 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.330+14909G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034046 | ||||||
chr4:54034100
|
T | C | 8 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0129others(5): Show | 8 | HG00544.hp1 HG00642.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+14855A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034100 | ||||||
chr4:54034120
|
C | T | 1 | a0001c0001t0002g0046 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.330+14835G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034120 | ||||||
chr4:54034124
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.330+14831C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034124 | ||||||
chr4:54034196
|
G | C | 4 | a0001c0002t0001g0215a0001c0002t0001g0216a0001c0002t0001g0217others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+14759C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034196 | ||||||
chr4:54034202
|
C | T | 4 | a0001c0002t0001g0215a0001c0002t0001g0216a0001c0002t0001g0217others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+14753G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034202 | ||||||
chr4:54034318
|
C | T | 59 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0008others(56): Show | 70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.330+14637G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034318 | ||||||
chr4:54034339
|
A | G | 87 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(84): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.330+14616T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034339 | ||||||
chr4:54034404
|
CA | C | 111 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(108): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.330+14550delT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034404 | ||||||
chr4:54034437
|
A | T | 109 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(106): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.330+14518T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034437 | ||||||
chr4:54034462
|
T | C | 1 | a0001c0001t0001g0016 | 2 | HG02809.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.330+14493A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034462 | ||||||
chr4:54034573
|
A | T | 1 | a0001c0001t0001g0212 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.330+14382T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034573 | ||||||
chr4:54034576
|
G | T | 1 | a0001c0001t0001g0212 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.330+14379C>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034576 | ||||||
chr4:54034577
|
T | TATTTTTT others(8): Show |
1 | a0001c0001t0001g0212 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.330+14377_330+1437 others(19): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034577 | ||||||
chr4:54034582
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.330+14373G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034582 | ||||||
chr4:54034585
|
T | G | 4 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+14370A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034585 | ||||||
chr4:54034636
|
T | C | 2 | a0001c0001t0003g0044a0001c0001t0003g0045 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.330+14319A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034636 | ||||||
chr4:54034720
|
C | A | 1 | a0001c0001t0001g0104 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.330+14235G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034720 | ||||||
chr4:54034724
|
A | G | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0097 | 3 | HG02615.hp2 HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.330+14231T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034724 | ||||||
chr4:54034849
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.330+14106A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034849 | ||||||
chr4:54035165
|
A | G | 1 | a0001c0001t0009g0117 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.330+13790T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54035165 | ||||||
chr4:54035242
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.330+13713C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54035242 | ||||||
chr4:54035309
|
T | C | 56 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0008others(53): Show | 67 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.330+13646A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54035309 | ||||||
chr4:54035317
|
A | G | 7 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(4): Show | 7 | HG02145.hp1 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.330+13638T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54035317 | ||||||
chr4:54035503
|
T | C | 4 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+13452A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54035503 | ||||||
chr4:54035634
|
C | T | 59 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0008others(56): Show | 70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.330+13321G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54035634 | ||||||
chr4:54035645
|
T | C | 1 | a0001c0001t0001g0208 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.330+13310A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54035645 | ||||||
chr4:54035684
|
T | C | 1 | a0001c0001t0002g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.330+13271A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54035684 | ||||||
chr4:54035737
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.330+13218G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54035737 | ||||||
chr4:54035795
|
G | A | 59 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0008others(56): Show | 70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.330+13160C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54035795 | ||||||
chr4:54035931
|
T | G | 1 | a0001c0001t0001g0114 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.330+13024A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54035931 | ||||||
chr4:54035971
|
C | T | 4 | a0001c0002t0001g0215a0001c0002t0001g0216a0001c0002t0001g0217others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+12984G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54035971 | ||||||
chr4:54036138
|
G | C | 3 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072 | 3 | HG02615.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.330+12817C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54036138 | ||||||
chr4:54036391
|
G | A | 8 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0149others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+12564C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54036391 | ||||||
chr4:54036403
|
T | G | 59 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0008others(56): Show | 70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.330+12552A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54036403 | ||||||
chr4:54036487
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.330+12468C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54036487 | ||||||
chr4:54036558
|
T | A | 1 | a0001c0001t0002g0133 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.330+12397A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54036558 | ||||||
chr4:54036577
|
G | A | 3 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072 | 3 | HG02615.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.330+12378C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54036577 | ||||||
chr4:54036701
|
C | T | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(15): Show | 20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.330+12254G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54036701 | ||||||
chr4:54036791
|
C | CA | 59 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0008others(56): Show | 70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.330+12163dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54036791 | ||||||
chr4:54036826
|
C | CA | 109 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(106): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.330+12128_330+1212 others(5): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54036826 | ||||||
chr4:54036962
|
T | C | 3 | a0001c0001t0001g0090a0001c0001t0002g0130a0001c0001t0003g0122 | 3 | HG02109.hp1 HG02132.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.330+11993A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54036962 | ||||||
chr4:54036997
|
A | G | 1 | a0001c0001t0002g0058 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.330+11958T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54036997 | ||||||
chr4:54037168
|
A | G | 2 | a0001c0001t0003g0121a0001c0001t0003g0123 | 2 | HG00642.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.330+11787T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54037168 | ||||||
chr4:54037209
|
A | C | 109 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(106): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.330+11746T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54037209 | ||||||
chr4:54037381
|
G | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0070others(3): Show | 8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+11574C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54037381 | ||||||
chr4:54037497
|
T | C | 59 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0008others(56): Show | 70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.330+11458A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54037497 | ||||||
chr4:54037657
|
T | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(15): Show | 20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.330+11298A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54037657 | ||||||
chr4:54037700
|
C | T | 1 | a0001c0001t0002g0116 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.330+11255G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54037700 | ||||||
chr4:54037839
|
G | C | 4 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+11116C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54037839 | ||||||
chr4:54037866
|
T | C | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0070others(3): Show | 8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+11089A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54037866 | ||||||
chr4:54038289
|
G | A | 5 | a0001c0001t0001g0073a0001c0001t0001g0087a0001c0001t0001g0088others(2): Show | 5 | HG01074.hp2 HG01167.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.330+10666C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54038289 | ||||||
chr4:54038399
|
T | C | 5 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0149others(2): Show | 5 | HG02109.hp2 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.330+10556A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54038399 | ||||||
chr4:54038432
|
T | C | 1 | a0001c0002t0005g0214 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.330+10523A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54038432 | ||||||
chr4:54038462
|
C | CA | 6 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(3): Show | 6 | HG01243.hp1 HG02055.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.330+10492dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54038462 | ||||||
chr4:54038609
|
T | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0148 | 5 | HG02717.hp2 HG02723.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.330+10346A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54038609 | ||||||
chr4:54039013
|
G | A | 10 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(7): Show | 10 | HG00642.hp2 HG01167.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.330+9942C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54039013 | ||||||
chr4:54039132
|
C | T | 4 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+9823G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54039132 | ||||||
chr4:54039169
|
T | C | 1 | a0001c0001t0002g0140 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.330+9786A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54039169 | ||||||
chr4:54039255
|
C | T | 2 | a0001c0001t0002g0058a0001c0001t0002g0059 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.330+9700G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54039255 | ||||||
chr4:54039268
|
G | A | 1 | a0001c0001t0007g0219 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.330+9687C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54039268 | ||||||
chr4:54039325
|
T | A | 57 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0008others(54): Show | 68 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.330+9630A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54039325 | ||||||
chr4:54039331
|
C | T | 1 | a0001c0001t0011g0096 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.330+9624G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54039331 | ||||||
chr4:54039572
|
C | T | 5 | a0001c0001t0001g0073a0001c0001t0001g0087a0001c0001t0001g0088others(2): Show | 5 | HG01074.hp2 HG01167.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.330+9383G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54039572 | ||||||
chr4:54039746
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.330+9209A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54039746 | ||||||
chr4:54039785
|
G | C | 214 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.330+9170C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54039785 | ||||||
chr4:54039807
|
T | C | 1 | a0001c0001t0001g0038 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.330+9148A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54039807 | ||||||
chr4:54039881
|
TAAAAG | T | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(15): Show | 20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.330+9069_330+9073d others(7): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54039881 | ||||||
chr4:54040041
|
C | A | 1 | a0001c0001t0009g0117 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.330+8914G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040041 | ||||||
chr4:54040194
|
T | C | 35 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0074others(32): Show | 39 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.330+8761A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040194 | ||||||
chr4:54040293
|
G | A | 1 | a0001c0001t0003g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.330+8662C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040293 | ||||||
chr4:54040372
|
G | C | 1 | a0001c0001t0002g0064 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.330+8583C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040372 | ||||||
chr4:54040396
|
G | A | 3 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072 | 3 | HG02615.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.330+8559C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040396 | ||||||
chr4:54040471
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.330+8484G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040471 | ||||||
chr4:54040665
|
T | G | 2 | a0001c0001t0001g0199a0001c0001t0001g0201 | 2 | HG01070.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.330+8290A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040665 | ||||||
chr4:54040703
|
C | CA | 40 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0017others(37): Show | 44 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.330+8251dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040703 | ||||||
chr4:54040703
|
C | CAA | 11 | a0001c0001t0001g0073a0001c0001t0001g0078a0001c0001t0001g0084others(8): Show | 11 | HG00323.hp1 HG00438.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.330+8250_330+8251d others(4): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040703 | ||||||
chr4:54040703
|
CA | C | 31 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0030others(28): Show | 33 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.330+8251delT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040703 | ||||||
chr4:54040703
|
CAA | C | 54 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0021others(51): Show | 65 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.330+8250_330+8251d others(4): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040703 | ||||||
chr4:54040703
|
CAAA | C | 7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0070others(4): Show | 9 | HG01255.hp1 HG02717.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.330+8249_330+8251d others(5): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040703 | ||||||
chr4:54040800
|
C | A | 57 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0008others(54): Show | 68 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.330+8155G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040800 | ||||||
chr4:54040973
|
AT | A | 8 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0149others(5): Show | 8 | HG01070.hp1 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+7981delA | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040973 | ||||||
chr4:54041020
|
G | A | 1 | a0001c0001t0002g0144 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.330+7935C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54041020 | ||||||
chr4:54041070
|
C | A | 8 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0149others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+7885G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54041070 | ||||||
chr4:54041311
|
A | C | 1 | a0001c0001t0002g0136 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.330+7644T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54041311 | ||||||
chr4:54041361
|
C | T | 1 | a0001c0001t0007g0218 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.330+7594G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54041361 | ||||||
chr4:54041384
|
T | C | 3 | a0001c0001t0002g0118a0001c0001t0002g0125a0001c0001t0009g0117 | 3 | HG01255.hp1 HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.330+7571A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54041384 | ||||||
chr4:54041391
|
C | G | 1 | a0001c0001t0001g0205 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.330+7564G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54041391 | ||||||
chr4:54042103
|
T | C | 1 | a0001c0002t0005g0214 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.330+6852A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042103 | ||||||
chr4:54042106
|
A | T | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(15): Show | 20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.330+6849T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042106 | ||||||
chr4:54042218
|
T | C | 4 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0103others(1): Show | 4 | HG02559.hp1 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+6737A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042218 | ||||||
chr4:54042314
|
C | T | 4 | a0001c0002t0001g0215a0001c0002t0001g0216a0001c0002t0001g0217others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+6641G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042314 | ||||||
chr4:54042316
|
T | C | 2 | a0001c0001t0002g0118a0001c0001t0002g0125 | 2 | HG01255.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.330+6639A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042316 | ||||||
chr4:54042339
|
G | T | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.330+6616C>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042339 | ||||||
chr4:54042397
|
A | C | 1 | a0001c0001t0001g0148 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.330+6558T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042397 | ||||||
chr4:54042460
|
G | A | 8 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0149others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+6495C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042460 | ||||||
chr4:54042524
|
A | T | 1 | a0001c0002t0001g0217 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.330+6431T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042524 | ||||||
chr4:54042587
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.330+6368C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042587 | ||||||
chr4:54042716
|
C | T | 2 | a0001c0001t0003g0122a0001c0001t0003g0124 | 2 | HG02109.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.330+6239G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042716 | ||||||
chr4:54042923
|
G | T | 2 | a0001c0001t0002g0008a0001c0001t0002g0048 | 3 | HG02683.hp1 HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.330+6032C>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042923 | ||||||
chr4:54042953
|
C | T | 3 | a0001c0001t0002g0011a0001c0001t0002g0056a0001c0001t0002g0064 | 4 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+6002G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042953 | ||||||
chr4:54043100
|
C | A | 1 | a0001c0001t0001g0175 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.330+5855G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54043100 | ||||||
chr4:54043139
|
C | T | 2 | a0001c0001t0001g0098a0001c0001t0001g0187 | 2 | HG01123.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.330+5816G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54043139 | ||||||
chr4:54043144
|
A | G | 107 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(104): Show | 122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.330+5811T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54043144 | ||||||
chr4:54043160
|
G | A | 3 | a0001c0001t0002g0050a0001c0001t0002g0051a0001c0001t0002g0063 | 3 | HG02074.hp1 NA18977.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.330+5795C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54043160 | ||||||
chr4:54043174
|
C | A | 3 | a0001c0001t0001g0092a0001c0001t0001g0103a0001c0001t0001g0114 | 3 | HG02559.hp1 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.330+5781G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54043174 | ||||||
chr4:54043255
|
A | C | 1 | a0001c0001t0002g0143 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.330+5700T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54043255 | ||||||
chr4:54043410
|
G | A | 1 | a0001c0001t0003g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.330+5545C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54043410 | ||||||
chr4:54043420
|
C | CA | 13 | a0001c0001t0001g0015a0001c0001t0001g0092a0001c0001t0001g0103others(10): Show | 14 | HG02145.hp2 HG02559.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.330+5534dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54043420 | ||||||
chr4:54043420
|
CA | C | 6 | a0001c0001t0001g0076a0001c0001t0001g0161a0001c0001t0001g0164others(3): Show | 6 | HG01943.hp1 HG02109.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.330+5534delT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54043420 | ||||||
chr4:54043531
|
C | G | 5 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0149others(2): Show | 5 | HG02109.hp2 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.330+5424G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54043531 | ||||||
chr4:54043538
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.330+5417T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54043538 | ||||||
chr4:54043645
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.330+5310G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54043645 | ||||||
chr4:54044041
|
T | A | 1 | a0001c0001t0001g0104 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.330+4914A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044041 | ||||||
chr4:54044118
|
C | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0070others(3): Show | 8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+4837G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044118 | ||||||
chr4:54044399
|
C | A | 1 | a0001c0001t0003g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.330+4556G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044399 | ||||||
chr4:54044504
|
T | C | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0070others(3): Show | 8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+4451A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044504 | ||||||
chr4:54044586
|
C | T | 107 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(104): Show | 122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.330+4369G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044586 | ||||||
chr4:54044648
|
G | A | 2 | a0001c0001t0001g0075a0001c0001t0001g0179 | 2 | HG00280.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.330+4307C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044648 | ||||||
chr4:54044648
|
G | C | 1 | a0001c0001t0001g0181 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.330+4307C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044648 | ||||||
chr4:54044704
|
T | C | 1 | a0001c0001t0002g0145 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.330+4251A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044704 | ||||||
chr4:54044896
|
C | T | 4 | a0001c0002t0001g0215a0001c0002t0001g0216a0001c0002t0001g0217others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+4059G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044896 | ||||||
chr4:54044911
|
TAAAG | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0070others(3): Show | 8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+4040_330+4043d others(6): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044911 | ||||||
chr4:54044976
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.330+3979C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044976 | ||||||
chr4:54044993
|
A | G | 2 | a0001c0001t0002g0005a0001c0001t0002g0135 | 4 | NA18975.hp2 NA18998.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+3962T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044993 | ||||||
chr4:54044998
|
C | A | 1 | a0001c0001t0002g0005 | 3 | NA18975.hp2 NA18998.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.330+3957G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044998 | ||||||
chr4:54045027
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.330+3928C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045027 | ||||||
chr4:54045046
|
C | G | 1 | a0001c0001t0001g0187 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.330+3909G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045046 | ||||||
chr4:54045129
|
A | G | 1 | a0001c0001t0009g0117 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.330+3826T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045129 | ||||||
chr4:54045217
|
G | A | 2 | a0001c0001t0003g0121a0001c0001t0003g0123 | 2 | HG00642.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.330+3738C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045217 | ||||||
chr4:54045223
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.330+3732T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045223 | ||||||
chr4:54045261
|
T | A | 1 | a0001c0001t0005g0120 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.330+3694A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045261 | ||||||
chr4:54045309
|
A | T | 14 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0069others(11): Show | 17 | HG00438.hp2 HG00597.hp1 HG02155.hp1 others(14): Show |
intron_variant | MODIFIER | c.330+3646T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045309 | ||||||
chr4:54045310
|
T | G | 1 | a0001c0001t0002g0057 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.330+3645A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045310 | ||||||
chr4:54045314
|
C | T | 14 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0069others(11): Show | 17 | HG00438.hp2 HG00597.hp1 HG02155.hp1 others(14): Show |
intron_variant | MODIFIER | c.330+3641G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045314 | ||||||
chr4:54045318
|
A | C | 6 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(3): Show | 6 | HG01243.hp1 HG02055.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.330+3637T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045318 | ||||||
chr4:54045344
|
A | C | 14 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0069others(11): Show | 17 | HG00438.hp2 HG00597.hp1 HG02155.hp1 others(14): Show |
intron_variant | MODIFIER | c.330+3611T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045344 | ||||||
chr4:54045395
|
T | G | 108 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(105): Show | 123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.330+3560A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045395 | ||||||
chr4:54045643
|
C | T | 1 | a0001c0001t0009g0117 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.330+3312G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045643 | ||||||
chr4:54045644
|
A | G | 1 | a0001c0001t0009g0117 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.330+3311T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045644 | ||||||
chr4:54045648
|
C | T | 1 | a0001c0001t0009g0117 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.330+3307G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045648 | ||||||
chr4:54045733
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.330+3222G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045733 | ||||||
chr4:54045741
|
A | C | 3 | a0001c0002t0001g0215a0001c0002t0001g0216a0001c0002t0001g0217 | 3 | HG02145.hp2 HG02559.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.330+3214T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045741 | ||||||
chr4:54045752
|
C | T | 4 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+3203G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045752 | ||||||
chr4:54045768
|
A | C | 1 | a0001c0001t0003g0124 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.330+3187T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045768 | ||||||
chr4:54045770
|
A | G | 1 | a0001c0001t0003g0124 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.330+3185T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045770 | ||||||
chr4:54045883
|
T | C | 1 | a0001c0001t0008g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.330+3072A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045883 | ||||||
chr4:54045905
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | NA18978.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.330+3050G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045905 | ||||||
chr4:54045971
|
G | T | 1 | a0001c0001t0002g0082 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.330+2984C>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045971 | ||||||
chr4:54046071
|
T | G | 1 | a0001c0002t0005g0214 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.330+2884A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54046071 | ||||||
chr4:54046139
|
G | T | 89 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(86): Show | 104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.330+2816C>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54046139 | ||||||
chr4:54046201
|
A | G | 2 | a0001c0001t0002g0099a0001c0001t0002g0100 | 2 | NA18747.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.330+2754T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54046201 | ||||||
chr4:54046381
|
C | T | 22 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(19): Show | 24 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.330+2574G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54046381 | ||||||
chr4:54046584
|
C | T | 7 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(4): Show | 7 | HG02145.hp1 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.330+2371G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54046584 | ||||||
chr4:54046601
|
C | G | 1 | a0001c0001t0003g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.330+2354G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54046601 | ||||||
chr4:54046678
|
C | G | 1 | a0001c0001t0002g0057 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.330+2277G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54046678 | ||||||
chr4:54046739
|
G | A | 1 | a0001c0001t0002g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.330+2216C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54046739 | ||||||
chr4:54046773
|
G | C | 101 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(98): Show | 116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.330+2182C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54046773 | ||||||
chr4:54047051
|
C | T | 3 | a0001c0001t0003g0040a0001c0001t0003g0042a0001c0001t0003g0043 | 3 | HG01243.hp1 HG02572.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.330+1904G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047051 | ||||||
chr4:54047095
|
A | T | 2 | a0001c0001t0003g0122a0001c0001t0003g0124 | 2 | HG02109.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.330+1860T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047095 | ||||||
chr4:54047102
|
C | T | 8 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(5): Show | 8 | HG00642.hp2 HG01167.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+1853G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047102 | ||||||
chr4:54047150
|
C | A | 4 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+1805G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047150 | ||||||
chr4:54047177
|
A | G | 59 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0008others(56): Show | 70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.330+1778T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047177 | ||||||
chr4:54047285
|
A | C | 22 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(19): Show | 24 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.330+1670T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047285 | ||||||
chr4:54047410
|
C | T | 22 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(19): Show | 24 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.330+1545G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047410 | ||||||
chr4:54047422
|
G | A | 1 | a0001c0001t0003g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.330+1533C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047422 | ||||||
chr4:54047543
|
G | A | 2 | a0001c0001t0003g0122a0001c0001t0003g0124 | 2 | HG02109.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.330+1412C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047543 | ||||||
chr4:54047591
|
T | C | 8 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0149others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+1364A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047591 | ||||||
chr4:54047632
|
C | T | 4 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+1323G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047632 | ||||||
chr4:54047663
|
G | T | 1 | a0001c0001t0001g0093 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.330+1292C>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047663 | ||||||
chr4:54047745
|
C | T | 5 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG00639.hp2 HG01070.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.330+1210G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047745 | ||||||
chr4:54047787
|
T | C | 109 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(106): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.330+1168A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047787 | ||||||
chr4:54047917
|
G | A | 217 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(214): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.330+1038C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047917 | ||||||
chr4:54047970
|
C | G | 1 | a0001c0002t0005g0214 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.330+985G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047970 | ||||||
chr4:54048008
|
G | A | 1 | a0001c0001t0002g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.330+947C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54048008 | ||||||
chr4:54048146
|
G | A | 2 | a0001c0001t0001g0075a0001c0001t0002g0126 | 2 | HG00280.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.330+809C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54048146 | ||||||
chr4:54048156
|
T | C | 3 | a0001c0001t0002g0011a0001c0001t0002g0056a0001c0001t0002g0064 | 4 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+799A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54048156 | ||||||
chr4:54048191
|
T | C | 1 | a0001c0001t0002g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.330+764A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54048191 | ||||||
chr4:54048544
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.330+411G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54048544 | ||||||
chr4:54048646
|
G | A | 6 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(3): Show | 6 | HG01243.hp1 HG02055.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.330+309C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54048646 | ||||||
chr4:54048698
|
T | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(180): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.330+257A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54048698 | ||||||
chr4:54048835
|
T | C | 5 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(2): Show | 5 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.330+120A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54048835 | ||||||
chr4:54049360
|
T | C | 2 | a0001c0001t0001g0196a0001c0001t0001g0213 | 2 | HG00099.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.120-55A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54049360 | ||||||
chr4:54049893
|
C | T | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(15): Show | 20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.120-588G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54049893 | ||||||
chr4:54050024
|
A | T | 1 | a0001c0001t0001g0080 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.120-719T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54050024 | ||||||
chr4:54050156
|
T | C | 87 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(84): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.120-851A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54050156 | ||||||
chr4:54050461
|
T | C | 1 | a0001c0002t0005g0214 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.120-1156A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54050461 | ||||||
chr4:54050543
|
C | G | 1 | a0001c0001t0004g0079 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.120-1238G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54050543 | ||||||
chr4:54050552
|
A | T | 1 | a0001c0001t0001g0206 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.120-1247T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54050552 | ||||||
chr4:54050644
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.120-1339A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54050644 | ||||||
chr4:54050758
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.120-1453C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54050758 | ||||||
chr4:54050783
|
T | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(15): Show | 20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.120-1478A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54050783 | ||||||
chr4:54051200
|
A | C | 59 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0008others(56): Show | 70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.120-1895T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54051200 | ||||||
chr4:54051229
|
A | G | 1 | a0001c0001t0002g0048 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.120-1924T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54051229 | ||||||
chr4:54051317
|
C | T | 87 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(84): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.120-2012G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54051317 | ||||||
chr4:54051517
|
C | T | 1 | a0001c0001t0007g0219 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.120-2212G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54051517 | ||||||
chr4:54051651
|
C | G | 2 | a0001c0001t0002g0134a0001c0001t0002g0139 | 2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.120-2346G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54051651 | ||||||
chr4:54051770
|
C | T | 21 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0014others(18): Show | 27 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.120-2465G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54051770 | ||||||
chr4:54051801
|
A | T | 2 | a0001c0001t0003g0121a0001c0001t0003g0123 | 2 | HG00642.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.120-2496T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54051801 | ||||||
chr4:54051864
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.120-2559C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54051864 | ||||||
chr4:54051900
|
T | C | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0070others(3): Show | 8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.120-2595A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54051900 | ||||||
chr4:54051915
|
T | C | 3 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072 | 3 | HG02615.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.120-2610A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54051915 | ||||||
chr4:54052068
|
T | A | 1 | a0001c0001t0001g0078 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.120-2763A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54052068 | ||||||
chr4:54052123
|
C | CCTT | 94 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(91): Show | 109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.120-2821_120-2819d others(5): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54052123 | ||||||
chr4:54052228
|
T | G | 1 | a0001c0001t0001g0020 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.120-2923A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54052228 | ||||||
chr4:54052460
|
G | C | 1 | a0001c0001t0001g0210 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.120-3155C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54052460 | ||||||
chr4:54052476
|
T | C | 109 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(106): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.120-3171A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54052476 | ||||||
chr4:54052731
|
G | A | 2 | a0001c0001t0001g0075a0001c0001t0001g0179 | 2 | HG00280.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.120-3426C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54052731 | ||||||
chr4:54052976
|
ATTATC | A | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(15): Show | 20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.120-3676_120-3672d others(7): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54052976 | ||||||
chr4:54053044
|
A | G | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(78): Show | 96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.120-3739T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54053044 | ||||||
chr4:54053164
|
C | G | 1 | a0001c0001t0002g0066 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.120-3859G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54053164 | ||||||
chr4:54053368
|
C | A | 4 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.120-4063G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54053368 | ||||||
chr4:54053530
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.120-4225C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54053530 | ||||||
chr4:54053551
|
A | G | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(15): Show | 20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.120-4246T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54053551 | ||||||
chr4:54053556
|
C | CA | 16 | a0001c0001t0001g0076a0001c0001t0001g0101a0001c0001t0001g0102others(13): Show | 16 | HG00597.hp1 HG00597.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.120-4252dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54053556 | ||||||
chr4:54053556
|
CA | C | 85 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(82): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.120-4252delT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54053556 | ||||||
chr4:54053556
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0002g0133a0001c0001t0002g0140 | 2 | HG00642.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.120-4261_120-4252d others(12): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54053556 | ||||||
chr4:54053838
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.120-4533A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54053838 | ||||||
chr4:54054054
|
T | C | 1 | a0001c0001t0002g0140 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.120-4749A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54054054 | ||||||
chr4:54054878
|
T | G | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.120-5573A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54054878 | ||||||
chr4:54054904
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.120-5599A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54054904 | ||||||
chr4:54055032
|
G | A | 1 | a0001c0001t0003g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.120-5727C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54055032 | ||||||
chr4:54055042
|
A | T | 1 | a0001c0001t0002g0066 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.120-5737T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54055042 | ||||||
chr4:54055326
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.120-6021G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54055326 | ||||||
chr4:54055327
|
G | A | 8 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0149others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.120-6022C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54055327 | ||||||
chr4:54055578
|
C | G | 1 | a0001c0001t0001g0078 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.120-6273G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54055578 | ||||||
chr4:54055735
|
T | C | 7 | a0001c0001t0001g0076a0001c0001t0003g0040a0001c0001t0003g0041others(4): Show | 7 | HG01243.hp1 HG02055.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.120-6430A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54055735 | ||||||
chr4:54055919
|
G | A | 6 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(3): Show | 6 | HG02647.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.120-6614C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54055919 | ||||||
chr4:54056315
|
T | C | 1 | a0001c0001t0001g0183 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.120-7010A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54056315 | ||||||
chr4:54056521
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.120-7216C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54056521 | ||||||
chr4:54056560
|
T | G | 4 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.120-7255A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54056560 | ||||||
chr4:54056980
|
C | T | 1 | a0001c0001t0005g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.119+7202G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54056980 | ||||||
chr4:54057015
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.119+7167T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54057015 | ||||||
chr4:54057038
|
G | C | 1 | a0001c0001t0003g0045 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.119+7144C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54057038 | ||||||
chr4:54057159
|
C | T | 4 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.119+7023G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54057159 | ||||||
chr4:54057725
|
C | G | 1 | a0001c0001t0001g0031 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.119+6457G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54057725 | ||||||
chr4:54057725
|
C | T | 1 | a0001c0001t0002g0127 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.119+6457G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54057725 | ||||||
chr4:54057780
|
T | C | 1 | a0001c0001t0001g0110 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.119+6402A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54057780 | ||||||
chr4:54058021
|
T | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0184a0001c0001t0001g0185others(2): Show | 6 | HG00741.hp2 HG01346.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.119+6161A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058021 | ||||||
chr4:54058041
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.119+6141G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058041 | ||||||
chr4:54058068
|
G | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0184a0001c0001t0001g0185others(2): Show | 6 | HG00741.hp2 HG01346.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.119+6114C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058068 | ||||||
chr4:54058423
|
G | A | 4 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.119+5759C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058423 | ||||||
chr4:54058447
|
T | C | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0070others(3): Show | 8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.119+5735A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058447 | ||||||
chr4:54058536
|
T | TCACATAC others(1): Show |
2 | a0001c0001t0002g0012a0001c0001t0002g0066 | 3 | HG01175.hp1 HG01192.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.119+5638_119+5645d others(10): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058536 | ||||||
chr4:54058549
|
T | TACACACA others(3): Show |
2 | a0001c0001t0002g0067a0001c0001t0002g0068 | 2 | HG02735.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.119+5632_119+5633i others(12): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058549 | ||||||
chr4:54058549
|
TAC | T | 9 | a0001c0001t0001g0037a0001c0001t0002g0005a0001c0001t0002g0125others(6): Show | 11 | HG00544.hp1 HG01255.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.119+5631_119+5632d others(4): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058549 | ||||||
chr4:54058551
|
C | CACACAT | 16 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0046others(13): Show | 18 | HG00099.hp1 HG00323.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.119+5630_119+5631i others(8): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058551 | ||||||
chr4:54058553
|
C | CACAT | 10 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0054others(7): Show | 10 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.119+5628_119+5629i others(6): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058553 | ||||||
chr4:54058553
|
CACACAT | C | 13 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(10): Show | 17 | HG02258.hp2 HG02622.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.119+5623_119+5628d others(8): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058553 | ||||||
chr4:54058555
|
C | CAT | 10 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0048others(7): Show | 12 | HG02572.hp2 HG02683.hp1 HG03927.hp1 others(9): Show |
intron_variant | MODIFIER | c.119+5626_119+5627i others(4): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058555 | ||||||
chr4:54058555
|
CACAT | C | 11 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(8): Show | 11 | HG02258.hp1 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.119+5623_119+5626d others(6): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058555 | ||||||
chr4:54058557
|
C | T | 11 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0047others(8): Show | 15 | HG00639.hp1 HG00642.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.119+5625G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058557 | ||||||
chr4:54058559
|
T | C | 52 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(49): Show | 61 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.119+5623A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058559 | ||||||
chr4:54058559
|
T | TAC | 9 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(6): Show | 9 | HG00639.hp2 HG01081.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.119+5621_119+5622d others(4): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058559 | ||||||
chr4:54058559
|
T | TACAC | 6 | a0001c0001t0003g0040a0001c0001t0003g0042a0001c0001t0003g0043others(3): Show | 6 | HG01243.hp1 HG02572.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.119+5619_119+5622d others(6): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058559 | ||||||
chr4:54058559
|
TAC | T | 45 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(42): Show | 50 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.119+5621_119+5622d others(4): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058559 | ||||||
chr4:54058559
|
TACAC | T | 12 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0149others(9): Show | 12 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.119+5619_119+5622d others(6): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058559 | ||||||
chr4:54058561
|
C | T | 11 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(8): Show | 11 | HG02258.hp1 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.119+5621G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058561 | ||||||
chr4:54058563
|
C | T | 13 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(10): Show | 17 | HG02258.hp2 HG02622.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.119+5619G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058563 | ||||||
chr4:54059027
|
A | C | 22 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(19): Show | 24 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.119+5155T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54059027 | ||||||
chr4:54059184
|
A | G | 1 | a0001c0001t0002g0046 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.119+4998T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54059184 | ||||||
chr4:54059251
|
G | A | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0207 | 3 | NA18950.hp1 NA18956.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.119+4931C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54059251 | ||||||
chr4:54059369
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.119+4813G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54059369 | ||||||
chr4:54059386
|
T | A | 5 | a0001c0001t0001g0039a0001c0001t0001g0119a0001c0001t0001g0153others(2): Show | 5 | HG02257.hp1 HG02523.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.119+4796A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54059386 | ||||||
chr4:54059444
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.119+4738T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54059444 | ||||||
chr4:54059585
|
T | TA | 11 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(8): Show | 11 | HG00642.hp2 HG01167.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.119+4596dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54059585 | ||||||
chr4:54059970
|
T | C | 4 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.119+4212A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54059970 | ||||||
chr4:54059978
|
T | A | 1 | a0001c0001t0002g0125 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.119+4204A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54059978 | ||||||
chr4:54059997
|
G | C | 4 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.119+4185C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54059997 | ||||||
chr4:54060019
|
T | C | 5 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG00639.hp2 HG01070.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.119+4163A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54060019 | ||||||
chr4:54060040
|
G | C | 1 | a0001c0001t0001g0204 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.119+4142C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54060040 | ||||||
chr4:54060073
|
G | A | 1 | a0001c0001t0002g0005 | 3 | NA18975.hp2 NA18998.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.119+4109C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54060073 | ||||||
chr4:54060207
|
ATCC | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037 | 3 | HG02145.hp1 HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.119+3972_119+3974d others(5): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54060207 | ||||||
chr4:54060208
|
TCCC | T | 15 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(12): Show | 17 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.119+3971_119+3973d others(5): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54060208 | ||||||
chr4:54060302
|
C | T | 51 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0008others(48): Show | 62 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.119+3880G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54060302 | ||||||
chr4:54060311
|
T | C | 4 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.119+3871A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54060311 | ||||||
chr4:54060506
|
G | C | 19 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0014others(16): Show | 25 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.119+3676C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54060506 | ||||||
chr4:54060744
|
T | G | 1 | a0001c0001t0001g0016 | 2 | HG02809.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.119+3438A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54060744 | ||||||
chr4:54060747
|
T | A | 1 | a0001c0001t0001g0205 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.119+3435A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54060747 | ||||||
chr4:54061344
|
G | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0148 | 5 | HG02717.hp2 HG02723.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.119+2838C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54061344 | ||||||
chr4:54061441
|
C | G | 1 | a0001c0001t0003g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.119+2741G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54061441 | ||||||
chr4:54061867
|
G | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0039 | 4 | HG02622.hp2 HG02809.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.119+2315C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54061867 | ||||||
chr4:54061867
|
G | T | 1 | a0001c0001t0001g0026 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.119+2315C>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54061867 | ||||||
chr4:54062151
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.119+2031A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54062151 | ||||||
chr4:54062159
|
A | C | 6 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(3): Show | 6 | HG01243.hp1 HG02055.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.119+2023T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54062159 | ||||||
chr4:54062302
|
G | C | 1 | a0001c0001t0001g0206 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.119+1880C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54062302 | ||||||
chr4:54062329
|
T | TTTTA | 10 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0207others(7): Show | 12 | HG02145.hp2 HG02559.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.119+1849_119+1852d others(6): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54062329 | ||||||
chr4:54062329
|
T | TTTTATTT others(1): Show |
3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 3 | HG02630.hp1 HG02717.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.119+1845_119+1852d others(10): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54062329 | ||||||
chr4:54062329
|
T | TTTTATTT others(5): Show |
2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.119+1841_119+1852d others(14): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54062329 | ||||||
chr4:54062329
|
T | TTTTATTT others(9): Show |
4 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0154others(1): Show | 4 | HG02257.hp1 HG02486.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.119+1837_119+1852d others(18): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54062329 | ||||||
chr4:54062329
|
TTTTA | T | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(15): Show | 20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.119+1849_119+1852d others(6): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54062329 | ||||||
chr4:54062522
|
C | T | 3 | a0001c0002t0001g0215a0001c0002t0001g0216a0001c0002t0001g0217 | 3 | HG02145.hp2 HG02559.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.119+1660G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54062522 | ||||||
chr4:54062812
|
A | T | 8 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(5): Show | 8 | HG02145.hp2 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.119+1370T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54062812 | ||||||
chr4:54063458
|
T | C | 1 | a0001c0001t0004g0155 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.119+724A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54063458 | ||||||
chr4:54064008
|
TC | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021 | 4 | HG02922.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.119+173delG | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54064008 | ||||||
chr4:54064009
|
C | A | 1 | a0001c0001t0001g0208 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.119+173G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54064009 | ||||||
chr4:54064050
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.119+132G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54064050 | ||||||
chr4:54064102
|
CAG | C | 56 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(53): Show | 61 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.119+78_119+79delCT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54064102 | ||||||
chr4:54064103
|
AG | A | 5 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 5 | HG00597.hp2 HG01258.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.119+78delC | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54064103 | ||||||
chr4:54064172
|
C | T | 1 | a0001c0002t0005g0214 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.119+10G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54064172 |