geneid | 134829 |
---|---|
ensemblid | ENSG00000146352.13 |
hgncid | 23046 |
symbol | CLVS2 |
name | clavesin 2 |
refseq_nuc | NM_001010852.4 |
refseq_prot | NP_001010852.2 |
ensembl_nuc | ENST00000275162.10 |
ensembl_prot | ENSP00000275162.4 |
mane_status | MANE Select |
chr | chr6 |
start | 122996235 |
end | 123072925 |
strand | + |
ver | v1.2 |
region | chr6:122996235-123072925 |
region5000 | chr6:122991235-123077925 |
regionname0 | CLVS2_chr6_122996235_123072925 |
regionname5000 | CLVS2_chr6_122991235_123077925 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 327 | 335 | 92 | 59 | 136 | 12 | 34 | 112 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0002 | 0/0 | 327 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 984 | 329 | 87 | 59 | 136 | 12 | 33 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
c0002 | 0/0 | 984 | 5 | 5 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
c0003 | 0/0 | 984 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
c0004 | 0/0 | 984 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 10236 | 44 | 6 | 6 | 28 | 1 | 3 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0002 | 0/0 | 10236 | 33 | 2 | 9 | 13 | 4 | 5 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0003 | 0/0 | 10236 | 28 | 4 | 11 | 8 | 1 | 4 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0004 | 0/0 | 10235 | 19 | 1 | 3 | 11 | 1 | 3 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0005 | 0/1 | 10236 | 18 | 2 | 5 | 8 | 0 | 2 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0006 | 0/0 | 10236 | 16 | 0 | 1 | 15 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0007 | 0/0 | 10240 | 10 | 0 | 1 | 8 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0008 | 0/0 | 10236 | 9 | 9 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0009 | 0/0 | 10244 | 7 | 1 | 0 | 1 | 0 | 5 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0010 | 0/0 | 10236 | 7 | 5 | 2 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0011 | 0/0 | 10236 | 7 | 0 | 0 | 7 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0012 | 0/0 | 10234 | 5 | 1 | 0 | 4 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0013 | 0/0 | 10236 | 5 | 0 | 0 | 4 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0014 | 0/0 | 10236 | 5 | 0 | 0 | 5 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0015 | 0/0 | 10235 | 4 | 4 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0016 | 0/0 | 10240 | 4 | 4 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0017 | 0/0 | 10238 | 4 | 4 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0018 | 0/0 | 10240 | 3 | 0 | 0 | 3 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0019 | 1/0 | 10236 | 3 | 0 | 2 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0020 | 0/0 | 10236 | 3 | 0 | 2 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0021 | 0/0 | 10242 | 3 | 0 | 3 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0022 | 0/0 | 10236 | 3 | 3 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0023 | 0/0 | 10236 | 3 | 0 | 2 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0024 | 0/0 | 10237 | 3 | 3 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0025 | 0/0 | 10244 | 3 | 0 | 3 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0026 | 0/0 | 10236 | 3 | 3 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0027 | 0/0 | 10234 | 3 | 0 | 2 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0028 | 0/0 | 10234 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0029 | 0/0 | 10237 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0030 | 0/0 | 10236 | 2 | 0 | 2 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0031 | 0/0 | 10236 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0032 | 0/0 | 10238 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0033 | 0/0 | 10236 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0034 | 0/0 | 10236 | 2 | 0 | 0 | 0 | 2 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0035 | 0/0 | 10238 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0036 | 0/0 | 10238 | 2 | 0 | 0 | 0 | 0 | 2 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0037 | 0/0 | 10235 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0038 | 0/0 | 10238 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0039 | 0/0 | 10236 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0040 | 0/0 | 10236 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0041 | 0/0 | 10244 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0042 | 0/0 | 10234 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0043 | 0/0 | 10234 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0044 | 0/0 | 10234 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0045 | 0/0 | 10245 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0046 | 0/0 | 10236 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0047 | 0/0 | 10236 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0048 | 0/0 | 10236 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0049 | 0/0 | 10235 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0050 | 0/0 | 10236 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0051 | 0/0 | 10236 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0052 | 0/0 | 10235 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0053 | 0/0 | 10236 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0054 | 0/0 | 10245 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0055 | 0/0 | 10236 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0056 | 0/0 | 10238 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0057 | 0/0 | 10238 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0058 | 0/0 | 10235 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0059 | 0/0 | 10235 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0060 | 0/0 | 10234 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0061 | 0/0 | 10236 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0062 | 0/0 | 10236 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0063 | 0/0 | 10236 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0064 | 0/0 | 10236 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0065 | 0/0 | 10218 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0066 | 0/0 | 10236 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0067 | 0/0 | 10236 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0068 | 0/0 | 10236 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0069 | 0/0 | 10244 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0070 | 0/0 | 10234 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0071 | 0/0 | 10240 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0072 | 0/0 | 10240 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0073 | 0/0 | 10238 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0074 | 0/0 | 10236 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0075 | 0/0 | 10235 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0076 | 0/0 | 10236 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0077 | 0/0 | 10236 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0078 | 0/0 | 10236 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0079 | 0/0 | 10236 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0080 | 0/0 | 10236 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0081 | 0/0 | 10247 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0082 | 0/0 | 10238 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0083 | 0/0 | 10234 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0084 | 0/0 | 10238 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0085 | 0/0 | 10236 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0086 | 0/0 | 10238 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0087 | 0/0 | 10236 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0088 | 0/0 | 10234 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0089 | 0/0 | 10236 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
t0090 | 0/0 | 10238 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0003 | 0/0 | 4 | 1 | 1 | 0 | 2 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0004 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0005 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0021 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0282 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 984 | 329 | 87 | 59 | 136 | 12 | 33 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0002 | 0/0 | 984 | 5 | 5 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0004 | 0/0 | 984 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0002c0003 | 0/0 | 984 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 11219 | 44 | 6 | 6 | 28 | 1 | 3 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0002 | 0/0 | 11219 | 33 | 2 | 9 | 13 | 4 | 5 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0003 | 0/0 | 11219 | 28 | 4 | 11 | 8 | 1 | 4 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0004 | 0/0 | 11218 | 19 | 1 | 3 | 11 | 1 | 3 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0005 | 0/1 | 11219 | 17 | 2 | 4 | 8 | 0 | 2 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0006 | 0/0 | 11219 | 16 | 0 | 1 | 15 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0007 | 0/0 | 11223 | 10 | 0 | 1 | 8 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0008 | 0/0 | 11219 | 9 | 9 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0009 | 0/0 | 11227 | 7 | 1 | 0 | 1 | 0 | 5 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0010 | 0/0 | 11219 | 7 | 5 | 2 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0011 | 0/0 | 11219 | 7 | 0 | 0 | 7 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0012 | 0/0 | 11217 | 5 | 1 | 0 | 4 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0013 | 0/0 | 11219 | 5 | 0 | 0 | 4 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0014 | 0/0 | 11219 | 5 | 0 | 0 | 5 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0015 | 0/0 | 11218 | 4 | 4 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0016 | 0/0 | 11223 | 4 | 4 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0017 | 0/0 | 11221 | 4 | 4 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0018 | 0/0 | 11223 | 3 | 0 | 0 | 3 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0019 | 1/0 | 11219 | 3 | 0 | 2 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0020 | 0/0 | 11219 | 3 | 0 | 2 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0021 | 0/0 | 11225 | 3 | 0 | 3 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0022 | 0/0 | 11219 | 3 | 3 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0023 | 0/0 | 11219 | 3 | 0 | 2 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0025 | 0/0 | 11227 | 3 | 0 | 3 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0026 | 0/0 | 11219 | 3 | 3 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0027 | 0/0 | 11217 | 3 | 0 | 2 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0028 | 0/0 | 11217 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0030 | 0/0 | 11219 | 2 | 0 | 2 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0031 | 0/0 | 11219 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0032 | 0/0 | 11221 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0033 | 0/0 | 11219 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0034 | 0/0 | 11219 | 2 | 0 | 0 | 0 | 2 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0035 | 0/0 | 11221 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0036 | 0/0 | 11221 | 2 | 0 | 0 | 0 | 0 | 2 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0037 | 0/0 | 11218 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0038 | 0/0 | 11221 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0039 | 0/0 | 11219 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0040 | 0/0 | 11219 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0041 | 0/0 | 11227 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0042 | 0/0 | 11217 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0043 | 0/0 | 11217 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0044 | 0/0 | 11217 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0045 | 0/0 | 11228 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0046 | 0/0 | 11219 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0047 | 0/0 | 11219 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0048 | 0/0 | 11219 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0049 | 0/0 | 11218 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0050 | 0/0 | 11219 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0051 | 0/0 | 11219 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0052 | 0/0 | 11218 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0053 | 0/0 | 11219 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0054 | 0/0 | 11228 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0055 | 0/0 | 11219 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0056 | 0/0 | 11221 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0057 | 0/0 | 11221 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0058 | 0/0 | 11218 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0059 | 0/0 | 11218 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0060 | 0/0 | 11217 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0061 | 0/0 | 11219 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0062 | 0/0 | 11219 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0063 | 0/0 | 11219 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0064 | 0/0 | 11219 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0065 | 0/0 | 11201 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0066 | 0/0 | 11219 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0067 | 0/0 | 11219 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0068 | 0/0 | 11219 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0069 | 0/0 | 11227 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0070 | 0/0 | 11217 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0071 | 0/0 | 11223 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0072 | 0/0 | 11223 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0073 | 0/0 | 11221 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0074 | 0/0 | 11219 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0075 | 0/0 | 11218 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0077 | 0/0 | 11219 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0078 | 0/0 | 11219 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0079 | 0/0 | 11219 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0080 | 0/0 | 11219 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0081 | 0/0 | 11230 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0082 | 0/0 | 11221 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0083 | 0/0 | 11217 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0084 | 0/0 | 11221 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0085 | 0/0 | 11219 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0086 | 0/0 | 11221 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0087 | 0/0 | 11219 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0088 | 0/0 | 11217 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0089 | 0/0 | 11219 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0001t0090 | 0/0 | 11221 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0002t0024 | 0/0 | 11220 | 3 | 3 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0002t0029 | 0/0 | 11220 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0001c0004t0076 | 0/0 | 11219 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
a0002c0003t0005 | 0/0 | 11219 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | copy fasta | chr6 | 122991235 | 123077925 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0003g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0004g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0005g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0005g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0005g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0005g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0005g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0005g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0005g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0005g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0005g0282 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0006g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0006g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0006g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0006g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0006g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0006g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0006g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0006g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0006g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0006g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0006g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0006g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0007g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0007g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0007g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0007g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0007g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0007g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0007g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0007g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0008g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0008g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0009g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0009g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0009g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0009g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0009g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0009g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0010g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0010g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0010g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0010g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0010g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0010g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0011g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0011g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0011g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0011g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0011g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0011g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0011g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0012g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0012g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0012g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0012g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0012g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0013g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0013g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0013g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0014g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0014g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0014g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0014g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0014g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0015g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0015g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0015g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0015g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0016g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0016g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0016g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0017g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0017g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0017g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0017g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0018g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0019g0021 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0019g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0020g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0020g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0021g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0021g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0022g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0022g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0022g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0023g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0023g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0023g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0025g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0025g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0025g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0026g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0026g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0026g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0027g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0027g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0027g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0028g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0028g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0030g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0031g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0031g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0032g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0032g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0033g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0033g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0034g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0035g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0035g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0036g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0036g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0037g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0037g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0038g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0038g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0039g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0039g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0040g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0040g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0041g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0041g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0042g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0042g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0043g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0043g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0044g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0045g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0045g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0046g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0047g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0048g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0049g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0050g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0051g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0052g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0053g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0054g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0055g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0056g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0057g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0058g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0059g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0060g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0061g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0062g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0063g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0064g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0065g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0066g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0067g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0068g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0069g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0070g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0071g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0072g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0073g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0074g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0075g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0077g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0078g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0079g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0080g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0081g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0082g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0083g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0084g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0085g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0086g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0087g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0088g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0089g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0001t0090g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0002t0024g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0002t0024g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0002t0024g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0002t0029g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0002t0029g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0001c0004t0076g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
a0002c0003t0005g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | GBR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00099 | hp2 | a0001 | c0001 | t0020 | g0281 | EUR | GBR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0114 | EUR | GBR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0024 | EUR | GBR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0024 | EUR | FIN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0104 | EUR | FIN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0228 | EUR | FIN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00323 | hp2 | a0001 | c0001 | t0023 | g0098 | EUR | FIN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00408 | hp2 | a0001 | c0001 | t0004 | g0105 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00423 | hp2 | a0001 | c0001 | t0006 | g0237 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00438 | hp1 | a0001 | c0001 | t0039 | g0233 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00438 | hp2 | a0001 | c0001 | t0067 | g0038 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00621 | hp1 | a0001 | c0001 | t0013 | g0030 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00639 | hp1 | a0001 | c0001 | t0020 | g0031 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00673 | hp2 | a0001 | c0001 | t0013 | g0030 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0131 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00735 | hp1 | a0001 | c0001 | t0027 | g0167 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0138 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00738 | hp1 | a0001 | c0001 | t0019 | g0021 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG00741 | hp2 | a0001 | c0001 | t0010 | g0161 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01070 | hp1 | a0001 | c0001 | t0023 | g0189 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01070 | hp2 | a0001 | c0001 | t0030 | g0010 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01071 | hp1 | a0001 | c0001 | t0030 | g0010 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01071 | hp2 | a0001 | c0001 | t0059 | g0279 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01099 | hp1 | a0001 | c0001 | t0007 | g0255 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01099 | hp2 | a0002 | c0003 | t0005 | g0269 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01106 | hp1 | a0001 | c0001 | t0062 | g0143 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01106 | hp2 | a0001 | c0001 | t0027 | g0168 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01109 | hp2 | a0001 | c0001 | t0025 | g0264 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01167 | hp1 | a0001 | c0001 | t0004 | g0103 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01167 | hp2 | a0001 | c0001 | t0025 | g0263 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01168 | hp2 | a0001 | c0001 | t0025 | g0260 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01192 | hp1 | a0001 | c0001 | t0006 | g0215 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0099 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01243 | hp1 | a0001 | c0001 | t0010 | g0019 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0112 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01256 | hp1 | a0001 | c0001 | t0023 | g0186 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0120 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0121 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01258 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0111 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01346 | hp1 | a0001 | c0001 | t0005 | g0280 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01346 | hp2 | a0001 | c0001 | t0074 | g0113 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01361 | hp1 | a0001 | c0001 | t0058 | g0278 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0097 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01496 | hp1 | a0001 | c0001 | t0075 | g0243 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01496 | hp2 | a0001 | c0001 | t0080 | g0200 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01515 | hp1 | a0001 | c0001 | t0034 | g0003 | EUR | IBS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01515 | hp2 | a0001 | c0001 | t0007 | g0250 | EUR | IBS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0224 | EUR | IBS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01517 | hp2 | a0001 | c0001 | t0034 | g0003 | EUR | IBS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01884 | hp2 | a0001 | c0001 | t0016 | g0027 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01891 | hp1 | a0001 | c0001 | t0032 | g0283 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01891 | hp2 | a0001 | c0001 | t0081 | g0035 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0146 | AMR | PEL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01934 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PEL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01975 | hp2 | a0001 | c0001 | t0021 | g0004 | AMR | PEL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01978 | hp1 | a0001 | c0001 | t0021 | g0005 | AMR | PEL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PEL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02004 | hp1 | a0001 | c0001 | t0020 | g0031 | AMR | PEL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02027 | hp1 | a0001 | c0001 | t0005 | g0028 | EAS | KHV | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02055 | hp1 | a0001 | c0001 | t0008 | g0002 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0123 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02074 | hp1 | a0001 | c0001 | t0006 | g0211 | EAS | KHV | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02074 | hp2 | a0001 | c0001 | t0039 | g0232 | EAS | KHV | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02083 | hp1 | a0001 | c0001 | t0009 | g0022 | EAS | KHV | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02083 | hp2 | a0001 | c0001 | t0004 | g0133 | EAS | KHV | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02145 | hp1 | a0001 | c0001 | t0035 | g0266 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0102 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | CDX | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02155 | hp2 | a0001 | c0001 | t0064 | g0180 | EAS | CDX | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02257 | hp1 | a0001 | c0001 | t0086 | g0150 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02257 | hp2 | a0001 | c0001 | t0015 | g0174 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02258 | hp1 | a0001 | c0001 | t0060 | g0247 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02273 | hp1 | a0001 | c0001 | t0005 | g0267 | AMR | PEL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PEL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02280 | hp1 | a0001 | c0001 | t0035 | g0265 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02280 | hp2 | a0001 | c0001 | t0045 | g0172 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02300 | hp2 | a0001 | c0001 | t0021 | g0004 | AMR | PEL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02451 | hp1 | a0001 | c0001 | t0015 | g0173 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02451 | hp2 | a0001 | c0001 | t0008 | g0001 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02523 | hp1 | a0001 | c0001 | t0049 | g0169 | EAS | KHV | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02523 | hp2 | a0001 | c0001 | t0055 | g0217 | EAS | KHV | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02615 | hp1 | a0001 | c0001 | t0042 | g0191 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02622 | hp1 | a0001 | c0001 | t0008 | g0045 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02622 | hp2 | a0001 | c0001 | t0041 | g0261 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02630 | hp1 | a0001 | c0001 | t0041 | g0262 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02630 | hp2 | a0001 | c0001 | t0026 | g0152 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02647 | hp1 | a0001 | c0001 | t0008 | g0002 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02647 | hp2 | a0001 | c0001 | t0087 | g0148 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02683 | hp1 | a0001 | c0001 | t0009 | g0037 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0119 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02698 | hp1 | a0001 | c0001 | t0069 | g0182 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02698 | hp2 | a0001 | c0001 | t0036 | g0089 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02717 | hp1 | a0001 | c0001 | t0044 | g0018 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02717 | hp2 | a0001 | c0002 | t0024 | g0259 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02723 | hp1 | a0001 | c0001 | t0010 | g0159 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02723 | hp2 | a0001 | c0001 | t0052 | g0147 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0125 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02735 | hp2 | a0001 | c0001 | t0053 | g0088 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02809 | hp1 | a0001 | c0001 | t0057 | g0164 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02818 | hp1 | a0001 | c0001 | t0082 | g0285 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02818 | hp2 | a0001 | c0001 | t0008 | g0002 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02895 | hp1 | a0001 | c0001 | t0028 | g0032 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02895 | hp2 | a0001 | c0001 | t0016 | g0244 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02896 | hp1 | a0001 | c0001 | t0026 | g0093 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02896 | hp2 | a0001 | c0002 | t0024 | g0258 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02897 | hp1 | a0001 | c0001 | t0028 | g0033 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02897 | hp2 | a0001 | c0002 | t0024 | g0257 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02922 | hp1 | a0001 | c0001 | t0010 | g0154 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02922 | hp2 | a0001 | c0001 | t0017 | g0100 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02965 | hp2 | a0001 | c0001 | t0010 | g0157 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02970 | hp1 | a0001 | c0001 | t0017 | g0149 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02970 | hp2 | a0001 | c0001 | t0022 | g0118 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02976 | hp1 | a0001 | c0001 | t0008 | g0043 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02976 | hp2 | a0001 | c0001 | t0073 | g0246 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0241 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03017 | hp2 | a0001 | c0001 | t0066 | g0015 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03041 | hp1 | a0001 | c0001 | t0040 | g0101 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03041 | hp2 | a0001 | c0001 | t0089 | g0156 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03098 | hp1 | a0001 | c0001 | t0088 | g0117 | AFR | MSL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03098 | hp2 | a0001 | c0001 | t0038 | g0095 | AFR | MSL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03130 | hp1 | a0001 | c0001 | t0022 | g0145 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03130 | hp2 | a0001 | c0001 | t0042 | g0284 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03139 | hp1 | a0001 | c0001 | t0017 | g0163 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03139 | hp2 | a0001 | c0001 | t0008 | g0001 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03209 | hp1 | a0001 | c0001 | t0010 | g0158 | AFR | MSL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | MSL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03225 | hp1 | a0001 | c0001 | t0044 | g0018 | AFR | MSL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03225 | hp2 | a0001 | c0001 | t0038 | g0094 | AFR | MSL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03239 | hp1 | a0001 | c0001 | t0068 | g0036 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03486 | hp1 | a0001 | c0001 | t0047 | g0046 | AFR | MSL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03486 | hp2 | a0001 | c0001 | t0005 | g0248 | AFR | MSL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03490 | hp1 | a0001 | c0001 | t0009 | g0181 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0132 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03492 | hp1 | a0001 | c0001 | t0009 | g0022 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03516 | hp1 | a0001 | c0001 | t0017 | g0170 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03516 | hp2 | a0001 | c0001 | t0045 | g0177 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0115 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03540 | hp2 | a0001 | c0001 | t0016 | g0162 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03579 | hp1 | a0001 | c0001 | t0015 | g0175 | AFR | MSL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0213 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03654 | hp2 | a0001 | c0001 | t0063 | g0142 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03704 | hp1 | a0001 | c0001 | t0027 | g0166 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0116 | SAS | BEB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03831 | hp2 | a0001 | c0001 | t0005 | g0275 | SAS | BEB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0205 | SAS | BEB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0096 | SAS | BEB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03927 | hp1 | a0001 | c0001 | t0036 | g0109 | SAS | BEB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03927 | hp2 | a0001 | c0004 | t0076 | g0192 | SAS | BEB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03942 | hp1 | a0001 | c0001 | t0013 | g0005 | SAS | BEB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03942 | hp2 | a0001 | c0001 | t0009 | g0183 | SAS | BEB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG04115 | hp1 | a0001 | c0001 | t0004 | g0141 | SAS | STU | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0239 | SAS | STU | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG04184 | hp1 | a0001 | c0001 | t0077 | g0222 | SAS | BEB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG04184 | hp2 | a0001 | c0001 | t0005 | g0268 | SAS | BEB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG04204 | hp1 | a0001 | c0001 | t0070 | g0050 | SAS | STU | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG04204 | hp2 | a0001 | c0001 | t0009 | g0184 | SAS | STU | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18522 | hp1 | a0001 | c0001 | t0090 | g0286 | AFR | YRI | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18522 | hp2 | a0001 | c0001 | t0008 | g0001 | AFR | YRI | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18906 | hp1 | a0001 | c0001 | t0016 | g0027 | AFR | YRI | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | YRI | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18942 | hp2 | a0001 | c0001 | t0014 | g0227 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18945 | hp2 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18947 | hp1 | a0001 | c0001 | t0013 | g0005 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18948 | hp1 | a0001 | c0001 | t0007 | g0254 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18950 | hp1 | a0001 | c0001 | t0018 | g0007 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18950 | hp2 | a0001 | c0001 | t0005 | g0272 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18951 | hp1 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18951 | hp2 | a0001 | c0001 | t0014 | g0196 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18952 | hp1 | a0001 | c0001 | t0011 | g0076 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18952 | hp2 | a0001 | c0001 | t0004 | g0134 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18953 | hp1 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18956 | hp1 | a0001 | c0001 | t0014 | g0201 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18956 | hp2 | a0001 | c0001 | t0007 | g0251 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18961 | hp2 | a0001 | c0001 | t0006 | g0242 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18962 | hp1 | a0001 | c0001 | t0011 | g0070 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18962 | hp2 | a0001 | c0001 | t0006 | g0193 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18963 | hp1 | a0001 | c0001 | t0011 | g0067 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18963 | hp2 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18967 | hp1 | a0001 | c0001 | t0048 | g0137 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18967 | hp2 | a0001 | c0001 | t0007 | g0252 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18972 | hp1 | a0001 | c0001 | t0006 | g0204 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18972 | hp2 | a0001 | c0001 | t0043 | g0234 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18973 | hp1 | a0001 | c0001 | t0018 | g0007 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18974 | hp1 | a0001 | c0001 | t0012 | g0083 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18977 | hp2 | a0001 | c0001 | t0011 | g0069 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18980 | hp2 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18981 | hp1 | a0001 | c0001 | t0005 | g0270 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18985 | hp1 | a0001 | c0001 | t0031 | g0188 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18986 | hp1 | a0001 | c0001 | t0018 | g0007 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18988 | hp1 | a0001 | c0001 | t0065 | g0128 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18990 | hp2 | a0001 | c0001 | t0012 | g0056 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18991 | hp1 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18994 | hp1 | a0001 | c0001 | t0037 | g0129 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18994 | hp2 | a0001 | c0001 | t0033 | g0271 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18995 | hp1 | a0001 | c0001 | t0006 | g0238 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18995 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18997 | hp1 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18997 | hp2 | a0001 | c0001 | t0007 | g0249 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18998 | hp1 | a0001 | c0001 | t0012 | g0059 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18998 | hp2 | a0001 | c0001 | t0046 | g0025 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18999 | hp1 | a0001 | c0001 | t0051 | g0057 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18999 | hp2 | a0001 | c0001 | t0043 | g0202 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19006 | hp1 | a0001 | c0001 | t0014 | g0230 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19006 | hp2 | a0001 | c0001 | t0005 | g0276 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19007 | hp2 | a0001 | c0001 | t0037 | g0126 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19009 | hp1 | a0001 | c0001 | t0006 | g0216 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19010 | hp1 | a0001 | c0001 | t0050 | g0006 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19010 | hp2 | a0001 | c0001 | t0006 | g0210 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19011 | hp1 | a0001 | c0001 | t0014 | g0198 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19012 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19030 | hp1 | a0001 | c0001 | t0012 | g0058 | AFR | LWK | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19030 | hp2 | a0001 | c0001 | t0072 | g0245 | AFR | LWK | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19043 | hp1 | a0001 | c0002 | t0029 | g0041 | AFR | LWK | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | LWK | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19054 | hp1 | a0001 | c0001 | t0031 | g0187 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19056 | hp1 | a0001 | c0001 | t0061 | g0028 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19058 | hp1 | a0001 | c0001 | t0013 | g0274 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19058 | hp2 | a0001 | c0001 | t0011 | g0084 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0107 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19063 | hp1 | a0001 | c0001 | t0007 | g0256 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19063 | hp2 | a0001 | c0001 | t0078 | g0223 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19065 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19065 | hp2 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19066 | hp2 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19068 | hp2 | a0001 | c0001 | t0006 | g0208 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19070 | hp1 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19076 | hp1 | a0001 | c0001 | t0012 | g0051 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19077 | hp2 | a0001 | c0001 | t0011 | g0064 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19080 | hp1 | a0001 | c0001 | t0006 | g0026 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19084 | hp1 | a0001 | c0001 | t0011 | g0012 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19084 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19085 | hp1 | a0001 | c0001 | t0033 | g0273 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19085 | hp2 | a0001 | c0001 | t0006 | g0212 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19087 | hp2 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19240 | hp1 | a0001 | c0001 | t0056 | g0048 | AFR | YRI | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA19240 | hp2 | a0001 | c0001 | t0079 | g0155 | AFR | YRI | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA20129 | hp1 | a0001 | c0001 | t0008 | g0001 | AFR | ASW | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA20129 | hp2 | a0001 | c0001 | t0009 | g0185 | AFR | ASW | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG01123 | hp2 | a0001 | c0001 | t0019 | g0190 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02109 | hp1 | a0001 | c0001 | t0054 | g0044 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02109 | hp2 | a0001 | c0001 | t0071 | g0178 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02486 | hp1 | a0001 | c0001 | t0010 | g0019 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02486 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02559 | hp1 | a0001 | c0001 | t0026 | g0151 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG02559 | hp2 | a0001 | c0001 | t0084 | g0287 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03471 | hp1 | a0001 | c0001 | t0085 | g0153 | AFR | MSL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG03471 | hp2 | a0001 | c0001 | t0022 | g0144 | AFR | MSL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG06807 | hp1 | a0001 | c0001 | t0015 | g0176 | AFR | USA | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
HG06807 | hp2 | a0001 | c0002 | t0029 | g0042 | AFR | USA | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA18955 | hp2 | a0001 | c0001 | t0006 | g0025 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA20300 | hp1 | a0001 | c0001 | t0083 | g0165 | AFR | USA | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA21309 | hp1 | a0001 | c0001 | t0032 | g0277 | AFR | LWK | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
NA21309 | hp2 | a0001 | c0001 | t0040 | g0160 | AFR | LWK | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0005 | g0282 | REF | REF | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0019 | g0021 | REF | REF | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:123055859
|
G | C | 1 | a0002 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.729G>C | p.Glu243Asp | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/6 | 1800/11219 | 729/984 | 243/327 | chr6 | 123055859 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:123055943
|
C | T | 1 | a0001c0004 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.813C>T | p.Asp271Asp | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/6 | 1884/11219 | 813/984 | 271/327 | chr6 | 123055943 | ||
chr6:123055961
|
T | C | 1 | a0001c0002 | 5 | HG02717.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
synonymous_variant | LOW | c.831T>C | p.Asn277Asn | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/6 | 1902/11219 | 831/984 | 277/327 | chr6 | 123055961 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:122996283
|
G | A | 21 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(18): Show | 91 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(88): Show |
5_prime_UTR_variant | MODIFIER | c.-1023G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/6 | 1495 | chr6 | 122996283 | |||||
chr6:122996286
|
A | C | 76 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(73): Show | 291 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(288): Show |
5_prime_UTR_variant | MODIFIER | c.-1020A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/6 | 1492 | chr6 | 122996286 | |||||
chr6:122996299
|
C | T | 1 | a0001c0001t0090 | 1 | NA18522.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1007C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/6 | 1479 | chr6 | 122996299 | |||||
chr6:122996434
|
C | G | 20 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(17): Show | 93 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(90): Show |
5_prime_UTR_variant | MODIFIER | c.-872C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/6 | 1344 | chr6 | 122996434 | |||||
chr6:122996532
|
A | G | 75 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(72): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-774A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/6 | chr6 | 122996532 | ||||||
chr6:122996553
|
G | T | 1 | a0001c0001t0089 | 1 | HG03041.hp2 | 5_prime_UTR_variant | MODIFIER | c.-753G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/6 | 1225 | chr6 | 122996553 | |||||
chr6:122996554
|
C | T | 1 | a0001c0001t0089 | 1 | HG03041.hp2 | 5_prime_UTR_variant | MODIFIER | c.-752C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/6 | 1224 | chr6 | 122996554 | |||||
chr6:122996686
|
C | T | 2 | a0001c0001t0087a0001c0001t0088 | 2 | HG02647.hp2 HG03098.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-620C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/6 | chr6 | 122996686 | ||||||
chr6:122996734
|
T | A | 1 | a0001c0001t0047 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-572T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/6 | 1044 | chr6 | 122996734 | |||||
chr6:122997224
|
C | G | 1 | a0001c0001t0035 | 2 | HG02145.hp1 HG02280.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-554C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/6 | chr6 | 122997224 | ||||||
chr6:122997333
|
C | T | 2 | a0001c0001t0027a0001c0001t0086 | 4 | HG00735.hp1 HG01106.hp2 HG02257.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-445C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/6 | 445 | chr6 | 122997333 | |||||
chr6:123063978
|
G | C | 80 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(77): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*217G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 217 | chr6 | 123063978 | |||||
chr6:123064100
|
C | T | 21 | a0001c0001t0009a0001c0001t0012a0001c0001t0025others(18): Show | 41 | HG00735.hp1 HG01106.hp2 HG01109.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*339C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 339 | chr6 | 123064100 | |||||
chr6:123064129
|
C | G | 3 | a0001c0001t0006a0001c0001t0046a0001c0001t0055 | 18 | HG00423.hp2 HG01192.hp1 HG02074.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*368C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 368 | chr6 | 123064129 | |||||
chr6:123064160
|
A | G | 1 | a0001c0001t0084 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*399A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 399 | chr6 | 123064160 | |||||
chr6:123064183
|
CT | C | 2 | a0001c0002t0024a0001c0002t0029 | 5 | HG02717.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*423delT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 423 | chr6 | 123064183 | |||||
chr6:123064297
|
G | A | 5 | a0001c0001t0016a0001c0001t0017a0001c0001t0057others(2): Show | 11 | HG01884.hp2 HG02109.hp2 HG02809.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*536G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 536 | chr6 | 123064297 | |||||
chr6:123064318
|
G | T | 2 | a0001c0001t0013a0001c0001t0031 | 7 | HG00621.hp1 HG00673.hp2 HG03942.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*557G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 557 | chr6 | 123064318 | |||||
chr6:123064433
|
C | T | 3 | a0001c0001t0045a0001c0001t0054a0001c0001t0081 | 4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*672C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 672 | chr6 | 123064433 | |||||
chr6:123064670
|
G | GTA | 9 | a0001c0001t0017a0001c0001t0032a0001c0001t0036others(6): Show | 18 | HG01891.hp1 HG02698.hp2 HG02717.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*925_*926dupAT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 927 | INFO_REALIGN_3_PRIME | chr6 | 123064670 | ||||
chr6:123064670
|
G | GTATA | 5 | a0001c0001t0016a0001c0001t0045a0001c0001t0054others(2): Show | 9 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*923_*926dupATAT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 927 | INFO_REALIGN_3_PRIME | chr6 | 123064670 | ||||
chr6:123064676
|
A | G | 1 | a0001c0001t0083 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*915A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 915 | chr6 | 123064676 | |||||
chr6:123064859
|
C | T | 2 | a0001c0001t0007a0001c0001t0018 | 13 | HG01099.hp1 HG01515.hp2 NA18948.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1098C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 1098 | chr6 | 123064859 | |||||
chr6:123064918
|
T | G | 18 | a0001c0001t0003a0001c0001t0004a0001c0001t0020others(15): Show | 68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1157T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 1157 | chr6 | 123064918 | |||||
chr6:123065135
|
C | T | 3 | a0001c0001t0007a0001c0001t0018a0001c0001t0073 | 14 | HG01099.hp1 HG01515.hp2 HG02976.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1374C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 1374 | chr6 | 123065135 | |||||
chr6:123065154
|
A | G | 3 | a0001c0001t0045a0001c0001t0054a0001c0001t0081 | 4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1393A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 1393 | chr6 | 123065154 | |||||
chr6:123065358
|
T | C | 3 | a0001c0001t0045a0001c0001t0054a0001c0001t0081 | 4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1597T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 1597 | chr6 | 123065358 | |||||
chr6:123065515
|
A | T | 21 | a0001c0001t0009a0001c0001t0012a0001c0001t0025others(18): Show | 41 | HG00735.hp1 HG01106.hp2 HG01109.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1754A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 1754 | chr6 | 123065515 | |||||
chr6:123065531
|
A | G | 1 | a0001c0001t0034 | 2 | HG01515.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1770A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 1770 | chr6 | 123065531 | |||||
chr6:123065958
|
A | G | 1 | a0001c0001t0053 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2197A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 2197 | chr6 | 123065958 | |||||
chr6:123066221
|
A | T | 1 | a0001c0001t0080 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2460A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 2460 | chr6 | 123066221 | |||||
chr6:123066264
|
A | T | 1 | a0001c0001t0081 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2503A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 2503 | chr6 | 123066264 | |||||
chr6:123066340
|
A | ACT | 19 | a0001c0001t0012a0001c0001t0027a0001c0001t0028others(16): Show | 31 | HG00735.hp1 HG01106.hp2 HG02109.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2595_*2596dupTC | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 2597 | INFO_REALIGN_3_PRIME | chr6 | 123066340 | ||||
chr6:123066356
|
T | TCTCATAC others(1): Show |
5 | a0001c0001t0009a0001c0001t0025a0001c0001t0041others(2): Show | 14 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2596_*2597insTCAT others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 2597 | INFO_REALIGN_3_PRIME | chr6 | 123066356 | ||||
chr6:123066357
|
C | CTCAT | 2 | a0001c0001t0007a0001c0001t0018 | 13 | HG01099.hp1 HG01515.hp2 NA18948.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2596_*2597insTCAT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 2597 | chr6 | 123066357 | |||||
chr6:123066359
|
T | C | 7 | a0001c0001t0007a0001c0001t0009a0001c0001t0018others(4): Show | 27 | HG01099.hp1 HG01109.hp2 HG01167.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2598T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 2598 | chr6 | 123066359 | |||||
chr6:123066391
|
C | T | 1 | a0001c0001t0030 | 2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2630C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 2630 | chr6 | 123066391 | |||||
chr6:123066700
|
A | G | 6 | a0001c0001t0035a0001c0001t0056a0001c0001t0082others(3): Show | 7 | HG02145.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2939A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 2939 | chr6 | 123066700 | |||||
chr6:123066869
|
G | A | 1 | a0001c0001t0061 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3108G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 3108 | chr6 | 123066869 | |||||
chr6:123066874
|
TACTC | T | 11 | a0001c0001t0012a0001c0001t0027a0001c0001t0028others(8): Show | 21 | HG00735.hp1 HG01106.hp2 HG02258.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3115_*3118delCTCA | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 3115 | INFO_REALIGN_3_PRIME | chr6 | 123066874 | ||||
chr6:123066926
|
T | C | 1 | a0001c0001t0088 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3165T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 3165 | chr6 | 123066926 | |||||
chr6:123066962
|
G | A | 6 | a0001c0001t0035a0001c0001t0056a0001c0001t0082others(3): Show | 7 | HG02145.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3201G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 3201 | chr6 | 123066962 | |||||
chr6:123067057
|
A | G | 1 | a0001c0001t0079 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3296A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 3296 | chr6 | 123067057 | |||||
chr6:123067083
|
T | C | 1 | a0001c0001t0050 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3322T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 3322 | chr6 | 123067083 | |||||
chr6:123067106
|
T | C | 21 | a0001c0001t0009a0001c0001t0012a0001c0001t0025others(18): Show | 41 | HG00735.hp1 HG01106.hp2 HG01109.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*3345T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 3345 | chr6 | 123067106 | |||||
chr6:123067173
|
A | T | 1 | a0001c0001t0066 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3412A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 3412 | chr6 | 123067173 | |||||
chr6:123067502
|
C | T | 4 | a0001c0001t0009a0001c0001t0025a0001c0001t0041others(1): Show | 13 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3741C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 3741 | chr6 | 123067502 | |||||
chr6:123067785
|
A | G | 2 | a0001c0001t0037a0001c0001t0065 | 3 | NA18988.hp1 NA18994.hp1 NA19007.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4024A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 4024 | chr6 | 123067785 | |||||
chr6:123067802
|
T | C | 2 | a0001c0002t0024a0001c0002t0029 | 5 | HG02717.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4041T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 4041 | chr6 | 123067802 | |||||
chr6:123067873
|
A | G | 3 | a0001c0001t0045a0001c0001t0054a0001c0001t0081 | 4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4112A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 4112 | chr6 | 123067873 | |||||
chr6:123068084
|
C | T | 2 | a0001c0001t0007a0001c0001t0018 | 13 | HG01099.hp1 HG01515.hp2 NA18948.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4323C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 4323 | chr6 | 123068084 | |||||
chr6:123068123
|
T | C | 3 | a0001c0001t0045a0001c0001t0054a0001c0001t0081 | 4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4362T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 4362 | chr6 | 123068123 | |||||
chr6:123068127
|
G | A | 1 | a0001c0004t0076 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4366G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 4366 | chr6 | 123068127 | |||||
chr6:123068141
|
T | A | 3 | a0001c0001t0045a0001c0001t0054a0001c0001t0081 | 4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4380T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 4380 | chr6 | 123068141 | |||||
chr6:123068290
|
A | G | 3 | a0001c0001t0045a0001c0001t0054a0001c0001t0081 | 4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4529A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 4529 | chr6 | 123068290 | |||||
chr6:123068488
|
G | A | 6 | a0001c0001t0035a0001c0001t0056a0001c0001t0082others(3): Show | 7 | HG02145.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4727G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 4727 | chr6 | 123068488 | |||||
chr6:123068761
|
C | T | 1 | a0001c0001t0059 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5000C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 5000 | chr6 | 123068761 | |||||
chr6:123068811
|
TA | T | 7 | a0001c0001t0004a0001c0001t0037a0001c0001t0049others(4): Show | 26 | HG00280.hp2 HG00408.hp2 HG00733.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*5052delA | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 5052 | INFO_REALIGN_3_PRIME | chr6 | 123068811 | ||||
chr6:123068917
|
T | C | 2 | a0001c0001t0010a0001c0001t0079 | 8 | HG00741.hp2 HG01243.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5156T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 5156 | chr6 | 123068917 | |||||
chr6:123069006
|
G | C | 1 | a0001c0001t0062 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5245G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 5245 | chr6 | 123069006 | |||||
chr6:123069115
|
G | A | 1 | a0001c0001t0077 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5354G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 5354 | chr6 | 123069115 | |||||
chr6:123069178
|
T | G | 2 | a0001c0001t0007a0001c0001t0018 | 13 | HG01099.hp1 HG01515.hp2 NA18948.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5417T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 5417 | chr6 | 123069178 | |||||
chr6:123069273
|
A | C | 1 | a0001c0001t0030 | 2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5512A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 5512 | chr6 | 123069273 | |||||
chr6:123069356
|
TA | T | 2 | a0001c0001t0015a0001c0001t0052 | 5 | HG02257.hp2 HG02451.hp1 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5605delA | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 5605 | INFO_REALIGN_3_PRIME | chr6 | 123069356 | ||||
chr6:123069385
|
A | G | 1 | a0001c0001t0044 | 2 | HG02717.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5624A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 5624 | chr6 | 123069385 | |||||
chr6:123069522
|
A | G | 2 | a0001c0002t0024a0001c0002t0029 | 5 | HG02717.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5761A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 5761 | chr6 | 123069522 | |||||
chr6:123069554
|
T | C | 80 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(77): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*5793T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 5793 | chr6 | 123069554 | |||||
chr6:123069721
|
T | C | 2 | a0001c0001t0010a0001c0001t0079 | 8 | HG00741.hp2 HG01243.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5960T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 5960 | chr6 | 123069721 | |||||
chr6:123070057
|
T | C | 3 | a0001c0001t0045a0001c0001t0054a0001c0001t0081 | 4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6296T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 6296 | chr6 | 123070057 | |||||
chr6:123070129
|
A | G | 26 | a0001c0001t0007a0001c0001t0009a0001c0001t0012others(23): Show | 58 | HG00735.hp1 HG01099.hp1 HG01106.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*6368A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 6368 | chr6 | 123070129 | |||||
chr6:123070153
|
A | G | 1 | a0001c0001t0041 | 2 | HG02622.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6392A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 6392 | chr6 | 123070153 | |||||
chr6:123070311
|
G | GTCATCC | 1 | a0001c0001t0021 | 3 | HG01975.hp2 HG01978.hp1 HG02300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6553_*6558dupATCC others(2): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 6559 | INFO_REALIGN_3_PRIME | chr6 | 123070311 | ||||
chr6:123070393
|
C | A | 2 | a0001c0001t0014a0001c0001t0051 | 6 | NA18942.hp2 NA18951.hp2 NA18956.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6632C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 6632 | chr6 | 123070393 | |||||
chr6:123070415
|
A | ATCT | 3 | a0001c0001t0045a0001c0001t0054a0001c0001t0081 | 4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6660_*6662dupTTC | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 6663 | INFO_REALIGN_3_PRIME | chr6 | 123070415 | ||||
chr6:123070547
|
C | T | 1 | a0001c0001t0085 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6786C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 6786 | chr6 | 123070547 | |||||
chr6:123070605
|
A | G | 26 | a0001c0001t0007a0001c0001t0009a0001c0001t0012others(23): Show | 58 | HG00735.hp1 HG01099.hp1 HG01106.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*6844A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 6844 | chr6 | 123070605 | |||||
chr6:123070706
|
G | T | 4 | a0001c0001t0012a0001c0001t0043a0001c0001t0068others(1): Show | 9 | HG03239.hp1 HG04204.hp1 NA18972.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6945G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 6945 | chr6 | 123070706 | |||||
chr6:123071152
|
G | T | 2 | a0001c0001t0016a0001c0001t0072 | 5 | HG01884.hp2 HG02895.hp2 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7391G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 7391 | chr6 | 123071152 | |||||
chr6:123071235
|
G | A | 1 | a0001c0001t0063 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7474G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 7474 | chr6 | 123071235 | |||||
chr6:123071582
|
AGGAAGTT others(10): Show |
A | 1 | a0001c0001t0065 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7822_*7838delGGAA others(13): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 7822 | chr6 | 123071582 | |||||
chr6:123071662
|
G | C | 26 | a0001c0001t0007a0001c0001t0009a0001c0001t0012others(23): Show | 58 | HG00735.hp1 HG01099.hp1 HG01106.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*7901G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 7901 | chr6 | 123071662 | |||||
chr6:123071784
|
A | T | 1 | a0001c0001t0064 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8023A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 8023 | chr6 | 123071784 | |||||
chr6:123071789
|
C | T | 1 | a0001c0001t0030 | 2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8028C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 8028 | chr6 | 123071789 | |||||
chr6:123071864
|
G | T | 1 | a0001c0001t0078 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8103G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 8103 | chr6 | 123071864 | |||||
chr6:123072052
|
T | G | 3 | a0001c0001t0045a0001c0001t0054a0001c0001t0081 | 4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8291T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 8291 | chr6 | 123072052 | |||||
chr6:123072097
|
G | A | 1 | a0001c0001t0072 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8336G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 8336 | chr6 | 123072097 | |||||
chr6:123072231
|
A | G | 18 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(15): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*8470A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 8470 | chr6 | 123072231 | |||||
chr6:123072237
|
T | G | 3 | a0001c0001t0045a0001c0001t0054a0001c0001t0081 | 4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8476T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 8476 | chr6 | 123072237 | |||||
chr6:123072555
|
A | G | 2 | a0001c0001t0039a0001c0001t0048 | 3 | HG00438.hp1 HG02074.hp2 NA18967.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8794A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 8794 | chr6 | 123072555 | |||||
chr6:123072607
|
C | T | 2 | a0001c0001t0007a0001c0001t0018 | 13 | HG01099.hp1 HG01515.hp2 NA18948.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*8846C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 8846 | chr6 | 123072607 | |||||
chr6:123072617
|
G | A | 3 | a0001c0001t0045a0001c0001t0054a0001c0001t0081 | 4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8856G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 8856 | chr6 | 123072617 | |||||
chr6:123072778
|
A | G | 2 | a0001c0002t0024a0001c0002t0029 | 5 | HG02717.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*9017A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 9017 | chr6 | 123072778 | |||||
chr6:123072873
|
T | G | 2 | a0001c0001t0045a0001c0001t0054 | 3 | HG02109.hp1 HG02280.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9112T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 9112 | chr6 | 123072873 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:122996879
|
G | C | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-560+133G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/5 | chr6 | 122996879 | ||||||
chr6:122996885
|
C | T | 4 | a0001c0001t0042g0284a0001c0001t0082g0285a0001c0001t0084g0287others(1): Show | 4 | HG02559.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-560+139C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/5 | chr6 | 122996885 | ||||||
chr6:122997156
|
C | G | 120 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0026others(117): Show | 135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.-559-63C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/5 | chr6 | 122997156 | ||||||
chr6:122997164
|
A | C | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-559-55A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/5 | chr6 | 122997164 | ||||||
chr6:122998237
|
C | T | 58 | a0001c0001t0002g0253a0001c0001t0005g0003a0001c0001t0005g0004others(55): Show | 70 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.389+71C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122998237 | ||||||
chr6:122998319
|
C | A | 1 | a0001c0001t0003g0034 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.389+153C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122998319 | ||||||
chr6:122998463
|
G | A | 59 | a0001c0001t0002g0253a0001c0001t0005g0003a0001c0001t0005g0004others(56): Show | 71 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.389+297G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122998463 | ||||||
chr6:122998541
|
C | T | 59 | a0001c0001t0002g0253a0001c0001t0005g0003a0001c0001t0005g0004others(56): Show | 71 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.389+375C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122998541 | ||||||
chr6:122998595
|
C | T | 57 | a0001c0001t0002g0253a0001c0001t0005g0003a0001c0001t0005g0004others(54): Show | 69 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.389+429C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122998595 | ||||||
chr6:122998646
|
C | T | 59 | a0001c0001t0002g0253a0001c0001t0005g0003a0001c0001t0005g0004others(56): Show | 71 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.389+480C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122998646 | ||||||
chr6:122998675
|
G | A | 1 | a0001c0001t0081g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.389+509G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122998675 | ||||||
chr6:122998761
|
G | A | 59 | a0001c0001t0002g0253a0001c0001t0005g0003a0001c0001t0005g0004others(56): Show | 71 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.389+595G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122998761 | ||||||
chr6:122998892
|
TGTCAGTT others(1): Show |
T | 59 | a0001c0001t0002g0253a0001c0001t0005g0003a0001c0001t0005g0004others(56): Show | 71 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.389+729_389+736del others(8): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 122998892 | |||||
chr6:122999042
|
T | C | 1 | a0001c0004t0076g0192 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.389+876T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122999042 | ||||||
chr6:122999191
|
T | G | 1 | a0001c0001t0006g0193 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.389+1025T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122999191 | ||||||
chr6:122999311
|
T | C | 59 | a0001c0001t0002g0253a0001c0001t0005g0003a0001c0001t0005g0004others(56): Show | 71 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.389+1145T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122999311 | ||||||
chr6:122999422
|
T | C | 57 | a0001c0001t0002g0253a0001c0001t0005g0003a0001c0001t0005g0004others(54): Show | 69 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.389+1256T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122999422 | ||||||
chr6:122999452
|
A | G | 59 | a0001c0001t0002g0253a0001c0001t0005g0003a0001c0001t0005g0004others(56): Show | 71 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.389+1286A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122999452 | ||||||
chr6:122999467
|
T | C | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.389+1301T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122999467 | ||||||
chr6:122999578
|
C | A | 5 | a0001c0001t0005g0003a0001c0001t0005g0248a0001c0001t0023g0186others(2): Show | 7 | HG01256.hp1 HG01258.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.389+1412C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122999578 | ||||||
chr6:122999633
|
A | G | 56 | a0001c0001t0002g0253a0001c0001t0005g0003a0001c0001t0005g0004others(53): Show | 68 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.389+1467A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122999633 | ||||||
chr6:122999653
|
A | G | 1 | a0001c0001t0032g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.389+1487A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122999653 | ||||||
chr6:122999668
|
A | C | 8 | a0001c0001t0005g0280a0001c0001t0005g0282a0001c0001t0019g0190others(5): Show | 9 | HG00099.hp2 HG00639.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.389+1502A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122999668 | ||||||
chr6:122999820
|
G | A | 1 | a0001c0001t0042g0284 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.389+1654G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122999820 | ||||||
chr6:122999929
|
T | A | 1 | a0001c0001t0006g0193 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.389+1763T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122999929 | ||||||
chr6:123000221
|
G | A | 1 | a0001c0001t0068g0036 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.389+2055G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123000221 | ||||||
chr6:123000265
|
A | G | 48 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(45): Show | 56 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.389+2099A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123000265 | ||||||
chr6:123000518
|
C | A | 1 | a0001c0001t0009g0037 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.389+2352C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123000518 | ||||||
chr6:123000706
|
C | G | 11 | a0001c0001t0002g0253a0001c0001t0007g0009a0001c0001t0007g0249others(8): Show | 15 | HG01099.hp1 HG01515.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.389+2540C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123000706 | ||||||
chr6:123000815
|
C | G | 1 | a0001c0001t0032g0277 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.389+2649C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123000815 | ||||||
chr6:123000900
|
G | A | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(122): Show | 141 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.389+2734G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123000900 | ||||||
chr6:123001245
|
A | G | 1 | a0001c0001t0006g0242 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.389+3079A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123001245 | ||||||
chr6:123001274
|
G | A | 3 | a0001c0002t0024g0257a0001c0002t0024g0258a0001c0002t0024g0259 | 3 | HG02717.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.389+3108G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123001274 | ||||||
chr6:123001635
|
C | T | 7 | a0001c0001t0009g0022a0001c0001t0009g0037a0001c0001t0009g0181others(4): Show | 8 | HG02083.hp1 HG02683.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.389+3469C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123001635 | ||||||
chr6:123001848
|
G | A | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(247): Show | 278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.389+3682G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123001848 | ||||||
chr6:123001870
|
A | G | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(236): Show | 263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.389+3704A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123001870 | ||||||
chr6:123001982
|
C | G | 3 | a0001c0001t0003g0020a0001c0001t0003g0179a0001c0001t0064g0180 | 4 | HG02155.hp2 NA18948.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.389+3816C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123001982 | ||||||
chr6:123002261
|
G | A | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(236): Show | 263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.389+4095G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123002261 | ||||||
chr6:123002262
|
C | T | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(236): Show | 263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.389+4096C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123002262 | ||||||
chr6:123002310
|
T | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(236): Show | 263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.389+4144T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123002310 | ||||||
chr6:123002331
|
T | C | 10 | a0001c0001t0002g0253a0001c0001t0007g0009a0001c0001t0007g0249others(7): Show | 14 | HG01099.hp1 HG01515.hp2 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.389+4165T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123002331 | ||||||
chr6:123002401
|
G | A | 1 | a0001c0001t0026g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.389+4235G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123002401 | ||||||
chr6:123002586
|
T | TAATAA | 4 | a0001c0001t0001g0013a0001c0001t0026g0093a0001c0001t0042g0191others(1): Show | 5 | HG02109.hp2 HG02602.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.389+4449_389+4453d others(7): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123002586 | |||||
chr6:123002586
|
T | TAATAAAA others(3): Show |
55 | a0001c0001t0002g0171a0001c0001t0002g0253a0001c0001t0007g0009others(52): Show | 62 | HG00735.hp1 HG00741.hp2 HG01099.hp1 others(59): Show |
intron_variant | MODIFIER | c.389+4444_389+4453d others(12): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123002586 | |||||
chr6:123002586
|
T | TAATAAAA others(8): Show |
174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.389+4439_389+4453d others(17): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123002586 | |||||
chr6:123002586
|
T | TAATAAAA others(13): Show |
15 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0002g0023others(12): Show | 16 | HG00438.hp2 HG00673.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.389+4434_389+4453d others(22): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123002586 | |||||
chr6:123002586
|
T | TAATAAAA others(18): Show |
2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG00741.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.389+4429_389+4453d others(27): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123002586 | |||||
chr6:123002692
|
A | G | 10 | a0001c0001t0002g0253a0001c0001t0007g0009a0001c0001t0007g0249others(7): Show | 14 | HG01099.hp1 HG01515.hp2 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.389+4526A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123002692 | ||||||
chr6:123002840
|
C | T | 1 | a0001c0001t0002g0241 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.389+4674C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123002840 | ||||||
chr6:123002851
|
T | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(257): Show | 288 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.389+4685T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123002851 | ||||||
chr6:123002912
|
G | C | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.389+4746G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123002912 | ||||||
chr6:123003168
|
A | C | 1 | a0001c0001t0001g0090 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.389+5002A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123003168 | ||||||
chr6:123003405
|
C | A | 1 | a0001c0001t0087g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.389+5239C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123003405 | ||||||
chr6:123003584
|
A | T | 1 | a0001c0001t0006g0193 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.389+5418A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123003584 | ||||||
chr6:123003593
|
T | TTTGG | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(236): Show | 263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.389+5430_389+5431i others(6): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123003593 | |||||
chr6:123003658
|
G | T | 1 | a0001c0001t0084g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.389+5492G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123003658 | ||||||
chr6:123004070
|
C | T | 1 | a0001c0001t0018g0007 | 3 | NA18950.hp1 NA18973.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.389+5904C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123004070 | ||||||
chr6:123004640
|
C | T | 1 | a0001c0001t0036g0089 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.390-6345C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123004640 | ||||||
chr6:123004667
|
C | G | 1 | a0001c0001t0002g0240 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.390-6318C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123004667 | ||||||
chr6:123004687
|
T | G | 2 | a0001c0001t0038g0094a0001c0001t0038g0095 | 2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.390-6298T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123004687 | ||||||
chr6:123004746
|
C | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(138): Show | 158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.390-6239C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123004746 | ||||||
chr6:123004892
|
G | T | 10 | a0001c0001t0002g0253a0001c0001t0007g0009a0001c0001t0007g0249others(7): Show | 14 | HG01099.hp1 HG01515.hp2 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.390-6093G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123004892 | ||||||
chr6:123004934
|
AAACAAAA others(9): Show |
A | 1 | a0001c0001t0082g0285 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.390-6048_390-6033d others(18): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123004934 | |||||
chr6:123004950
|
CA | C | 8 | a0001c0001t0025g0260a0001c0001t0025g0263a0001c0001t0025g0264others(5): Show | 8 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.390-6021delA | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123004950 | |||||
chr6:123004950
|
CAA | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(138): Show | 158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.390-6022_390-6021d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123004950 | |||||
chr6:123004950
|
CAAA | C | 27 | a0001c0001t0002g0253a0001c0001t0007g0009a0001c0001t0007g0249others(24): Show | 33 | HG00741.hp2 HG01099.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.390-6023_390-6021d others(5): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123004950 | |||||
chr6:123004950
|
CAAAA | C | 80 | a0001c0001t0002g0171a0001c0001t0003g0014a0001c0001t0003g0015others(77): Show | 85 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.390-6024_390-6021d others(6): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123004950 | |||||
chr6:123004952
|
A | C | 1 | a0001c0001t0053g0088 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.390-6033A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123004952 | ||||||
chr6:123004954
|
A | C | 2 | a0001c0001t0005g0276a0001c0001t0082g0285 | 2 | HG02818.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.390-6031A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123004954 | ||||||
chr6:123004955
|
A | C | 1 | a0001c0001t0023g0186 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.390-6030A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123004955 | ||||||
chr6:123004957
|
A | C | 1 | a0001c0001t0005g0275 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.390-6028A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123004957 | ||||||
chr6:123004959
|
A | C | 1 | a0001c0001t0002g0239 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.390-6026A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123004959 | ||||||
chr6:123004964
|
A | C | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | NA19007.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.390-6021A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123004964 | ||||||
chr6:123005113
|
C | T | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(236): Show | 263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.390-5872C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123005113 | ||||||
chr6:123005130
|
C | T | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(236): Show | 263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.390-5855C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123005130 | ||||||
chr6:123005422
|
G | A | 4 | a0001c0001t0042g0284a0001c0001t0082g0285a0001c0001t0084g0287others(1): Show | 4 | HG02559.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.390-5563G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123005422 | ||||||
chr6:123005577
|
G | A | 5 | a0001c0001t0025g0260a0001c0001t0025g0263a0001c0001t0025g0264others(2): Show | 5 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.390-5408G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123005577 | ||||||
chr6:123005611
|
A | G | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(236): Show | 263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.390-5374A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123005611 | ||||||
chr6:123005921
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.390-5064C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123005921 | ||||||
chr6:123005985
|
C | T | 32 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(29): Show | 34 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.390-5000C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123005985 | ||||||
chr6:123006068
|
C | A | 5 | a0001c0001t0026g0151a0001c0001t0026g0152a0001c0001t0044g0018others(2): Show | 6 | HG02257.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.390-4917C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006068 | ||||||
chr6:123006110
|
C | T | 1 | a0001c0001t0045g0177 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.390-4875C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006110 | ||||||
chr6:123006178
|
G | A | 3 | a0001c0001t0016g0162a0001c0001t0017g0149a0001c0001t0071g0178 | 3 | HG02109.hp2 HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.390-4807G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006178 | ||||||
chr6:123006276
|
G | C | 1 | a0001c0001t0006g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.390-4709G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006276 | ||||||
chr6:123006401
|
C | A | 1 | a0001c0001t0004g0097 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.390-4584C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006401 | ||||||
chr6:123006537
|
G | T | 11 | a0001c0001t0002g0253a0001c0001t0007g0009a0001c0001t0007g0249others(8): Show | 15 | HG01099.hp1 HG01515.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.390-4448G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006537 | ||||||
chr6:123006555
|
A | G | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(235): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.390-4430A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006555 | ||||||
chr6:123006607
|
G | T | 1 | a0001c0001t0006g0238 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.390-4378G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006607 | ||||||
chr6:123006659
|
G | A | 1 | a0001c0001t0002g0205 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.390-4326G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006659 | ||||||
chr6:123006721
|
G | C | 5 | a0001c0001t0026g0151a0001c0001t0026g0152a0001c0001t0044g0018others(2): Show | 6 | HG02257.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.390-4264G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006721 | ||||||
chr6:123006808
|
C | T | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.390-4177C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006808 | ||||||
chr6:123006910
|
A | G | 1 | a0001c0001t0007g0256 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.390-4075A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006910 | ||||||
chr6:123006912
|
G | A | 1 | a0001c0001t0003g0034 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.390-4073G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006912 | ||||||
chr6:123006922
|
G | A | 7 | a0001c0001t0009g0022a0001c0001t0009g0037a0001c0001t0009g0181others(4): Show | 8 | HG02083.hp1 HG02683.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.390-4063G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006922 | ||||||
chr6:123007001
|
T | C | 2 | a0001c0001t0003g0014a0001c0001t0003g0099 | 3 | HG01123.hp1 HG01168.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.390-3984T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123007001 | ||||||
chr6:123007250
|
G | A | 2 | a0001c0001t0002g0206a0001c0001t0002g0207 | 2 | NA18969.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.390-3735G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123007250 | ||||||
chr6:123007525
|
A | G | 1 | a0001c0001t0006g0237 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.390-3460A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123007525 | ||||||
chr6:123007546
|
G | A | 2 | a0001c0001t0035g0265a0001c0001t0035g0266 | 2 | HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.390-3439G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123007546 | ||||||
chr6:123007993
|
A | G | 1 | a0001c0001t0003g0146 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.390-2992A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123007993 | ||||||
chr6:123008009
|
A | C | 1 | a0001c0001t0002g0236 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.390-2976A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123008009 | ||||||
chr6:123008026
|
T | G | 1 | a0001c0001t0006g0242 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.390-2959T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123008026 | ||||||
chr6:123008110
|
T | C | 1 | a0001c0001t0006g0208 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.390-2875T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123008110 | ||||||
chr6:123008202
|
C | T | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.390-2783C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123008202 | ||||||
chr6:123008214
|
A | G | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(248): Show | 279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.390-2771A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123008214 | ||||||
chr6:123008307
|
A | G | 2 | a0001c0001t0022g0144a0001c0001t0022g0145 | 2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.390-2678A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123008307 | ||||||
chr6:123008377
|
C | T | 2 | a0001c0001t0038g0094a0001c0001t0038g0095 | 2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.390-2608C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123008377 | ||||||
chr6:123008558
|
G | A | 10 | a0001c0001t0002g0253a0001c0001t0007g0009a0001c0001t0007g0249others(7): Show | 14 | HG01099.hp1 HG01515.hp2 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.390-2427G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123008558 | ||||||
chr6:123008563
|
T | G | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.390-2422T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123008563 | ||||||
chr6:123008653
|
C | A | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(235): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.390-2332C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123008653 | ||||||
chr6:123008685
|
C | CT | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(235): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.390-2289dupT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123008685 | |||||
chr6:123008838
|
A | G | 2 | a0001c0001t0002g0171a0001c0001t0017g0170 | 2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.390-2147A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123008838 | ||||||
chr6:123008886
|
C | T | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(248): Show | 279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.390-2099C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123008886 | ||||||
chr6:123009281
|
A | G | 10 | a0001c0001t0002g0253a0001c0001t0007g0009a0001c0001t0007g0249others(7): Show | 14 | HG01099.hp1 HG01515.hp2 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.390-1704A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123009281 | ||||||
chr6:123009355
|
A | G | 2 | a0001c0001t0001g0039a0001c0001t0001g0085 | 2 | HG02300.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.390-1630A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123009355 | ||||||
chr6:123009523
|
T | C | 1 | a0001c0001t0002g0209 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.390-1462T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123009523 | ||||||
chr6:123009605
|
C | A | 1 | a0001c0001t0002g0024 | 2 | HG00140.hp2 HG00280.hp1 |
intron_variant | MODIFIER | c.390-1380C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123009605 | ||||||
chr6:123009727
|
C | T | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(238): Show | 265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.390-1258C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123009727 | ||||||
chr6:123010191
|
C | A | 8 | a0001c0001t0016g0162a0001c0001t0017g0100a0001c0001t0017g0149others(5): Show | 8 | HG02109.hp2 HG02809.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.390-794C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123010191 | ||||||
chr6:123010336
|
G | A | 2 | a0001c0002t0029g0041a0001c0002t0029g0042 | 2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.390-649G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123010336 | ||||||
chr6:123010622
|
C | T | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.390-363C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123010622 | ||||||
chr6:123010670
|
A | C | 1 | a0001c0001t0062g0143 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.390-315A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123010670 | ||||||
chr6:123010768
|
G | A | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(237): Show | 264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.390-217G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123010768 | ||||||
chr6:123010797
|
T | TAAATTCG others(6): Show |
1 | a0001c0001t0071g0178 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390-187_390-175dup others(13): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123010797 | |||||
chr6:123010803
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0063 | 2 | HG00099.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.390-182C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123010803 | ||||||
chr6:123011706
|
A | G | 1 | a0001c0001t0009g0185 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.564+547A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123011706 | ||||||
chr6:123012080
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0008g0001others(5): Show | 16 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.564+921G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123012080 | ||||||
chr6:123012234
|
C | A | 1 | a0001c0001t0004g0102 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.564+1075C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123012234 | ||||||
chr6:123012442
|
G | A | 4 | a0001c0001t0006g0008a0001c0001t0006g0210a0001c0001t0006g0211others(1): Show | 6 | HG02074.hp1 NA18945.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.564+1283G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123012442 | ||||||
chr6:123012485
|
C | T | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(234): Show | 261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.564+1326C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123012485 | ||||||
chr6:123012649
|
G | C | 2 | a0001c0001t0002g0213a0001c0001t0002g0214 | 2 | HG02602.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.564+1490G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123012649 | ||||||
chr6:123012962
|
T | G | 1 | a0001c0001t0071g0178 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.564+1803T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123012962 | ||||||
chr6:123013092
|
C | A | 4 | a0001c0001t0042g0284a0001c0001t0082g0285a0001c0001t0084g0287others(1): Show | 4 | HG02559.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.564+1933C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013092 | ||||||
chr6:123013130
|
G | A | 1 | a0001c0001t0010g0154 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.564+1971G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013130 | ||||||
chr6:123013183
|
C | T | 1 | a0001c0001t0011g0084 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.564+2024C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013183 | ||||||
chr6:123013191
|
C | A | 1 | a0001c0001t0087g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.564+2032C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013191 | ||||||
chr6:123013240
|
T | A | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.564+2081T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013240 | ||||||
chr6:123013254
|
A | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(235): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.564+2095A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013254 | ||||||
chr6:123013528
|
A | C | 1 | a0001c0001t0067g0038 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.564+2369A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013528 | ||||||
chr6:123013654
|
AT | A | 10 | a0001c0001t0010g0019a0001c0001t0010g0154a0001c0001t0010g0157others(7): Show | 11 | HG00741.hp2 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.564+2502delT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123013654 | |||||
chr6:123013683
|
A | T | 2 | a0001c0001t0002g0206a0001c0001t0002g0207 | 2 | NA18969.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.564+2524A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013683 | ||||||
chr6:123013691
|
G | T | 1 | a0001c0001t0007g0255 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.564+2532G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013691 | ||||||
chr6:123013723
|
A | G | 1 | a0001c0001t0052g0147 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.564+2564A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013723 | ||||||
chr6:123013738
|
T | C | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(248): Show | 279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.564+2579T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013738 | ||||||
chr6:123013767
|
G | C | 13 | a0001c0001t0006g0008a0001c0001t0006g0025a0001c0001t0006g0193others(10): Show | 15 | HG01192.hp1 HG02074.hp1 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.564+2608G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013767 | ||||||
chr6:123013817
|
C | G | 1 | a0001c0002t0024g0259 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.564+2658C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013817 | ||||||
chr6:123013817
|
C | T | 4 | a0001c0001t0016g0027a0001c0001t0016g0244a0001c0001t0072g0245others(1): Show | 5 | HG01884.hp2 HG02895.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.564+2658C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013817 | ||||||
chr6:123014040
|
T | G | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(235): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.564+2881T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123014040 | ||||||
chr6:123014123
|
C | T | 58 | a0001c0001t0001g0061a0001c0001t0003g0014a0001c0001t0003g0015others(55): Show | 62 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.564+2964C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123014123 | ||||||
chr6:123014318
|
C | A | 1 | a0001c0004t0076g0192 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.564+3159C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123014318 | ||||||
chr6:123014320
|
C | T | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(235): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.564+3161C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123014320 | ||||||
chr6:123014335
|
CT | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(235): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.564+3185delT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123014335 | |||||
chr6:123014549
|
C | T | 1 | a0001c0001t0005g0275 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.564+3390C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123014549 | ||||||
chr6:123014626
|
G | A | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+3467G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123014626 | ||||||
chr6:123014632
|
A | G | 1 | a0001c0001t0063g0142 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.564+3473A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123014632 | ||||||
chr6:123014887
|
C | A | 2 | a0001c0001t0031g0187a0001c0001t0031g0188 | 2 | NA18985.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.564+3728C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123014887 | ||||||
chr6:123014994
|
G | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(235): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.564+3835G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123014994 | ||||||
chr6:123015027
|
T | G | 1 | a0001c0001t0032g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.564+3868T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123015027 | ||||||
chr6:123015035
|
AG | A | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(235): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.564+3877delG | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123015035 | ||||||
chr6:123015046
|
T | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(137): Show | 157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.564+3887T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123015046 | ||||||
chr6:123015515
|
C | T | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+4356C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123015515 | ||||||
chr6:123015604
|
C | A | 1 | a0001c0001t0079g0155 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.564+4445C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123015604 | ||||||
chr6:123015710
|
G | A | 2 | a0001c0001t0004g0103a0001c0001t0004g0104 | 2 | HG00280.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.564+4551G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123015710 | ||||||
chr6:123015848
|
G | A | 1 | a0001c0001t0008g0043 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.564+4689G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123015848 | ||||||
chr6:123015905
|
G | C | 2 | a0001c0001t0031g0187a0001c0001t0031g0188 | 2 | NA18985.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.564+4746G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123015905 | ||||||
chr6:123015996
|
G | A | 1 | a0001c0001t0004g0105 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.564+4837G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123015996 | ||||||
chr6:123016021
|
C | CT | 76 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(73): Show | 93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.564+4889dupT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123016021 | |||||
chr6:123016021
|
C | CTT | 77 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0049others(74): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.564+4888_564+4889d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123016021 | |||||
chr6:123016021
|
C | CTTT | 24 | a0001c0001t0001g0055a0001c0001t0001g0090a0001c0001t0002g0195others(21): Show | 25 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.564+4887_564+4889d others(5): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123016021 | |||||
chr6:123016021
|
C | CTTTT | 6 | a0001c0001t0001g0060a0001c0001t0002g0235a0001c0001t0006g0204others(3): Show | 6 | NA18953.hp2 NA18972.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.564+4886_564+4889d others(6): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123016021 | |||||
chr6:123016021
|
CT | C | 14 | a0001c0001t0003g0020a0001c0001t0003g0135a0001c0001t0003g0136others(11): Show | 15 | HG00735.hp1 HG00735.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.564+4889delT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123016021 | |||||
chr6:123016021
|
CTT | C | 56 | a0001c0001t0001g0061a0001c0001t0003g0014a0001c0001t0003g0015others(53): Show | 61 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.564+4888_564+4889d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123016021 | |||||
chr6:123016021
|
CTTT | C | 11 | a0001c0001t0003g0106a0001c0001t0003g0146a0001c0001t0004g0107others(8): Show | 11 | HG01934.hp1 HG02647.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+4887_564+4889d others(5): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123016021 | |||||
chr6:123016021
|
CTTTTT | C | 10 | a0001c0001t0002g0253a0001c0001t0007g0009a0001c0001t0007g0249others(7): Show | 14 | HG01099.hp1 HG01515.hp2 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.564+4885_564+4889d others(7): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123016021 | |||||
chr6:123016113
|
G | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(120): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.564+4954G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123016113 | ||||||
chr6:123016152
|
C | A | 4 | a0001c0001t0042g0284a0001c0001t0082g0285a0001c0001t0084g0287others(1): Show | 4 | HG02559.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.564+4993C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123016152 | ||||||
chr6:123016158
|
A | G | 2 | a0001c0001t0038g0094a0001c0001t0038g0095 | 2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.564+4999A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123016158 | ||||||
chr6:123016237
|
C | T | 1 | a0001c0002t0029g0042 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.564+5078C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123016237 | ||||||
chr6:123016339
|
T | TG | 9 | a0001c0001t0002g0205a0001c0001t0026g0151a0001c0001t0026g0152others(6): Show | 10 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.564+5187dupG | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123016339 | |||||
chr6:123016339
|
T | TGG | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(218): Show | 248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.564+5186_564+5187d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123016339 | |||||
chr6:123016339
|
T | TTG | 5 | a0001c0001t0042g0284a0001c0001t0045g0177a0001c0001t0082g0285others(2): Show | 5 | HG02559.hp2 HG02818.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.564+5180_564+5181i others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123016339 | ||||||
chr6:123016340
|
G | A | 2 | a0001c0001t0084g0287a0001c0001t0090g0286 | 2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.564+5181G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123016340 | ||||||
chr6:123016340
|
G | T | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.564+5181G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123016340 | ||||||
chr6:123016453
|
T | A | 1 | a0001c0001t0073g0246 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.564+5294T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123016453 | ||||||
chr6:123016625
|
G | C | 1 | a0001c0001t0023g0098 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.564+5466G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123016625 | ||||||
chr6:123016653
|
C | T | 2 | a0001c0001t0002g0206a0001c0001t0002g0207 | 2 | NA18969.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.564+5494C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123016653 | ||||||
chr6:123016669
|
A | C | 5 | a0001c0001t0002g0171a0001c0001t0026g0093a0001c0001t0027g0166others(2): Show | 5 | HG00735.hp1 HG01106.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.564+5510A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123016669 | ||||||
chr6:123017088
|
A | ATG | 13 | a0001c0001t0002g0171a0001c0001t0002g0253a0001c0001t0005g0029others(10): Show | 18 | HG01099.hp1 HG02896.hp2 HG02897.hp2 others(15): Show |
intron_variant | MODIFIER | c.564+5956_564+5957d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123017088 | |||||
chr6:123017088
|
ATG | A | 94 | a0001c0001t0001g0061a0001c0001t0003g0014a0001c0001t0003g0015others(91): Show | 100 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.564+5956_564+5957d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123017088 | |||||
chr6:123017088
|
ATGTG | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(135): Show | 156 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.564+5954_564+5957d others(6): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123017088 | |||||
chr6:123017133
|
G | A | 1 | a0001c0001t0004g0102 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.564+5974G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123017133 | ||||||
chr6:123017147
|
G | T | 1 | a0001c0001t0053g0088 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.564+5988G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123017147 | ||||||
chr6:123017208
|
T | C | 1 | a0001c0001t0026g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.564+6049T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123017208 | ||||||
chr6:123017228
|
T | C | 5 | a0001c0001t0002g0171a0001c0001t0026g0093a0001c0001t0027g0166others(2): Show | 5 | HG00735.hp1 HG01106.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.564+6069T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123017228 | ||||||
chr6:123017354
|
C | G | 5 | a0001c0001t0002g0171a0001c0001t0026g0093a0001c0001t0027g0166others(2): Show | 5 | HG00735.hp1 HG01106.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.564+6195C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123017354 | ||||||
chr6:123017369
|
T | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(128): Show | 147 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.564+6210T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123017369 | ||||||
chr6:123017788
|
T | C | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.564+6629T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123017788 | ||||||
chr6:123017920
|
T | G | 15 | a0001c0001t0002g0171a0001c0001t0002g0253a0001c0001t0007g0009others(12): Show | 19 | HG00735.hp1 HG01099.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.564+6761T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123017920 | ||||||
chr6:123017945
|
T | A | 1 | a0001c0001t0060g0247 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.564+6786T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123017945 | ||||||
chr6:123018118
|
T | C | 2 | a0001c0001t0038g0094a0001c0001t0038g0095 | 2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.564+6959T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123018118 | ||||||
chr6:123018262
|
G | T | 2 | a0001c0001t0001g0077a0001c0001t0011g0076 | 2 | HG00408.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.564+7103G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123018262 | ||||||
chr6:123018273
|
G | C | 1 | a0001c0001t0010g0161 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.564+7114G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123018273 | ||||||
chr6:123018276
|
T | A | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.564+7117T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123018276 | ||||||
chr6:123018384
|
G | A | 4 | a0001c0001t0042g0284a0001c0001t0082g0285a0001c0001t0084g0287others(1): Show | 4 | HG02559.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.564+7225G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123018384 | ||||||
chr6:123018465
|
A | G | 94 | a0001c0001t0001g0061a0001c0001t0003g0014a0001c0001t0003g0015others(91): Show | 101 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.564+7306A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123018465 | ||||||
chr6:123018469
|
C | T | 94 | a0001c0001t0001g0061a0001c0001t0003g0014a0001c0001t0003g0015others(91): Show | 101 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.564+7310C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123018469 | ||||||
chr6:123018668
|
C | CT | 36 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(33): Show | 44 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.564+7526dupT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123018668 | |||||
chr6:123018668
|
CT | C | 94 | a0001c0001t0001g0061a0001c0001t0002g0171a0001c0001t0003g0014others(91): Show | 102 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.564+7526delT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123018668 | |||||
chr6:123018668
|
CTT | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(138): Show | 157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.564+7525_564+7526d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123018668 | |||||
chr6:123018684
|
T | A | 15 | a0001c0001t0002g0171a0001c0001t0002g0206a0001c0001t0002g0219others(12): Show | 19 | HG01099.hp1 HG01515.hp2 HG03209.hp2 others(16): Show |
intron_variant | MODIFIER | c.564+7525T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123018684 | ||||||
chr6:123018685
|
T | A | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(215): Show | 245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.564+7526T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123018685 | ||||||
chr6:123019203
|
G | A | 2 | a0001c0001t0036g0089a0001c0001t0036g0109 | 2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.564+8044G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123019203 | ||||||
chr6:123019212
|
A | G | 298 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(295): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.564+8053A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123019212 | ||||||
chr6:123019531
|
T | G | 1 | a0001c0001t0035g0265 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.564+8372T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123019531 | ||||||
chr6:123019688
|
G | A | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+8529G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123019688 | ||||||
chr6:123019733
|
G | C | 2 | a0001c0001t0022g0144a0001c0001t0022g0145 | 2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.564+8574G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123019733 | ||||||
chr6:123019969
|
CT | C | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(289): Show | 328 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.564+8820delT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123019969 | |||||
chr6:123020247
|
AT | A | 4 | a0001c0001t0003g0106a0001c0001t0003g0110a0001c0001t0003g0135others(1): Show | 4 | NA18961.hp1 NA18977.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.564+9090delT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123020247 | |||||
chr6:123020361
|
C | A | 2 | a0001c0001t0036g0089a0001c0001t0036g0109 | 2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.564+9202C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123020361 | ||||||
chr6:123020375
|
T | A | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+9216T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123020375 | ||||||
chr6:123020547
|
A | G | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+9388A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123020547 | ||||||
chr6:123020558
|
C | A | 1 | a0001c0001t0001g0078 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.564+9399C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123020558 | ||||||
chr6:123020860
|
T | G | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.564+9701T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123020860 | ||||||
chr6:123020946
|
G | A | 1 | a0001c0001t0005g0270 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.564+9787G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123020946 | ||||||
chr6:123021051
|
T | TG | 98 | a0001c0001t0001g0061a0001c0001t0002g0253a0001c0001t0003g0014others(95): Show | 109 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.564+9900dupG | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123021051 | |||||
chr6:123021060
|
T | G | 96 | a0001c0001t0001g0061a0001c0001t0003g0014a0001c0001t0003g0015others(93): Show | 103 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.564+9901T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123021060 | ||||||
chr6:123021061
|
A | G | 3 | a0001c0001t0004g0134a0001c0001t0022g0144a0001c0001t0022g0145 | 3 | HG03130.hp1 HG03471.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.564+9902A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123021061 | ||||||
chr6:123021550
|
G | A | 4 | a0001c0001t0016g0027a0001c0001t0016g0244a0001c0001t0072g0245others(1): Show | 5 | HG01884.hp2 HG02895.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.564+10391G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123021550 | ||||||
chr6:123021569
|
T | C | 15 | a0001c0001t0002g0171a0001c0001t0002g0253a0001c0001t0007g0009others(12): Show | 19 | HG00735.hp1 HG01099.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.564+10410T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123021569 | ||||||
chr6:123021591
|
G | A | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(246): Show | 277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.564+10432G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123021591 | ||||||
chr6:123021729
|
C | T | 1 | a0001c0001t0027g0168 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.564+10570C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123021729 | ||||||
chr6:123021848
|
A | AT | 5 | a0001c0001t0026g0151a0001c0001t0026g0152a0001c0001t0044g0018others(2): Show | 6 | HG02257.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.564+10698dupT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123021848 | |||||
chr6:123021891
|
C | A | 2 | a0001c0001t0006g0216a0001c0001t0006g0238 | 2 | NA18995.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.564+10732C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123021891 | ||||||
chr6:123022052
|
T | G | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+10893T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123022052 | ||||||
chr6:123022053
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0068 | 2 | HG01433.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.564+10894G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123022053 | ||||||
chr6:123022121
|
C | T | 3 | a0001c0001t0016g0027a0001c0001t0016g0244a0001c0001t0072g0245 | 4 | HG01884.hp2 HG02895.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.564+10962C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123022121 | ||||||
chr6:123022203
|
C | T | 2 | a0001c0001t0022g0144a0001c0001t0022g0145 | 2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.564+11044C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123022203 | ||||||
chr6:123022316
|
C | T | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(248): Show | 279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.564+11157C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123022316 | ||||||
chr6:123022458
|
G | C | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+11299G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123022458 | ||||||
chr6:123022607
|
C | T | 1 | a0001c0001t0017g0170 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.564+11448C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123022607 | ||||||
chr6:123022845
|
A | G | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(246): Show | 277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.564+11686A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123022845 | ||||||
chr6:123022861
|
C | T | 1 | a0001c0001t0004g0133 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.564+11702C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123022861 | ||||||
chr6:123022949
|
G | A | 96 | a0001c0001t0001g0061a0001c0001t0003g0014a0001c0001t0003g0015others(93): Show | 103 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.564+11790G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123022949 | ||||||
chr6:123023124
|
C | T | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(246): Show | 277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.564+11965C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123023124 | ||||||
chr6:123023254
|
G | C | 1 | a0001c0001t0002g0218 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.564+12095G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123023254 | ||||||
chr6:123023374
|
T | C | 1 | a0001c0001t0002g0226 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.564+12215T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123023374 | ||||||
chr6:123023526
|
A | T | 1 | a0001c0001t0009g0183 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.564+12367A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123023526 | ||||||
chr6:123023647
|
C | T | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(246): Show | 277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.564+12488C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123023647 | ||||||
chr6:123023850
|
C | A | 1 | a0001c0001t0037g0126 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.564+12691C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123023850 | ||||||
chr6:123023875
|
C | A | 5 | a0001c0001t0002g0171a0001c0001t0026g0093a0001c0001t0027g0166others(2): Show | 5 | HG00735.hp1 HG01106.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.564+12716C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123023875 | ||||||
chr6:123023909
|
TAC | T | 10 | a0001c0001t0002g0253a0001c0001t0007g0009a0001c0001t0007g0249others(7): Show | 14 | HG01099.hp1 HG01515.hp2 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.564+12752_564+1275 others(6): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123023909 | |||||
chr6:123023945
|
A | G | 1 | a0001c0001t0003g0124 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.564+12786A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123023945 | ||||||
chr6:123024034
|
C | G | 1 | a0001c0001t0080g0200 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.564+12875C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123024034 | ||||||
chr6:123024083
|
C | G | 4 | a0001c0001t0002g0199a0001c0001t0002g0203a0001c0001t0039g0232others(1): Show | 4 | HG00438.hp1 HG02074.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.564+12924C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123024083 | ||||||
chr6:123024216
|
C | T | 10 | a0001c0001t0002g0253a0001c0001t0007g0009a0001c0001t0007g0249others(7): Show | 14 | HG01099.hp1 HG01515.hp2 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.564+13057C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123024216 | ||||||
chr6:123024235
|
A | G | 1 | a0001c0001t0087g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.564+13076A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123024235 | ||||||
chr6:123024450
|
A | G | 4 | a0001c0001t0016g0027a0001c0001t0016g0244a0001c0001t0072g0245others(1): Show | 5 | HG01884.hp2 HG02895.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.564+13291A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123024450 | ||||||
chr6:123024766
|
A | G | 1 | a0001c0001t0042g0284 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.564+13607A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123024766 | ||||||
chr6:123024832
|
G | A | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+13673G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123024832 | ||||||
chr6:123024870
|
C | T | 1 | a0001c0001t0087g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.564+13711C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123024870 | ||||||
chr6:123024958
|
T | G | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+13799T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123024958 | ||||||
chr6:123024968
|
C | A | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(246): Show | 277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.564+13809C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123024968 | ||||||
chr6:123024971
|
C | T | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(246): Show | 277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.564+13812C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123024971 | ||||||
chr6:123025217
|
G | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(120): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.564+14058G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123025217 | ||||||
chr6:123025538
|
G | A | 1 | a0001c0001t0005g0275 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.564+14379G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123025538 | ||||||
chr6:123025627
|
C | G | 6 | a0001c0001t0038g0094a0001c0001t0038g0095a0001c0001t0042g0284others(3): Show | 6 | HG02559.hp2 HG02818.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.564+14468C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123025627 | ||||||
chr6:123025774
|
C | T | 59 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(56): Show | 63 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.564+14615C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123025774 | ||||||
chr6:123025777
|
C | G | 96 | a0001c0001t0001g0061a0001c0001t0003g0014a0001c0001t0003g0015others(93): Show | 103 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.564+14618C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123025777 | ||||||
chr6:123026055
|
A | T | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(246): Show | 277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.564+14896A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123026055 | ||||||
chr6:123026056
|
A | G | 1 | a0001c0001t0004g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.564+14897A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123026056 | ||||||
chr6:123026125
|
A | C | 1 | a0001c0001t0014g0198 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.564+14966A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123026125 | ||||||
chr6:123026421
|
T | G | 1 | a0001c0001t0010g0161 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.564+15262T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123026421 | ||||||
chr6:123026513
|
G | A | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+15354G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123026513 | ||||||
chr6:123026817
|
T | C | 9 | a0001c0001t0016g0162a0001c0001t0017g0100a0001c0001t0017g0149others(6): Show | 9 | HG02109.hp2 HG02809.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.564+15658T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123026817 | ||||||
chr6:123027002
|
T | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(230): Show | 257 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.564+15843T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123027002 | ||||||
chr6:123027016
|
C | T | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.564+15857C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123027016 | ||||||
chr6:123027077
|
T | G | 1 | a0001c0001t0045g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.564+15918T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123027077 | ||||||
chr6:123027132
|
A | G | 2 | a0001c0001t0030g0010a0001c0001t0053g0088 | 3 | HG01070.hp2 HG01071.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.564+15973A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123027132 | ||||||
chr6:123027199
|
A | G | 2 | a0001c0001t0003g0122a0001c0001t0003g0123 | 2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.564+16040A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123027199 | ||||||
chr6:123027434
|
G | A | 6 | a0001c0001t0038g0094a0001c0001t0038g0095a0001c0001t0042g0284others(3): Show | 6 | HG02559.hp2 HG02818.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.564+16275G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123027434 | ||||||
chr6:123027913
|
A | G | 1 | a0001c0001t0008g0045 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.564+16754A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123027913 | ||||||
chr6:123028243
|
T | TA | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(252): Show | 283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.564+17086dupA | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123028243 | |||||
chr6:123028365
|
G | T | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+17206G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123028365 | ||||||
chr6:123028419
|
G | A | 1 | a0001c0001t0048g0137 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.564+17260G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123028419 | ||||||
chr6:123028422
|
G | C | 1 | a0001c0001t0087g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.564+17263G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123028422 | ||||||
chr6:123028458
|
G | A | 6 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0201others(3): Show | 6 | NA18942.hp2 NA18951.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.564+17299G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123028458 | ||||||
chr6:123028694
|
T | A | 1 | a0001c0001t0001g0052 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.564+17535T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123028694 | ||||||
chr6:123029233
|
G | A | 1 | a0001c0001t0002g0220 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.564+18074G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123029233 | ||||||
chr6:123029306
|
G | A | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+18147G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123029306 | ||||||
chr6:123029375
|
T | A | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+18216T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123029375 | ||||||
chr6:123029413
|
T | C | 4 | a0001c0001t0042g0284a0001c0001t0082g0285a0001c0001t0084g0287others(1): Show | 4 | HG02559.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.564+18254T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123029413 | ||||||
chr6:123029459
|
T | C | 5 | a0001c0001t0026g0151a0001c0001t0026g0152a0001c0001t0044g0018others(2): Show | 6 | HG02257.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.564+18300T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123029459 | ||||||
chr6:123029545
|
C | T | 252 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(249): Show | 280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.564+18386C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123029545 | ||||||
chr6:123029590
|
G | A | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+18431G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123029590 | ||||||
chr6:123029984
|
C | T | 1 | a0001c0001t0056g0048 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.565-18638C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123029984 | ||||||
chr6:123029989
|
A | C | 1 | a0001c0001t0087g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.565-18633A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123029989 | ||||||
chr6:123030053
|
G | A | 5 | a0001c0001t0002g0171a0001c0001t0026g0093a0001c0001t0027g0166others(2): Show | 5 | HG00735.hp1 HG01106.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.565-18569G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123030053 | ||||||
chr6:123030144
|
A | G | 15 | a0001c0001t0002g0171a0001c0001t0002g0253a0001c0001t0007g0009others(12): Show | 19 | HG00735.hp1 HG01099.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.565-18478A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123030144 | ||||||
chr6:123030151
|
A | T | 252 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(249): Show | 280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.565-18471A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123030151 | ||||||
chr6:123030585
|
C | A | 1 | a0001c0001t0003g0112 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.565-18037C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123030585 | ||||||
chr6:123030818
|
A | AAT | 15 | a0001c0001t0002g0171a0001c0001t0002g0253a0001c0001t0007g0009others(12): Show | 19 | HG00735.hp1 HG01099.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.565-17788_565-1778 others(6): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123030818 | |||||
chr6:123030837
|
A | AAT | 95 | a0001c0001t0001g0061a0001c0001t0003g0014a0001c0001t0003g0015others(92): Show | 102 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.565-17773_565-1777 others(6): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123030837 | |||||
chr6:123030837
|
A | T | 1 | a0001c0001t0082g0285 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.565-17785A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123030837 | ||||||
chr6:123030968
|
T | C | 7 | a0001c0001t0015g0173a0001c0001t0015g0174a0001c0001t0015g0175others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.565-17654T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123030968 | ||||||
chr6:123030982
|
G | A | 2 | a0001c0001t0038g0094a0001c0001t0038g0095 | 2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.565-17640G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123030982 | ||||||
chr6:123031056
|
C | T | 1 | a0001c0001t0003g0016 | 2 | HG01175.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.565-17566C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031056 | ||||||
chr6:123031104
|
T | A | 15 | a0001c0001t0002g0171a0001c0001t0002g0253a0001c0001t0007g0009others(12): Show | 19 | HG00735.hp1 HG01099.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.565-17518T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031104 | ||||||
chr6:123031139
|
T | G | 1 | a0001c0001t0004g0130 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.565-17483T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031139 | ||||||
chr6:123031255
|
G | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(109): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.565-17367G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031255 | ||||||
chr6:123031326
|
G | A | 10 | a0001c0001t0010g0019a0001c0001t0010g0154a0001c0001t0010g0157others(7): Show | 11 | HG00741.hp2 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.565-17296G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031326 | ||||||
chr6:123031393
|
C | G | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(247): Show | 278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.565-17229C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031393 | ||||||
chr6:123031447
|
G | A | 1 | a0001c0001t0026g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.565-17175G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031447 | ||||||
chr6:123031507
|
T | C | 1 | a0001c0001t0004g0102 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.565-17115T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031507 | ||||||
chr6:123031652
|
T | C | 2 | a0001c0001t0011g0069a0001c0001t0011g0084 | 2 | NA18977.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.565-16970T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031652 | ||||||
chr6:123031709
|
C | T | 1 | a0001c0001t0002g0225 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.565-16913C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031709 | ||||||
chr6:123031715
|
C | A | 1 | a0001c0004t0076g0192 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.565-16907C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031715 | ||||||
chr6:123031832
|
G | A | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(247): Show | 278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.565-16790G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031832 | ||||||
chr6:123031957
|
G | C | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.565-16665G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031957 | ||||||
chr6:123031979
|
T | G | 1 | a0001c0001t0001g0091 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.565-16643T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031979 | ||||||
chr6:123032202
|
C | T | 1 | a0001c0001t0002g0231 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.565-16420C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123032202 | ||||||
chr6:123032248
|
A | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(137): Show | 157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.565-16374A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123032248 | ||||||
chr6:123032262
|
G | A | 1 | a0001c0001t0070g0050 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.565-16360G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123032262 | ||||||
chr6:123032306
|
A | C | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(247): Show | 278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.565-16316A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123032306 | ||||||
chr6:123032360
|
T | A | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.565-16262T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123032360 | ||||||
chr6:123032630
|
T | C | 1 | a0001c0001t0005g0268 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.565-15992T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123032630 | ||||||
chr6:123032778
|
C | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(231): Show | 258 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.565-15844C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123032778 | ||||||
chr6:123032841
|
C | T | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.565-15781C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123032841 | ||||||
chr6:123032873
|
G | A | 1 | a0001c0001t0081g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.565-15749G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123032873 | ||||||
chr6:123032916
|
A | T | 13 | a0001c0001t0010g0019a0001c0001t0010g0154a0001c0001t0010g0157others(10): Show | 14 | HG00741.hp2 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.565-15706A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123032916 | ||||||
chr6:123032937
|
T | A | 1 | a0001c0001t0001g0011 | 2 | NA18988.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.565-15685T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123032937 | ||||||
chr6:123033391
|
C | T | 93 | a0001c0001t0001g0061a0001c0001t0003g0014a0001c0001t0003g0015others(90): Show | 99 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.565-15231C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123033391 | ||||||
chr6:123033561
|
T | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(231): Show | 258 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.565-15061T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123033561 | ||||||
chr6:123033645
|
A | G | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.565-14977A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123033645 | ||||||
chr6:123033703
|
T | A | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565-14919T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123033703 | ||||||
chr6:123033873
|
A | G | 2 | a0001c0001t0004g0107a0001c0001t0004g0108 | 2 | NA18995.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.565-14749A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123033873 | ||||||
chr6:123033909
|
G | A | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.565-14713G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123033909 | ||||||
chr6:123034217
|
C | T | 4 | a0001c0001t0016g0027a0001c0001t0016g0244a0001c0001t0072g0245others(1): Show | 5 | HG01884.hp2 HG02895.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-14405C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123034217 | ||||||
chr6:123034321
|
T | C | 1 | a0001c0001t0035g0266 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.565-14301T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123034321 | ||||||
chr6:123034358
|
A | G | 1 | a0001c0001t0035g0266 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.565-14264A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123034358 | ||||||
chr6:123034391
|
T | C | 1 | a0001c0001t0074g0113 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.565-14231T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123034391 | ||||||
chr6:123034408
|
C | T | 5 | a0001c0001t0025g0260a0001c0001t0025g0263a0001c0001t0025g0264others(2): Show | 5 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-14214C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123034408 | ||||||
chr6:123034672
|
T | C | 1 | a0001c0001t0002g0171 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.565-13950T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123034672 | ||||||
chr6:123034752
|
C | T | 2 | a0001c0001t0003g0112a0001c0001t0063g0142 | 2 | HG01255.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.565-13870C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123034752 | ||||||
chr6:123034965
|
A | G | 1 | a0001c0001t0005g0280 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.565-13657A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123034965 | ||||||
chr6:123035124
|
T | C | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.565-13498T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123035124 | ||||||
chr6:123035235
|
G | A | 235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(232): Show | 259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.565-13387G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123035235 | ||||||
chr6:123035335
|
C | T | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.565-13287C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123035335 | ||||||
chr6:123035347
|
C | A | 1 | a0001c0001t0002g0171 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.565-13275C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123035347 | ||||||
chr6:123035441
|
G | A | 1 | a0001c0001t0002g0024 | 2 | HG00140.hp2 HG00280.hp1 |
intron_variant | MODIFIER | c.565-13181G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123035441 | ||||||
chr6:123035902
|
C | G | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.565-12720C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123035902 | ||||||
chr6:123035903
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.565-12719A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123035903 | ||||||
chr6:123035980
|
G | A | 4 | a0001c0001t0016g0027a0001c0001t0016g0244a0001c0001t0072g0245others(1): Show | 5 | HG01884.hp2 HG02895.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-12642G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123035980 | ||||||
chr6:123036292
|
A | C | 4 | a0001c0001t0042g0284a0001c0001t0082g0285a0001c0001t0084g0287others(1): Show | 4 | HG02559.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.565-12330A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123036292 | ||||||
chr6:123036570
|
CT | C | 8 | a0001c0001t0002g0253a0001c0001t0007g0009a0001c0001t0007g0249others(5): Show | 12 | NA18947.hp2 NA18948.hp1 NA18950.hp1 others(9): Show |
intron_variant | MODIFIER | c.565-12051delT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123036570 | ||||||
chr6:123036647
|
G | A | 7 | a0001c0001t0009g0022a0001c0001t0009g0037a0001c0001t0009g0181others(4): Show | 8 | HG02083.hp1 HG02683.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.565-11975G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123036647 | ||||||
chr6:123036652
|
A | G | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565-11970A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123036652 | ||||||
chr6:123036778
|
G | T | 2 | a0001c0001t0025g0260a0001c0001t0025g0263 | 2 | HG01167.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.565-11844G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123036778 | ||||||
chr6:123036866
|
G | A | 2 | a0001c0001t0004g0107a0001c0001t0004g0108 | 2 | NA18995.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.565-11756G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123036866 | ||||||
chr6:123037104
|
C | T | 4 | a0001c0001t0042g0284a0001c0001t0082g0285a0001c0001t0084g0287others(1): Show | 4 | HG02559.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.565-11518C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123037104 | ||||||
chr6:123037235
|
G | C | 1 | a0001c0001t0027g0166 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.565-11387G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123037235 | ||||||
chr6:123037438
|
A | G | 2 | a0001c0001t0002g0205a0001c0001t0002g0228 | 2 | HG00323.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.565-11184A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123037438 | ||||||
chr6:123038357
|
G | C | 252 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(249): Show | 280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.565-10265G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123038357 | ||||||
chr6:123038490
|
G | T | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565-10132G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123038490 | ||||||
chr6:123038662
|
A | G | 1 | a0001c0001t0005g0248 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.565-9960A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123038662 | ||||||
chr6:123038670
|
C | G | 1 | a0001c0001t0011g0069 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.565-9952C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123038670 | ||||||
chr6:123038914
|
G | A | 1 | a0001c0001t0002g0221 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.565-9708G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123038914 | ||||||
chr6:123038991
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(120): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.565-9631T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123038991 | ||||||
chr6:123039015
|
C | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(137): Show | 157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.565-9607C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123039015 | ||||||
chr6:123039305
|
C | A | 1 | a0001c0001t0007g0252 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.565-9317C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123039305 | ||||||
chr6:123039890
|
C | T | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.565-8732C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123039890 | ||||||
chr6:123039921
|
G | A | 1 | a0001c0001t0003g0111 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.565-8701G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123039921 | ||||||
chr6:123039952
|
T | C | 2 | a0001c0001t0011g0064a0001c0001t0011g0070 | 2 | NA18962.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.565-8670T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123039952 | ||||||
chr6:123040060
|
G | T | 2 | a0001c0001t0003g0120a0001c0001t0003g0121 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.565-8562G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123040060 | ||||||
chr6:123040092
|
G | A | 10 | a0001c0001t0010g0019a0001c0001t0010g0154a0001c0001t0010g0157others(7): Show | 11 | HG00741.hp2 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.565-8530G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123040092 | ||||||
chr6:123040160
|
G | T | 59 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(56): Show | 63 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.565-8462G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123040160 | ||||||
chr6:123040174
|
T | C | 1 | a0001c0001t0012g0058 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.565-8448T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123040174 | ||||||
chr6:123040234
|
G | A | 1 | a0001c0001t0009g0037 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.565-8388G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123040234 | ||||||
chr6:123040603
|
G | A | 1 | a0001c0001t0043g0234 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.565-8019G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123040603 | ||||||
chr6:123040693
|
G | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(120): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.565-7929G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123040693 | ||||||
chr6:123040717
|
G | A | 1 | a0001c0001t0004g0105 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.565-7905G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123040717 | ||||||
chr6:123040769
|
A | AAAAAG | 18 | a0001c0001t0001g0074a0001c0001t0003g0114a0001c0001t0006g0193others(15): Show | 18 | HG00140.hp1 HG00735.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.565-7820_565-7816d others(7): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123040769 | |||||
chr6:123040769
|
A | AAAAAGAA others(3): Show |
22 | a0001c0001t0001g0011a0001c0001t0001g0073a0001c0001t0002g0171others(19): Show | 25 | HG00609.hp1 HG00733.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.565-7825_565-7816d others(12): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123040769 | |||||
chr6:123040769
|
A | AAAAAGAA others(8): Show |
88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(85): Show | 101 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.565-7830_565-7816d others(17): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123040769 | |||||
chr6:123040769
|
A | AAAAAGAA others(13): Show |
15 | a0001c0001t0001g0040a0001c0001t0001g0055a0001c0001t0001g0062others(12): Show | 16 | HG00099.hp1 HG00673.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.565-7835_565-7816d others(22): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123040769 | |||||
chr6:123040769
|
A | AAAAAGAA others(18): Show |
2 | a0001c0001t0002g0195a0001c0001t0012g0056 | 2 | HG00741.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.565-7840_565-7816d others(27): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123040769 | |||||
chr6:123040769
|
A | AAAAAGAA others(23): Show |
7 | a0001c0001t0001g0082a0001c0001t0002g0229a0001c0001t0012g0051others(4): Show | 7 | NA18906.hp2 NA18972.hp2 NA18998.hp1 others(4): Show |
intron_variant | MODIFIER | c.565-7845_565-7816d others(32): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123040769 | |||||
chr6:123040769
|
A | AAAAAGAA others(28): Show |
3 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0070g0050 | 3 | HG04204.hp1 NA19007.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.565-7850_565-7816d others(37): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123040769 | |||||
chr6:123040769
|
A | AAAAAGAA others(33): Show |
1 | a0001c0001t0068g0036 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.565-7816_565-7815i others(42): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123040769 | |||||
chr6:123040769
|
AAAAAG | A | 4 | a0001c0001t0005g0268a0001c0001t0016g0027a0001c0001t0016g0244others(1): Show | 5 | HG01884.hp2 HG02895.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-7820_565-7816d others(7): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123040769 | |||||
chr6:123040961
|
C | A | 3 | a0001c0001t0027g0166a0001c0001t0027g0167a0001c0001t0027g0168 | 3 | HG00735.hp1 HG01106.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.565-7661C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123040961 | ||||||
chr6:123041047
|
C | A | 1 | a0001c0001t0042g0284 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.565-7575C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041047 | ||||||
chr6:123041091
|
G | T | 4 | a0001c0001t0042g0284a0001c0001t0082g0285a0001c0001t0084g0287others(1): Show | 4 | HG02559.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.565-7531G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041091 | ||||||
chr6:123041366
|
T | G | 5 | a0001c0001t0002g0023a0001c0001t0002g0194a0001c0001t0002g0195others(2): Show | 6 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.565-7256T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041366 | ||||||
chr6:123041440
|
A | G | 9 | a0001c0001t0010g0019a0001c0001t0010g0154a0001c0001t0010g0157others(6): Show | 10 | HG00741.hp2 HG01243.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.565-7182A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041440 | ||||||
chr6:123041446
|
G | T | 94 | a0001c0001t0001g0061a0001c0001t0003g0014a0001c0001t0003g0015others(91): Show | 101 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.565-7176G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041446 | ||||||
chr6:123041531
|
T | G | 1 | a0001c0001t0002g0218 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.565-7091T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041531 | ||||||
chr6:123041577
|
A | G | 4 | a0001c0001t0016g0027a0001c0001t0016g0244a0001c0001t0072g0245others(1): Show | 5 | HG01884.hp2 HG02895.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-7045A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041577 | ||||||
chr6:123041732
|
A | T | 3 | a0001c0001t0017g0163a0001c0001t0040g0101a0001c0001t0083g0165 | 3 | HG03041.hp1 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.565-6890A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041732 | ||||||
chr6:123041817
|
A | G | 1 | a0001c0001t0017g0149 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.565-6805A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041817 | ||||||
chr6:123041830
|
T | C | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.565-6792T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041830 | ||||||
chr6:123041911
|
G | A | 1 | a0001c0001t0017g0100 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.565-6711G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041911 | ||||||
chr6:123041949
|
A | G | 1 | a0001c0001t0003g0119 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.565-6673A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041949 | ||||||
chr6:123041956
|
A | G | 1 | a0001c0001t0025g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.565-6666A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041956 | ||||||
chr6:123042130
|
C | T | 1 | a0001c0001t0005g0280 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.565-6492C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123042130 | ||||||
chr6:123042346
|
T | C | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.565-6276T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123042346 | ||||||
chr6:123042398
|
A | G | 13 | a0001c0001t0010g0019a0001c0001t0010g0154a0001c0001t0010g0157others(10): Show | 14 | HG00741.hp2 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.565-6224A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123042398 | ||||||
chr6:123042780
|
C | T | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565-5842C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123042780 | ||||||
chr6:123043001
|
C | A | 3 | a0001c0001t0025g0264a0001c0001t0041g0261a0001c0001t0041g0262 | 3 | HG01109.hp2 HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565-5621C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123043001 | ||||||
chr6:123043113
|
T | C | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(146): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.565-5509T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123043113 | ||||||
chr6:123043147
|
C | T | 1 | a0001c0001t0039g0233 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.565-5475C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123043147 | ||||||
chr6:123043403
|
A | G | 6 | a0001c0001t0002g0171a0001c0001t0027g0166a0001c0001t0027g0167others(3): Show | 6 | HG00735.hp1 HG01106.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.565-5219A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123043403 | ||||||
chr6:123043642
|
A | C | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565-4980A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123043642 | ||||||
chr6:123043702
|
T | G | 3 | a0001c0001t0082g0285a0001c0001t0084g0287a0001c0001t0090g0286 | 3 | HG02559.hp2 HG02818.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.565-4920T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123043702 | ||||||
chr6:123043825
|
G | T | 7 | a0001c0001t0004g0017a0001c0001t0004g0105a0001c0001t0004g0107others(4): Show | 8 | HG00408.hp2 NA18952.hp2 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.565-4797G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123043825 | ||||||
chr6:123043873
|
G | A | 5 | a0001c0001t0025g0260a0001c0001t0025g0263a0001c0001t0025g0264others(2): Show | 5 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-4749G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123043873 | ||||||
chr6:123043946
|
A | T | 1 | a0001c0001t0002g0224 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.565-4676A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123043946 | ||||||
chr6:123043984
|
A | G | 10 | a0001c0001t0002g0253a0001c0001t0007g0009a0001c0001t0007g0249others(7): Show | 14 | HG01099.hp1 HG01515.hp2 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.565-4638A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123043984 | ||||||
chr6:123044064
|
C | T | 3 | a0001c0001t0027g0166a0001c0001t0027g0167a0001c0001t0027g0168 | 3 | HG00735.hp1 HG01106.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.565-4558C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123044064 | ||||||
chr6:123044403
|
G | A | 5 | a0001c0001t0025g0260a0001c0001t0025g0263a0001c0001t0025g0264others(2): Show | 5 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-4219G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123044403 | ||||||
chr6:123044667
|
GTAAATCT others(15): Show |
G | 2 | a0001c0001t0001g0061a0001c0001t0003g0034 | 2 | HG00544.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.565-3954_565-3933d others(24): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123044667 | ||||||
chr6:123044690
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0003g0034 | 2 | HG00544.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.565-3932G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123044690 | ||||||
chr6:123044691
|
G | C | 2 | a0001c0001t0001g0061a0001c0001t0003g0034 | 2 | HG00544.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.565-3931G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123044691 | ||||||
chr6:123044696
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0003g0034 | 2 | HG00544.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.565-3926G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123044696 | ||||||
chr6:123045142
|
G | GAC | 11 | a0001c0001t0001g0052a0001c0001t0001g0082a0001c0001t0002g0224others(8): Show | 11 | HG01517.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.565-3455_565-3454d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123045142 | |||||
chr6:123045142
|
G | GACAC | 7 | a0001c0001t0016g0027a0001c0001t0016g0244a0001c0001t0035g0265others(4): Show | 8 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.565-3457_565-3454d others(6): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123045142 | |||||
chr6:123045142
|
G | GACACAC | 5 | a0001c0002t0024g0257a0001c0002t0024g0258a0001c0002t0024g0259others(2): Show | 5 | HG02717.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-3459_565-3454d others(8): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123045142 | |||||
chr6:123045142
|
GAC | G | 15 | a0001c0001t0002g0253a0001c0001t0007g0009a0001c0001t0007g0249others(12): Show | 19 | HG01099.hp1 HG01109.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.565-3455_565-3454d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123045142 | |||||
chr6:123045271
|
C | T | 2 | a0001c0002t0024g0257a0001c0002t0024g0258 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.565-3351C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123045271 | ||||||
chr6:123045304
|
A | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(185): Show | 211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.565-3318A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123045304 | ||||||
chr6:123045339
|
G | A | 8 | a0001c0001t0035g0265a0001c0001t0035g0266a0001c0001t0056g0048others(5): Show | 8 | HG02145.hp1 HG02280.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.565-3283G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123045339 | ||||||
chr6:123045588
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.565-3034C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123045588 | ||||||
chr6:123046480
|
T | G | 3 | a0001c0001t0045g0172a0001c0001t0045g0177a0001c0001t0054g0044 | 3 | HG02109.hp1 HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.565-2142T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123046480 | ||||||
chr6:123046490
|
T | C | 66 | a0001c0001t0001g0061a0001c0001t0001g0078a0001c0001t0003g0014others(63): Show | 70 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.565-2132T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123046490 | ||||||
chr6:123046573
|
C | T | 9 | a0001c0001t0009g0022a0001c0001t0009g0037a0001c0001t0009g0181others(6): Show | 11 | HG01891.hp2 HG02083.hp1 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.565-2049C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123046573 | ||||||
chr6:123046658
|
CA | C | 19 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0072others(16): Show | 19 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.565-1949delA | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123046658 | |||||
chr6:123046658
|
CAA | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(232): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.565-1950_565-1949d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123046658 | |||||
chr6:123046671
|
A | T | 2 | a0001c0001t0002g0213a0001c0001t0002g0214 | 2 | HG02602.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.565-1951A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123046671 | ||||||
chr6:123046674
|
T | A | 1 | a0001c0001t0026g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.565-1948T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123046674 | ||||||
chr6:123046729
|
A | C | 35 | a0001c0001t0010g0019a0001c0001t0010g0154a0001c0001t0010g0157others(32): Show | 37 | HG00741.hp2 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.565-1893A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123046729 | ||||||
chr6:123046866
|
G | A | 5 | a0001c0002t0024g0257a0001c0002t0024g0258a0001c0002t0024g0259others(2): Show | 5 | HG02717.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-1756G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123046866 | ||||||
chr6:123046878
|
T | C | 1 | a0001c0001t0003g0020 | 2 | NA19009.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.565-1744T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123046878 | ||||||
chr6:123047051
|
G | T | 1 | a0001c0001t0016g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.565-1571G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123047051 | ||||||
chr6:123047141
|
G | C | 5 | a0001c0002t0024g0257a0001c0002t0024g0258a0001c0002t0024g0259others(2): Show | 5 | HG02717.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-1481G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123047141 | ||||||
chr6:123047250
|
T | C | 1 | a0001c0001t0040g0160 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.565-1372T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123047250 | ||||||
chr6:123047263
|
T | G | 40 | a0001c0001t0010g0019a0001c0001t0010g0154a0001c0001t0010g0157others(37): Show | 42 | HG00741.hp2 HG01243.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.565-1359T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123047263 | ||||||
chr6:123047300
|
T | C | 10 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0040others(7): Show | 12 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.565-1322T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123047300 | ||||||
chr6:123047362
|
A | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(111): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.565-1260A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123047362 | ||||||
chr6:123047365
|
T | C | 40 | a0001c0001t0010g0019a0001c0001t0010g0154a0001c0001t0010g0157others(37): Show | 42 | HG00741.hp2 HG01243.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.565-1257T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123047365 | ||||||
chr6:123047475
|
A | G | 7 | a0001c0001t0035g0265a0001c0001t0035g0266a0001c0001t0056g0048others(4): Show | 7 | HG02145.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.565-1147A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123047475 | ||||||
chr6:123047535
|
T | A | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565-1087T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123047535 | ||||||
chr6:123047703
|
C | T | 40 | a0001c0001t0010g0019a0001c0001t0010g0154a0001c0001t0010g0157others(37): Show | 42 | HG00741.hp2 HG01243.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.565-919C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123047703 | ||||||
chr6:123047745
|
G | GT | 67 | a0001c0001t0001g0061a0001c0001t0001g0078a0001c0001t0002g0197others(64): Show | 71 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.565-867dupT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123047745 | |||||
chr6:123047891
|
C | G | 4 | a0001c0001t0002g0253a0001c0001t0007g0249a0001c0001t0007g0254others(1): Show | 4 | NA18947.hp2 NA18948.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.565-731C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123047891 | ||||||
chr6:123048026
|
T | TCCTTAAG others(18): Show |
1 | a0001c0001t0004g0141 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.565-595_565-571dup others(25): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123048026 | |||||
chr6:123048209
|
T | G | 5 | a0001c0001t0025g0260a0001c0001t0025g0263a0001c0001t0025g0264others(2): Show | 5 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-413T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123048209 | ||||||
chr6:123048271
|
A | T | 5 | a0001c0001t0025g0260a0001c0001t0025g0263a0001c0001t0025g0264others(2): Show | 5 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-351A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123048271 | ||||||
chr6:123048353
|
T | G | 5 | a0001c0001t0015g0173a0001c0001t0015g0174a0001c0001t0015g0175others(2): Show | 5 | HG02257.hp2 HG02451.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-269T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123048353 | ||||||
chr6:123048403
|
C | A | 65 | a0001c0001t0001g0061a0001c0001t0003g0014a0001c0001t0003g0015others(62): Show | 69 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.565-219C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123048403 | ||||||
chr6:123048465
|
G | A | 40 | a0001c0001t0010g0019a0001c0001t0010g0154a0001c0001t0010g0157others(37): Show | 42 | HG00741.hp2 HG01243.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.565-157G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123048465 | ||||||
chr6:123048543
|
G | A | 40 | a0001c0001t0010g0019a0001c0001t0010g0154a0001c0001t0010g0157others(37): Show | 42 | HG00741.hp2 HG01243.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.565-79G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123048543 | ||||||
chr6:123048561
|
CCTAAA | C | 40 | a0001c0001t0010g0019a0001c0001t0010g0154a0001c0001t0010g0157others(37): Show | 42 | HG00741.hp2 HG01243.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.565-59_565-55delTA others(3): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123048561 | |||||
chr6:123048765
|
T | C | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(289): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.675+33T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123048765 | ||||||
chr6:123048788
|
T | TGCATAAT others(15): Show |
1 | a0001c0001t0004g0127 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.675+59_675+80dupAT others(20): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 123048788 | |||||
chr6:123048800
|
A | G | 1 | a0001c0001t0010g0159 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.675+68A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123048800 | ||||||
chr6:123048867
|
G | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(111): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.675+135G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123048867 | ||||||
chr6:123049026
|
T | C | 3 | a0001c0002t0024g0259a0001c0002t0029g0041a0001c0002t0029g0042 | 3 | HG02717.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.675+294T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049026 | ||||||
chr6:123049074
|
T | A | 1 | a0001c0001t0002g0240 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.675+342T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049074 | ||||||
chr6:123049121
|
G | A | 1 | a0001c0001t0003g0138 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.675+389G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049121 | ||||||
chr6:123049403
|
A | C | 40 | a0001c0001t0010g0019a0001c0001t0010g0154a0001c0001t0010g0157others(37): Show | 42 | HG00741.hp2 HG01243.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.675+671A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049403 | ||||||
chr6:123049478
|
G | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(111): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.675+746G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049478 | ||||||
chr6:123049532
|
C | T | 1 | a0001c0001t0003g0124 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.675+800C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049532 | ||||||
chr6:123049562
|
A | G | 1 | a0001c0001t0045g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.675+830A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049562 | ||||||
chr6:123049674
|
A | G | 40 | a0001c0001t0010g0019a0001c0001t0010g0154a0001c0001t0010g0157others(37): Show | 42 | HG00741.hp2 HG01243.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.675+942A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049674 | ||||||
chr6:123049684
|
C | T | 2 | a0001c0001t0001g0047a0001c0001t0001g0049 | 2 | HG01175.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.675+952C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049684 | ||||||
chr6:123049701
|
C | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(111): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.675+969C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049701 | ||||||
chr6:123049732
|
T | C | 5 | a0001c0001t0025g0260a0001c0001t0025g0263a0001c0001t0025g0264others(2): Show | 5 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.675+1000T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049732 | ||||||
chr6:123049789
|
G | T | 1 | a0001c0001t0001g0081 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.675+1057G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049789 | ||||||
chr6:123049804
|
T | TG | 12 | a0001c0001t0003g0020a0001c0001t0003g0096a0001c0001t0003g0120others(9): Show | 13 | HG00408.hp2 HG01256.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.675+1078dupG | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 123049804 | |||||
chr6:123049804
|
T | TGG | 42 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0016others(39): Show | 45 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.675+1077_675+1078d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 123049804 | |||||
chr6:123049804
|
T | TGGG | 21 | a0001c0001t0001g0061a0001c0001t0001g0078a0001c0001t0003g0099others(18): Show | 21 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.675+1076_675+1078d others(5): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 123049804 | |||||
chr6:123049807
|
G | GGA | 8 | a0001c0001t0012g0051a0001c0001t0012g0056a0001c0001t0012g0058others(5): Show | 8 | HG03239.hp1 HG04204.hp1 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.675+1076_675+1077i others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 123049807 | |||||
chr6:123049809
|
GGC | G | 40 | a0001c0001t0010g0019a0001c0001t0010g0154a0001c0001t0010g0157others(37): Show | 42 | HG00741.hp2 HG01243.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.675+1079_675+1080d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 123049809 | |||||
chr6:123049810
|
G | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(119): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.675+1078G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049810 | ||||||
chr6:123049810
|
GC | G | 3 | a0001c0001t0045g0172a0001c0001t0045g0177a0001c0001t0054g0044 | 3 | HG02109.hp1 HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.675+1079delC | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049810 | ||||||
chr6:123049811
|
C | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(217): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.675+1079C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049811 | ||||||
chr6:123049852
|
A | T | 5 | a0001c0001t0025g0260a0001c0001t0025g0263a0001c0001t0025g0264others(2): Show | 5 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.675+1120A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049852 | ||||||
chr6:123049886
|
A | G | 1 | a0001c0001t0026g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.675+1154A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049886 | ||||||
chr6:123049958
|
G | T | 1 | a0001c0001t0002g0240 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.675+1226G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049958 | ||||||
chr6:123049972
|
C | T | 1 | a0001c0001t0003g0096 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.675+1240C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049972 | ||||||
chr6:123049976
|
T | C | 45 | a0001c0001t0010g0019a0001c0001t0010g0154a0001c0001t0010g0157others(42): Show | 47 | HG00741.hp2 HG01109.hp2 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.675+1244T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049976 | ||||||
chr6:123050007
|
T | C | 106 | a0001c0001t0001g0061a0001c0001t0001g0078a0001c0001t0003g0014others(103): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.675+1275T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123050007 | ||||||
chr6:123050154
|
G | A | 45 | a0001c0001t0010g0019a0001c0001t0010g0154a0001c0001t0010g0157others(42): Show | 47 | HG00741.hp2 HG01109.hp2 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.675+1422G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123050154 | ||||||
chr6:123050445
|
T | C | 1 | a0001c0001t0057g0164 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.675+1713T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123050445 | ||||||
chr6:123050679
|
G | C | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.675+1947G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123050679 | ||||||
chr6:123050705
|
C | T | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(260): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.675+1973C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123050705 | ||||||
chr6:123050714
|
A | G | 116 | a0001c0001t0001g0061a0001c0001t0001g0078a0001c0001t0002g0253others(113): Show | 126 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.675+1982A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123050714 | ||||||
chr6:123050725
|
C | A | 1 | a0001c0001t0001g0065 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.675+1993C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123050725 | ||||||
chr6:123050981
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0063 | 2 | HG00099.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.675+2249G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123050981 | ||||||
chr6:123051055
|
T | C | 1 | a0001c0001t0048g0137 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.675+2323T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123051055 | ||||||
chr6:123051126
|
TACTC | T | 4 | a0001c0001t0016g0027a0001c0001t0016g0244a0001c0001t0072g0245others(1): Show | 5 | HG01884.hp2 HG02895.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.675+2397_675+2400d others(6): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 123051126 | |||||
chr6:123051174
|
G | A | 40 | a0001c0001t0010g0019a0001c0001t0010g0154a0001c0001t0010g0157others(37): Show | 42 | HG00741.hp2 HG01243.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.675+2442G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123051174 | ||||||
chr6:123051196
|
A | G | 40 | a0001c0001t0010g0019a0001c0001t0010g0154a0001c0001t0010g0157others(37): Show | 42 | HG00741.hp2 HG01243.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.675+2464A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123051196 | ||||||
chr6:123051336
|
C | T | 1 | a0001c0001t0002g0024 | 2 | HG00140.hp2 HG00280.hp1 |
intron_variant | MODIFIER | c.675+2604C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123051336 | ||||||
chr6:123051391
|
A | G | 8 | a0001c0001t0010g0019a0001c0001t0010g0154a0001c0001t0010g0157others(5): Show | 9 | HG00741.hp2 HG01243.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.675+2659A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123051391 | ||||||
chr6:123051601
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.675+2869T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123051601 | ||||||
chr6:123051885
|
A | G | 18 | a0001c0001t0002g0253a0001c0001t0007g0009a0001c0001t0007g0249others(15): Show | 23 | HG01099.hp1 HG01515.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.675+3153A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123051885 | ||||||
chr6:123051948
|
T | G | 25 | a0001c0001t0012g0051a0001c0001t0012g0056a0001c0001t0012g0058others(22): Show | 26 | HG00735.hp1 HG01106.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.675+3216T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123051948 | ||||||
chr6:123052102
|
T | TA | 109 | a0001c0001t0001g0061a0001c0001t0001g0078a0001c0001t0002g0253others(106): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.675+3371dupA | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 123052102 | |||||
chr6:123052169
|
A | G | 1 | a0001c0001t0015g0176 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.675+3437A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123052169 | ||||||
chr6:123052179
|
A | G | 2 | a0001c0001t0022g0144a0001c0001t0022g0145 | 2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.675+3447A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123052179 | ||||||
chr6:123052376
|
T | G | 51 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0009g0022others(48): Show | 54 | HG00741.hp2 HG01109.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.676-3430T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123052376 | ||||||
chr6:123052665
|
T | G | 1 | a0001c0001t0006g0211 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.676-3141T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123052665 | ||||||
chr6:123052729
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.676-3077G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123052729 | ||||||
chr6:123052736
|
TAGTGA | T | 25 | a0001c0001t0012g0051a0001c0001t0012g0056a0001c0001t0012g0058others(22): Show | 26 | HG00735.hp1 HG01106.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.676-3069_676-3065d others(7): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123052736 | ||||||
chr6:123052745
|
C | T | 25 | a0001c0001t0012g0051a0001c0001t0012g0056a0001c0001t0012g0058others(22): Show | 26 | HG00735.hp1 HG01106.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.676-3061C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123052745 | ||||||
chr6:123052748
|
TAACTGAT others(324): Show |
T | 25 | a0001c0001t0012g0051a0001c0001t0012g0056a0001c0001t0012g0058others(22): Show | 26 | HG00735.hp1 HG01106.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.676-3057_676-2727d others(2): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123052748 | ||||||
chr6:123052800
|
A | G | 24 | a0001c0001t0009g0022a0001c0001t0009g0037a0001c0001t0009g0181others(21): Show | 26 | HG01884.hp2 HG01891.hp1 HG02083.hp1 others(23): Show |
intron_variant | MODIFIER | c.676-3006A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123052800 | ||||||
chr6:123053069
|
A | C | 5 | a0001c0001t0015g0173a0001c0001t0015g0174a0001c0001t0015g0175others(2): Show | 5 | HG02257.hp2 HG02451.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.676-2737A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123053069 | ||||||
chr6:123053174
|
G | A | 2 | a0001c0001t0004g0127a0001c0001t0004g0140 | 2 | NA18953.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.676-2632G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123053174 | ||||||
chr6:123053397
|
C | A | 1 | a0001c0001t0002g0213 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.676-2409C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123053397 | ||||||
chr6:123053416
|
A | G | 1 | a0001c0001t0038g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.676-2390A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123053416 | ||||||
chr6:123053537
|
C | G | 1 | a0001c0001t0006g0210 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.676-2269C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123053537 | ||||||
chr6:123053543
|
G | T | 2 | a0001c0001t0041g0261a0001c0001t0041g0262 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.676-2263G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123053543 | ||||||
chr6:123053880
|
G | C | 3 | a0001c0001t0003g0115a0001c0001t0003g0122a0001c0001t0003g0123 | 3 | HG02055.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.676-1926G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123053880 | ||||||
chr6:123054083
|
G | A | 1 | a0001c0001t0014g0227 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.676-1723G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123054083 | ||||||
chr6:123054111
|
G | A | 4 | a0001c0001t0003g0106a0001c0001t0003g0110a0001c0001t0003g0135others(1): Show | 4 | NA18961.hp1 NA18977.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.676-1695G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123054111 | ||||||
chr6:123054139
|
TGAA | T | 10 | a0001c0001t0002g0253a0001c0001t0007g0009a0001c0001t0007g0249others(7): Show | 14 | HG01099.hp1 HG01515.hp2 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.676-1661_676-1659d others(5): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 123054139 | |||||
chr6:123054257
|
C | A | 1 | a0001c0001t0081g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.676-1549C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123054257 | ||||||
chr6:123054539
|
T | C | 1 | a0001c0001t0003g0124 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.676-1267T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123054539 | ||||||
chr6:123054823
|
G | GT | 24 | a0001c0001t0012g0051a0001c0001t0012g0056a0001c0001t0012g0058others(21): Show | 25 | HG00735.hp1 HG01106.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.676-970dupT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 123054823 | |||||
chr6:123054913
|
T | C | 2 | a0001c0001t0002g0225a0001c0001t0002g0239 | 2 | HG00733.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.676-893T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123054913 | ||||||
chr6:123055101
|
A | G | 1 | a0001c0001t0006g0210 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.676-705A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123055101 | ||||||
chr6:123055302
|
G | A | 1 | a0001c0001t0012g0056 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.676-504G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123055302 | ||||||
chr6:123055319
|
AT | A | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(226): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.676-482delT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 123055319 | |||||
chr6:123055541
|
T | C | 4 | a0001c0001t0082g0285a0001c0001t0084g0287a0001c0001t0086g0150others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-265T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123055541 | ||||||
chr6:123055577
|
C | T | 1 | a0001c0001t0087g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.676-229C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123055577 | ||||||
chr6:123055661
|
C | A | 2 | a0001c0001t0002g0205a0001c0001t0002g0228 | 2 | HG00323.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.676-145C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123055661 | ||||||
chr6:123055798
|
A | G | 1 | a0001c0001t0002g0024 | 2 | HG00140.hp2 HG00280.hp1 |
splice_region_variant&intron_variant | LOW | c.676-8A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123055798 | ||||||
chr6:123056137
|
A | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(226): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.896+111A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123056137 | ||||||
chr6:123056372
|
C | A | 2 | a0001c0001t0003g0114a0001c0001t0062g0143 | 2 | HG00140.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.896+346C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123056372 | ||||||
chr6:123056372
|
C | G | 1 | a0001c0001t0071g0178 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.896+346C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123056372 | ||||||
chr6:123056438
|
G | A | 31 | a0001c0001t0009g0022a0001c0001t0009g0037a0001c0001t0009g0181others(28): Show | 33 | HG00735.hp1 HG01106.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.896+412G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123056438 | ||||||
chr6:123056655
|
G | T | 1 | a0001c0001t0003g0116 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.896+629G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123056655 | ||||||
chr6:123056665
|
G | A | 1 | a0001c0001t0081g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.896+639G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123056665 | ||||||
chr6:123056700
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.896+674G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123056700 | ||||||
chr6:123056989
|
A | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(223): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.896+963A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123056989 | ||||||
chr6:123057038
|
A | G | 1 | a0001c0001t0004g0102 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.896+1012A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123057038 | ||||||
chr6:123057071
|
A | G | 6 | a0001c0001t0003g0119a0001c0001t0003g0120a0001c0001t0003g0121others(3): Show | 7 | HG00639.hp1 HG00735.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.896+1045A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123057071 | ||||||
chr6:123057099
|
C | T | 5 | a0001c0001t0015g0173a0001c0001t0015g0174a0001c0001t0015g0175others(2): Show | 5 | HG02257.hp2 HG02451.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.896+1073C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123057099 | ||||||
chr6:123057163
|
G | A | 266 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(263): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.896+1137G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123057163 | ||||||
chr6:123057261
|
A | G | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(222): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.896+1235A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123057261 | ||||||
chr6:123057334
|
CT | C | 24 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(21): Show | 30 | HG01070.hp1 HG01099.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.896+1339delT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 123057334 | |||||
chr6:123057334
|
CTTT | C | 11 | a0001c0001t0007g0009a0001c0001t0007g0249a0001c0001t0007g0250others(8): Show | 15 | HG01099.hp1 HG01515.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.896+1337_896+1339d others(5): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 123057334 | |||||
chr6:123057334
|
CTTTTT | C | 23 | a0001c0001t0009g0022a0001c0001t0009g0037a0001c0001t0009g0181others(20): Show | 25 | HG01109.hp2 HG01167.hp2 HG02083.hp1 others(22): Show |
intron_variant | MODIFIER | c.896+1335_896+1339d others(7): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 123057334 | |||||
chr6:123057334
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0004g0141a0001c0001t0074g0113 | 2 | HG01346.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.896+1330_896+1339d others(12): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 123057334 | |||||
chr6:123057334
|
CTTTTTTT others(4): Show |
C | 65 | a0001c0001t0001g0060a0001c0001t0001g0078a0001c0001t0001g0082others(62): Show | 70 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.896+1329_896+1339d others(13): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 123057334 | |||||
chr6:123057334
|
CTTTTTTT others(5): Show |
C | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(145): Show | 166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.896+1328_896+1339d others(14): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 123057334 | |||||
chr6:123057334
|
CTTTTTTT others(6): Show |
C | 7 | a0001c0001t0001g0065a0001c0001t0006g0193a0001c0001t0011g0064others(4): Show | 7 | HG02647.hp2 HG02897.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.896+1327_896+1339d others(15): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 123057334 | |||||
chr6:123057410
|
G | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(250): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.896+1384G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123057410 | ||||||
chr6:123057596
|
G | A | 2 | a0001c0001t0028g0032a0001c0001t0028g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.896+1570G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123057596 | ||||||
chr6:123057783
|
T | G | 9 | a0001c0001t0007g0009a0001c0001t0007g0249a0001c0001t0007g0250others(6): Show | 13 | HG01099.hp1 HG01515.hp2 NA18948.hp1 others(10): Show |
intron_variant | MODIFIER | c.896+1757T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123057783 | ||||||
chr6:123057841
|
C | G | 7 | a0001c0001t0010g0019a0001c0001t0010g0154a0001c0001t0010g0157others(4): Show | 8 | HG00741.hp2 HG01243.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.896+1815C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123057841 | ||||||
chr6:123057911
|
T | A | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(222): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.896+1885T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123057911 | ||||||
chr6:123058145
|
C | CT | 9 | a0001c0001t0007g0009a0001c0001t0007g0249a0001c0001t0007g0250others(6): Show | 13 | HG01099.hp1 HG01515.hp2 NA18948.hp1 others(10): Show |
intron_variant | MODIFIER | c.896+2127dupT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 123058145 | |||||
chr6:123058209
|
C | T | 1 | a0001c0001t0063g0142 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.896+2183C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123058209 | ||||||
chr6:123058210
|
G | A | 1 | a0001c0001t0052g0147 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.896+2184G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123058210 | ||||||
chr6:123058233
|
A | G | 3 | a0001c0001t0012g0051a0001c0001t0012g0059a0001c0001t0043g0202 | 3 | NA18998.hp1 NA18999.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.896+2207A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123058233 | ||||||
chr6:123058280
|
C | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(212): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.896+2254C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123058280 | ||||||
chr6:123058631
|
C | G | 3 | a0001c0001t0006g0025a0001c0001t0006g0242a0001c0001t0046g0025 | 3 | NA18955.hp2 NA18961.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.896+2605C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123058631 | ||||||
chr6:123058664
|
T | A | 4 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0225others(1): Show | 4 | HG00733.hp2 HG02602.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+2638T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123058664 | ||||||
chr6:123058756
|
A | G | 1 | a0001c0001t0081g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.896+2730A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123058756 | ||||||
chr6:123058992
|
A | G | 1 | a0001c0001t0081g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.896+2966A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123058992 | ||||||
chr6:123059108
|
T | C | 3 | a0001c0001t0045g0172a0001c0001t0045g0177a0001c0001t0054g0044 | 3 | HG02109.hp1 HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.896+3082T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123059108 | ||||||
chr6:123059135
|
C | T | 1 | a0001c0001t0059g0279 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.896+3109C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123059135 | ||||||
chr6:123059202
|
AAG | A | 9 | a0001c0001t0007g0009a0001c0001t0007g0249a0001c0001t0007g0250others(6): Show | 13 | HG01099.hp1 HG01515.hp2 NA18948.hp1 others(10): Show |
intron_variant | MODIFIER | c.896+3179_896+3180d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 123059202 | |||||
chr6:123059214
|
A | G | 20 | a0001c0001t0012g0051a0001c0001t0012g0056a0001c0001t0012g0058others(17): Show | 21 | HG00735.hp1 HG01106.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.896+3188A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123059214 | ||||||
chr6:123059222
|
C | T | 1 | a0002c0003t0005g0269 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.896+3196C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123059222 | ||||||
chr6:123059652
|
G | A | 1 | a0001c0001t0083g0165 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.896+3626G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123059652 | ||||||
chr6:123059814
|
G | T | 6 | a0001c0001t0006g0008a0001c0001t0006g0193a0001c0001t0006g0210others(3): Show | 8 | HG00423.hp2 HG02074.hp1 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.896+3788G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123059814 | ||||||
chr6:123059825
|
C | A | 2 | a0001c0001t0001g0074a0001c0001t0002g0253 | 2 | NA18947.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.896+3799C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123059825 | ||||||
chr6:123059892
|
G | A | 1 | a0001c0001t0081g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.897-3782G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123059892 | ||||||
chr6:123060125
|
T | A | 1 | a0001c0001t0001g0062 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.897-3549T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123060125 | ||||||
chr6:123060417
|
C | G | 7 | a0001c0001t0035g0265a0001c0001t0035g0266a0001c0001t0056g0048others(4): Show | 7 | HG02145.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.897-3257C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123060417 | ||||||
chr6:123060598
|
C | T | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(110): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.897-3076C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123060598 | ||||||
chr6:123060674
|
A | C | 4 | a0001c0001t0045g0172a0001c0001t0045g0177a0001c0001t0054g0044others(1): Show | 4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.897-3000A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123060674 | ||||||
chr6:123060699
|
C | T | 2 | a0001c0001t0038g0094a0001c0001t0038g0095 | 2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.897-2975C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123060699 | ||||||
chr6:123060713
|
G | A | 1 | a0001c0001t0025g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.897-2961G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123060713 | ||||||
chr6:123060797
|
G | A | 12 | a0001c0001t0009g0022a0001c0001t0009g0037a0001c0001t0009g0181others(9): Show | 13 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.897-2877G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123060797 | ||||||
chr6:123060873
|
C | T | 1 | a0001c0001t0038g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.897-2801C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123060873 | ||||||
chr6:123061192
|
T | C | 1 | a0001c0001t0002g0253 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.897-2482T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123061192 | ||||||
chr6:123061219
|
C | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(211): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.897-2455C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123061219 | ||||||
chr6:123061246
|
G | A | 2 | a0001c0001t0041g0261a0001c0001t0041g0262 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.897-2428G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123061246 | ||||||
chr6:123061262
|
A | G | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.897-2412A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123061262 | ||||||
chr6:123061311
|
C | T | 1 | a0001c0001t0060g0247 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.897-2363C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123061311 | ||||||
chr6:123061312
|
G | GA | 9 | a0001c0001t0004g0017a0001c0001t0004g0130a0001c0001t0004g0134others(6): Show | 10 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.897-2351dupA | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 123061312 | |||||
chr6:123061312
|
GA | G | 17 | a0001c0001t0002g0219a0001c0001t0002g0226a0001c0001t0002g0235others(14): Show | 18 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.897-2351delA | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 123061312 | |||||
chr6:123061324
|
C | A | 4 | a0001c0001t0045g0172a0001c0001t0045g0177a0001c0001t0054g0044others(1): Show | 4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.897-2350C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123061324 | ||||||
chr6:123061441
|
C | G | 1 | a0001c0001t0081g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.897-2233C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123061441 | ||||||
chr6:123061799
|
T | C | 9 | a0001c0001t0012g0051a0001c0001t0012g0056a0001c0001t0012g0058others(6): Show | 9 | HG03239.hp1 HG04204.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.897-1875T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123061799 | ||||||
chr6:123061868
|
T | TATATA | 52 | a0001c0001t0007g0009a0001c0001t0007g0249a0001c0001t0007g0250others(49): Show | 58 | HG00735.hp1 HG01099.hp1 HG01106.hp2 others(55): Show |
intron_variant | MODIFIER | c.897-1805_897-1801d others(7): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 123061868 | |||||
chr6:123061922
|
A | G | 1 | a0001c0001t0006g0237 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.897-1752A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123061922 | ||||||
chr6:123062081
|
T | C | 1 | a0001c0001t0081g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.897-1593T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123062081 | ||||||
chr6:123062107
|
G | A | 1 | a0001c0001t0074g0113 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.897-1567G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123062107 | ||||||
chr6:123062503
|
C | G | 1 | a0001c0001t0062g0143 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.897-1171C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123062503 | ||||||
chr6:123062551
|
A | G | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | NA19007.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.897-1123A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123062551 | ||||||
chr6:123062564
|
C | T | 1 | a0001c0001t0081g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.897-1110C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123062564 | ||||||
chr6:123062618
|
A | G | 9 | a0001c0001t0007g0009a0001c0001t0007g0249a0001c0001t0007g0250others(6): Show | 13 | HG01099.hp1 HG01515.hp2 NA18948.hp1 others(10): Show |
intron_variant | MODIFIER | c.897-1056A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123062618 | ||||||
chr6:123062750
|
G | T | 12 | a0001c0001t0009g0022a0001c0001t0009g0037a0001c0001t0009g0181others(9): Show | 13 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.897-924G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123062750 | ||||||
chr6:123063010
|
T | C | 9 | a0001c0001t0007g0009a0001c0001t0007g0249a0001c0001t0007g0250others(6): Show | 13 | HG01099.hp1 HG01515.hp2 NA18948.hp1 others(10): Show |
intron_variant | MODIFIER | c.897-664T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123063010 |