geneid | 57703 |
---|---|
ensemblid | ENSG00000163510.14 |
hgncid | 29322 |
symbol | CWC22 |
name | CWC22 spliceosome associated protein homolog |
refseq_nuc | NM_020943.3 |
refseq_prot | NP_065994.1 |
ensembl_nuc | ENST00000410053.8 |
ensembl_prot | ENSP00000387006.3 |
mane_status | MANE Select |
chr | chr2 |
start | 179944876 |
end | 180007297 |
strand | - |
ver | v1.2 |
region | chr2:179944876-180007297 |
region5000 | chr2:179939876-180012297 |
regionname0 | CWC22_chr2_179944876_180007297 |
regionname5000 | CWC22_chr2_179939876_180012297 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 908 | 186 | 52 | 24 | 82 | 8 | 19 | 64 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0002 | 0/0 | 908 | 82 | 14 | 17 | 44 | 1 | 6 | 37 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0003 | 0/0 | 908 | 64 | 4 | 8 | 48 | 1 | 3 | 39 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0004 | 1/0 | 908 | 29 | 13 | 8 | 0 | 3 | 4 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0005 | 0/0 | 908 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0006 | 0/0 | 908 | 3 | 0 | 0 | 2 | 0 | 1 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0007 | 0/0 | 908 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0008 | 0/0 | 908 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0009 | 0/0 | 908 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0010 | 0/0 | 908 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0011 | 0/0 | 529 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0012 | 0/0 | 908 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0013 | 0/0 | 908 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2727 | 174 | 41 | 24 | 81 | 8 | 19 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
c0002 | 0/0 | 2727 | 81 | 14 | 17 | 43 | 1 | 6 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
c0003 | 0/0 | 2727 | 64 | 4 | 8 | 48 | 1 | 3 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
c0004 | 1/0 | 2727 | 28 | 12 | 8 | 0 | 3 | 4 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
c0005 | 0/0 | 2727 | 4 | 4 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
c0006 | 0/0 | 2727 | 3 | 0 | 0 | 2 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
c0007 | 0/0 | 2727 | 3 | 3 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
c0008 | 0/0 | 2727 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
c0009 | 0/0 | 2727 | 2 | 0 | 2 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
c0010 | 0/0 | 2727 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
c0011 | 0/0 | 2727 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
c0012 | 0/0 | 2727 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
c0013 | 0/0 | 2727 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
c0014 | 0/0 | 2727 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
c0015 | 0/0 | 2727 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
c0016 | 0/0 | 2727 | 1 | 0 | 0 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
c0017 | 0/0 | 2727 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
c0018 | 0/0 | 2727 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
c0019 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
c0020 | 0/0 | 2727 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
c0021 | 0/0 | 2727 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
c0022 | 0/0 | 2727 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
c0023 | 0/0 | 2727 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
c0024 | 0/0 | 2727 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 798 | 188 | 49 | 25 | 84 | 8 | 20 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
t0002 | 0/0 | 798 | 176 | 36 | 33 | 90 | 5 | 12 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
t0003 | 0/0 | 798 | 3 | 0 | 1 | 0 | 1 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
t0004 | 0/0 | 798 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
t0005 | 0/0 | 798 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
t0006 | 0/0 | 798 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
t0007 | 0/0 | 798 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
t0008 | 0/0 | 798 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
t0009 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
t0010 | 0/0 | 798 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 9 | 0 | 6 | 3 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0002 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0003 | 0/0 | 7 | 0 | 3 | 1 | 2 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0004 | 0/0 | 7 | 0 | 0 | 5 | 2 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0005 | 0/0 | 6 | 0 | 0 | 5 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0008 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0009 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0014 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0034 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0102 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0146 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2727 | 174 | 41 | 24 | 81 | 8 | 19 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0001c0005 | 0/0 | 2727 | 4 | 4 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0001c0008 | 0/0 | 2727 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0001c0011 | 0/0 | 2727 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0001c0012 | 0/0 | 2727 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0001c0014 | 0/0 | 2727 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0001c0015 | 0/0 | 2727 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0001c0017 | 0/0 | 2727 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0001c0022 | 0/0 | 2727 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0002c0002 | 0/0 | 2727 | 81 | 14 | 17 | 43 | 1 | 6 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0002c0013 | 0/0 | 2727 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0003c0003 | 0/0 | 2727 | 64 | 4 | 8 | 48 | 1 | 3 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0004c0004 | 1/0 | 2727 | 28 | 12 | 8 | 0 | 3 | 4 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0004c0018 | 0/0 | 2727 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0005c0007 | 0/0 | 2727 | 3 | 3 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0005c0020 | 0/0 | 2727 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0006c0006 | 0/0 | 2727 | 3 | 0 | 0 | 2 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0007c0009 | 0/0 | 2727 | 2 | 0 | 2 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0008c0024 | 0/0 | 2727 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0009c0023 | 0/0 | 2727 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0010c0021 | 0/0 | 2727 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0011c0019 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0012c0016 | 0/0 | 2727 | 1 | 0 | 0 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0013c0010 | 0/0 | 2727 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3524 | 169 | 41 | 22 | 80 | 7 | 18 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0001c0001t0002 | 0/0 | 3524 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0001c0001t0003 | 0/0 | 3524 | 3 | 0 | 1 | 0 | 1 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0001c0001t0006 | 0/0 | 3524 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0001c0005t0001 | 0/0 | 3524 | 4 | 4 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0001c0008t0002 | 0/0 | 3524 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0001c0011t0001 | 0/0 | 3524 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0001c0012t0001 | 0/0 | 3524 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0001c0014t0002 | 0/0 | 3524 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0001c0015t0002 | 0/0 | 3524 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0001c0017t0009 | 0/0 | 3524 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0001c0022t0001 | 0/0 | 3524 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0002c0002t0002 | 0/0 | 3524 | 78 | 14 | 17 | 41 | 1 | 5 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0002c0002t0007 | 0/0 | 3524 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0002c0002t0008 | 0/0 | 3524 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0002c0002t0010 | 0/0 | 3524 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0002c0013t0002 | 0/0 | 3524 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0003c0003t0002 | 0/0 | 3524 | 62 | 4 | 8 | 46 | 1 | 3 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0003c0003t0005 | 0/0 | 3524 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0004c0004t0001 | 1/0 | 3524 | 1 | 0 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0004c0004t0002 | 0/0 | 3524 | 25 | 10 | 8 | 0 | 3 | 4 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0004c0004t0004 | 0/0 | 3524 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0004c0018t0001 | 0/0 | 3524 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0005c0007t0002 | 0/0 | 3524 | 3 | 3 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0005c0020t0002 | 0/0 | 3524 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0006c0006t0001 | 0/0 | 3524 | 3 | 0 | 0 | 2 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0007c0009t0001 | 0/0 | 3524 | 2 | 0 | 2 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0008c0024t0002 | 0/0 | 3524 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0009c0023t0001 | 0/0 | 3524 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0010c0021t0001 | 0/0 | 3524 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0011c0019t0001 | 0/0 | 3548 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0012c0016t0001 | 0/0 | 3524 | 1 | 0 | 0 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
a0013c0010t0001 | 0/0 | 3524 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | copy fasta | chr2 | 179939876 | 180012297 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0003 | 0/0 | 7 | 0 | 3 | 1 | 2 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 5 | 2 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0102 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0003g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0001t0006g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0005t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0005t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0005t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0005t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0008t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0008t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0011t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0012t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0014t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0015t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0017t0009g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0001c0022t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0001 | 0/0 | 9 | 0 | 6 | 3 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0005 | 0/0 | 6 | 0 | 0 | 5 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0007g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0008g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0002t0010g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0002c0013t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0014 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0034 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0003c0003t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0004c0004t0001g0146 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0004c0004t0002g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0004c0004t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0004c0004t0002g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0004c0004t0002g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0004c0004t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0004c0004t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0004c0004t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0004c0004t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0004c0004t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0004c0004t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0004c0004t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0004c0004t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0004c0004t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0004c0004t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0004c0004t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0004c0004t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0004c0004t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0004c0004t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0004c0004t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0004c0004t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0004c0004t0004g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0004c0018t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0005c0007t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0005c0007t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0005c0020t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0006c0006t0001g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0006c0006t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0007c0009t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0007c0009t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0008c0024t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0009c0023t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0010c0021t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0011c0019t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0012c0016t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
a0013c0010t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0003 | c0003 | t0002 | g0014 | EUR | GBR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00140 | hp2 | a0012 | c0016 | t0001 | g0059 | EUR | GBR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0172 | EUR | FIN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00280 | hp2 | a0004 | c0004 | t0002 | g0214 | EUR | FIN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | FIN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00408 | hp1 | a0003 | c0003 | t0002 | g0206 | EAS | CHS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00438 | hp1 | a0003 | c0003 | t0002 | g0197 | EAS | CHS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00544 | hp1 | a0003 | c0003 | t0002 | g0007 | EAS | CHS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00558 | hp2 | a0006 | c0006 | t0001 | g0105 | EAS | CHS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00597 | hp2 | a0003 | c0003 | t0002 | g0012 | EAS | CHS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0237 | EAS | CHS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00733 | hp1 | a0002 | c0002 | t0002 | g0021 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00738 | hp1 | a0004 | c0004 | t0002 | g0213 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0261 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01069 | hp1 | a0001 | c0001 | t0006 | g0171 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01099 | hp1 | a0004 | c0004 | t0002 | g0038 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01106 | hp2 | a0003 | c0003 | t0002 | g0187 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01109 | hp1 | a0002 | c0002 | t0002 | g0243 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01168 | hp2 | a0002 | c0002 | t0002 | g0021 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01169 | hp2 | a0002 | c0002 | t0002 | g0021 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01175 | hp1 | a0009 | c0023 | t0001 | g0067 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01175 | hp2 | a0003 | c0003 | t0002 | g0014 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01243 | hp1 | a0003 | c0003 | t0002 | g0182 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0263 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01256 | hp1 | a0007 | c0009 | t0001 | g0161 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01256 | hp2 | a0003 | c0003 | t0002 | g0210 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01258 | hp2 | a0007 | c0009 | t0001 | g0162 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01261 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01358 | hp1 | a0003 | c0003 | t0002 | g0194 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01361 | hp1 | a0004 | c0004 | t0002 | g0222 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0233 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01496 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01516 | hp1 | a0004 | c0004 | t0002 | g0219 | EUR | IBS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01934 | hp1 | a0003 | c0003 | t0002 | g0188 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01934 | hp2 | a0002 | c0002 | t0002 | g0241 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01943 | hp1 | a0004 | c0004 | t0002 | g0017 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01943 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01975 | hp2 | a0004 | c0004 | t0002 | g0017 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01981 | hp1 | a0004 | c0004 | t0002 | g0037 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01993 | hp1 | a0002 | c0002 | t0002 | g0239 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01993 | hp2 | a0002 | c0002 | t0002 | g0260 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02027 | hp1 | a0002 | c0002 | t0002 | g0245 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02027 | hp2 | a0003 | c0003 | t0002 | g0199 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02055 | hp1 | a0002 | c0002 | t0002 | g0046 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02055 | hp2 | a0003 | c0003 | t0002 | g0014 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0244 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02074 | hp1 | a0003 | c0003 | t0002 | g0205 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02080 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02132 | hp1 | a0008 | c0024 | t0002 | g0255 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02132 | hp2 | a0003 | c0003 | t0002 | g0200 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02135 | hp1 | a0003 | c0003 | t0002 | g0035 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02145 | hp1 | a0002 | c0002 | t0002 | g0227 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02148 | hp1 | a0003 | c0003 | t0002 | g0181 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02148 | hp2 | a0002 | c0002 | t0002 | g0258 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CDX | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02155 | hp2 | a0002 | c0002 | t0002 | g0041 | EAS | CDX | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CDX | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02165 | hp2 | a0003 | c0003 | t0002 | g0198 | EAS | CDX | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02257 | hp1 | a0004 | c0004 | t0002 | g0273 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02280 | hp2 | a0004 | c0004 | t0002 | g0176 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02300 | hp1 | a0004 | c0004 | t0002 | g0038 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02300 | hp2 | a0004 | c0004 | t0002 | g0215 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02451 | hp1 | a0004 | c0004 | t0002 | g0033 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02602 | hp2 | a0002 | c0002 | t0002 | g0231 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02615 | hp1 | a0001 | c0005 | t0001 | g0149 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02630 | hp1 | a0002 | c0002 | t0002 | g0044 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02647 | hp1 | a0002 | c0002 | t0002 | g0265 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02717 | hp2 | a0002 | c0002 | t0002 | g0044 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02735 | hp2 | a0004 | c0004 | t0002 | g0017 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02809 | hp1 | a0002 | c0002 | t0002 | g0266 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02809 | hp2 | a0001 | c0022 | t0001 | g0087 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02886 | hp1 | a0002 | c0002 | t0002 | g0264 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02895 | hp1 | a0004 | c0004 | t0002 | g0178 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02896 | hp1 | a0004 | c0004 | t0004 | g0032 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02896 | hp2 | a0001 | c0005 | t0001 | g0150 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02897 | hp1 | a0004 | c0004 | t0004 | g0032 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02897 | hp2 | a0004 | c0004 | t0002 | g0177 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02965 | hp1 | a0003 | c0003 | t0002 | g0034 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02970 | hp1 | a0003 | c0003 | t0002 | g0185 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02976 | hp1 | a0002 | c0002 | t0002 | g0019 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03017 | hp2 | a0004 | c0004 | t0002 | g0221 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03098 | hp2 | a0004 | c0004 | t0002 | g0272 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03130 | hp2 | a0002 | c0002 | t0002 | g0046 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03139 | hp2 | a0004 | c0004 | t0002 | g0217 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03195 | hp1 | a0001 | c0012 | t0001 | g0054 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03195 | hp2 | a0005 | c0007 | t0002 | g0039 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03209 | hp1 | a0005 | c0007 | t0002 | g0039 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03209 | hp2 | a0004 | c0004 | t0002 | g0033 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03225 | hp2 | a0002 | c0002 | t0002 | g0268 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03239 | hp1 | a0004 | c0004 | t0002 | g0216 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03453 | hp2 | a0001 | c0008 | t0002 | g0174 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03486 | hp2 | a0001 | c0005 | t0001 | g0148 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03490 | hp2 | a0002 | c0002 | t0002 | g0040 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03491 | hp1 | a0002 | c0002 | t0002 | g0256 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03492 | hp2 | a0002 | c0002 | t0002 | g0040 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03540 | hp1 | a0001 | c0015 | t0002 | g0271 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03540 | hp2 | a0001 | c0008 | t0002 | g0179 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03579 | hp2 | a0013 | c0010 | t0001 | g0117 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03654 | hp1 | a0002 | c0002 | t0008 | g0229 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03669 | hp1 | a0003 | c0003 | t0002 | g0211 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03688 | hp1 | a0010 | c0021 | t0001 | g0111 | SAS | STU | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0031 | SAS | STU | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03710 | hp1 | a0003 | c0003 | t0002 | g0034 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03834 | hp1 | a0006 | c0006 | t0001 | g0028 | SAS | BEB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03834 | hp2 | a0004 | c0004 | t0002 | g0220 | SAS | BEB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG04204 | hp2 | a0003 | c0003 | t0002 | g0209 | SAS | STU | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0257 | SAS | STU | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | STU | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18522 | hp1 | a0005 | c0007 | t0002 | g0225 | AFR | YRI | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | YRI | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | CHB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18939 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18941 | hp2 | a0003 | c0003 | t0002 | g0196 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18943 | hp1 | a0003 | c0003 | t0002 | g0207 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18943 | hp2 | a0002 | c0002 | t0002 | g0236 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18946 | hp1 | a0006 | c0006 | t0001 | g0028 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18946 | hp2 | a0003 | c0003 | t0002 | g0189 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18948 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0234 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18951 | hp1 | a0002 | c0002 | t0002 | g0242 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18952 | hp1 | a0003 | c0003 | t0002 | g0007 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0259 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18954 | hp1 | a0003 | c0003 | t0002 | g0012 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18957 | hp2 | a0003 | c0003 | t0002 | g0195 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18960 | hp2 | a0003 | c0003 | t0002 | g0036 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18961 | hp1 | a0003 | c0003 | t0002 | g0208 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18965 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18966 | hp1 | a0003 | c0003 | t0005 | g0277 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18967 | hp1 | a0003 | c0003 | t0002 | g0191 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18968 | hp1 | a0001 | c0011 | t0001 | g0072 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18968 | hp2 | a0002 | c0002 | t0002 | g0251 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18970 | hp1 | a0003 | c0003 | t0002 | g0007 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18970 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18971 | hp2 | a0003 | c0003 | t0002 | g0018 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18973 | hp2 | a0002 | c0002 | t0010 | g0278 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18975 | hp1 | a0003 | c0003 | t0002 | g0202 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18978 | hp2 | a0003 | c0003 | t0002 | g0193 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18979 | hp1 | a0003 | c0003 | t0002 | g0035 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18980 | hp1 | a0003 | c0003 | t0002 | g0012 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18980 | hp2 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18984 | hp2 | a0003 | c0003 | t0002 | g0015 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18986 | hp1 | a0002 | c0002 | t0002 | g0232 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0228 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18987 | hp1 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18987 | hp2 | a0003 | c0003 | t0002 | g0203 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18989 | hp1 | a0003 | c0003 | t0002 | g0015 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18990 | hp1 | a0003 | c0003 | t0002 | g0018 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18992 | hp1 | a0003 | c0003 | t0002 | g0201 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18992 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18994 | hp1 | a0002 | c0002 | t0002 | g0240 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18998 | hp2 | a0003 | c0003 | t0002 | g0190 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18999 | hp1 | a0002 | c0002 | t0002 | g0247 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA18999 | hp2 | a0003 | c0003 | t0002 | g0016 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19001 | hp2 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19002 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19002 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19003 | hp1 | a0003 | c0003 | t0002 | g0018 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19004 | hp1 | a0003 | c0003 | t0002 | g0270 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19004 | hp2 | a0002 | c0002 | t0002 | g0230 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19005 | hp1 | a0003 | c0003 | t0002 | g0204 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0254 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19009 | hp2 | a0003 | c0003 | t0002 | g0016 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19010 | hp1 | a0002 | c0002 | t0002 | g0246 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19010 | hp2 | a0003 | c0003 | t0002 | g0012 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19011 | hp1 | a0003 | c0003 | t0005 | g0276 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19030 | hp1 | a0001 | c0005 | t0001 | g0134 | AFR | LWK | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19030 | hp2 | a0002 | c0002 | t0002 | g0019 | AFR | LWK | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19054 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19056 | hp2 | a0003 | c0003 | t0002 | g0007 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19058 | hp1 | a0003 | c0003 | t0002 | g0016 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19060 | hp1 | a0003 | c0003 | t0002 | g0192 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19062 | hp1 | a0003 | c0003 | t0002 | g0015 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19068 | hp1 | a0003 | c0003 | t0002 | g0036 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19068 | hp2 | a0002 | c0002 | t0002 | g0253 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19074 | hp1 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19078 | hp2 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19079 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19080 | hp1 | a0003 | c0003 | t0002 | g0223 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19081 | hp1 | a0011 | c0019 | t0001 | g0086 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19081 | hp2 | a0002 | c0013 | t0002 | g0267 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19082 | hp1 | a0003 | c0003 | t0002 | g0184 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19082 | hp2 | a0002 | c0002 | t0007 | g0173 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19085 | hp2 | a0003 | c0003 | t0002 | g0269 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19087 | hp1 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0235 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19088 | hp2 | a0003 | c0003 | t0002 | g0007 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19089 | hp1 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19089 | hp2 | a0003 | c0003 | t0002 | g0183 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA19240 | hp2 | a0002 | c0002 | t0002 | g0019 | AFR | YRI | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0005 | EUR | TSI | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA20752 | hp2 | a0004 | c0004 | t0002 | g0037 | EUR | TSI | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01123 | hp1 | a0003 | c0003 | t0002 | g0212 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02109 | hp1 | a0004 | c0004 | t0002 | g0218 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02109 | hp2 | a0002 | c0002 | t0002 | g0226 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02486 | hp1 | a0002 | c0002 | t0002 | g0262 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03471 | hp1 | a0004 | c0004 | t0002 | g0175 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG03471 | hp2 | a0003 | c0003 | t0002 | g0186 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG06807 | hp1 | a0005 | c0020 | t0002 | g0224 | AFR | USA | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | USA | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA20300 | hp1 | a0004 | c0018 | t0001 | g0080 | AFR | USA | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | USA | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA21309 | hp1 | a0001 | c0017 | t0009 | g0275 | AFR | LWK | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
NA21309 | hp2 | a0001 | c0014 | t0002 | g0180 | AFR | LWK | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0102 | REF | REF | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
homoSapiens_grch38 | hp1 | a0004 | c0004 | t0001 | g0146 | REF | REF | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:179945475
|
C | T | 1 | a0003 | 64 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(61): Show |
missense_variant | MODERATE | c.2381G>A | p.Arg794Gln | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 20/20 | 2925/3524 | 2381/2727 | 794/908 | chr2 | 179945475 | ||
chr2:179945537
|
A | T | 12 | a0001a0002a0003others(9): Show | 347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
missense_variant | MODERATE | c.2319T>A | p.Ser773Arg | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 20/20 | 2863/3524 | 2319/2727 | 773/908 | chr2 | 179945537 | ||
chr2:179945631
|
C | T | 2 | a0002a0008 | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
missense_variant | MODERATE | c.2225G>A | p.Arg742Lys | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 20/20 | 2769/3524 | 2225/2727 | 742/908 | chr2 | 179945631 | ||
chr2:179945634
|
T | A | 1 | a0005 | 4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
missense_variant | MODERATE | c.2222A>T | p.Asp741Val | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 20/20 | 2766/3524 | 2222/2727 | 741/908 | chr2 | 179945634 | ||
chr2:179950602
|
C | T | 1 | a0006 | 3 | HG00558.hp2 HG03834.hp1 NA18946.hp1 |
missense_variant | MODERATE | c.2050G>A | p.Asp684Asn | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/20 | 2594/3524 | 2050/2727 | 684/908 | chr2 | 179950602 | ||
chr2:179950686
|
C | T | 1 | a0012 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.1966G>A | p.Ala656Thr | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/20 | 2510/3524 | 1966/2727 | 656/908 | chr2 | 179950686 | ||
chr2:179954220
|
A | AAAATTCC others(17): Show |
1 | a0011 | 1 | NA19081.hp1 | disruptive_inframe_insertion | MODERATE | c.1673_1674insGAATTT others(18): Show |
p.Asp558delinsGluAsn others(21): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2217/3524 | 1673/2727 | 558/908 | chr2 | 179954220 | ||
chr2:179954224
|
G | C | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1670C>G | p.Thr557Ser | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2214/3524 | 1670/2727 | 557/908 | chr2 | 179954224 | ||
chr2:179954239
|
G | C | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1655C>G | p.Ala552Gly | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2199/3524 | 1655/2727 | 552/908 | chr2 | 179954239 | ||
chr2:179954246
|
T | A | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1648A>T | p.Met550Leu | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2192/3524 | 1648/2727 | 550/908 | chr2 | 179954246 | ||
chr2:179954248
|
T | A | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1646A>T | p.Lys549Met | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2190/3524 | 1646/2727 | 549/908 | chr2 | 179954248 | ||
chr2:179954252
|
C | G | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1642G>C | p.Ala548Pro | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2186/3524 | 1642/2727 | 548/908 | chr2 | 179954252 | ||
chr2:179954254
|
A | C | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1640T>G | p.Val547Gly | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2184/3524 | 1640/2727 | 547/908 | chr2 | 179954254 | ||
chr2:179954256
|
A | T | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1638T>A | p.Asn546Lys | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2182/3524 | 1638/2727 | 546/908 | chr2 | 179954256 | ||
chr2:179954258
|
T | A | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1636A>T | p.Asn546Tyr | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2180/3524 | 1636/2727 | 546/908 | chr2 | 179954258 | ||
chr2:179954263
|
A | C | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1631T>G | p.Leu544Trp | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2175/3524 | 1631/2727 | 544/908 | chr2 | 179954263 | ||
chr2:179954268
|
G | C | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1626C>G | p.Asn542Lys | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2170/3524 | 1626/2727 | 542/908 | chr2 | 179954268 | ||
chr2:179954270
|
T | C | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1624A>G | p.Asn542Asp | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2168/3524 | 1624/2727 | 542/908 | chr2 | 179954270 | ||
chr2:179954275
|
T | A | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1619A>T | p.Glu540Val | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2163/3524 | 1619/2727 | 540/908 | chr2 | 179954275 | ||
chr2:179954281
|
C | T | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1613G>A | p.Arg538His | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2157/3524 | 1613/2727 | 538/908 | chr2 | 179954281 | ||
chr2:179954282
|
G | C | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1612C>G | p.Arg538Gly | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2156/3524 | 1612/2727 | 538/908 | chr2 | 179954282 | ||
chr2:179954285
|
G | T | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1609C>A | p.His537Asn | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2153/3524 | 1609/2727 | 537/908 | chr2 | 179954285 | ||
chr2:179954287
|
A | T | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1607T>A | p.Ile536Asn | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2151/3524 | 1607/2727 | 536/908 | chr2 | 179954287 | ||
chr2:179954288
|
T | G | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1606A>C | p.Ile536Leu | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2150/3524 | 1606/2727 | 536/908 | chr2 | 179954288 | ||
chr2:179954292
|
A | T | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1602T>A | p.Asp534Glu | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2146/3524 | 1602/2727 | 534/908 | chr2 | 179954292 | ||
chr2:179954295
|
A | C | 1 | a0011 | 1 | NA19081.hp1 | stop_gained | HIGH | c.1599T>G | p.Tyr533* | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2143/3524 | 1599/2727 | 533/908 | chr2 | 179954295 | ||
chr2:179954296
|
T | C | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1598A>G | p.Tyr533Cys | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2142/3524 | 1598/2727 | 533/908 | chr2 | 179954296 | ||
chr2:179954305
|
T | C | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1589A>G | p.Lys530Arg | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2133/3524 | 1589/2727 | 530/908 | chr2 | 179954305 | ||
chr2:179954306
|
T | A | 1 | a0011 | 1 | NA19081.hp1 | stop_gained | HIGH | c.1588A>T | p.Lys530* | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2132/3524 | 1588/2727 | 530/908 | chr2 | 179954306 | ||
chr2:179954308
|
A | C | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1586T>G | p.Phe529Cys | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2130/3524 | 1586/2727 | 529/908 | chr2 | 179954308 | ||
chr2:179954310
|
T | C | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1584A>G | p.Ile528Met | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2128/3524 | 1584/2727 | 528/908 | chr2 | 179954310 | ||
chr2:179954315
|
C | A | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1579G>T | p.Gly527Cys | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2123/3524 | 1579/2727 | 527/908 | chr2 | 179954315 | ||
chr2:179954320
|
A | T | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1574T>A | p.Phe525Tyr | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2118/3524 | 1574/2727 | 525/908 | chr2 | 179954320 | ||
chr2:179954324
|
A | T | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1570T>A | p.Ser524Thr | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2114/3524 | 1570/2727 | 524/908 | chr2 | 179954324 | ||
chr2:179954326
|
T | A | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1568A>T | p.Glu523Val | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2112/3524 | 1568/2727 | 523/908 | chr2 | 179954326 | ||
chr2:179954328
|
C | G | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1566G>C | p.Met522Ile | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2110/3524 | 1566/2727 | 522/908 | chr2 | 179954328 | ||
chr2:179954329
|
A | G | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1565T>C | p.Met522Thr | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2109/3524 | 1565/2727 | 522/908 | chr2 | 179954329 | ||
chr2:179954333
|
A | C | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1561T>G | p.Tyr521Asp | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2105/3524 | 1561/2727 | 521/908 | chr2 | 179954333 | ||
chr2:179954337
|
T | A | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1557A>T | p.Lys519Asn | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2101/3524 | 1557/2727 | 519/908 | chr2 | 179954337 | ||
chr2:179954346
|
C | G | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1548G>C | p.Met516Ile | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2092/3524 | 1548/2727 | 516/908 | chr2 | 179954346 | ||
chr2:179954347
|
A | T | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1547T>A | p.Met516Lys | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2091/3524 | 1547/2727 | 516/908 | chr2 | 179954347 | ||
chr2:179954352
|
A | C | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1542T>G | p.Phe514Leu | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2086/3524 | 1542/2727 | 514/908 | chr2 | 179954352 | ||
chr2:179954354
|
A | T | 1 | a0011 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1540T>A | p.Phe514Ile | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2084/3524 | 1540/2727 | 514/908 | chr2 | 179954354 | ||
chr2:179954356
|
C | T | 1 | a0011 | 1 | NA19081.hp1 | missense_variant&splice_region_variant | MODERATE | c.1538G>A | p.Arg513Gln | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2082/3524 | 1538/2727 | 513/908 | chr2 | 179954356 | ||
chr2:179954357
|
G | C | 1 | a0011 | 1 | NA19081.hp1 | missense_variant&splice_region_variant | MODERATE | c.1537C>G | p.Arg513Gly | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2081/3524 | 1537/2727 | 513/908 | chr2 | 179954357 | ||
chr2:179970716
|
C | G | 1 | a0007 | 2 | HG01256.hp1 HG01258.hp2 |
missense_variant | MODERATE | c.1081G>C | p.Glu361Gln | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 10/20 | 1625/3524 | 1081/2727 | 361/908 | chr2 | 179970716 | ||
chr2:179970773
|
C | A | 1 | a0010 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.1024G>T | p.Val342Leu | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 10/20 | 1568/3524 | 1024/2727 | 342/908 | chr2 | 179970773 | ||
chr2:179986767
|
T | C | 1 | a0009 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.134A>G | p.Tyr45Cys | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/20 | 678/3524 | 134/2727 | 45/908 | chr2 | 179986767 | ||
chr2:179988629
|
C | T | 1 | a0013 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.43G>A | p.Asp15Asn | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/20 | 587/3524 | 43/2727 | 15/908 | chr2 | 179988629 | ||
chr2:179988635
|
C | A | 1 | a0008 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.37G>T | p.Gly13Cys | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/20 | 581/3524 | 37/2727 | 13/908 | chr2 | 179988635 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:179945231
|
G | A | 1 | a0001c0014 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.2625C>T | p.Ala875Ala | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 20/20 | 3169/3524 | 2625/2727 | 875/908 | chr2 | 179945231 | ||
chr2:179945453
|
C | T | 12 | a0001c0001a0001c0005a0001c0011others(9): Show | 191 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(188): Show |
synonymous_variant | LOW | c.2403G>A | p.Ala801Ala | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 20/20 | 2947/3524 | 2403/2727 | 801/908 | chr2 | 179945453 | ||
chr2:179954232
|
A | G | 1 | a0011c0019 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.1662T>C | p.Leu554Leu | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2206/3524 | 1662/2727 | 554/908 | chr2 | 179954232 | ||
chr2:179954253
|
A | G | 1 | a0011c0019 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.1641T>C | p.Val547Val | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2185/3524 | 1641/2727 | 547/908 | chr2 | 179954253 | ||
chr2:179954259
|
T | G | 1 | a0011c0019 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.1635A>C | p.Arg545Arg | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2179/3524 | 1635/2727 | 545/908 | chr2 | 179954259 | ||
chr2:179954271
|
T | A | 1 | a0011c0019 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.1623A>T | p.Thr541Thr | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2167/3524 | 1623/2727 | 541/908 | chr2 | 179954271 | ||
chr2:179954286
|
G | T | 1 | a0011c0019 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.1608C>A | p.Ile536Ile | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2152/3524 | 1608/2727 | 536/908 | chr2 | 179954286 | ||
chr2:179964597
|
T | C | 1 | a0005c0020 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.1347A>G | p.Glu449Glu | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/20 | 1891/3524 | 1347/2727 | 449/908 | chr2 | 179964597 | ||
chr2:179970702
|
T | C | 1 | a0001c0015 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.1095A>G | p.Gln365Gln | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 10/20 | 1639/3524 | 1095/2727 | 365/908 | chr2 | 179970702 | ||
chr2:179971038
|
G | C | 1 | a0001c0005 | 4 | HG02615.hp1 HG02896.hp2 HG03486.hp2 others(1): Show |
synonymous_variant | LOW | c.843C>G | p.Leu281Leu | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 9/20 | 1387/3524 | 843/2727 | 281/908 | chr2 | 179971038 | ||
chr2:179971065
|
T | A | 18 | a0001c0001a0001c0005a0001c0011others(15): Show | 279 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(276): Show |
synonymous_variant | LOW | c.816A>T | p.Val272Val | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 9/20 | 1360/3524 | 816/2727 | 272/908 | chr2 | 179971065 | ||
chr2:179971071
|
G | A | 1 | a0001c0022 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.810C>T | p.His270His | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 9/20 | 1354/3524 | 810/2727 | 270/908 | chr2 | 179971071 | ||
chr2:179978219
|
C | T | 1 | a0001c0012 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.552G>A | p.Glu184Glu | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/20 | 1096/3524 | 552/2727 | 184/908 | chr2 | 179978219 | ||
chr2:179978303
|
C | T | 1 | a0001c0011 | 1 | NA18968.hp1 | synonymous_variant | LOW | c.468G>A | p.Arg156Arg | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/20 | 1012/3524 | 468/2727 | 156/908 | chr2 | 179978303 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:179993410
|
C | T | 1 | a0002c0002t0008 | 1 | HG03654.hp1 | 5_prime_UTR_variant | MODIFIER | c.-69G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/20 | 69 | chr2 | 179993410 | |||||
chr2:180006897
|
C | A | 1 | a0001c0001t0006 | 1 | HG01069.hp1 | 5_prime_UTR_variant | MODIFIER | c.-144G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/20 | 13556 | chr2 | 180006897 | |||||
chr2:180006908
|
G | C | 1 | a0001c0001t0003 | 3 | HG00280.hp1 HG01069.hp2 HG03688.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-155C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/20 | chr2 | 180006908 | ||||||
chr2:180007008
|
G | A | 1 | a0001c0017t0009 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-255C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/20 | 13667 | chr2 | 180007008 | |||||
chr2:180007102
|
C | T | 1 | a0004c0004t0004 | 2 | HG02896.hp1 HG02897.hp1 |
5_prime_UTR_variant | MODIFIER | c.-349G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/20 | 13761 | chr2 | 180007102 | |||||
chr2:180007192
|
G | A | 1 | a0003c0003t0005 | 2 | NA18966.hp1 NA19011.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-439C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/20 | chr2 | 180007192 | ||||||
chr2:180007259
|
A | G | 1 | a0002c0002t0007 | 1 | NA19082.hp2 | 5_prime_UTR_variant | MODIFIER | c.-506T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/20 | 13918 | chr2 | 180007259 | |||||
chr2:180007267
|
G | C | 17 | a0001c0001t0002a0001c0008t0002a0001c0014t0002others(14): Show | 184 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(181): Show |
5_prime_UTR_variant | MODIFIER | c.-514C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/20 | 13926 | chr2 | 180007267 | |||||
chr2:180007296
|
T | C | 1 | a0002c0002t0010 | 1 | NA18973.hp2 | 5_prime_UTR_variant | MODIFIER | c.-543A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/20 | 13955 | chr2 | 180007296 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:179945831
|
A | C | 1 | a0001c0001t0001g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2141-116T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179945831 | ||||||
chr2:179945936
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0142 | 2 | NA18951.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.2141-221C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179945936 | ||||||
chr2:179945940
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2141-225A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179945940 | ||||||
chr2:179945969
|
G | A | 1 | a0002c0002t0002g0242 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2141-254C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179945969 | ||||||
chr2:179946097
|
G | A | 1 | a0004c0018t0001g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2141-382C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946097 | ||||||
chr2:179946171
|
C | G | 1 | a0004c0004t0004g0032 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2141-456G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946171 | ||||||
chr2:179946213
|
G | T | 1 | a0004c0004t0004g0032 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2141-498C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946213 | ||||||
chr2:179946216
|
G | A | 1 | a0001c0017t0009g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2141-501C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946216 | ||||||
chr2:179946232
|
T | C | 51 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(48): Show | 75 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.2141-517A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946232 | ||||||
chr2:179946233
|
T | C | 1 | a0001c0008t0002g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2141-518A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946233 | ||||||
chr2:179946265
|
C | T | 1 | a0003c0003t0002g0194 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2141-550G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946265 | ||||||
chr2:179946266
|
G | A | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2141-551C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946266 | ||||||
chr2:179946418
|
C | G | 1 | a0001c0001t0001g0152 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2141-703G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946418 | ||||||
chr2:179946449
|
C | CA | 83 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0047others(80): Show | 111 | HG00597.hp1 HG00621.hp1 HG00642.hp1 others(108): Show |
intron_variant | MODIFIER | c.2141-735dupT | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946449 | ||||||
chr2:179946449
|
C | CAA | 7 | a0001c0014t0002g0180a0002c0002t0002g0227a0002c0002t0002g0244others(4): Show | 8 | HG01175.hp1 HG02056.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.2141-736_2141-735d others(4): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946449 | ||||||
chr2:179946464
|
A | AG | 28 | a0003c0003t0002g0007a0003c0003t0002g0018a0003c0003t0002g0034others(25): Show | 36 | HG00280.hp2 HG00544.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.2141-750dupC | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946464 | ||||||
chr2:179946464
|
A | AGG | 28 | a0003c0003t0002g0012a0003c0003t0002g0014a0003c0003t0002g0016others(25): Show | 39 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.2141-751_2141-750d others(4): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946464 | ||||||
chr2:179946465
|
G | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 249 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.2141-750C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946465 | ||||||
chr2:179946466
|
G | A | 57 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(54): Show | 85 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.2141-751C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946466 | ||||||
chr2:179946467
|
G | C | 1 | a0002c0002t0002g0247 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2141-752C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946467 | ||||||
chr2:179946468
|
G | C | 56 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(53): Show | 82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.2141-753C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946468 | ||||||
chr2:179946473
|
G | T | 1 | a0001c0008t0002g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2141-758C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946473 | ||||||
chr2:179946476
|
A | G | 3 | a0005c0007t0002g0039a0005c0007t0002g0225a0005c0020t0002g0224 | 4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2141-761T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946476 | ||||||
chr2:179946486
|
G | A | 1 | a0003c0003t0002g0188 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2141-771C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946486 | ||||||
chr2:179946487
|
A | G | 1 | a0003c0003t0002g0188 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2141-772T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946487 | ||||||
chr2:179946509
|
T | C | 1 | a0001c0017t0009g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2141-794A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946509 | ||||||
chr2:179946517
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2141-802G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946517 | ||||||
chr2:179946539
|
T | C | 1 | a0004c0018t0001g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2141-824A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946539 | ||||||
chr2:179946558
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | HG02145.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.2141-843G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946558 | ||||||
chr2:179946961
|
A | G | 3 | a0005c0007t0002g0039a0005c0007t0002g0225a0005c0020t0002g0224 | 4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2141-1246T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946961 | ||||||
chr2:179947113
|
T | C | 46 | a0003c0003t0002g0007a0003c0003t0002g0012a0003c0003t0002g0014others(43): Show | 64 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.2141-1398A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179947113 | ||||||
chr2:179947140
|
T | C | 1 | a0001c0017t0009g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2141-1425A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179947140 | ||||||
chr2:179947718
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2141-2003A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179947718 | ||||||
chr2:179947849
|
T | C | 4 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(1): Show | 4 | NA18947.hp2 NA18985.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.2141-2134A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179947849 | ||||||
chr2:179947927
|
T | C | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 192 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.2141-2212A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179947927 | ||||||
chr2:179947971
|
G | A | 1 | a0001c0008t0002g0179 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2141-2256C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179947971 | ||||||
chr2:179948138
|
T | C | 4 | a0001c0017t0009g0275a0005c0007t0002g0039a0005c0007t0002g0225others(1): Show | 5 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.2140+2374A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179948138 | ||||||
chr2:179948295
|
CTAAA | C | 56 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(53): Show | 82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.2140+2213_2140+221 others(8): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179948295 | ||||||
chr2:179948335
|
T | C | 3 | a0001c0008t0002g0174a0001c0008t0002g0179a0001c0014t0002g0180 | 3 | HG03453.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2140+2177A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179948335 | ||||||
chr2:179948396
|
G | A | 56 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(53): Show | 82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.2140+2116C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179948396 | ||||||
chr2:179948397
|
A | AT | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 192 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.2140+2114dupA | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179948397 | ||||||
chr2:179948403
|
TA | T | 56 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(53): Show | 82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.2140+2108delT | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179948403 | ||||||
chr2:179948409
|
T | A | 56 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(53): Show | 82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.2140+2103A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179948409 | ||||||
chr2:179948679
|
C | T | 7 | a0002c0002t0002g0001a0002c0002t0002g0233a0002c0002t0002g0239others(4): Show | 15 | HG00642.hp1 HG01258.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.2140+1833G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179948679 | ||||||
chr2:179948918
|
T | A | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 192 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.2140+1594A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179948918 | ||||||
chr2:179948978
|
T | C | 3 | a0001c0008t0002g0174a0001c0008t0002g0179a0001c0014t0002g0180 | 3 | HG03453.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2140+1534A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179948978 | ||||||
chr2:179949133
|
A | G | 1 | a0002c0002t0002g0044 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2140+1379T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179949133 | ||||||
chr2:179949184
|
T | C | 1 | a0001c0001t0001g0119 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2140+1328A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179949184 | ||||||
chr2:179949233
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2140+1279A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179949233 | ||||||
chr2:179949350
|
C | T | 56 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(53): Show | 82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.2140+1162G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179949350 | ||||||
chr2:179949360
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2140+1152A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179949360 | ||||||
chr2:179949440
|
G | T | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2140+1072C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179949440 | ||||||
chr2:179949467
|
G | A | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(249): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.2140+1045C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179949467 | ||||||
chr2:179949468
|
C | T | 1 | a0003c0003t0002g0201 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2140+1044G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179949468 | ||||||
chr2:179949546
|
A | C | 1 | a0002c0002t0002g0228 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2140+966T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179949546 | ||||||
chr2:179949861
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0159 | 3 | NA18967.hp2 NA18988.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.2140+651G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179949861 | ||||||
chr2:179949892
|
A | C | 1 | a0001c0001t0001g0074 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2140+620T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179949892 | ||||||
chr2:179950130
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2140+382A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179950130 | ||||||
chr2:179950345
|
G | T | 1 | a0002c0002t0002g0043 | 2 | HG02080.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.2140+167C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179950345 | ||||||
chr2:179950801
|
A | T | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(141): Show | 191 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.1919+24T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 18/19 | chr2 | 179950801 | ||||||
chr2:179951122
|
A | C | 3 | a0005c0007t0002g0039a0005c0007t0002g0225a0005c0020t0002g0224 | 4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1818-196T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179951122 | ||||||
chr2:179951144
|
A | G | 3 | a0005c0007t0002g0039a0005c0007t0002g0225a0005c0020t0002g0224 | 4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1818-218T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179951144 | ||||||
chr2:179951328
|
T | A | 1 | a0002c0002t0002g0259 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1818-402A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179951328 | ||||||
chr2:179951428
|
AC | A | 50 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(47): Show | 74 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.1818-503delG | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179951428 | ||||||
chr2:179951531
|
A | C | 3 | a0001c0001t0001g0009a0001c0001t0001g0114a0001c0001t0001g0115 | 6 | HG01081.hp1 HG01123.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1818-605T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179951531 | ||||||
chr2:179951542
|
A | G | 3 | a0005c0007t0002g0039a0005c0007t0002g0225a0005c0020t0002g0224 | 4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1818-616T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179951542 | ||||||
chr2:179951689
|
A | C | 1 | a0002c0002t0002g0265 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1818-763T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179951689 | ||||||
chr2:179951950
|
A | G | 1 | a0003c0003t0002g0193 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1817+521T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179951950 | ||||||
chr2:179951962
|
G | T | 56 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(53): Show | 82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.1817+509C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179951962 | ||||||
chr2:179952016
|
C | T | 56 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(53): Show | 82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.1817+455G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179952016 | ||||||
chr2:179952038
|
G | A | 56 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(53): Show | 82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.1817+433C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179952038 | ||||||
chr2:179952084
|
T | C | 1 | a0004c0004t0002g0273 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1817+387A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179952084 | ||||||
chr2:179952131
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1817+340A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179952131 | ||||||
chr2:179952249
|
T | C | 1 | a0002c0002t0002g0045 | 2 | NA18992.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1817+222A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179952249 | ||||||
chr2:179952344
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1817+127A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179952344 | ||||||
chr2:179953030
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1690-432A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/19 | chr2 | 179953030 | ||||||
chr2:179953175
|
A | AT | 13 | a0004c0004t0002g0017a0004c0004t0002g0037a0004c0004t0002g0038others(10): Show | 17 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.1690-578dupA | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/19 | chr2 | 179953175 | ||||||
chr2:179953215
|
C | A | 7 | a0002c0002t0002g0044a0002c0002t0002g0046a0002c0002t0002g0262others(4): Show | 9 | HG02055.hp1 HG02486.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1690-617G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/19 | chr2 | 179953215 | ||||||
chr2:179953567
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1689+638G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/19 | chr2 | 179953567 | ||||||
chr2:179953816
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1689+389T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/19 | chr2 | 179953816 | ||||||
chr2:179953922
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1689+283T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/19 | chr2 | 179953922 | ||||||
chr2:179954143
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1689+62G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/19 | chr2 | 179954143 | ||||||
chr2:179954358
|
C | T | 1 | a0011c0019t0001g0086 | 1 | NA19081.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.1537-1G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 15/19 | chr2 | 179954358 | ||||||
chr2:179954359
|
TAATAAAT others(6): Show |
T | 1 | a0011c0019t0001g0086 | 1 | NA19081.hp1 | splice_region_variant&intron_variant | LOW | c.1537-15_1537-3delT others(12): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 15/19 | chr2 | 179954359 | ||||||
chr2:179954378
|
A | T | 1 | a0011c0019t0001g0086 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1537-21T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 15/19 | chr2 | 179954378 | ||||||
chr2:179954379
|
C | A | 1 | a0011c0019t0001g0086 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1537-22G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 15/19 | chr2 | 179954379 | ||||||
chr2:179954427
|
A | T | 1 | a0002c0002t0002g0044 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1537-70T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 15/19 | chr2 | 179954427 | ||||||
chr2:179954865
|
A | G | 6 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(3): Show | 6 | HG01361.hp2 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1536+92T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 15/19 | chr2 | 179954865 | ||||||
chr2:179955251
|
T | G | 47 | a0002c0013t0002g0267a0003c0003t0002g0007a0003c0003t0002g0012others(44): Show | 65 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1459-217A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179955251 | ||||||
chr2:179955253
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1459-219G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179955253 | ||||||
chr2:179955419
|
T | C | 6 | a0002c0013t0002g0267a0003c0003t0002g0016a0003c0003t0002g0184others(3): Show | 8 | NA18941.hp2 NA18957.hp2 NA18998.hp2 others(5): Show |
intron_variant | MODIFIER | c.1459-385A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179955419 | ||||||
chr2:179955742
|
C | T | 1 | a0001c0017t0009g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1459-708G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179955742 | ||||||
chr2:179955777
|
T | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0156a0001c0001t0001g0157others(1): Show | 7 | HG02622.hp2 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1459-743A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179955777 | ||||||
chr2:179955877
|
C | A | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(141): Show | 191 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.1459-843G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179955877 | ||||||
chr2:179956149
|
T | A | 56 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(53): Show | 82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.1459-1115A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179956149 | ||||||
chr2:179956384
|
T | C | 1 | a0001c0001t0001g0056 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1459-1350A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179956384 | ||||||
chr2:179956412
|
T | C | 1 | a0001c0001t0001g0096 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1459-1378A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179956412 | ||||||
chr2:179956582
|
C | CTA | 3 | a0001c0017t0009g0275a0005c0007t0002g0039a0005c0007t0002g0225 | 4 | HG03195.hp2 HG03209.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1459-1550_1459-154 others(6): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179956582 | ||||||
chr2:179956630
|
A | C | 56 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(53): Show | 82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.1459-1596T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179956630 | ||||||
chr2:179956773
|
T | C | 1 | a0003c0003t0002g0197 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1459-1739A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179956773 | ||||||
chr2:179956784
|
C | CT | 48 | a0002c0002t0002g0261a0002c0013t0002g0267a0003c0003t0002g0007others(45): Show | 66 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1459-1751dupA | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179956784 | ||||||
chr2:179956918
|
G | A | 1 | a0003c0003t0002g0191 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1459-1884C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179956918 | ||||||
chr2:179957271
|
A | G | 3 | a0001c0008t0002g0174a0001c0008t0002g0179a0001c0014t0002g0180 | 3 | HG03453.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1458+1751T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179957271 | ||||||
chr2:179957293
|
G | A | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(141): Show | 191 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.1458+1729C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179957293 | ||||||
chr2:179957297
|
T | A | 4 | a0001c0017t0009g0275a0005c0007t0002g0039a0005c0007t0002g0225others(1): Show | 5 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1458+1725A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179957297 | ||||||
chr2:179957545
|
A | T | 2 | a0004c0004t0002g0214a0004c0004t0002g0215 | 2 | HG00280.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1458+1477T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179957545 | ||||||
chr2:179957748
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1458+1274G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179957748 | ||||||
chr2:179957828
|
T | C | 56 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(53): Show | 82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.1458+1194A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179957828 | ||||||
chr2:179957839
|
T | C | 3 | a0001c0008t0002g0174a0001c0008t0002g0179a0001c0014t0002g0180 | 3 | HG03453.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1458+1183A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179957839 | ||||||
chr2:179957842
|
GA | G | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 277 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.1458+1179delT | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179957842 | ||||||
chr2:179958106
|
A | G | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(269): Show | 369 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.1458+916T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958106 | ||||||
chr2:179958163
|
G | T | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 282 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.1458+859C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958163 | ||||||
chr2:179958330
|
C | CA | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(150): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1458+691dupT | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958330 | ||||||
chr2:179958330
|
C | CAA | 8 | a0001c0001t0001g0055a0001c0001t0001g0100a0001c0001t0001g0155others(5): Show | 8 | HG01169.hp1 HG01243.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.1458+690_1458+691d others(4): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958330 | ||||||
chr2:179958350
|
AG | A | 50 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(47): Show | 76 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.1458+671delC | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958350 | ||||||
chr2:179958351
|
G | A | 5 | a0002c0002t0002g0234a0002c0002t0002g0235a0002c0002t0002g0243others(2): Show | 5 | HG01109.hp1 HG02056.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1458+671C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958351 | ||||||
chr2:179958513
|
A | T | 14 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0071others(11): Show | 21 | HG00558.hp1 HG01496.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.1458+509T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958513 | ||||||
chr2:179958546
|
T | G | 1 | a0001c0001t0001g0092 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1458+476A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958546 | ||||||
chr2:179958547
|
T | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0131 | 2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1458+475A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958547 | ||||||
chr2:179958656
|
T | C | 2 | a0003c0003t0002g0192a0003c0003t0002g0200 | 2 | HG02132.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1458+366A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958656 | ||||||
chr2:179958820
|
A | C | 1 | a0002c0002t0002g0044 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1458+202T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958820 | ||||||
chr2:179958856
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1458+166T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958856 | ||||||
chr2:179958863
|
C | T | 84 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(81): Show | 103 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.1458+159G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958863 | ||||||
chr2:179958910
|
T | C | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1458+112A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958910 | ||||||
chr2:179959138
|
T | C | 2 | a0002c0002t0002g0046a0002c0002t0002g0268 | 3 | HG02055.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1398-56A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179959138 | ||||||
chr2:179959447
|
G | A | 1 | a0001c0017t0009g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1398-365C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179959447 | ||||||
chr2:179959507
|
A | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | NA18944.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1398-425T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179959507 | ||||||
chr2:179959681
|
A | G | 1 | a0002c0002t0002g0044 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1398-599T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179959681 | ||||||
chr2:179959754
|
A | T | 1 | a0001c0001t0001g0170 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1398-672T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179959754 | ||||||
chr2:179959761
|
G | C | 1 | a0001c0001t0001g0085 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1398-679C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179959761 | ||||||
chr2:179959772
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1398-690C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179959772 | ||||||
chr2:179959816
|
T | C | 1 | a0001c0017t0009g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1398-734A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179959816 | ||||||
chr2:179959870
|
T | C | 23 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(20): Show | 39 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1398-788A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179959870 | ||||||
chr2:179959887
|
G | A | 3 | a0005c0007t0002g0039a0005c0007t0002g0225a0005c0020t0002g0224 | 4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1398-805C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179959887 | ||||||
chr2:179959933
|
T | C | 1 | a0001c0001t0001g0057 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1398-851A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179959933 | ||||||
chr2:179959942
|
A | T | 46 | a0002c0013t0002g0267a0003c0003t0002g0007a0003c0003t0002g0012others(43): Show | 64 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1398-860T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179959942 | ||||||
chr2:179960044
|
T | A | 5 | a0003c0003t0002g0192a0003c0003t0002g0198a0003c0003t0002g0199others(2): Show | 5 | HG00408.hp1 HG02027.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1398-962A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179960044 | ||||||
chr2:179960172
|
T | C | 1 | a0001c0014t0002g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1398-1090A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179960172 | ||||||
chr2:179960436
|
G | A | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 192 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.1398-1354C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179960436 | ||||||
chr2:179960626
|
T | C | 1 | a0002c0002t0002g0259 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1398-1544A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179960626 | ||||||
chr2:179960673
|
T | C | 1 | a0003c0003t0002g0203 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1398-1591A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179960673 | ||||||
chr2:179960715
|
T | C | 1 | a0001c0008t0002g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1398-1633A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179960715 | ||||||
chr2:179960775
|
T | C | 47 | a0002c0013t0002g0267a0003c0003t0002g0007a0003c0003t0002g0012others(44): Show | 65 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1398-1693A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179960775 | ||||||
chr2:179960913
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1398-1831A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179960913 | ||||||
chr2:179960957
|
C | T | 1 | a0002c0002t0002g0044 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1398-1875G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179960957 | ||||||
chr2:179960958
|
G | A | 255 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.1398-1876C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179960958 | ||||||
chr2:179960977
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1398-1895A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179960977 | ||||||
chr2:179961280
|
A | C | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(249): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1398-2198T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179961280 | ||||||
chr2:179961563
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1398-2481T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179961563 | ||||||
chr2:179961603
|
C | T | 1 | a0002c0002t0002g0262 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1398-2521G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179961603 | ||||||
chr2:179961724
|
G | A | 49 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(46): Show | 74 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.1398-2642C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179961724 | ||||||
chr2:179961785
|
C | T | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(269): Show | 369 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.1398-2703G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179961785 | ||||||
chr2:179961897
|
T | C | 1 | a0001c0008t0002g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1397+2650A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179961897 | ||||||
chr2:179961903
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1397+2644A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179961903 | ||||||
chr2:179961985
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1397+2562G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179961985 | ||||||
chr2:179962007
|
C | T | 3 | a0001c0008t0002g0174a0001c0008t0002g0179a0001c0014t0002g0180 | 3 | HG03453.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1397+2540G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179962007 | ||||||
chr2:179962054
|
A | G | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(249): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1397+2493T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179962054 | ||||||
chr2:179962061
|
T | A | 1 | a0002c0002t0002g0260 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1397+2486A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179962061 | ||||||
chr2:179962250
|
T | A | 3 | a0005c0007t0002g0039a0005c0007t0002g0225a0005c0020t0002g0224 | 4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1397+2297A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179962250 | ||||||
chr2:179962329
|
G | C | 1 | a0001c0014t0002g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1397+2218C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179962329 | ||||||
chr2:179962398
|
C | G | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1397+2149G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179962398 | ||||||
chr2:179962404
|
C | A | 1 | a0001c0001t0001g0143 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1397+2143G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179962404 | ||||||
chr2:179962475
|
G | C | 57 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.1397+2072C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179962475 | ||||||
chr2:179962641
|
A | AT | 7 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(4): Show | 7 | HG01361.hp2 HG01884.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1397+1905dupA | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179962641 | ||||||
chr2:179962819
|
T | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 192 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.1397+1728A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179962819 | ||||||
chr2:179962952
|
A | G | 1 | a0003c0003t0002g0192 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1397+1595T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179962952 | ||||||
chr2:179963052
|
T | G | 1 | a0001c0008t0002g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1397+1495A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963052 | ||||||
chr2:179963092
|
C | T | 57 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.1397+1455G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963092 | ||||||
chr2:179963107
|
A | G | 1 | a0002c0002t0010g0278 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1397+1440T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963107 | ||||||
chr2:179963219
|
T | TG | 57 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.1397+1327dupC | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963219 | ||||||
chr2:179963276
|
A | C | 57 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.1397+1271T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963276 | ||||||
chr2:179963284
|
G | C | 57 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.1397+1263C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963284 | ||||||
chr2:179963285
|
A | G | 3 | a0005c0007t0002g0039a0005c0007t0002g0225a0005c0020t0002g0224 | 4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1397+1262T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963285 | ||||||
chr2:179963328
|
T | G | 46 | a0003c0003t0002g0007a0003c0003t0002g0012a0003c0003t0002g0014others(43): Show | 64 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1397+1219A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963328 | ||||||
chr2:179963335
|
C | CT | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 214 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.1397+1211dupA | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963335 | ||||||
chr2:179963335
|
C | CTT | 86 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0047others(83): Show | 115 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1397+1210_1397+121 others(6): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963335 | ||||||
chr2:179963335
|
C | CTTT | 16 | a0001c0001t0001g0137a0002c0002t0002g0234a0002c0002t0002g0236others(13): Show | 17 | HG01243.hp2 HG01934.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.1397+1209_1397+121 others(7): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963335 | ||||||
chr2:179963436
|
A | G | 2 | a0004c0004t0002g0214a0004c0004t0002g0215 | 2 | HG00280.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1397+1111T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963436 | ||||||
chr2:179963447
|
A | C | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1397+1100T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963447 | ||||||
chr2:179963448
|
T | C | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1397+1099A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963448 | ||||||
chr2:179963457
|
C | T | 1 | a0006c0006t0001g0028 | 2 | HG03834.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.1397+1090G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963457 | ||||||
chr2:179963695
|
T | A | 1 | a0002c0002t0002g0262 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1397+852A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963695 | ||||||
chr2:179963705
|
A | G | 2 | a0002c0002t0002g0045a0002c0013t0002g0267 | 3 | NA18992.hp2 NA19002.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1397+842T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963705 | ||||||
chr2:179963765
|
A | G | 1 | a0005c0020t0002g0224 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1397+782T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963765 | ||||||
chr2:179964056
|
CAA | C | 2 | a0002c0002t0002g0046a0002c0002t0002g0268 | 3 | HG02055.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1397+489_1397+490d others(4): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179964056 | ||||||
chr2:179964079
|
A | C | 1 | a0001c0001t0001g0088 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1397+468T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179964079 | ||||||
chr2:179964089
|
C | A | 1 | a0004c0004t0002g0220 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1397+458G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179964089 | ||||||
chr2:179964466
|
G | A | 3 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0053 | 3 | NA18947.hp2 NA18985.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1397+81C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179964466 | ||||||
chr2:179964480
|
T | C | 1 | a0002c0002t0002g0250 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1397+67A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179964480 | ||||||
chr2:179964655
|
A | G | 3 | a0005c0007t0002g0039a0005c0007t0002g0225a0005c0020t0002g0224 | 4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1316-27T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179964655 | ||||||
chr2:179964731
|
T | C | 1 | a0001c0017t0009g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1316-103A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179964731 | ||||||
chr2:179964744
|
A | C | 2 | a0002c0002t0002g0040a0002c0002t0002g0238 | 3 | HG03490.hp2 HG03492.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1316-116T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179964744 | ||||||
chr2:179964825
|
G | C | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1316-197C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179964825 | ||||||
chr2:179964977
|
G | A | 256 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(253): Show | 348 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.1316-349C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179964977 | ||||||
chr2:179965074
|
C | G | 1 | a0002c0002t0002g0240 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1316-446G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179965074 | ||||||
chr2:179965076
|
CT | C | 57 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.1316-449delA | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179965076 | ||||||
chr2:179965226
|
G | A | 2 | a0004c0004t0002g0214a0004c0004t0002g0215 | 2 | HG00280.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1316-598C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179965226 | ||||||
chr2:179965248
|
T | C | 1 | a0002c0002t0002g0262 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1316-620A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179965248 | ||||||
chr2:179965371
|
G | C | 1 | a0003c0003t0002g0208 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1315+507C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179965371 | ||||||
chr2:179965430
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1315+448A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179965430 | ||||||
chr2:179965438
|
T | C | 2 | a0002c0002t0002g0230a0002c0002t0002g0232 | 2 | NA18986.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1315+440A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179965438 | ||||||
chr2:179965490
|
T | C | 1 | a0001c0012t0001g0054 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1315+388A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179965490 | ||||||
chr2:179965524
|
A | G | 57 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.1315+354T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179965524 | ||||||
chr2:179966178
|
TG | T | 39 | a0003c0003t0002g0007a0003c0003t0002g0012a0003c0003t0002g0015others(36): Show | 54 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.1211-197delC | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179966178 | ||||||
chr2:179966231
|
A | G | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(249): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1211-249T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179966231 | ||||||
chr2:179966274
|
G | C | 39 | a0003c0003t0002g0007a0003c0003t0002g0012a0003c0003t0002g0015others(36): Show | 54 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.1211-292C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179966274 | ||||||
chr2:179966296
|
T | G | 1 | a0001c0008t0002g0179 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1211-314A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179966296 | ||||||
chr2:179966494
|
A | G | 9 | a0001c0001t0001g0011a0001c0001t0001g0049a0001c0001t0001g0139others(6): Show | 12 | HG02615.hp2 HG02622.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1211-512T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179966494 | ||||||
chr2:179966603
|
T | C | 1 | a0001c0014t0002g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1211-621A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179966603 | ||||||
chr2:179966650
|
T | C | 39 | a0003c0003t0002g0007a0003c0003t0002g0012a0003c0003t0002g0015others(36): Show | 54 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.1211-668A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179966650 | ||||||
chr2:179966672
|
T | A | 3 | a0005c0007t0002g0039a0005c0007t0002g0225a0005c0020t0002g0224 | 4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1211-690A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179966672 | ||||||
chr2:179966687
|
T | G | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1211-705A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179966687 | ||||||
chr2:179966898
|
T | C | 57 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.1211-916A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179966898 | ||||||
chr2:179966996
|
G | C | 1 | a0001c0001t0001g0083 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1211-1014C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179966996 | ||||||
chr2:179967072
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1211-1090C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967072 | ||||||
chr2:179967178
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1211-1196C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967178 | ||||||
chr2:179967200
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1211-1218C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967200 | ||||||
chr2:179967212
|
T | C | 2 | a0007c0009t0001g0161a0007c0009t0001g0162 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1211-1230A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967212 | ||||||
chr2:179967337
|
T | A | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(269): Show | 369 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.1211-1355A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967337 | ||||||
chr2:179967373
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1211-1391C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967373 | ||||||
chr2:179967719
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1211-1737A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967719 | ||||||
chr2:179967746
|
C | CAT | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(131): Show | 178 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.1211-1766_1211-176 others(6): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967746 | ||||||
chr2:179967755
|
A | G | 13 | a0004c0004t0002g0017a0004c0004t0002g0037a0004c0004t0002g0038others(10): Show | 17 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.1211-1773T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967755 | ||||||
chr2:179967782
|
C | T | 46 | a0003c0003t0002g0007a0003c0003t0002g0012a0003c0003t0002g0014others(43): Show | 64 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1211-1800G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967782 | ||||||
chr2:179967820
|
A | G | 2 | a0003c0003t0002g0185a0003c0003t0002g0186 | 2 | HG02970.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1211-1838T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967820 | ||||||
chr2:179967883
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1211-1901G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967883 | ||||||
chr2:179967945
|
C | T | 16 | a0004c0004t0002g0017a0004c0004t0002g0037a0004c0004t0002g0038others(13): Show | 21 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1211-1963G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967945 | ||||||
chr2:179967948
|
T | C | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(249): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1211-1966A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967948 | ||||||
chr2:179967977
|
T | C | 3 | a0001c0008t0002g0174a0001c0008t0002g0179a0001c0014t0002g0180 | 3 | HG03453.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1211-1995A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967977 | ||||||
chr2:179968020
|
A | G | 2 | a0004c0004t0002g0214a0004c0004t0002g0215 | 2 | HG00280.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1211-2038T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968020 | ||||||
chr2:179968027
|
G | C | 57 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.1211-2045C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968027 | ||||||
chr2:179968453
|
A | G | 4 | a0002c0002t0002g0231a0002c0002t0002g0256a0002c0002t0002g0257others(1): Show | 4 | HG02602.hp2 HG03491.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1210+2048T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968453 | ||||||
chr2:179968478
|
T | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0156a0001c0001t0001g0157others(1): Show | 7 | HG02622.hp2 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1210+2023A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968478 | ||||||
chr2:179968535
|
C | T | 46 | a0003c0003t0002g0007a0003c0003t0002g0012a0003c0003t0002g0014others(43): Show | 64 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1210+1966G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968535 | ||||||
chr2:179968590
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1210+1911G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968590 | ||||||
chr2:179968591
|
G | A | 2 | a0001c0001t0003g0031a0001c0001t0003g0172 | 3 | HG00280.hp1 HG01069.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1210+1910C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968591 | ||||||
chr2:179968599
|
G | A | 2 | a0002c0002t0002g0256a0002c0002t0002g0257 | 2 | HG03491.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1210+1902C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968599 | ||||||
chr2:179968759
|
G | A | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1210+1742C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968759 | ||||||
chr2:179968788
|
G | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0094a0005c0007t0002g0039others(1): Show | 6 | HG03195.hp2 HG03209.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.1210+1713C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968788 | ||||||
chr2:179968802
|
G | A | 1 | a0001c0017t0009g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1210+1699C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968802 | ||||||
chr2:179968808
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1210+1693G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968808 | ||||||
chr2:179968861
|
C | T | 1 | a0003c0003t0002g0206 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1210+1640G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968861 | ||||||
chr2:179969065
|
C | T | 1 | a0004c0004t0002g0213 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1210+1436G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179969065 | ||||||
chr2:179969076
|
G | C | 1 | a0003c0003t0002g0184 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1210+1425C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179969076 | ||||||
chr2:179969103
|
T | G | 80 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(77): Show | 99 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1210+1398A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179969103 | ||||||
chr2:179969207
|
C | T | 1 | a0001c0017t0009g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1210+1294G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179969207 | ||||||
chr2:179969216
|
T | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0064 | 2 | HG01169.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.1210+1285A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179969216 | ||||||
chr2:179969234
|
G | C | 45 | a0002c0013t0002g0267a0003c0003t0002g0007a0003c0003t0002g0012others(42): Show | 63 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1210+1267C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179969234 | ||||||
chr2:179969354
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1210+1147C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179969354 | ||||||
chr2:179969721
|
C | T | 46 | a0003c0003t0002g0007a0003c0003t0002g0012a0003c0003t0002g0014others(43): Show | 64 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1210+780G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179969721 | ||||||
chr2:179969898
|
C | T | 1 | a0001c0017t0009g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1210+603G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179969898 | ||||||
chr2:179969919
|
T | C | 57 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.1210+582A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179969919 | ||||||
chr2:179970647
|
T | TA | 3 | a0005c0007t0002g0039a0005c0007t0002g0225a0005c0020t0002g0224 | 4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
splice_donor_variant&intron_variant | HIGH | c.1147+2dupT | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 10/19 | chr2 | 179970647 | ||||||
chr2:179970862
|
A | G | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(269): Show | 369 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(366): Show |
splice_region_variant&intron_variant | LOW | c.941-6T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 9/19 | chr2 | 179970862 | ||||||
chr2:179971095
|
A | T | 56 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(53): Show | 82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.805-19T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179971095 | ||||||
chr2:179971265
|
G | A | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 283 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.805-189C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179971265 | ||||||
chr2:179971293
|
T | C | 103 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(100): Show | 147 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.805-217A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179971293 | ||||||
chr2:179971316
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.805-240A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179971316 | ||||||
chr2:179971474
|
C | T | 3 | a0001c0001t0001g0049a0001c0001t0001g0140a0001c0001t0001g0141 | 3 | HG02615.hp2 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.805-398G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179971474 | ||||||
chr2:179971538
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.805-462C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179971538 | ||||||
chr2:179971698
|
G | C | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.805-622C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179971698 | ||||||
chr2:179971753
|
C | A | 1 | a0001c0017t0009g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.805-677G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179971753 | ||||||
chr2:179972251
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.804+942G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179972251 | ||||||
chr2:179972299
|
A | G | 80 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(77): Show | 99 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.804+894T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179972299 | ||||||
chr2:179972342
|
A | T | 1 | a0001c0001t0001g0147 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.804+851T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179972342 | ||||||
chr2:179972376
|
A | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0053 | 2 | NA18985.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.804+817T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179972376 | ||||||
chr2:179972640
|
T | A | 1 | a0001c0001t0001g0065 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.804+553A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179972640 | ||||||
chr2:179972723
|
T | C | 1 | a0001c0017t0009g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.804+470A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179972723 | ||||||
chr2:179972815
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090 | 3 | HG01081.hp2 HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.804+378C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179972815 | ||||||
chr2:179972860
|
C | A | 2 | a0005c0007t0002g0039a0005c0007t0002g0225 | 3 | HG03195.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.804+333G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179972860 | ||||||
chr2:179972886
|
G | A | 1 | a0001c0017t0009g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.804+307C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179972886 | ||||||
chr2:179972995
|
T | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(250): Show | 345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.804+198A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179972995 | ||||||
chr2:179973049
|
T | G | 47 | a0002c0013t0002g0267a0003c0003t0002g0007a0003c0003t0002g0012others(44): Show | 65 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.804+144A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179973049 | ||||||
chr2:179973079
|
T | A | 253 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(250): Show | 345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.804+114A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179973079 | ||||||
chr2:179973096
|
T | C | 1 | a0001c0001t0001g0119 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.804+97A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179973096 | ||||||
chr2:179973147
|
G | C | 1 | a0001c0001t0001g0168 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.804+46C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179973147 | ||||||
chr2:179973317
|
C | T | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.751-71G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 7/19 | chr2 | 179973317 | ||||||
chr2:179973332
|
A | G | 1 | a0002c0002t0008g0229 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.751-86T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 7/19 | chr2 | 179973332 | ||||||
chr2:179973360
|
T | C | 1 | a0004c0018t0001g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.751-114A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 7/19 | chr2 | 179973360 | ||||||
chr2:179973386
|
A | C | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.751-140T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 7/19 | chr2 | 179973386 | ||||||
chr2:179973578
|
C | A | 1 | a0001c0008t0002g0179 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.750+56G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 7/19 | chr2 | 179973578 | ||||||
chr2:179973857
|
C | G | 1 | a0001c0014t0002g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.582-55G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179973857 | ||||||
chr2:179973857
|
C | T | 1 | a0009c0023t0001g0067 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.582-55G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179973857 | ||||||
chr2:179973924
|
A | G | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.582-122T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179973924 | ||||||
chr2:179973935
|
G | A | 1 | a0001c0001t0001g0022 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.582-133C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179973935 | ||||||
chr2:179973950
|
A | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(48): Show | 76 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.582-148T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179973950 | ||||||
chr2:179974031
|
C | T | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.582-229G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179974031 | ||||||
chr2:179974281
|
A | G | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.582-479T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179974281 | ||||||
chr2:179974382
|
C | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 192 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.582-580G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179974382 | ||||||
chr2:179974452
|
T | G | 1 | a0001c0001t0001g0102 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.582-650A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179974452 | ||||||
chr2:179974514
|
A | G | 57 | a0001c0015t0002g0271a0002c0002t0002g0001a0002c0002t0002g0005others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.582-712T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179974514 | ||||||
chr2:179974530
|
A | G | 4 | a0001c0017t0009g0275a0005c0007t0002g0039a0005c0007t0002g0225others(1): Show | 5 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.582-728T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179974530 | ||||||
chr2:179974762
|
G | A | 1 | a0003c0003t0002g0202 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.582-960C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179974762 | ||||||
chr2:179974854
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.582-1052G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179974854 | ||||||
chr2:179974893
|
T | C | 58 | a0001c0015t0002g0271a0002c0002t0002g0001a0002c0002t0002g0005others(55): Show | 84 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(81): Show |
intron_variant | MODIFIER | c.582-1091A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179974893 | ||||||
chr2:179974942
|
T | G | 2 | a0001c0001t0001g0136a0006c0006t0001g0105 | 2 | HG00558.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.582-1140A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179974942 | ||||||
chr2:179974980
|
G | A | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 280 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.582-1178C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179974980 | ||||||
chr2:179975065
|
T | A | 1 | a0002c0002t0002g0238 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.582-1263A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179975065 | ||||||
chr2:179975066
|
T | A | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 280 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.582-1264A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179975066 | ||||||
chr2:179975198
|
T | C | 3 | a0002c0002t0002g0042a0002c0002t0002g0246a0002c0002t0002g0247 | 4 | NA18960.hp1 NA18999.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.582-1396A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179975198 | ||||||
chr2:179975341
|
C | T | 1 | a0001c0017t0009g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.582-1539G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179975341 | ||||||
chr2:179975413
|
C | T | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.582-1611G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179975413 | ||||||
chr2:179975439
|
G | C | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 192 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.582-1637C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179975439 | ||||||
chr2:179975678
|
T | C | 22 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(19): Show | 38 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.582-1876A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179975678 | ||||||
chr2:179975695
|
G | C | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 283 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.582-1893C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179975695 | ||||||
chr2:179975752
|
G | A | 57 | a0001c0015t0002g0271a0002c0002t0002g0001a0002c0002t0002g0005others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.582-1950C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179975752 | ||||||
chr2:179975784
|
T | C | 56 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(53): Show | 82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.582-1982A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179975784 | ||||||
chr2:179976381
|
A | C | 1 | a0001c0008t0002g0179 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.581+1809T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179976381 | ||||||
chr2:179976506
|
A | AC | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 280 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.581+1683dupG | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179976506 | ||||||
chr2:179976597
|
A | AACG | 108 | a0001c0015t0002g0271a0001c0017t0009g0275a0002c0002t0002g0001others(105): Show | 153 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.581+1592_581+1593i others(5): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179976597 | ||||||
chr2:179976687
|
T | C | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.581+1503A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179976687 | ||||||
chr2:179976710
|
A | T | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.581+1480T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179976710 | ||||||
chr2:179976728
|
G | C | 1 | a0001c0001t0001g0075 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.581+1462C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179976728 | ||||||
chr2:179976827
|
T | G | 58 | a0001c0015t0002g0271a0002c0002t0002g0001a0002c0002t0002g0005others(55): Show | 84 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(81): Show |
intron_variant | MODIFIER | c.581+1363A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179976827 | ||||||
chr2:179976947
|
G | C | 1 | a0001c0001t0001g0076 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.581+1243C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179976947 | ||||||
chr2:179976973
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.581+1217C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179976973 | ||||||
chr2:179977118
|
G | A | 1 | a0002c0002t0002g0262 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.581+1072C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179977118 | ||||||
chr2:179977187
|
T | G | 256 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(253): Show | 348 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.581+1003A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179977187 | ||||||
chr2:179977693
|
T | C | 1 | a0003c0003t0002g0203 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.581+497A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179977693 | ||||||
chr2:179977776
|
T | C | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.581+414A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179977776 | ||||||
chr2:179977817
|
C | T | 1 | a0004c0004t0002g0222 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.581+373G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179977817 | ||||||
chr2:179977899
|
C | G | 1 | a0001c0001t0001g0154 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.581+291G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179977899 | ||||||
chr2:179977900
|
G | A | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 193 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.581+290C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179977900 | ||||||
chr2:179978047
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.581+143T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179978047 | ||||||
chr2:179978399
|
C | T | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(249): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.453-81G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179978399 | ||||||
chr2:179978483
|
TC | T | 56 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(53): Show | 82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.453-166delG | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179978483 | ||||||
chr2:179978681
|
T | G | 2 | a0004c0004t0002g0175a0004c0004t0002g0176 | 2 | HG02280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.453-363A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179978681 | ||||||
chr2:179978806
|
C | G | 1 | a0001c0001t0001g0143 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.453-488G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179978806 | ||||||
chr2:179978809
|
C | G | 1 | a0002c0002t0002g0239 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.453-491G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179978809 | ||||||
chr2:179978862
|
TTACC | T | 103 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(100): Show | 147 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.453-548_453-545del others(4): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179978862 | ||||||
chr2:179979031
|
T | C | 4 | a0001c0017t0009g0275a0005c0007t0002g0039a0005c0007t0002g0225others(1): Show | 5 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.453-713A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179979031 | ||||||
chr2:179979148
|
A | C | 57 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.453-830T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179979148 | ||||||
chr2:179979282
|
A | AAAC | 256 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(253): Show | 348 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.453-967_453-965dup others(3): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179979282 | ||||||
chr2:179979300
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.453-982A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179979300 | ||||||
chr2:179979343
|
C | T | 3 | a0005c0007t0002g0039a0005c0007t0002g0225a0005c0020t0002g0224 | 4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.453-1025G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179979343 | ||||||
chr2:179979436
|
G | A | 1 | a0001c0008t0002g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.453-1118C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179979436 | ||||||
chr2:179979576
|
T | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(250): Show | 345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.453-1258A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179979576 | ||||||
chr2:179979631
|
G | T | 3 | a0001c0008t0002g0174a0001c0008t0002g0179a0001c0014t0002g0180 | 3 | HG03453.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.453-1313C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179979631 | ||||||
chr2:179979655
|
G | A | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(249): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.453-1337C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179979655 | ||||||
chr2:179979853
|
T | C | 1 | a0002c0002t0002g0265 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.453-1535A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179979853 | ||||||
chr2:179979862
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.453-1544C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179979862 | ||||||
chr2:179980055
|
C | G | 49 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(46): Show | 74 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.452+1697G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980055 | ||||||
chr2:179980114
|
C | T | 1 | a0002c0002t0002g0232 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.452+1638G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980114 | ||||||
chr2:179980419
|
A | AT | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 263 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.452+1332dupA | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980419 | ||||||
chr2:179980419
|
A | ATT | 10 | a0001c0001t0001g0091a0001c0001t0001g0104a0001c0001t0001g0154others(7): Show | 12 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.452+1331_452+1332d others(4): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980419 | ||||||
chr2:179980513
|
G | C | 2 | a0002c0002t0002g0244a0002c0002t0002g0245 | 2 | HG02027.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.452+1239C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980513 | ||||||
chr2:179980518
|
T | C | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(269): Show | 369 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.452+1234A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980518 | ||||||
chr2:179980527
|
T | C | 1 | a0001c0017t0009g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.452+1225A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980527 | ||||||
chr2:179980637
|
C | T | 1 | a0003c0003t0002g0181 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.452+1115G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980637 | ||||||
chr2:179980661
|
C | T | 3 | a0005c0007t0002g0039a0005c0007t0002g0225a0005c0020t0002g0224 | 4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.452+1091G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980661 | ||||||
chr2:179980671
|
C | T | 3 | a0001c0008t0002g0174a0001c0008t0002g0179a0001c0014t0002g0180 | 3 | HG03453.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.452+1081G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980671 | ||||||
chr2:179980680
|
T | C | 1 | a0001c0017t0009g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.452+1072A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980680 | ||||||
chr2:179980833
|
C | T | 1 | a0001c0001t0001g0013 | 3 | HG02486.hp2 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.452+919G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980833 | ||||||
chr2:179980965
|
T | C | 6 | a0002c0002t0002g0041a0002c0002t0002g0043a0002c0002t0002g0251others(3): Show | 8 | HG02080.hp2 HG02155.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.452+787A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980965 | ||||||
chr2:179981053
|
T | TA | 3 | a0002c0002t0002g0042a0002c0002t0002g0246a0002c0002t0002g0247 | 4 | NA18960.hp1 NA18999.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.452+698dupT | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179981053 | ||||||
chr2:179981610
|
T | C | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.452+142A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179981610 | ||||||
chr2:179982016
|
G | T | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 283 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.207-19C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179982016 | ||||||
chr2:179982091
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.207-94G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179982091 | ||||||
chr2:179982355
|
A | G | 2 | a0005c0007t0002g0039a0005c0007t0002g0225 | 3 | HG03195.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.207-358T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179982355 | ||||||
chr2:179982720
|
T | C | 3 | a0004c0004t0002g0272a0004c0004t0002g0273a0004c0004t0004g0032 | 4 | HG02257.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.207-723A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179982720 | ||||||
chr2:179982862
|
C | G | 2 | a0001c0001t0001g0139a0001c0001t0001g0143 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.207-865G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179982862 | ||||||
chr2:179983147
|
T | G | 1 | a0002c0002t0002g0253 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.207-1150A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179983147 | ||||||
chr2:179983179
|
T | C | 194 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.207-1182A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179983179 | ||||||
chr2:179983309
|
T | C | 4 | a0002c0002t0002g0020a0002c0002t0002g0248a0002c0002t0002g0249others(1): Show | 6 | NA18747.hp1 NA18939.hp1 NA18987.hp1 others(3): Show |
intron_variant | MODIFIER | c.207-1312A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179983309 | ||||||
chr2:179983311
|
T | A | 2 | a0001c0015t0002g0271a0002c0002t0002g0044 | 3 | HG02630.hp1 HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.207-1314A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179983311 | ||||||
chr2:179983463
|
A | G | 1 | a0002c0002t0002g0236 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.207-1466T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179983463 | ||||||
chr2:179983487
|
C | T | 13 | a0004c0004t0002g0017a0004c0004t0002g0037a0004c0004t0002g0038others(10): Show | 17 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.207-1490G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179983487 | ||||||
chr2:179983564
|
T | C | 57 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.207-1567A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179983564 | ||||||
chr2:179983758
|
T | C | 1 | a0002c0002t0002g0261 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.207-1761A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179983758 | ||||||
chr2:179983761
|
C | A | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 284 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.207-1764G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179983761 | ||||||
chr2:179983802
|
A | G | 57 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.207-1805T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179983802 | ||||||
chr2:179983924
|
C | T | 13 | a0004c0004t0002g0017a0004c0004t0002g0037a0004c0004t0002g0038others(10): Show | 17 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.207-1927G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179983924 | ||||||
chr2:179983961
|
T | C | 3 | a0005c0007t0002g0039a0005c0007t0002g0225a0005c0020t0002g0224 | 4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.207-1964A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179983961 | ||||||
chr2:179984055
|
C | A | 4 | a0001c0017t0009g0275a0004c0004t0002g0272a0004c0004t0002g0273others(1): Show | 5 | HG02257.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.207-2058G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984055 | ||||||
chr2:179984165
|
C | T | 1 | a0001c0017t0009g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.207-2168G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984165 | ||||||
chr2:179984223
|
T | C | 1 | a0002c0002t0002g0231 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.207-2226A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984223 | ||||||
chr2:179984227
|
T | C | 1 | a0001c0008t0002g0179 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.207-2230A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984227 | ||||||
chr2:179984257
|
C | T | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(146): Show | 197 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.207-2260G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984257 | ||||||
chr2:179984363
|
A | T | 60 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(57): Show | 87 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.206+2332T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984363 | ||||||
chr2:179984472
|
T | C | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.206+2223A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984472 | ||||||
chr2:179984496
|
T | C | 56 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(53): Show | 82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.206+2199A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984496 | ||||||
chr2:179984539
|
A | G | 57 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.206+2156T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984539 | ||||||
chr2:179984548
|
G | A | 1 | a0001c0014t0002g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.206+2147C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984548 | ||||||
chr2:179984775
|
A | C | 1 | a0002c0002t0002g0251 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.206+1920T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984775 | ||||||
chr2:179984935
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.206+1760A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984935 | ||||||
chr2:179984978
|
C | A | 1 | a0001c0001t0001g0137 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.206+1717G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984978 | ||||||
chr2:179985286
|
T | C | 3 | a0001c0001t0001g0049a0001c0001t0001g0140a0001c0001t0001g0141 | 3 | HG02615.hp2 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.206+1409A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179985286 | ||||||
chr2:179985353
|
T | G | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(196): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.206+1342A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179985353 | ||||||
chr2:179985539
|
G | A | 1 | a0001c0017t0009g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.206+1156C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179985539 | ||||||
chr2:179985820
|
G | GTA | 66 | a0001c0001t0001g0053a0001c0001t0001g0113a0001c0008t0002g0174others(63): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.206+873_206+874dup others(2): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179985820 | ||||||
chr2:179985902
|
G | A | 1 | a0001c0001t0001g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.206+793C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179985902 | ||||||
chr2:179985978
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.206+717A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179985978 | ||||||
chr2:179986183
|
G | T | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 192 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.206+512C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179986183 | ||||||
chr2:179986386
|
A | G | 3 | a0004c0004t0002g0272a0004c0004t0002g0273a0004c0004t0004g0032 | 4 | HG02257.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.206+309T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179986386 | ||||||
chr2:179986389
|
G | A | 1 | a0002c0002t0002g0265 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.206+306C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179986389 | ||||||
chr2:179986434
|
A | G | 1 | a0001c0017t0009g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.206+261T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179986434 | ||||||
chr2:179986475
|
A | T | 13 | a0004c0004t0002g0017a0004c0004t0002g0037a0004c0004t0002g0038others(10): Show | 17 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.206+220T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179986475 | ||||||
chr2:179987139
|
T | C | 5 | a0002c0002t0002g0043a0002c0002t0002g0251a0002c0002t0002g0252others(2): Show | 6 | HG02080.hp2 NA18965.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.96-334A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179987139 | ||||||
chr2:179987223
|
T | C | 47 | a0002c0013t0002g0267a0003c0003t0002g0007a0003c0003t0002g0012others(44): Show | 65 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.96-418A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179987223 | ||||||
chr2:179987450
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.96-645T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179987450 | ||||||
chr2:179987555
|
T | C | 1 | a0002c0002t0002g0232 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.96-750A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179987555 | ||||||
chr2:179987646
|
G | C | 1 | a0002c0002t0002g0254 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.96-841C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179987646 | ||||||
chr2:179987692
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.95+885G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179987692 | ||||||
chr2:179987700
|
AT | A | 46 | a0003c0003t0002g0007a0003c0003t0002g0012a0003c0003t0002g0014others(43): Show | 64 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.95+876delA | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179987700 | ||||||
chr2:179988000
|
T | C | 57 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.95+577A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179988000 | ||||||
chr2:179988040
|
A | G | 256 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(253): Show | 349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.95+537T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179988040 | ||||||
chr2:179988179
|
G | A | 1 | a0001c0008t0002g0179 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.95+398C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179988179 | ||||||
chr2:179988232
|
C | A | 3 | a0004c0004t0002g0272a0004c0004t0002g0273a0004c0004t0004g0032 | 4 | HG02257.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95+345G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179988232 | ||||||
chr2:179988281
|
G | A | 57 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.95+296C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179988281 | ||||||
chr2:179988455
|
T | C | 7 | a0001c0017t0009g0275a0004c0004t0002g0272a0004c0004t0002g0273others(4): Show | 9 | HG02257.hp1 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.95+122A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179988455 | ||||||
chr2:179988740
|
A | C | 2 | a0003c0003t0002g0018a0003c0003t0002g0223 | 4 | NA18971.hp2 NA18990.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-96T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179988740 | ||||||
chr2:179988888
|
T | G | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.28-244A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179988888 | ||||||
chr2:179988940
|
G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 180 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.28-296C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179988940 | ||||||
chr2:179989067
|
C | G | 4 | a0001c0001t0001g0070a0001c0001t0001g0088a0001c0001t0001g0089others(1): Show | 4 | HG01081.hp2 HG01884.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-423G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989067 | ||||||
chr2:179989074
|
C | G | 1 | a0001c0001t0001g0103 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.28-430G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989074 | ||||||
chr2:179989115
|
T | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 180 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.28-471A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989115 | ||||||
chr2:179989241
|
TATA | T | 267 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(264): Show | 363 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.28-600_28-598delTA others(1): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989241 | ||||||
chr2:179989250
|
A | T | 268 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(265): Show | 361 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.28-606T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989250 | ||||||
chr2:179989284
|
G | T | 1 | a0001c0001t0001g0058 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.28-640C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989284 | ||||||
chr2:179989503
|
C | T | 1 | a0003c0003t0002g0181 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.28-859G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989503 | ||||||
chr2:179989590
|
A | T | 2 | a0002c0002t0002g0234a0002c0002t0002g0235 | 2 | NA18950.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.28-946T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989590 | ||||||
chr2:179989710
|
T | C | 1 | a0002c0002t0002g0262 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.28-1066A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989710 | ||||||
chr2:179989893
|
A | G | 57 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.28-1249T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989893 | ||||||
chr2:179989930
|
T | C | 2 | a0002c0002t0002g0256a0002c0002t0002g0257 | 2 | HG03491.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.28-1286A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989930 | ||||||
chr2:179989938
|
G | T | 3 | a0001c0001t0001g0049a0001c0001t0001g0140a0001c0001t0001g0141 | 3 | HG02615.hp2 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.28-1294C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989938 | ||||||
chr2:179989984
|
C | G | 57 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.28-1340G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989984 | ||||||
chr2:179990317
|
C | G | 1 | a0002c0002t0002g0233 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.28-1673G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179990317 | ||||||
chr2:179990505
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.28-1861T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179990505 | ||||||
chr2:179990542
|
C | T | 3 | a0001c0001t0001g0009a0001c0001t0001g0114a0001c0001t0001g0115 | 6 | HG01081.hp1 HG01123.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-1898G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179990542 | ||||||
chr2:179990546
|
C | CAG | 3 | a0001c0001t0001g0100a0001c0001t0001g0139a0004c0004t0002g0037 | 4 | HG01981.hp1 HG02922.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-1904_28-1903dup others(2): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179990546 | ||||||
chr2:179990546
|
CAG | C | 35 | a0001c0001t0001g0008a0001c0001t0001g0029a0001c0001t0001g0050others(32): Show | 41 | HG00558.hp2 HG02056.hp1 HG02074.hp2 others(38): Show |
intron_variant | MODIFIER | c.28-1904_28-1903del others(2): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179990546 | ||||||
chr2:179990546
|
CAGAG | C | 216 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.28-1906_28-1903del others(4): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179990546 | ||||||
chr2:179990556
|
G | C | 1 | a0001c0001t0001g0077 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.28-1912C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179990556 | ||||||
chr2:179990743
|
G | A | 56 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(53): Show | 82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.28-2099C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179990743 | ||||||
chr2:179990773
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.28-2129A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179990773 | ||||||
chr2:179990830
|
A | G | 1 | a0001c0001t0003g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.28-2186T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179990830 | ||||||
chr2:179990874
|
T | C | 2 | a0001c0001t0001g0138a0001c0001t0001g0142 | 2 | NA18951.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.28-2230A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179990874 | ||||||
chr2:179990899
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.28-2255C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179990899 | ||||||
chr2:179991136
|
C | T | 47 | a0002c0013t0002g0267a0003c0003t0002g0007a0003c0003t0002g0012others(44): Show | 65 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.27+2179G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179991136 | ||||||
chr2:179991169
|
C | T | 271 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(268): Show | 368 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(365): Show |
intron_variant | MODIFIER | c.27+2146G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179991169 | ||||||
chr2:179991266
|
C | CT | 47 | a0002c0013t0002g0267a0003c0003t0002g0007a0003c0003t0002g0012others(44): Show | 65 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.27+2048dupA | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179991266 | ||||||
chr2:179991319
|
G | A | 1 | a0003c0003t0002g0204 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.27+1996C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179991319 | ||||||
chr2:179991345
|
T | C | 1 | a0001c0017t0009g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.27+1970A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179991345 | ||||||
chr2:179991529
|
G | A | 1 | a0005c0020t0002g0224 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.27+1786C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179991529 | ||||||
chr2:179991674
|
G | A | 3 | a0002c0002t0002g0019a0002c0002t0002g0226a0002c0002t0002g0227 | 5 | HG02109.hp2 HG02145.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+1641C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179991674 | ||||||
chr2:179991687
|
A | G | 1 | a0001c0008t0002g0179 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.27+1628T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179991687 | ||||||
chr2:179991729
|
G | A | 11 | a0001c0001t0001g0011a0001c0001t0001g0049a0001c0001t0001g0139others(8): Show | 14 | HG02145.hp2 HG02257.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.27+1586C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179991729 | ||||||
chr2:179991732
|
T | C | 255 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 348 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.27+1583A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179991732 | ||||||
chr2:179991789
|
A | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | NA19079.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.27+1526T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179991789 | ||||||
chr2:179991931
|
T | C | 5 | a0002c0002t0002g0021a0002c0002t0002g0258a0002c0002t0002g0259others(2): Show | 7 | HG00733.hp1 HG00741.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.27+1384A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179991931 | ||||||
chr2:179992149
|
T | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(19): Show | 38 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.27+1166A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179992149 | ||||||
chr2:179992498
|
C | A | 1 | a0001c0001t0001g0096 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.27+817G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179992498 | ||||||
chr2:179992545
|
T | G | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(269): Show | 369 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.27+770A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179992545 | ||||||
chr2:179992548
|
C | T | 56 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(53): Show | 82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.27+767G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179992548 | ||||||
chr2:179992742
|
A | G | 1 | a0002c0002t0002g0262 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.27+573T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179992742 | ||||||
chr2:179992856
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.27+459G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179992856 | ||||||
chr2:179992869
|
A | G | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.27+446T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179992869 | ||||||
chr2:179992940
|
T | G | 1 | a0001c0001t0001g0142 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.27+375A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179992940 | ||||||
chr2:179992986
|
C | T | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(141): Show | 191 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.27+329G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179992986 | ||||||
chr2:179993004
|
TAC | T | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(141): Show | 191 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.27+309_27+310delGT | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179993004 | ||||||
chr2:179993004
|
TACAC | T | 4 | a0001c0017t0009g0275a0004c0004t0002g0272a0004c0004t0002g0273others(1): Show | 5 | HG02257.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+307_27+310delGT others(2): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179993004 | ||||||
chr2:179993020
|
C | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090 | 3 | HG01081.hp2 HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.27+295G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179993020 | ||||||
chr2:179993030
|
C | T | 13 | a0004c0004t0002g0017a0004c0004t0002g0037a0004c0004t0002g0038others(10): Show | 17 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.27+285G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179993030 | ||||||
chr2:179993048
|
T | G | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.27+267A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179993048 | ||||||
chr2:179993465
|
T | C | 1 | a0001c0014t0002g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-113-11A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179993465 | ||||||
chr2:179993729
|
A | G | 19 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0024others(16): Show | 28 | HG00280.hp1 HG00558.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.-113-275T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179993729 | ||||||
chr2:179994119
|
G | A | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-113-665C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994119 | ||||||
chr2:179994221
|
CAAAAATA others(5): Show |
C | 1 | a0001c0022t0001g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-113-779_-113-768d others(14): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994221 | ||||||
chr2:179994255
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-113-801A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994255 | ||||||
chr2:179994264
|
T | C | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-113-810A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994264 | ||||||
chr2:179994311
|
GA | G | 45 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0020others(42): Show | 67 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.-113-858delT | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994311 | ||||||
chr2:179994546
|
C | T | 3 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099 | 3 | HG01361.hp2 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-113-1092G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994546 | ||||||
chr2:179994549
|
C | A | 1 | a0001c0001t0001g0144 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-113-1095G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994549 | ||||||
chr2:179994567
|
G | A | 56 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(53): Show | 82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.-113-1113C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994567 | ||||||
chr2:179994598
|
T | G | 1 | a0003c0003t0002g0205 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-113-1144A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994598 | ||||||
chr2:179994612
|
T | C | 3 | a0001c0001t0001g0024a0001c0001t0001g0078a0001c0001t0001g0079 | 4 | HG00558.hp1 HG02135.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.-113-1158A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994612 | ||||||
chr2:179994832
|
C | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(268): Show | 368 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(365): Show |
intron_variant | MODIFIER | c.-113-1378G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994832 | ||||||
chr2:179994901
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02040.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.-113-1447C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994901 | ||||||
chr2:179994940
|
C | A | 1 | a0001c0014t0002g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-113-1486G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994940 | ||||||
chr2:179995005
|
C | T | 1 | a0002c0002t0002g0228 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-113-1551G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179995005 | ||||||
chr2:179995012
|
G | A | 46 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(43): Show | 71 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.-113-1558C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179995012 | ||||||
chr2:179995112
|
C | T | 56 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(53): Show | 82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.-113-1658G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179995112 | ||||||
chr2:179995113
|
G | A | 1 | a0001c0008t0002g0179 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-113-1659C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179995113 | ||||||
chr2:179995219
|
T | C | 57 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.-113-1765A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179995219 | ||||||
chr2:179995588
|
T | C | 1 | a0003c0003t0002g0206 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-113-2134A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179995588 | ||||||
chr2:179995670
|
A | C | 1 | a0003c0003t0002g0181 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-113-2216T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179995670 | ||||||
chr2:179995761
|
G | A | 56 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(53): Show | 82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.-113-2307C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179995761 | ||||||
chr2:179996007
|
T | C | 1 | a0003c0003t0002g0207 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-113-2553A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179996007 | ||||||
chr2:179996218
|
A | G | 57 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.-113-2764T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179996218 | ||||||
chr2:179996277
|
A | T | 2 | a0003c0003t0002g0209a0003c0003t0002g0210 | 2 | HG01256.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-113-2823T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179996277 | ||||||
chr2:179996312
|
C | T | 3 | a0002c0002t0002g0019a0002c0002t0002g0226a0002c0002t0002g0227 | 5 | HG02109.hp2 HG02145.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-113-2858G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179996312 | ||||||
chr2:179996386
|
A | C | 47 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(44): Show | 72 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.-113-2932T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179996386 | ||||||
chr2:179996725
|
G | A | 13 | a0004c0004t0002g0017a0004c0004t0002g0037a0004c0004t0002g0038others(10): Show | 17 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.-113-3271C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179996725 | ||||||
chr2:179996731
|
G | C | 1 | a0004c0018t0001g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-113-3277C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179996731 | ||||||
chr2:179996761
|
A | G | 3 | a0001c0001t0001g0145a0001c0001t0003g0031a0001c0001t0003g0172 | 4 | HG00280.hp1 HG01069.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.-113-3307T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179996761 | ||||||
chr2:179996788
|
G | C | 7 | a0001c0017t0009g0275a0004c0004t0002g0272a0004c0004t0002g0273others(4): Show | 9 | HG02257.hp1 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.-113-3334C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179996788 | ||||||
chr2:179996831
|
T | TA | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 198 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-113-3378dupT | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179996831 | ||||||
chr2:179996831
|
T | TTA | 2 | a0005c0007t0002g0039a0005c0007t0002g0225 | 3 | HG03195.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-113-3378_-113-337 others(6): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179996831 | ||||||
chr2:179996883
|
C | CA | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 192 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.-113-3430dupT | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179996883 | ||||||
chr2:179997259
|
A | G | 1 | a0001c0008t0002g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-113-3805T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179997259 | ||||||
chr2:179997337
|
C | T | 1 | a0001c0017t0009g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-113-3883G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179997337 | ||||||
chr2:179997406
|
C | G | 13 | a0004c0004t0002g0017a0004c0004t0002g0037a0004c0004t0002g0038others(10): Show | 17 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.-113-3952G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179997406 | ||||||
chr2:179997468
|
C | G | 1 | a0002c0002t0002g0226 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-113-4014G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179997468 | ||||||
chr2:179997593
|
T | G | 13 | a0004c0004t0002g0017a0004c0004t0002g0037a0004c0004t0002g0038others(10): Show | 17 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.-113-4139A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179997593 | ||||||
chr2:179997610
|
T | C | 57 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.-113-4156A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179997610 | ||||||
chr2:179997879
|
A | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 284 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.-113-4425T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179997879 | ||||||
chr2:179997927
|
C | G | 13 | a0004c0004t0002g0017a0004c0004t0002g0037a0004c0004t0002g0038others(10): Show | 17 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.-113-4473G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179997927 | ||||||
chr2:179998340
|
C | T | 57 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.-113-4886G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179998340 | ||||||
chr2:179998357
|
T | G | 3 | a0001c0001t0001g0145a0001c0001t0003g0031a0001c0001t0003g0172 | 4 | HG00280.hp1 HG01069.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.-113-4903A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179998357 | ||||||
chr2:179998373
|
A | C | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-113-4919T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179998373 | ||||||
chr2:179998441
|
A | T | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 201 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.-113-4987T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179998441 | ||||||
chr2:179998459
|
T | G | 57 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.-113-5005A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179998459 | ||||||
chr2:179998787
|
T | A | 1 | a0002c0002t0002g0266 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-113-5333A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179998787 | ||||||
chr2:179998793
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-113-5339C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179998793 | ||||||
chr2:179998829
|
T | C | 1 | a0001c0014t0002g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-113-5375A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179998829 | ||||||
chr2:179998934
|
T | C | 3 | a0001c0005t0001g0148a0001c0005t0001g0149a0001c0005t0001g0150 | 3 | HG02615.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-113-5480A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179998934 | ||||||
chr2:179998946
|
A | C | 7 | a0001c0001t0001g0070a0001c0001t0001g0082a0001c0001t0001g0088others(4): Show | 7 | HG01081.hp2 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-113-5492T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179998946 | ||||||
chr2:179998981
|
G | A | 56 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(53): Show | 82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.-113-5527C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179998981 | ||||||
chr2:179999273
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-113-5819A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179999273 | ||||||
chr2:179999382
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | HG02145.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-113-5928G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179999382 | ||||||
chr2:179999826
|
C | A | 1 | a0003c0003t0002g0208 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-113-6372G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179999826 | ||||||
chr2:179999954
|
G | C | 4 | a0003c0003t0002g0209a0003c0003t0002g0210a0003c0003t0002g0211others(1): Show | 4 | HG01123.hp1 HG01256.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.-113-6500C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179999954 | ||||||
chr2:180000069
|
C | T | 2 | a0005c0007t0002g0039a0005c0007t0002g0225 | 3 | HG03195.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-113-6615G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180000069 | ||||||
chr2:180000240
|
A | G | 60 | a0002c0013t0002g0267a0003c0003t0002g0007a0003c0003t0002g0012others(57): Show | 82 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.-114+6627T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180000240 | ||||||
chr2:180000244
|
G | C | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-114+6623C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180000244 | ||||||
chr2:180000406
|
T | G | 1 | a0001c0001t0001g0152 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-114+6461A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180000406 | ||||||
chr2:180000481
|
G | T | 3 | a0004c0004t0002g0272a0004c0004t0002g0273a0004c0004t0004g0032 | 4 | HG02257.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-114+6386C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180000481 | ||||||
chr2:180000767
|
G | C | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-114+6100C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180000767 | ||||||
chr2:180000770
|
T | C | 1 | a0003c0003t0002g0223 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-114+6097A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180000770 | ||||||
chr2:180000820
|
GAA | G | 6 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0083others(3): Show | 14 | NA18942.hp1 NA18948.hp1 NA18950.hp1 others(11): Show |
intron_variant | MODIFIER | c.-114+6045_-114+604 others(6): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180000820 | ||||||
chr2:180000872
|
A | C | 2 | a0003c0003t0002g0269a0003c0003t0002g0270 | 2 | NA19004.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-114+5995T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180000872 | ||||||
chr2:180000898
|
T | G | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-114+5969A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180000898 | ||||||
chr2:180000940
|
A | G | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-114+5927T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180000940 | ||||||
chr2:180001006
|
T | A | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-114+5861A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180001006 | ||||||
chr2:180001037
|
C | T | 3 | a0004c0004t0002g0272a0004c0004t0002g0273a0004c0004t0004g0032 | 4 | HG02257.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-114+5830G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180001037 | ||||||
chr2:180001048
|
C | A | 1 | a0005c0020t0002g0224 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-114+5819G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180001048 | ||||||
chr2:180001157
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-114+5710A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180001157 | ||||||
chr2:180001420
|
G | T | 3 | a0004c0004t0002g0272a0004c0004t0002g0273a0004c0004t0004g0032 | 4 | HG02257.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-114+5447C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180001420 | ||||||
chr2:180001519
|
G | A | 8 | a0001c0008t0002g0174a0001c0008t0002g0179a0001c0014t0002g0180others(5): Show | 9 | HG02280.hp2 HG02451.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-114+5348C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180001519 | ||||||
chr2:180001519
|
G | T | 2 | a0005c0007t0002g0039a0005c0007t0002g0225 | 3 | HG03195.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-114+5348C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180001519 | ||||||
chr2:180001527
|
G | A | 22 | a0001c0008t0002g0174a0001c0008t0002g0179a0001c0014t0002g0180others(19): Show | 27 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.-114+5340C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180001527 | ||||||
chr2:180001634
|
G | T | 1 | a0001c0001t0001g0025 | 2 | NA18948.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-114+5233C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180001634 | ||||||
chr2:180001814
|
C | T | 2 | a0003c0003t0002g0181a0003c0003t0002g0182 | 2 | HG01243.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.-114+5053G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180001814 | ||||||
chr2:180001894
|
T | C | 2 | a0005c0007t0002g0039a0005c0007t0002g0225 | 3 | HG03195.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-114+4973A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180001894 | ||||||
chr2:180001928
|
C | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0164 | 2 | NA18972.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.-114+4939G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180001928 | ||||||
chr2:180002024
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-114+4843G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180002024 | ||||||
chr2:180002328
|
A | G | 2 | a0003c0003t0005g0276a0003c0003t0005g0277 | 2 | NA18966.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-114+4539T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180002328 | ||||||
chr2:180002367
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-114+4500G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180002367 | ||||||
chr2:180002469
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-114+4398A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180002469 | ||||||
chr2:180002515
|
G | T | 1 | a0001c0017t0009g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-114+4352C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180002515 | ||||||
chr2:180002695
|
T | C | 6 | a0001c0008t0002g0174a0004c0004t0002g0033a0004c0004t0002g0175others(3): Show | 7 | HG02280.hp2 HG02451.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-114+4172A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180002695 | ||||||
chr2:180002793
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0156a0001c0001t0001g0157others(1): Show | 7 | HG02622.hp2 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-114+4074C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180002793 | ||||||
chr2:180002847
|
A | G | 1 | a0001c0015t0002g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-114+4020T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180002847 | ||||||
chr2:180002901
|
A | C | 1 | a0004c0018t0001g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-114+3966T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180002901 | ||||||
chr2:180002919
|
G | C | 7 | a0001c0017t0009g0275a0004c0004t0002g0272a0004c0004t0002g0273others(4): Show | 9 | HG02257.hp1 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.-114+3948C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180002919 | ||||||
chr2:180003063
|
T | C | 1 | a0002c0002t0002g0045 | 2 | NA18992.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.-114+3804A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180003063 | ||||||
chr2:180003115
|
G | A | 1 | a0002c0013t0002g0267 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-114+3752C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180003115 | ||||||
chr2:180003176
|
T | G | 1 | a0001c0001t0001g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-114+3691A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180003176 | ||||||
chr2:180003301
|
C | A | 1 | a0004c0004t0002g0222 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-114+3566G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180003301 | ||||||
chr2:180003666
|
C | T | 46 | a0003c0003t0002g0007a0003c0003t0002g0012a0003c0003t0002g0014others(43): Show | 64 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.-114+3201G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180003666 | ||||||
chr2:180003731
|
A | G | 14 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0071others(11): Show | 21 | HG00558.hp1 HG01496.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.-114+3136T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180003731 | ||||||
chr2:180003759
|
A | C | 1 | a0001c0001t0001g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-114+3108T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180003759 | ||||||
chr2:180003901
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-114+2966T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180003901 | ||||||
chr2:180003915
|
A | C | 1 | a0001c0001t0001g0160 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-114+2952T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180003915 | ||||||
chr2:180004035
|
T | C | 1 | a0001c0001t0001g0159 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-114+2832A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004035 | ||||||
chr2:180004060
|
G | T | 1 | a0001c0017t0009g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-114+2807C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004060 | ||||||
chr2:180004111
|
A | C | 133 | a0001c0001t0001g0068a0001c0008t0002g0174a0001c0008t0002g0179others(130): Show | 184 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.-114+2756T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004111 | ||||||
chr2:180004361
|
T | G | 2 | a0002c0002t0002g0046a0002c0002t0002g0268 | 3 | HG02055.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-114+2506A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004361 | ||||||
chr2:180004418
|
G | A | 68 | a0001c0008t0002g0174a0001c0008t0002g0179a0001c0014t0002g0180others(65): Show | 91 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.-114+2449C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004418 | ||||||
chr2:180004430
|
C | T | 19 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0055others(16): Show | 26 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.-114+2437G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004430 | ||||||
chr2:180004457
|
G | T | 57 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0019others(54): Show | 83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.-114+2410C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004457 | ||||||
chr2:180004461
|
A | G | 129 | a0001c0008t0002g0174a0001c0008t0002g0179a0001c0014t0002g0180others(126): Show | 179 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.-114+2406T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004461 | ||||||
chr2:180004500
|
T | G | 3 | a0001c0001t0001g0160a0007c0009t0001g0161a0007c0009t0001g0162 | 3 | HG00738.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-114+2367A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004500 | ||||||
chr2:180004610
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-114+2257C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004610 | ||||||
chr2:180004683
|
C | G | 1 | a0001c0012t0001g0054 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-114+2184G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004683 | ||||||
chr2:180004808
|
A | G | 4 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(1): Show | 4 | NA18947.hp2 NA18985.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-114+2059T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004808 | ||||||
chr2:180004822
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-114+2045C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004822 | ||||||
chr2:180004841
|
G | A | 1 | a0001c0001t0001g0013 | 3 | HG02486.hp2 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-114+2026C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004841 | ||||||
chr2:180004873
|
G | T | 1 | a0001c0001t0001g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-114+1994C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004873 | ||||||
chr2:180004893
|
C | T | 8 | a0001c0008t0002g0174a0001c0008t0002g0179a0001c0014t0002g0180others(5): Show | 9 | HG02280.hp2 HG02451.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-114+1974G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004893 | ||||||
chr2:180004909
|
G | A | 1 | a0001c0017t0009g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-114+1958C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004909 | ||||||
chr2:180005024
|
A | G | 1 | a0001c0017t0009g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-114+1843T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180005024 | ||||||
chr2:180005135
|
T | C | 1 | a0001c0001t0001g0164 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-114+1732A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180005135 | ||||||
chr2:180005303
|
A | C | 128 | a0001c0008t0002g0174a0001c0008t0002g0179a0001c0014t0002g0180others(125): Show | 178 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.-114+1564T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180005303 | ||||||
chr2:180005405
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-114+1462C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180005405 | ||||||
chr2:180005560
|
A | G | 3 | a0005c0007t0002g0039a0005c0007t0002g0225a0005c0020t0002g0224 | 4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-114+1307T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180005560 | ||||||
chr2:180005567
|
C | G | 1 | a0001c0001t0001g0048 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-114+1300G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180005567 | ||||||
chr2:180005742
|
C | T | 6 | a0001c0008t0002g0174a0004c0004t0002g0033a0004c0004t0002g0175others(3): Show | 7 | HG02280.hp2 HG02451.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-114+1125G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180005742 | ||||||
chr2:180005782
|
T | C | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | HG02145.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-114+1085A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180005782 | ||||||
chr2:180005785
|
A | G | 1 | a0001c0001t0001g0022 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-114+1082T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180005785 | ||||||
chr2:180005800
|
G | A | 2 | a0003c0003t0002g0018a0003c0003t0002g0223 | 4 | NA18971.hp2 NA18990.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.-114+1067C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180005800 | ||||||
chr2:180005863
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-114+1004G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180005863 | ||||||
chr2:180005940
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-114+927A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180005940 | ||||||
chr2:180006166
|
G | A | 65 | a0001c0008t0002g0174a0001c0008t0002g0179a0001c0014t0002g0180others(62): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.-114+701C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180006166 | ||||||
chr2:180006168
|
GTC | G | 65 | a0001c0008t0002g0174a0001c0008t0002g0179a0001c0014t0002g0180others(62): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.-114+697_-114+698d others(4): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180006168 | ||||||
chr2:180006331
|
T | A | 1 | a0001c0001t0001g0169 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-114+536A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180006331 | ||||||
chr2:180006448
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-114+419C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180006448 | ||||||
chr2:180006668
|
A | G | 132 | a0001c0008t0002g0174a0001c0008t0002g0179a0001c0014t0002g0180others(129): Show | 183 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.-114+199T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180006668 |