geneid | 80157 |
---|---|
ensemblid | ENSG00000109182.12 |
hgncid | 26133 |
symbol | CWH43 |
name | cell wall biogenesis 43 C-terminal homolog |
refseq_nuc | NM_025087.3 |
refseq_prot | NP_079363.2 |
ensembl_nuc | ENST00000226432.9 |
ensembl_prot | ENSP00000226432.4 |
mane_status | MANE Select |
chr | chr4 |
start | 48986275 |
end | 49062079 |
strand | + |
ver | v1.2 |
region | chr4:48986275-49062079 |
region5000 | chr4:48981275-49067079 |
regionname0 | CWH43_chr4_48986275_49062079 |
regionname5000 | CWH43_chr4_48981275_49067079 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 699 | 126 | 48 | 6 | 55 | 1 | 14 | 43 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0002 | 0/0 | 699 | 85 | 10 | 26 | 33 | 7 | 9 | 25 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0003 | 0/0 | 699 | 67 | 7 | 18 | 29 | 6 | 7 | 20 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0004 | 0/0 | 532 | 9 | 0 | 5 | 1 | 2 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0005 | 0/0 | 699 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0006 | 0/0 | 699 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0007 | 0/0 | 699 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0008 | 0/0 | 699 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0009 | 0/0 | 699 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2100 | 124 | 48 | 6 | 55 | 1 | 12 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
c0002 | 0/0 | 2100 | 85 | 10 | 26 | 33 | 7 | 9 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
c0003 | 0/0 | 2100 | 67 | 7 | 18 | 29 | 6 | 7 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
c0004 | 0/0 | 2099 | 9 | 0 | 5 | 1 | 2 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
c0005 | 0/0 | 2100 | 3 | 0 | 3 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
c0006 | 0/0 | 2100 | 2 | 0 | 2 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
c0007 | 0/0 | 2100 | 2 | 0 | 0 | 0 | 0 | 2 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
c0008 | 0/0 | 2100 | 2 | 2 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
c0009 | 0/0 | 2100 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
c0010 | 0/0 | 2100 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 345 | 291 | 66 | 60 | 116 | 16 | 31 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
t0002 | 0/0 | 345 | 3 | 0 | 0 | 2 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
t0003 | 0/0 | 345 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
t0004 | 0/0 | 345 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0002 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0240 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2100 | 124 | 48 | 6 | 55 | 1 | 12 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0001c0007 | 0/0 | 2100 | 2 | 0 | 0 | 0 | 0 | 2 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0002c0002 | 0/0 | 2100 | 85 | 10 | 26 | 33 | 7 | 9 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0003c0003 | 0/0 | 2100 | 67 | 7 | 18 | 29 | 6 | 7 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0004c0004 | 0/0 | 2099 | 9 | 0 | 5 | 1 | 2 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0005c0005 | 0/0 | 2100 | 3 | 0 | 3 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0006c0008 | 0/0 | 2100 | 2 | 2 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0007c0006 | 0/0 | 2100 | 2 | 0 | 2 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0008c0009 | 0/0 | 2100 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0009c0010 | 0/0 | 2100 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2444 | 122 | 46 | 6 | 55 | 1 | 12 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0001c0001t0003 | 0/0 | 2444 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0001c0001t0004 | 0/0 | 2444 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0001c0007t0001 | 0/0 | 2444 | 2 | 0 | 0 | 0 | 0 | 2 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0002c0002t0001 | 0/0 | 2444 | 85 | 10 | 26 | 33 | 7 | 9 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0003c0003t0001 | 0/0 | 2444 | 64 | 7 | 18 | 27 | 6 | 6 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0003c0003t0002 | 0/0 | 2444 | 3 | 0 | 0 | 2 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0004c0004t0001 | 0/0 | 2443 | 9 | 0 | 5 | 1 | 2 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0005c0005t0001 | 0/0 | 2444 | 3 | 0 | 3 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0006c0008t0001 | 0/0 | 2444 | 2 | 2 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0007c0006t0001 | 0/0 | 2444 | 2 | 0 | 2 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0008c0009t0001 | 0/0 | 2444 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
a0009c0010t0001 | 0/0 | 2444 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | copy fasta | chr4 | 48981275 | 49067079 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0240 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0001t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0001c0007t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0003c0003t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0004c0004t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0004c0004t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0004c0004t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0004c0004t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0004c0004t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0004c0004t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0004c0004t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0005c0005t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0005c0005t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0006c0008t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0006c0008t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0007c0006t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0007c0006t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0008c0009t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
a0009c0010t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0003 | t0001 | g0189 | EUR | GBR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0102 | EUR | GBR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0264 | EUR | GBR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0086 | EUR | GBR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0112 | EUR | FIN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG00280 | hp2 | a0003 | c0003 | t0001 | g0035 | EUR | FIN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0106 | EUR | FIN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG00323 | hp2 | a0003 | c0003 | t0001 | g0031 | EUR | FIN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | CHS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | CHS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | CHS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | CHS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG00558 | hp2 | a0003 | c0003 | t0001 | g0133 | EAS | CHS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | CHS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG00639 | hp1 | a0003 | c0003 | t0001 | g0116 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0074 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG00735 | hp1 | a0003 | c0003 | t0001 | g0044 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG00735 | hp2 | a0007 | c0006 | t0001 | g0144 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0093 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG00738 | hp2 | a0004 | c0004 | t0001 | g0154 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG00741 | hp1 | a0003 | c0003 | t0001 | g0127 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG00741 | hp2 | a0003 | c0003 | t0001 | g0188 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0067 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01069 | hp2 | a0004 | c0004 | t0001 | g0011 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01070 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0090 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01071 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0062 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01074 | hp1 | a0003 | c0003 | t0001 | g0121 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01074 | hp2 | a0007 | c0006 | t0001 | g0134 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0103 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01109 | hp1 | a0004 | c0004 | t0001 | g0011 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0111 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01167 | hp2 | a0003 | c0003 | t0001 | g0043 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0142 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01192 | hp1 | a0003 | c0003 | t0001 | g0024 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0105 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0109 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0143 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01257 | hp1 | a0004 | c0004 | t0001 | g0012 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0104 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0101 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01258 | hp2 | a0004 | c0004 | t0001 | g0012 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01346 | hp2 | a0003 | c0003 | t0001 | g0141 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0087 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01358 | hp2 | a0003 | c0003 | t0001 | g0005 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01361 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0088 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01433 | hp2 | a0003 | c0003 | t0001 | g0029 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0092 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01496 | hp2 | a0003 | c0003 | t0001 | g0140 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0113 | EUR | IBS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01515 | hp2 | a0003 | c0003 | t0001 | g0003 | EUR | IBS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01517 | hp1 | a0003 | c0003 | t0001 | g0003 | EUR | IBS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0073 | EUR | IBS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01884 | hp1 | a0006 | c0008 | t0001 | g0146 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01891 | hp2 | a0003 | c0003 | t0001 | g0058 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01928 | hp1 | a0005 | c0005 | t0001 | g0244 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0095 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01952 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01975 | hp1 | a0005 | c0005 | t0001 | g0020 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0089 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01978 | hp1 | a0003 | c0003 | t0001 | g0030 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01981 | hp1 | a0005 | c0005 | t0001 | g0020 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0096 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01993 | hp1 | a0003 | c0003 | t0001 | g0045 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0094 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02004 | hp1 | a0003 | c0003 | t0001 | g0128 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0078 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02027 | hp2 | a0004 | c0004 | t0001 | g0150 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0110 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02056 | hp1 | a0003 | c0003 | t0001 | g0038 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02056 | hp2 | a0003 | c0003 | t0001 | g0185 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02129 | hp1 | a0003 | c0003 | t0001 | g0132 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02129 | hp2 | a0003 | c0003 | t0001 | g0046 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02132 | hp2 | a0003 | c0003 | t0002 | g0153 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0138 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02155 | hp1 | a0003 | c0003 | t0001 | g0184 | EAS | CDX | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02155 | hp2 | a0003 | c0003 | t0001 | g0026 | EAS | CDX | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0270 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0097 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0070 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02523 | hp1 | a0003 | c0003 | t0001 | g0123 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02572 | hp2 | a0003 | c0003 | t0001 | g0118 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02630 | hp2 | a0003 | c0003 | t0001 | g0119 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02698 | hp2 | a0008 | c0009 | t0001 | g0033 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02735 | hp1 | a0003 | c0003 | t0001 | g0120 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02735 | hp2 | a0003 | c0003 | t0001 | g0028 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0049 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0114 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0115 | AFR | ESN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ESN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0052 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03130 | hp1 | a0006 | c0008 | t0001 | g0147 | AFR | ESN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0108 | AFR | ESN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03195 | hp2 | a0002 | c0002 | t0001 | g0100 | AFR | ESN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0099 | AFR | MSL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0139 | AFR | MSL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0010 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03490 | hp2 | a0004 | c0004 | t0001 | g0155 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0010 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0048 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03654 | hp2 | a0003 | c0003 | t0001 | g0039 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03710 | hp1 | a0003 | c0003 | t0001 | g0034 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0055 | SAS | BEB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03831 | hp2 | a0001 | c0007 | t0001 | g0015 | SAS | BEB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03834 | hp2 | a0003 | c0003 | t0001 | g0124 | SAS | BEB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03927 | hp2 | a0003 | c0003 | t0002 | g0157 | SAS | BEB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG03942 | hp2 | a0003 | c0003 | t0001 | g0027 | SAS | BEB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | STU | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0117 | SAS | STU | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0071 | SAS | BEB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0084 | SAS | STU | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG04204 | hp2 | a0001 | c0007 | t0001 | g0015 | SAS | STU | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18522 | hp1 | a0003 | c0003 | t0001 | g0158 | AFR | YRI | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | YRI | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | CHB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | YRI | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | YRI | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18946 | hp2 | a0003 | c0003 | t0001 | g0014 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18951 | hp1 | a0003 | c0003 | t0001 | g0032 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18954 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18956 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18959 | hp1 | a0003 | c0003 | t0001 | g0211 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18968 | hp1 | a0003 | c0003 | t0001 | g0190 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18969 | hp2 | a0003 | c0003 | t0001 | g0126 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18971 | hp1 | a0003 | c0003 | t0001 | g0037 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18971 | hp2 | a0003 | c0003 | t0001 | g0191 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18980 | hp2 | a0003 | c0003 | t0001 | g0187 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18983 | hp2 | a0003 | c0003 | t0001 | g0210 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18986 | hp2 | a0003 | c0003 | t0001 | g0042 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18990 | hp2 | a0003 | c0003 | t0001 | g0014 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18997 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18999 | hp2 | a0003 | c0003 | t0001 | g0186 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19000 | hp1 | a0003 | c0003 | t0002 | g0156 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19001 | hp1 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19011 | hp2 | a0003 | c0003 | t0001 | g0183 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | LWK | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19030 | hp2 | a0003 | c0003 | t0001 | g0085 | AFR | LWK | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | LWK | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19043 | hp2 | a0009 | c0010 | t0001 | g0145 | AFR | LWK | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19070 | hp1 | a0003 | c0003 | t0001 | g0036 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19075 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19076 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19082 | hp2 | a0003 | c0003 | t0001 | g0122 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19083 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19091 | hp1 | a0003 | c0003 | t0001 | g0041 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ASW | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0107 | AFR | ASW | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA20752 | hp1 | a0004 | c0004 | t0001 | g0151 | EUR | TSI | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0091 | EUR | TSI | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA20805 | hp1 | a0003 | c0003 | t0001 | g0131 | EUR | TSI | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA20805 | hp2 | a0004 | c0004 | t0001 | g0152 | EUR | TSI | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0220 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | USA | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
HG06807 | hp2 | a0003 | c0003 | t0001 | g0159 | AFR | USA | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18955 | hp1 | a0003 | c0003 | t0001 | g0125 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA20300 | hp1 | a0003 | c0003 | t0001 | g0023 | AFR | USA | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | USA | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0240 | REF | REF | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0002 | REF | REF | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:48986433
|
C | A | 2 | a0002a0007 | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
missense_variant | MODERATE | c.4C>A | p.Pro2Thr | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/16 | 159/2444 | 4/2100 | 2/699 | chr4 | 48986433 | ||
chr4:48988665
|
A | G | 2 | a0006a0009 | 3 | HG01884.hp1 HG03130.hp1 NA19043.hp2 |
missense_variant | MODERATE | c.232A>G | p.Ile78Val | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/16 | 387/2444 | 232/2100 | 78/699 | chr4 | 48988665 | ||
chr4:48992079
|
G | A | 1 | a0008 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.500G>A | p.Arg167His | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/16 | 655/2444 | 500/2100 | 167/699 | chr4 | 48992079 | ||
chr4:49032652
|
CA | C | 1 | a0004 | 9 | HG00738.hp2 HG01069.hp2 HG01109.hp1 others(6): Show |
frameshift_variant | HIGH | c.1596delA | p.Leu533fs | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/16 | 1751/2444 | 1596/2100 | 532/699 | chr4 | 49032652 | ||
chr4:49050705
|
C | T | 1 | a0005 | 3 | HG01928.hp1 HG01975.hp1 HG01981.hp1 |
missense_variant | MODERATE | c.1877C>T | p.Ala626Val | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/16 | 2032/2444 | 1877/2100 | 626/699 | chr4 | 49050705 | ||
chr4:49061855
|
C | A | 4 | a0002a0003a0008others(1): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
missense_variant | MODERATE | c.2065C>A | p.His689Asn | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 16/16 | 2220/2444 | 2065/2100 | 689/699 | chr4 | 49061855 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:48986462
|
G | A | 1 | a0001c0007 | 2 | HG03831.hp2 HG04204.hp2 |
synonymous_variant | LOW | c.33G>A | p.Glu11Glu | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/16 | 188/2444 | 33/2100 | 11/699 | chr4 | 48986462 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:49061941
|
T | C | 1 | a0001c0001t0003 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*51T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 16/16 | 51 | chr4 | 49061941 | |||||
chr4:49062016
|
T | A | 1 | a0003c0003t0002 | 3 | HG02132.hp2 HG03927.hp2 NA19000.hp1 |
3_prime_UTR_variant | MODIFIER | c.*126T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 16/16 | 126 | chr4 | 49062016 | |||||
chr4:49062018
|
T | C | 1 | a0001c0001t0004 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*128T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 16/16 | 128 | chr4 | 49062018 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:48986554
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.43+82G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48986554 | ||||||
chr4:48986556
|
T | G | 1 | a0001c0001t0001g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.43+84T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48986556 | ||||||
chr4:48986588
|
G | T | 1 | a0001c0001t0001g0274 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.43+116G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48986588 | ||||||
chr4:48986657
|
G | A | 1 | a0003c0003t0001g0023 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.43+185G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48986657 | ||||||
chr4:48986688
|
G | A | 131 | a0001c0001t0001g0040a0001c0001t0001g0129a0001c0001t0001g0130others(128): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.43+216G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48986688 | ||||||
chr4:48986876
|
C | T | 1 | a0007c0006t0001g0144 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.43+404C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48986876 | ||||||
chr4:48987244
|
C | T | 131 | a0001c0001t0001g0040a0001c0001t0001g0129a0001c0001t0001g0130others(128): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.43+772C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48987244 | ||||||
chr4:48987341
|
A | G | 131 | a0001c0001t0001g0040a0001c0001t0001g0129a0001c0001t0001g0130others(128): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.43+869A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48987341 | ||||||
chr4:48987591
|
C | T | 1 | a0002c0002t0001g0143 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.44-886C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48987591 | ||||||
chr4:48987707
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.44-770A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48987707 | ||||||
chr4:48987837
|
C | T | 4 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(1): Show | 4 | HG02258.hp2 HG03540.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-640C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48987837 | ||||||
chr4:48988084
|
C | CA | 3 | a0006c0008t0001g0146a0006c0008t0001g0147a0009c0010t0001g0145 | 3 | HG01884.hp1 HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.44-392dupA | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 48988084 | |||||
chr4:48988222
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG01099.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.44-255G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48988222 | ||||||
chr4:48988291
|
C | T | 1 | a0002c0002t0001g0142 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.44-186C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48988291 | ||||||
chr4:48988459
|
CT | C | 132 | a0001c0001t0001g0021a0001c0001t0001g0040a0001c0001t0001g0129others(129): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
splice_region_variant&intron_variant | LOW | c.44-5delT | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 48988459 | |||||
chr4:48988868
|
T | G | 165 | a0001c0001t0001g0021a0001c0001t0001g0040a0001c0001t0001g0129others(162): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.235+200T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48988868 | ||||||
chr4:48988994
|
A | G | 133 | a0001c0001t0001g0040a0001c0001t0001g0129a0001c0001t0001g0130others(130): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.235+326A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48988994 | ||||||
chr4:48989140
|
A | G | 2 | a0003c0003t0001g0140a0003c0003t0001g0141 | 2 | HG01346.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.235+472A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989140 | ||||||
chr4:48989165
|
A | C | 134 | a0001c0001t0001g0021a0001c0001t0001g0040a0001c0001t0001g0129others(131): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.235+497A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989165 | ||||||
chr4:48989474
|
A | G | 2 | a0006c0008t0001g0146a0006c0008t0001g0147 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.235+806A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989474 | ||||||
chr4:48989494
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.235+826G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989494 | ||||||
chr4:48989523
|
G | A | 131 | a0001c0001t0001g0040a0001c0001t0001g0129a0001c0001t0001g0130others(128): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.235+855G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989523 | ||||||
chr4:48989535
|
C | T | 1 | a0002c0002t0001g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.235+867C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989535 | ||||||
chr4:48989556
|
T | C | 9 | a0001c0001t0001g0013a0001c0001t0001g0174a0001c0001t0001g0175others(6): Show | 10 | NA18968.hp2 NA18980.hp1 NA18982.hp2 others(7): Show |
intron_variant | MODIFIER | c.235+888T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989556 | ||||||
chr4:48989582
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.235+914A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989582 | ||||||
chr4:48989809
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.235+1141C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989809 | ||||||
chr4:48989820
|
G | C | 131 | a0001c0001t0001g0040a0001c0001t0001g0129a0001c0001t0001g0130others(128): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.235+1152G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989820 | ||||||
chr4:48989872
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.235+1204A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989872 | ||||||
chr4:48989876
|
T | G | 2 | a0003c0003t0001g0001a0003c0003t0001g0024 | 4 | HG01070.hp1 HG01071.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+1208T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989876 | ||||||
chr4:48989881
|
C | A | 1 | a0002c0002t0001g0025 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.235+1213C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989881 | ||||||
chr4:48989910
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.235+1242C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989910 | ||||||
chr4:48989992
|
G | A | 2 | a0006c0008t0001g0146a0006c0008t0001g0147 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.235+1324G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989992 | ||||||
chr4:48990175
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.236-1279G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48990175 | ||||||
chr4:48990239
|
A | C | 132 | a0001c0001t0001g0021a0001c0001t0001g0040a0001c0001t0001g0129others(129): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.236-1215A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48990239 | ||||||
chr4:48990331
|
C | T | 1 | a0002c0002t0001g0138 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.236-1123C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48990331 | ||||||
chr4:48990401
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.236-1053C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48990401 | ||||||
chr4:48990731
|
G | A | 131 | a0001c0001t0001g0040a0001c0001t0001g0129a0001c0001t0001g0130others(128): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.236-723G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48990731 | ||||||
chr4:48990744
|
T | A | 132 | a0001c0001t0001g0021a0001c0001t0001g0040a0001c0001t0001g0129others(129): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.236-710T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48990744 | ||||||
chr4:48990756
|
A | T | 1 | a0001c0001t0001g0169 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.236-698A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48990756 | ||||||
chr4:48991001
|
G | T | 2 | a0006c0008t0001g0146a0006c0008t0001g0147 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.236-453G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48991001 | ||||||
chr4:48991593
|
G | A | 9 | a0003c0003t0002g0153a0003c0003t0002g0156a0004c0004t0001g0011others(6): Show | 11 | HG00738.hp2 HG01069.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.356+19G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 3/15 | chr4 | 48991593 | ||||||
chr4:48991600
|
T | C | 1 | a0003c0003t0001g0026 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.356+26T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 3/15 | chr4 | 48991600 | ||||||
chr4:48991724
|
A | T | 1 | a0003c0003t0002g0156 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.356+150A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 3/15 | chr4 | 48991724 | ||||||
chr4:48991790
|
T | C | 1 | a0003c0003t0001g0027 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.357-146T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 3/15 | chr4 | 48991790 | ||||||
chr4:48991879
|
G | T | 1 | a0001c0001t0001g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.357-57G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 3/15 | chr4 | 48991879 | ||||||
chr4:48991893
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.357-43G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 3/15 | chr4 | 48991893 | ||||||
chr4:48992121
|
G | T | 131 | a0001c0001t0001g0040a0001c0001t0001g0129a0001c0001t0001g0130others(128): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.511+31G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48992121 | ||||||
chr4:48992147
|
G | A | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.511+57G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48992147 | ||||||
chr4:48992376
|
A | G | 1 | a0002c0002t0001g0137 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.511+286A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48992376 | ||||||
chr4:48992450
|
C | A | 1 | a0004c0004t0001g0150 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.511+360C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48992450 | ||||||
chr4:48992470
|
TAAC | T | 3 | a0006c0008t0001g0146a0006c0008t0001g0147a0009c0010t0001g0145 | 3 | HG01884.hp1 HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.511+382_511+384del others(3): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 48992470 | |||||
chr4:48992729
|
G | T | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(9): Show | 12 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.511+639G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48992729 | ||||||
chr4:48992857
|
G | A | 3 | a0006c0008t0001g0146a0006c0008t0001g0147a0009c0010t0001g0145 | 3 | HG01884.hp1 HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.511+767G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48992857 | ||||||
chr4:48993026
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.511+936A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48993026 | ||||||
chr4:48993269
|
T | G | 27 | a0001c0001t0001g0040a0003c0003t0001g0001a0003c0003t0001g0003others(24): Show | 32 | HG00280.hp2 HG00323.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.511+1179T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48993269 | ||||||
chr4:48993366
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.512-1253C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48993366 | ||||||
chr4:48993482
|
T | C | 160 | a0001c0001t0001g0021a0001c0001t0001g0040a0001c0001t0001g0129others(157): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.512-1137T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48993482 | ||||||
chr4:48993599
|
G | A | 141 | a0001c0001t0001g0040a0001c0001t0001g0129a0001c0001t0001g0130others(138): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.512-1020G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48993599 | ||||||
chr4:48993683
|
G | A | 140 | a0001c0001t0001g0040a0001c0001t0001g0129a0001c0001t0001g0130others(137): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.512-936G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48993683 | ||||||
chr4:48993707
|
A | G | 1 | a0002c0002t0001g0135 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.512-912A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48993707 | ||||||
chr4:48993784
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.512-835C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48993784 | ||||||
chr4:48993795
|
C | G | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.512-824C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48993795 | ||||||
chr4:48994099
|
C | A | 140 | a0001c0001t0001g0040a0001c0001t0001g0129a0001c0001t0001g0130others(137): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.512-520C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48994099 | ||||||
chr4:48994159
|
G | A | 3 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195 | 3 | HG01255.hp1 HG02897.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.512-460G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48994159 | ||||||
chr4:48994349
|
C | A | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.512-270C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48994349 | ||||||
chr4:48994390
|
C | G | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.512-229C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48994390 | ||||||
chr4:48994604
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.512-15A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48994604 | ||||||
chr4:48994882
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.713+62C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48994882 | ||||||
chr4:48995103
|
A | T | 1 | a0003c0003t0001g0046 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.713+283A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48995103 | ||||||
chr4:48995195
|
T | G | 3 | a0001c0001t0001g0160a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG02258.hp1 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.713+375T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48995195 | ||||||
chr4:48995333
|
T | A | 147 | a0001c0001t0001g0021a0001c0001t0001g0040a0001c0001t0001g0129others(144): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.713+513T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48995333 | ||||||
chr4:48995613
|
C | T | 4 | a0003c0003t0001g0005a0003c0003t0001g0043a0003c0003t0001g0044others(1): Show | 5 | HG00735.hp1 HG01167.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.713+793C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48995613 | ||||||
chr4:48996241
|
T | A | 1 | a0001c0001t0001g0196 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.713+1421T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48996241 | ||||||
chr4:48996298
|
T | TAC | 13 | a0001c0001t0001g0021a0001c0001t0001g0148a0001c0001t0001g0149others(10): Show | 13 | HG00609.hp2 HG01099.hp1 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.713+1510_713+1511d others(4): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr4 | 48996298 | |||||
chr4:48996298
|
TAC | T | 15 | a0001c0001t0001g0168a0001c0001t0001g0171a0001c0001t0001g0260others(12): Show | 15 | HG01884.hp1 HG02258.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.713+1510_713+1511d others(4): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr4 | 48996298 | |||||
chr4:48996298
|
TACAC | T | 2 | a0002c0002t0001g0047a0004c0004t0001g0012 | 3 | HG01257.hp1 HG01258.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.713+1508_713+1511d others(6): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr4 | 48996298 | |||||
chr4:48996298
|
TACACAC | T | 94 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0008others(91): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.713+1506_713+1511d others(8): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr4 | 48996298 | |||||
chr4:48996298
|
TACACACA others(1): Show |
T | 3 | a0002c0002t0001g0117a0003c0003t0001g0116a0009c0010t0001g0145 | 3 | HG00639.hp1 HG04115.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.713+1504_713+1511d others(10): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr4 | 48996298 | |||||
chr4:48996298
|
TACACACA others(3): Show |
T | 42 | a0001c0001t0001g0040a0001c0001t0001g0129a0001c0001t0001g0130others(39): Show | 47 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.713+1502_713+1511d others(12): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr4 | 48996298 | |||||
chr4:48996328
|
C | T | 3 | a0003c0003t0001g0026a0003c0003t0001g0132a0003c0003t0001g0133 | 3 | HG00558.hp2 HG02129.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.713+1508C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48996328 | ||||||
chr4:48996330
|
C | T | 123 | a0001c0001t0001g0040a0001c0001t0001g0129a0001c0001t0001g0130others(120): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.713+1510C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48996330 | ||||||
chr4:48996715
|
T | C | 2 | a0003c0003t0001g0027a0003c0003t0001g0028 | 2 | HG02735.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.714-1745T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48996715 | ||||||
chr4:48996757
|
A | T | 139 | a0001c0001t0001g0040a0001c0001t0001g0129a0001c0001t0001g0130others(136): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.714-1703A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48996757 | ||||||
chr4:48996984
|
G | C | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(9): Show | 12 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.714-1476G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48996984 | ||||||
chr4:48997082
|
A | G | 2 | a0002c0002t0001g0114a0002c0002t0001g0115 | 2 | HG02886.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.714-1378A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48997082 | ||||||
chr4:48997225
|
C | CT | 158 | a0001c0001t0001g0021a0001c0001t0001g0040a0001c0001t0001g0129others(155): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.714-1221dupT | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr4 | 48997225 | |||||
chr4:48997319
|
A | G | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(9): Show | 12 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.714-1141A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48997319 | ||||||
chr4:48997418
|
C | G | 1 | a0001c0001t0001g0259 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.714-1042C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48997418 | ||||||
chr4:48997669
|
A | G | 1 | a0004c0004t0001g0155 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.714-791A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48997669 | ||||||
chr4:48997704
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.714-756T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48997704 | ||||||
chr4:48997711
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.714-749C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48997711 | ||||||
chr4:48997825
|
G | A | 159 | a0001c0001t0001g0021a0001c0001t0001g0040a0001c0001t0001g0129others(156): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.714-635G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48997825 | ||||||
chr4:48997946
|
C | T | 139 | a0001c0001t0001g0040a0001c0001t0001g0129a0001c0001t0001g0130others(136): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.714-514C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48997946 | ||||||
chr4:48998235
|
T | C | 4 | a0003c0003t0002g0153a0003c0003t0002g0156a0003c0003t0002g0157others(1): Show | 4 | HG02027.hp2 HG02132.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.714-225T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48998235 | ||||||
chr4:48998582
|
T | A | 1 | a0003c0003t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.802+34T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48998582 | ||||||
chr4:48998623
|
G | A | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(9): Show | 12 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.802+75G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48998623 | ||||||
chr4:48998635
|
A | T | 2 | a0002c0002t0001g0112a0002c0002t0001g0113 | 2 | HG00280.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.802+87A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48998635 | ||||||
chr4:48998754
|
C | T | 7 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.802+206C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48998754 | ||||||
chr4:48998833
|
A | G | 143 | a0001c0001t0001g0040a0001c0001t0001g0129a0001c0001t0001g0130others(140): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.802+285A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48998833 | ||||||
chr4:48998935
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.802+387C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48998935 | ||||||
chr4:48998974
|
T | G | 2 | a0002c0002t0001g0056a0002c0002t0001g0057 | 2 | NA19010.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.802+426T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48998974 | ||||||
chr4:48999046
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.802+498A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48999046 | ||||||
chr4:48999327
|
A | G | 1 | a0003c0003t0001g0131 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.802+779A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48999327 | ||||||
chr4:48999388
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.802+840C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48999388 | ||||||
chr4:48999610
|
C | G | 8 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(5): Show | 8 | HG01255.hp1 HG01884.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.802+1062C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48999610 | ||||||
chr4:48999761
|
C | T | 1 | a0001c0001t0001g0254 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.802+1213C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48999761 | ||||||
chr4:48999790
|
G | T | 157 | a0001c0001t0001g0040a0001c0001t0001g0129a0001c0001t0001g0130others(154): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.802+1242G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48999790 | ||||||
chr4:48999917
|
G | T | 1 | a0002c0002t0001g0113 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.802+1369G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48999917 | ||||||
chr4:48999962
|
G | A | 2 | a0003c0003t0001g0188a0003c0003t0001g0189 | 2 | HG00099.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.802+1414G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48999962 | ||||||
chr4:49000066
|
A | C | 1 | a0003c0003t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.802+1518A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49000066 | ||||||
chr4:49000067
|
C | A | 1 | a0001c0001t0001g0271 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.802+1519C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49000067 | ||||||
chr4:49000204
|
T | A | 139 | a0001c0001t0001g0040a0001c0001t0001g0129a0001c0001t0001g0130others(136): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.802+1656T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49000204 | ||||||
chr4:49000241
|
T | C | 1 | a0001c0001t0001g0197 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.802+1693T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49000241 | ||||||
chr4:49000337
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.802+1789G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49000337 | ||||||
chr4:49000529
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.802+1981T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49000529 | ||||||
chr4:49000839
|
ACT | A | 139 | a0001c0001t0001g0040a0001c0001t0001g0129a0001c0001t0001g0130others(136): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.802+2294_802+2295d others(4): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 49000839 | |||||
chr4:49001034
|
C | CTG | 19 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(16): Show | 19 | HG01884.hp1 HG02145.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.802+2489_802+2490d others(4): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 49001034 | |||||
chr4:49001172
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.803-2563G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49001172 | ||||||
chr4:49001206
|
A | T | 7 | a0001c0001t0001g0021a0001c0001t0001g0250a0001c0001t0001g0251others(4): Show | 7 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.803-2529A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49001206 | ||||||
chr4:49001222
|
T | C | 1 | a0002c0002t0001g0138 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.803-2513T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49001222 | ||||||
chr4:49001365
|
T | C | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | HG02572.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.803-2370T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49001365 | ||||||
chr4:49001520
|
T | C | 2 | a0006c0008t0001g0146a0006c0008t0001g0147 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.803-2215T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49001520 | ||||||
chr4:49001871
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.803-1864G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49001871 | ||||||
chr4:49001972
|
C | T | 3 | a0003c0003t0001g0004a0003c0003t0001g0041a0003c0003t0001g0042 | 4 | NA18954.hp1 NA18956.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-1763C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49001972 | ||||||
chr4:49002150
|
T | A | 1 | a0003c0003t0001g0058 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.803-1585T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49002150 | ||||||
chr4:49002414
|
A | G | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.803-1321A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49002414 | ||||||
chr4:49002642
|
A | T | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.803-1093A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49002642 | ||||||
chr4:49002817
|
C | T | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.803-918C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49002817 | ||||||
chr4:49002831
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.803-904G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49002831 | ||||||
chr4:49002846
|
G | A | 16 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0059others(13): Show | 18 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.803-889G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49002846 | ||||||
chr4:49003224
|
A | G | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | NA18986.hp1 NA19011.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.803-511A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49003224 | ||||||
chr4:49003281
|
T | C | 6 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(3): Show | 6 | HG01884.hp1 HG03130.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.803-454T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49003281 | ||||||
chr4:49003505
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.803-230T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49003505 | ||||||
chr4:49003600
|
G | C | 1 | a0003c0003t0001g0210 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.803-135G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49003600 | ||||||
chr4:49004168
|
T | C | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1060+176T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49004168 | ||||||
chr4:49004374
|
T | A | 1 | a0001c0001t0001g0264 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1060+382T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49004374 | ||||||
chr4:49004614
|
T | G | 155 | a0001c0001t0001g0021a0001c0001t0001g0040a0001c0001t0001g0129others(152): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1060+622T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49004614 | ||||||
chr4:49004665
|
C | G | 8 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(5): Show | 8 | HG01255.hp1 HG01884.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1060+673C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49004665 | ||||||
chr4:49004739
|
G | C | 1 | a0002c0002t0001g0070 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1060+747G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49004739 | ||||||
chr4:49004799
|
A | T | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1060+807A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49004799 | ||||||
chr4:49004951
|
T | C | 162 | a0001c0001t0001g0021a0001c0001t0001g0040a0001c0001t0001g0129others(159): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1060+959T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49004951 | ||||||
chr4:49005100
|
A | C | 1 | a0001c0001t0001g0249 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1060+1108A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49005100 | ||||||
chr4:49005391
|
A | G | 2 | a0004c0004t0001g0151a0004c0004t0001g0152 | 2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1060+1399A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49005391 | ||||||
chr4:49005433
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1060+1441C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49005433 | ||||||
chr4:49005563
|
CT | C | 6 | a0001c0001t0001g0161a0001c0001t0001g0170a0002c0002t0001g0056others(3): Show | 6 | HG02145.hp2 HG03041.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060+1585delT | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr4 | 49005563 | |||||
chr4:49005757
|
C | T | 1 | a0003c0003t0001g0058 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1061-1444C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49005757 | ||||||
chr4:49005810
|
G | C | 2 | a0001c0001t0001g0165a0001c0001t0001g0170 | 2 | HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1061-1391G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49005810 | ||||||
chr4:49005958
|
A | C | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1061-1243A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49005958 | ||||||
chr4:49005996
|
T | C | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | NA18946.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1061-1205T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49005996 | ||||||
chr4:49006013
|
C | G | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1061-1188C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49006013 | ||||||
chr4:49006412
|
T | C | 2 | a0002c0002t0001g0073a0002c0002t0001g0074 | 2 | HG00639.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1061-789T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49006412 | ||||||
chr4:49006558
|
T | C | 1 | a0001c0001t0001g0214 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1061-643T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49006558 | ||||||
chr4:49006600
|
T | G | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1061-601T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49006600 | ||||||
chr4:49006639
|
T | A | 2 | a0003c0003t0001g0118a0003c0003t0001g0119 | 2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1061-562T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49006639 | ||||||
chr4:49006639
|
T | G | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1061-562T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49006639 | ||||||
chr4:49006749
|
A | T | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1061-452A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49006749 | ||||||
chr4:49006892
|
C | G | 1 | a0001c0001t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1061-309C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49006892 | ||||||
chr4:49006957
|
A | G | 1 | a0003c0003t0001g0210 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1061-244A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49006957 | ||||||
chr4:49007161
|
G | C | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1061-40G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49007161 | ||||||
chr4:49007543
|
G | A | 1 | a0002c0002t0001g0142 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1186+217G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49007543 | ||||||
chr4:49007625
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0001g0181 | 2 | NA18612.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.1186+299C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49007625 | ||||||
chr4:49007750
|
T | G | 1 | a0001c0001t0001g0215 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1186+424T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49007750 | ||||||
chr4:49007816
|
G | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0170 | 2 | HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1186+490G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49007816 | ||||||
chr4:49007832
|
T | C | 1 | a0003c0003t0001g0058 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1186+506T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49007832 | ||||||
chr4:49007871
|
T | C | 1 | a0002c0002t0001g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1186+545T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49007871 | ||||||
chr4:49007933
|
C | T | 3 | a0001c0001t0001g0160a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG02258.hp1 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1186+607C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49007933 | ||||||
chr4:49008094
|
T | C | 56 | a0002c0002t0001g0008a0002c0002t0001g0075a0002c0002t0001g0076others(53): Show | 62 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.1186+768T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49008094 | ||||||
chr4:49008243
|
T | A | 1 | a0001c0001t0001g0160 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1186+917T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49008243 | ||||||
chr4:49008514
|
G | A | 2 | a0003c0003t0001g0132a0003c0003t0001g0133 | 2 | HG00558.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1186+1188G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49008514 | ||||||
chr4:49008521
|
T | C | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1186+1195T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49008521 | ||||||
chr4:49008598
|
A | G | 4 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(1): Show | 4 | HG02145.hp2 HG02486.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1186+1272A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49008598 | ||||||
chr4:49008734
|
C | G | 1 | a0003c0003t0001g0039 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1186+1408C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49008734 | ||||||
chr4:49008907
|
C | A | 1 | a0001c0001t0001g0265 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1186+1581C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49008907 | ||||||
chr4:49008935
|
C | T | 151 | a0001c0001t0001g0021a0001c0001t0001g0271a0001c0001t0001g0272others(148): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1186+1609C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49008935 | ||||||
chr4:49008957
|
G | T | 3 | a0003c0003t0001g0014a0003c0003t0001g0186a0003c0003t0001g0187 | 4 | NA18946.hp2 NA18980.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.1186+1631G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49008957 | ||||||
chr4:49008991
|
G | C | 1 | a0002c0002t0001g0070 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1186+1665G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49008991 | ||||||
chr4:49009103
|
A | G | 1 | a0003c0003t0001g0038 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1186+1777A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49009103 | ||||||
chr4:49009116
|
A | G | 6 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1186+1790A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49009116 | ||||||
chr4:49009412
|
C | T | 1 | a0002c0002t0001g0117 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1186+2086C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49009412 | ||||||
chr4:49009564
|
C | T | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1186+2238C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49009564 | ||||||
chr4:49009645
|
A | G | 152 | a0001c0001t0001g0021a0001c0001t0001g0149a0001c0001t0001g0271others(149): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1186+2319A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49009645 | ||||||
chr4:49009813
|
C | T | 145 | a0001c0001t0001g0021a0002c0002t0001g0006a0002c0002t0001g0007others(142): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1186+2487C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49009813 | ||||||
chr4:49010009
|
T | G | 1 | a0003c0003t0001g0023 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1186+2683T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49010009 | ||||||
chr4:49010115
|
T | G | 145 | a0001c0001t0001g0149a0002c0002t0001g0006a0002c0002t0001g0007others(142): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1186+2789T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49010115 | ||||||
chr4:49010229
|
A | G | 1 | a0002c0002t0001g0069 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1186+2903A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49010229 | ||||||
chr4:49010334
|
T | C | 2 | a0006c0008t0001g0146a0006c0008t0001g0147 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1186+3008T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49010334 | ||||||
chr4:49010776
|
T | C | 1 | a0002c0002t0001g0084 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1186+3450T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49010776 | ||||||
chr4:49010794
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1186+3468G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49010794 | ||||||
chr4:49010823
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1186+3497G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49010823 | ||||||
chr4:49010847
|
G | T | 1 | a0001c0001t0001g0247 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1186+3521G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49010847 | ||||||
chr4:49011153
|
G | A | 1 | a0006c0008t0001g0146 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1186+3827G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49011153 | ||||||
chr4:49011173
|
A | G | 1 | a0002c0002t0001g0083 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1186+3847A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49011173 | ||||||
chr4:49011841
|
C | T | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1186+4515C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49011841 | ||||||
chr4:49011922
|
A | G | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1186+4596A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49011922 | ||||||
chr4:49011959
|
G | A | 1 | a0003c0003t0001g0085 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1186+4633G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49011959 | ||||||
chr4:49012039
|
G | C | 1 | a0002c0002t0001g0070 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1186+4713G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49012039 | ||||||
chr4:49012075
|
C | T | 1 | a0003c0003t0001g0058 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1186+4749C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49012075 | ||||||
chr4:49012370
|
G | C | 3 | a0003c0003t0001g0116a0003c0003t0001g0120a0003c0003t0001g0131 | 3 | HG00639.hp1 HG02735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1187-4879G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49012370 | ||||||
chr4:49012668
|
C | T | 1 | a0002c0002t0001g0111 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1187-4581C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49012668 | ||||||
chr4:49012674
|
T | G | 1 | a0002c0002t0001g0111 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1187-4575T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49012674 | ||||||
chr4:49012777
|
G | A | 2 | a0002c0002t0001g0075a0002c0002t0001g0076 | 2 | HG00408.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.1187-4472G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49012777 | ||||||
chr4:49012786
|
G | A | 3 | a0003c0003t0001g0116a0003c0003t0001g0120a0003c0003t0001g0131 | 3 | HG00639.hp1 HG02735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1187-4463G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49012786 | ||||||
chr4:49012921
|
G | A | 2 | a0006c0008t0001g0146a0006c0008t0001g0147 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1187-4328G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49012921 | ||||||
chr4:49012937
|
A | G | 1 | a0002c0002t0001g0082 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1187-4312A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49012937 | ||||||
chr4:49012997
|
G | A | 1 | a0001c0001t0001g0254 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1187-4252G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49012997 | ||||||
chr4:49013147
|
C | T | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1187-4102C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49013147 | ||||||
chr4:49013226
|
C | T | 1 | a0003c0003t0001g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1187-4023C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49013226 | ||||||
chr4:49013227
|
G | T | 2 | a0002c0002t0001g0112a0002c0002t0001g0113 | 2 | HG00280.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1187-4022G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49013227 | ||||||
chr4:49013364
|
C | T | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1187-3885C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49013364 | ||||||
chr4:49013421
|
G | A | 1 | a0002c0002t0001g0117 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1187-3828G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49013421 | ||||||
chr4:49013467
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1187-3782C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49013467 | ||||||
chr4:49013500
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1187-3749C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49013500 | ||||||
chr4:49013595
|
A | C | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1187-3654A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49013595 | ||||||
chr4:49013631
|
CT | C | 152 | a0001c0001t0001g0021a0001c0001t0001g0130a0001c0001t0001g0271others(149): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1187-3608delT | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 49013631 | |||||
chr4:49013654
|
A | C | 1 | a0001c0001t0001g0246 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1187-3595A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49013654 | ||||||
chr4:49013802
|
T | C | 1 | a0002c0002t0001g0086 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1187-3447T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49013802 | ||||||
chr4:49013818
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1187-3431G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49013818 | ||||||
chr4:49013896
|
A | C | 6 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0252others(3): Show | 6 | HG01243.hp1 HG02622.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1187-3353A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49013896 | ||||||
chr4:49014035
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1187-3214A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49014035 | ||||||
chr4:49014139
|
T | A | 2 | a0001c0001t0001g0203a0001c0001t0001g0204 | 2 | NA19011.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1187-3110T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49014139 | ||||||
chr4:49014290
|
A | C | 1 | a0001c0001t0001g0196 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1187-2959A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49014290 | ||||||
chr4:49014360
|
C | A | 1 | a0001c0001t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1187-2889C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49014360 | ||||||
chr4:49014439
|
A | T | 1 | a0002c0002t0001g0055 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1187-2810A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49014439 | ||||||
chr4:49014443
|
A | C | 1 | a0002c0002t0001g0055 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1187-2806A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49014443 | ||||||
chr4:49014458
|
C | CA | 114 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(111): Show | 123 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.1187-2774dupA | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 49014458 | |||||
chr4:49014465
|
A | G | 145 | a0001c0001t0001g0021a0002c0002t0001g0006a0002c0002t0001g0007others(142): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1187-2784A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49014465 | ||||||
chr4:49014656
|
C | A | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1187-2593C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49014656 | ||||||
chr4:49014744
|
A | G | 145 | a0001c0001t0001g0021a0002c0002t0001g0006a0002c0002t0001g0007others(142): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1187-2505A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49014744 | ||||||
chr4:49014977
|
T | A | 1 | a0001c0001t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1187-2272T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49014977 | ||||||
chr4:49015055
|
C | A | 9 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(6): Show | 9 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1187-2194C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49015055 | ||||||
chr4:49015071
|
G | A | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1187-2178G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49015071 | ||||||
chr4:49015202
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1187-2047T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49015202 | ||||||
chr4:49015262
|
GT | G | 7 | a0001c0001t0001g0013a0001c0001t0001g0174a0001c0001t0001g0175others(4): Show | 8 | HG02258.hp2 NA18968.hp2 NA18980.hp1 others(5): Show |
intron_variant | MODIFIER | c.1187-1977delT | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 49015262 | |||||
chr4:49015441
|
A | C | 3 | a0003c0003t0001g0014a0003c0003t0001g0186a0003c0003t0001g0187 | 4 | NA18946.hp2 NA18980.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.1187-1808A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49015441 | ||||||
chr4:49015714
|
C | T | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1187-1535C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49015714 | ||||||
chr4:49015824
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1187-1425A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49015824 | ||||||
chr4:49016289
|
T | C | 146 | a0001c0001t0001g0021a0001c0001t0001g0149a0002c0002t0001g0006others(143): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1187-960T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016289 | ||||||
chr4:49016317
|
G | C | 146 | a0001c0001t0001g0021a0001c0001t0001g0149a0002c0002t0001g0006others(143): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1187-932G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016317 | ||||||
chr4:49016417
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1187-832G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016417 | ||||||
chr4:49016427
|
C | T | 1 | a0001c0001t0001g0178 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1187-822C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016427 | ||||||
chr4:49016439
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1187-810G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016439 | ||||||
chr4:49016654
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1187-595G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016654 | ||||||
chr4:49016754
|
C | G | 1 | a0001c0001t0001g0040 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1187-495C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016754 | ||||||
chr4:49016764
|
A | G | 1 | a0001c0001t0001g0178 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1187-485A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016764 | ||||||
chr4:49016790
|
T | A | 1 | a0001c0001t0001g0161 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1187-459T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016790 | ||||||
chr4:49016869
|
G | A | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1187-380G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016869 | ||||||
chr4:49016897
|
T | C | 152 | a0001c0001t0001g0021a0001c0001t0001g0149a0001c0001t0001g0271others(149): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1187-352T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016897 | ||||||
chr4:49016915
|
C | T | 2 | a0006c0008t0001g0146a0006c0008t0001g0147 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1187-334C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016915 | ||||||
chr4:49016958
|
G | A | 1 | a0002c0002t0001g0059 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1187-291G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016958 | ||||||
chr4:49017101
|
T | A | 4 | a0004c0004t0001g0011a0004c0004t0001g0012a0004c0004t0001g0154others(1): Show | 6 | HG00738.hp2 HG01069.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1187-148T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49017101 | ||||||
chr4:49017130
|
A | G | 1 | a0003c0003t0001g0189 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1187-119A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49017130 | ||||||
chr4:49017215
|
T | A | 56 | a0002c0002t0001g0008a0002c0002t0001g0075a0002c0002t0001g0076others(53): Show | 62 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.1187-34T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49017215 | ||||||
chr4:49017588
|
T | G | 1 | a0001c0001t0001g0040 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1266+260T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49017588 | ||||||
chr4:49017682
|
C | G | 145 | a0001c0001t0001g0149a0002c0002t0001g0006a0002c0002t0001g0007others(142): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1266+354C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49017682 | ||||||
chr4:49017685
|
T | C | 152 | a0001c0001t0001g0021a0001c0001t0001g0149a0001c0001t0001g0271others(149): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1266+357T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49017685 | ||||||
chr4:49017875
|
G | A | 1 | a0002c0002t0001g0087 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1266+547G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49017875 | ||||||
chr4:49017897
|
C | T | 3 | a0001c0001t0001g0263a0005c0005t0001g0020a0005c0005t0001g0244 | 4 | HG01928.hp1 HG01975.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266+569C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49017897 | ||||||
chr4:49018031
|
G | A | 4 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(1): Show | 4 | HG02145.hp2 HG02486.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1266+703G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49018031 | ||||||
chr4:49018089
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1266+761C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49018089 | ||||||
chr4:49018106
|
A | G | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1266+778A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49018106 | ||||||
chr4:49018154
|
C | G | 146 | a0001c0001t0001g0021a0001c0001t0001g0149a0002c0002t0001g0006others(143): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1266+826C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49018154 | ||||||
chr4:49018214
|
C | CATTT | 2 | a0003c0003t0001g0003a0003c0003t0001g0029 | 3 | HG01433.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1266+906_1266+909d others(6): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49018214 | |||||
chr4:49018333
|
T | C | 1 | a0003c0003t0001g0030 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1266+1005T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49018333 | ||||||
chr4:49018649
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1266+1321C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49018649 | ||||||
chr4:49018761
|
C | T | 2 | a0006c0008t0001g0146a0006c0008t0001g0147 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1266+1433C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49018761 | ||||||
chr4:49018762
|
G | A | 1 | a0001c0001t0003g0220 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1266+1434G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49018762 | ||||||
chr4:49018792
|
A | T | 1 | a0001c0001t0001g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1266+1464A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49018792 | ||||||
chr4:49019082
|
A | G | 152 | a0001c0001t0001g0021a0001c0001t0001g0149a0001c0001t0001g0271others(149): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1266+1754A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49019082 | ||||||
chr4:49019094
|
A | G | 1 | a0002c0002t0001g0137 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1266+1766A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49019094 | ||||||
chr4:49019243
|
G | A | 1 | a0003c0003t0001g0039 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1266+1915G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49019243 | ||||||
chr4:49019243
|
G | T | 1 | a0002c0002t0001g0054 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1266+1915G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49019243 | ||||||
chr4:49019462
|
T | C | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1266+2134T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49019462 | ||||||
chr4:49019465
|
C | T | 1 | a0001c0001t0001g0243 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1266+2137C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49019465 | ||||||
chr4:49019511
|
T | C | 1 | a0002c0002t0001g0077 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1266+2183T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49019511 | ||||||
chr4:49019569
|
A | G | 1 | a0002c0002t0001g0137 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1266+2241A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49019569 | ||||||
chr4:49019724
|
C | T | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1266+2396C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49019724 | ||||||
chr4:49019741
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1266+2413A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49019741 | ||||||
chr4:49019890
|
G | A | 4 | a0002c0002t0001g0088a0002c0002t0001g0089a0002c0002t0001g0090others(1): Show | 4 | HG01070.hp2 HG01433.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1266+2562G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49019890 | ||||||
chr4:49020039
|
A | G | 1 | a0001c0001t0001g0242 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1266+2711A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49020039 | ||||||
chr4:49020289
|
G | A | 7 | a0004c0004t0001g0011a0004c0004t0001g0012a0004c0004t0001g0150others(4): Show | 9 | HG00738.hp2 HG01069.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1266+2961G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49020289 | ||||||
chr4:49020306
|
G | A | 145 | a0001c0001t0001g0021a0002c0002t0001g0006a0002c0002t0001g0007others(142): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1266+2978G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49020306 | ||||||
chr4:49020326
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1266+2998C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49020326 | ||||||
chr4:49020384
|
T | TAC | 5 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0221others(2): Show | 5 | HG00558.hp1 HG02523.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.1266+3088_1266+308 others(6): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020384 | |||||
chr4:49020384
|
T | TACAC | 6 | a0001c0001t0001g0148a0001c0001t0001g0207a0001c0001t0001g0208others(3): Show | 6 | HG01891.hp1 HG02572.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1266+3086_1266+308 others(8): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020384 | |||||
chr4:49020384
|
TAC | T | 9 | a0001c0001t0001g0040a0001c0001t0001g0170a0001c0001t0001g0202others(6): Show | 9 | HG01074.hp2 HG02738.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.1266+3088_1266+308 others(6): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020384 | |||||
chr4:49020384
|
TACAC | T | 5 | a0001c0001t0001g0195a0001c0001t0001g0263a0002c0002t0001g0081others(2): Show | 6 | HG01928.hp1 HG01975.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1266+3086_1266+308 others(8): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020384 | |||||
chr4:49020384
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0169 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1266+3080_1266+308 others(14): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020384 | |||||
chr4:49020414
|
C | CATATAT | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1266+3087_1266+308 others(10): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020414 | |||||
chr4:49020414
|
C | T | 1 | a0002c0002t0001g0081 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1266+3086C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49020414 | ||||||
chr4:49020416
|
C | CACACACA others(15): Show |
1 | a0002c0002t0001g0078 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1266+3089_1266+309 others(26): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | |||||
chr4:49020416
|
C | CACACACA others(17): Show |
2 | a0002c0002t0001g0006a0002c0002t0001g0060 | 3 | NA18940.hp1 NA18994.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1266+3089_1266+309 others(28): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | |||||
chr4:49020416
|
C | CACACACA others(13): Show |
1 | a0003c0003t0001g0183 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1266+3089_1266+309 others(24): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | |||||
chr4:49020416
|
C | CACACACA others(15): Show |
5 | a0002c0002t0001g0092a0002c0002t0001g0093a0002c0002t0001g0113others(2): Show | 5 | HG00738.hp1 HG01496.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.1266+3089_1266+309 others(26): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | |||||
chr4:49020416
|
C | CACACACA others(11): Show |
1 | a0003c0003t0001g0121 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1266+3089_1266+309 others(22): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | |||||
chr4:49020416
|
C | CACACACA others(13): Show |
20 | a0002c0002t0001g0047a0002c0002t0001g0048a0002c0002t0001g0061others(17): Show | 20 | HG00099.hp1 HG00280.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1266+3089_1266+309 others(24): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | |||||
chr4:49020416
|
C | CACACACA others(9): Show |
1 | a0003c0003t0001g0123 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1266+3089_1266+309 others(20): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | |||||
chr4:49020416
|
C | CACACACA others(11): Show |
65 | a0001c0001t0001g0021a0001c0001t0004g0270a0002c0002t0001g0007others(62): Show | 72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.1266+3089_1266+309 others(22): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | |||||
chr4:49020416
|
C | CACACACA others(13): Show |
1 | a0003c0003t0001g0118 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1266+3089_1266+309 others(24): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | |||||
chr4:49020416
|
C | CACACACA others(7): Show |
2 | a0003c0003t0001g0085a0003c0003t0001g0127 | 2 | HG00741.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1266+3089_1266+309 others(18): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | |||||
chr4:49020416
|
C | CACACACA others(9): Show |
28 | a0002c0002t0001g0010a0002c0002t0001g0069a0002c0002t0001g0070others(25): Show | 30 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.1266+3089_1266+309 others(20): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | |||||
chr4:49020416
|
C | CACACACA others(11): Show |
2 | a0002c0002t0001g0068a0009c0010t0001g0145 | 2 | NA18982.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1266+3089_1266+309 others(22): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | |||||
chr4:49020416
|
C | CACACACA others(7): Show |
13 | a0002c0002t0001g0008a0002c0002t0001g0055a0002c0002t0001g0072others(10): Show | 14 | HG00558.hp2 HG00735.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1266+3089_1266+309 others(18): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | |||||
chr4:49020416
|
C | CACACACA others(9): Show |
2 | a0002c0002t0001g0090a0002c0002t0001g0091 | 2 | HG01070.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1266+3089_1266+309 others(20): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | |||||
chr4:49020416
|
C | CACACACA others(3): Show |
1 | a0001c0001t0001g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1266+3089_1266+309 others(14): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | |||||
chr4:49020416
|
C | CACACACA others(5): Show |
1 | a0002c0002t0001g0110 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1266+3089_1266+309 others(16): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | |||||
chr4:49020416
|
C | CACACACA others(3): Show |
2 | a0006c0008t0001g0146a0006c0008t0001g0147 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1266+3089_1266+309 others(14): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | |||||
chr4:49020416
|
C | CACAT | 8 | a0001c0001t0001g0130a0001c0001t0001g0168a0004c0004t0001g0011others(5): Show | 10 | HG00738.hp2 HG01069.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1266+3089_1266+309 others(8): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | |||||
chr4:49020416
|
C | CAT | 4 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0166others(1): Show | 4 | HG02258.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266+3100_1266+310 others(6): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | |||||
chr4:49020416
|
C | T | 8 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0169others(5): Show | 8 | HG02145.hp2 HG03041.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1266+3088C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49020416 | ||||||
chr4:49020453
|
G | T | 2 | a0006c0008t0001g0146a0006c0008t0001g0147 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1266+3125G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49020453 | ||||||
chr4:49020638
|
T | A | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1266+3310T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49020638 | ||||||
chr4:49020742
|
T | G | 4 | a0002c0002t0001g0070a0002c0002t0001g0106a0002c0002t0001g0111others(1): Show | 4 | HG00323.hp1 HG01109.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266+3414T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49020742 | ||||||
chr4:49021161
|
G | A | 1 | a0001c0001t0001g0271 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1266+3833G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49021161 | ||||||
chr4:49021189
|
G | T | 1 | a0001c0001t0001g0243 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1266+3861G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49021189 | ||||||
chr4:49021315
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1266+3987T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49021315 | ||||||
chr4:49021407
|
C | G | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1266+4079C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49021407 | ||||||
chr4:49021435
|
T | A | 1 | a0003c0003t0001g0124 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1266+4107T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49021435 | ||||||
chr4:49021999
|
C | A | 4 | a0001c0001t0001g0130a0001c0001t0001g0165a0001c0001t0001g0169others(1): Show | 4 | HG03041.hp1 HG03139.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266+4671C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49021999 | ||||||
chr4:49022002
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1266+4674C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49022002 | ||||||
chr4:49022173
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1266+4845T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49022173 | ||||||
chr4:49022340
|
G | T | 1 | a0001c0001t0001g0241 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1266+5012G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49022340 | ||||||
chr4:49022415
|
G | A | 2 | a0002c0002t0001g0112a0002c0002t0001g0113 | 2 | HG00280.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1266+5087G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49022415 | ||||||
chr4:49022438
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1266+5110G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49022438 | ||||||
chr4:49022532
|
A | G | 1 | a0001c0001t0001g0259 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1266+5204A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49022532 | ||||||
chr4:49022836
|
A | G | 5 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(2): Show | 5 | HG01884.hp1 HG03130.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1266+5508A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49022836 | ||||||
chr4:49022870
|
A | G | 4 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(1): Show | 4 | HG02145.hp2 HG02486.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1266+5542A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49022870 | ||||||
chr4:49023062
|
C | A | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1267-5567C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49023062 | ||||||
chr4:49023248
|
T | A | 4 | a0002c0002t0001g0078a0003c0003t0001g0121a0003c0003t0001g0123others(1): Show | 4 | HG00741.hp1 HG01074.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1267-5381T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49023248 | ||||||
chr4:49023258
|
G | A | 2 | a0006c0008t0001g0146a0006c0008t0001g0147 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1267-5371G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49023258 | ||||||
chr4:49023566
|
G | A | 1 | a0002c0002t0001g0107 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1267-5063G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49023566 | ||||||
chr4:49023704
|
C | T | 9 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(6): Show | 9 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1267-4925C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49023704 | ||||||
chr4:49023951
|
C | A | 8 | a0002c0002t0001g0087a0002c0002t0001g0092a0002c0002t0001g0094others(5): Show | 8 | HG01358.hp1 HG01496.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1267-4678C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49023951 | ||||||
chr4:49024078
|
C | T | 1 | a0002c0002t0001g0053 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1267-4551C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49024078 | ||||||
chr4:49024087
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1267-4542G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49024087 | ||||||
chr4:49024195
|
A | T | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1267-4434A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49024195 | ||||||
chr4:49024270
|
A | G | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1267-4359A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49024270 | ||||||
chr4:49024359
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1267-4270C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49024359 | ||||||
chr4:49024579
|
T | A | 152 | a0001c0001t0001g0021a0001c0001t0001g0149a0001c0001t0001g0271others(149): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1267-4050T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49024579 | ||||||
chr4:49024582
|
T | A | 152 | a0001c0001t0001g0021a0001c0001t0001g0149a0001c0001t0001g0271others(149): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1267-4047T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49024582 | ||||||
chr4:49024714
|
T | A | 152 | a0001c0001t0001g0021a0001c0001t0001g0149a0001c0001t0001g0271others(149): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1267-3915T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49024714 | ||||||
chr4:49025060
|
C | A | 1 | a0001c0001t0001g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1267-3569C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025060 | ||||||
chr4:49025127
|
T | C | 1 | a0001c0001t0001g0259 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1267-3502T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025127 | ||||||
chr4:49025159
|
G | A | 2 | a0006c0008t0001g0146a0006c0008t0001g0147 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1267-3470G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025159 | ||||||
chr4:49025173
|
T | C | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1267-3456T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025173 | ||||||
chr4:49025179
|
C | T | 3 | a0002c0002t0001g0115a0003c0003t0001g0034a0003c0003t0001g0035 | 3 | HG00280.hp2 HG02965.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1267-3450C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025179 | ||||||
chr4:49025251
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1267-3378A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025251 | ||||||
chr4:49025384
|
A | G | 1 | a0002c0002t0001g0056 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1267-3245A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025384 | ||||||
chr4:49025516
|
G | A | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1267-3113G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025516 | ||||||
chr4:49025539
|
T | C | 1 | a0003c0003t0001g0085 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1267-3090T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025539 | ||||||
chr4:49025621
|
T | C | 152 | a0001c0001t0001g0021a0001c0001t0001g0149a0001c0001t0001g0271others(149): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1267-3008T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025621 | ||||||
chr4:49025698
|
G | A | 3 | a0001c0001t0004g0270a0006c0008t0001g0146a0006c0008t0001g0147 | 3 | HG01884.hp1 HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1267-2931G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025698 | ||||||
chr4:49025823
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1267-2806G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025823 | ||||||
chr4:49025936
|
G | T | 1 | a0001c0001t0001g0269 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1267-2693G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025936 | ||||||
chr4:49025968
|
T | C | 1 | a0003c0003t0001g0123 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1267-2661T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025968 | ||||||
chr4:49025989
|
C | T | 144 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0008others(141): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1267-2640C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025989 | ||||||
chr4:49025999
|
A | T | 1 | a0002c0002t0001g0109 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1267-2630A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025999 | ||||||
chr4:49026053
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1267-2576C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49026053 | ||||||
chr4:49026100
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1267-2529T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49026100 | ||||||
chr4:49026120
|
A | G | 152 | a0001c0001t0001g0021a0001c0001t0001g0149a0001c0001t0001g0271others(149): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1267-2509A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49026120 | ||||||
chr4:49026202
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1267-2427C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49026202 | ||||||
chr4:49026632
|
C | T | 7 | a0001c0001t0001g0261a0001c0001t0001g0271a0001c0001t0001g0272others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1267-1997C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49026632 | ||||||
chr4:49027121
|
C | T | 4 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0254others(1): Show | 4 | HG02622.hp2 HG03516.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1267-1508C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49027121 | ||||||
chr4:49027328
|
T | C | 1 | a0002c0002t0001g0070 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1267-1301T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49027328 | ||||||
chr4:49027406
|
G | A | 4 | a0003c0003t0001g0005a0003c0003t0001g0043a0003c0003t0001g0044others(1): Show | 5 | HG00735.hp1 HG01167.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1267-1223G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49027406 | ||||||
chr4:49027474
|
C | T | 2 | a0006c0008t0001g0146a0006c0008t0001g0147 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1267-1155C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49027474 | ||||||
chr4:49027552
|
A | T | 2 | a0001c0001t0001g0237a0001c0001t0001g0242 | 2 | NA19002.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1267-1077A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49027552 | ||||||
chr4:49027683
|
G | A | 1 | a0003c0003t0001g0184 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1267-946G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49027683 | ||||||
chr4:49027690
|
A | G | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1267-939A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49027690 | ||||||
chr4:49027884
|
C | T | 151 | a0001c0001t0001g0021a0001c0001t0001g0271a0001c0001t0001g0272others(148): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1267-745C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49027884 | ||||||
chr4:49027957
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1267-672C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49027957 | ||||||
chr4:49028213
|
T | A | 1 | a0002c0002t0001g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1267-416T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49028213 | ||||||
chr4:49028222
|
A | G | 2 | a0002c0002t0001g0112a0002c0002t0001g0113 | 2 | HG00280.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1267-407A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49028222 | ||||||
chr4:49028446
|
G | T | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1267-183G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49028446 | ||||||
chr4:49028566
|
G | A | 1 | a0003c0003t0001g0085 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1267-63G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49028566 | ||||||
chr4:49028854
|
G | A | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1372+120G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | chr4 | 49028854 | ||||||
chr4:49028985
|
A | G | 1 | a0003c0003t0001g0190 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1372+251A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | chr4 | 49028985 | ||||||
chr4:49029409
|
G | C | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1372+675G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | chr4 | 49029409 | ||||||
chr4:49029690
|
G | A | 1 | a0002c0002t0001g0111 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1372+956G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | chr4 | 49029690 | ||||||
chr4:49029838
|
G | A | 143 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0008others(140): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1373-987G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | chr4 | 49029838 | ||||||
chr4:49029849
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1373-976G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | chr4 | 49029849 | ||||||
chr4:49029910
|
T | C | 1 | a0003c0003t0001g0041 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1373-915T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | chr4 | 49029910 | ||||||
chr4:49030055
|
T | A | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1373-770T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | chr4 | 49030055 | ||||||
chr4:49030303
|
G | C | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1373-522G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | chr4 | 49030303 | ||||||
chr4:49030336
|
T | G | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1373-489T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | chr4 | 49030336 | ||||||
chr4:49030378
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1373-447T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | chr4 | 49030378 | ||||||
chr4:49030465
|
T | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG01167.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1373-360T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | chr4 | 49030465 | ||||||
chr4:49030806
|
CT | C | 4 | a0002c0002t0001g0062a0002c0002t0001g0090a0003c0003t0001g0001others(1): Show | 6 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1373-9delT | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr4 | 49030806 | |||||
chr4:49031197
|
C | A | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1508+237C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 11/15 | chr4 | 49031197 | ||||||
chr4:49031348
|
G | T | 1 | a0001c0001t0001g0243 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1508+388G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 11/15 | chr4 | 49031348 | ||||||
chr4:49031378
|
T | C | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1508+418T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 11/15 | chr4 | 49031378 | ||||||
chr4:49031511
|
TG | T | 146 | a0001c0001t0001g0021a0001c0001t0001g0237a0001c0001t0001g0242others(143): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1508+557delG | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 49031511 | |||||
chr4:49031525
|
G | A | 1 | a0003c0003t0001g0185 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1508+565G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 11/15 | chr4 | 49031525 | ||||||
chr4:49031854
|
C | T | 3 | a0002c0002t0001g0048a0002c0002t0001g0052a0002c0002t0001g0055 | 3 | HG03017.hp2 HG03654.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1509-712C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 11/15 | chr4 | 49031854 | ||||||
chr4:49031915
|
A | C | 1 | a0004c0004t0001g0154 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1509-651A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 11/15 | chr4 | 49031915 | ||||||
chr4:49032206
|
G | A | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1509-360G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 11/15 | chr4 | 49032206 | ||||||
chr4:49032279
|
C | T | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1509-287C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 11/15 | chr4 | 49032279 | ||||||
chr4:49032291
|
G | T | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1509-275G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 11/15 | chr4 | 49032291 | ||||||
chr4:49032538
|
G | A | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1509-28G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 11/15 | chr4 | 49032538 | ||||||
chr4:49032891
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1658+176G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49032891 | ||||||
chr4:49032915
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1658+200C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49032915 | ||||||
chr4:49032933
|
C | T | 1 | a0003c0003t0001g0026 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1658+218C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49032933 | ||||||
chr4:49033105
|
T | C | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1658+390T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49033105 | ||||||
chr4:49033204
|
A | G | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1658+489A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49033204 | ||||||
chr4:49033356
|
T | A | 1 | a0001c0001t0001g0195 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1658+641T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49033356 | ||||||
chr4:49033377
|
A | G | 1 | a0003c0003t0001g0005 | 2 | HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1658+662A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49033377 | ||||||
chr4:49033470
|
C | T | 2 | a0006c0008t0001g0146a0006c0008t0001g0147 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1658+755C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49033470 | ||||||
chr4:49033672
|
C | A | 2 | a0006c0008t0001g0146a0006c0008t0001g0147 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1658+957C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49033672 | ||||||
chr4:49033801
|
A | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0249a0001c0001t0001g0265 | 4 | HG02074.hp2 NA18956.hp2 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1658+1086A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49033801 | ||||||
chr4:49033916
|
A | G | 1 | a0002c0002t0001g0109 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1658+1201A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49033916 | ||||||
chr4:49034035
|
C | G | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1658+1320C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49034035 | ||||||
chr4:49034273
|
T | C | 144 | a0001c0001t0001g0149a0002c0002t0001g0006a0002c0002t0001g0007others(141): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1658+1558T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49034273 | ||||||
chr4:49034868
|
A | T | 2 | a0001c0001t0001g0214a0001c0001t0001g0240 | 2 | NA18943.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1658+2153A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49034868 | ||||||
chr4:49034906
|
G | T | 7 | a0004c0004t0001g0011a0004c0004t0001g0012a0004c0004t0001g0150others(4): Show | 9 | HG00738.hp2 HG01069.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1658+2191G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49034906 | ||||||
chr4:49035022
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1658+2307A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49035022 | ||||||
chr4:49035078
|
C | A | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1658+2363C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49035078 | ||||||
chr4:49035094
|
G | A | 8 | a0001c0001t0001g0219a0001c0001t0001g0226a0001c0001t0001g0227others(5): Show | 9 | HG00140.hp1 HG01175.hp1 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.1658+2379G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49035094 | ||||||
chr4:49035203
|
C | T | 1 | a0007c0006t0001g0134 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1658+2488C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49035203 | ||||||
chr4:49035571
|
T | C | 151 | a0001c0001t0001g0021a0001c0001t0001g0149a0001c0001t0001g0271others(148): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1659-2465T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49035571 | ||||||
chr4:49035634
|
C | A | 1 | a0002c0002t0001g0050 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1659-2402C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49035634 | ||||||
chr4:49035924
|
T | C | 151 | a0001c0001t0001g0021a0001c0001t0001g0149a0001c0001t0001g0271others(148): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1659-2112T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49035924 | ||||||
chr4:49036029
|
G | A | 2 | a0002c0002t0001g0112a0002c0002t0001g0113 | 2 | HG00280.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1659-2007G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49036029 | ||||||
chr4:49036039
|
C | A | 1 | a0003c0003t0001g0116 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1659-1997C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49036039 | ||||||
chr4:49036039
|
C | T | 9 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(6): Show | 9 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1659-1997C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49036039 | ||||||
chr4:49036296
|
A | C | 1 | a0001c0001t0001g0236 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1659-1740A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49036296 | ||||||
chr4:49036334
|
A | G | 7 | a0001c0001t0001g0021a0001c0001t0001g0271a0001c0001t0001g0272others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1659-1702A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49036334 | ||||||
chr4:49036851
|
G | T | 1 | a0001c0001t0001g0019 | 2 | NA18956.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1659-1185G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49036851 | ||||||
chr4:49037174
|
G | C | 1 | a0001c0001t0001g0198 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1659-862G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49037174 | ||||||
chr4:49037185
|
A | T | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1659-851A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49037185 | ||||||
chr4:49037233
|
G | A | 2 | a0006c0008t0001g0146a0006c0008t0001g0147 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1659-803G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49037233 | ||||||
chr4:49037424
|
G | A | 1 | a0002c0002t0001g0087 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1659-612G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49037424 | ||||||
chr4:49037569
|
C | CA | 152 | a0001c0001t0001g0021a0001c0001t0001g0149a0001c0001t0001g0202others(149): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1659-453dupA | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 49037569 | |||||
chr4:49037652
|
T | A | 1 | a0001c0001t0001g0149 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1659-384T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49037652 | ||||||
chr4:49037791
|
T | C | 3 | a0002c0002t0001g0008a0002c0002t0001g0077a0002c0002t0001g0082 | 4 | NA18943.hp1 NA18964.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1659-245T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49037791 | ||||||
chr4:49037913
|
C | T | 1 | a0006c0008t0001g0146 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1659-123C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49037913 | ||||||
chr4:49037941
|
C | G | 5 | a0003c0003t0001g0001a0003c0003t0001g0024a0003c0003t0001g0027others(2): Show | 7 | HG01070.hp1 HG01071.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.1659-95C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49037941 | ||||||
chr4:49037942
|
T | C | 4 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(1): Show | 4 | HG02486.hp1 HG03486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1659-94T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49037942 | ||||||
chr4:49037958
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1659-78T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49037958 | ||||||
chr4:49038008
|
T | C | 2 | a0003c0003t0001g0014a0003c0003t0001g0186 | 3 | NA18946.hp2 NA18990.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1659-28T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49038008 | ||||||
chr4:49038647
|
T | G | 150 | a0001c0001t0001g0021a0001c0001t0001g0271a0001c0001t0001g0272others(147): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.1803+467T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49038647 | ||||||
chr4:49038914
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1803+734C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49038914 | ||||||
chr4:49038940
|
C | A | 1 | a0001c0001t0001g0193 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1803+760C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49038940 | ||||||
chr4:49039051
|
C | G | 2 | a0001c0001t0001g0214a0001c0001t0001g0240 | 2 | NA18943.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1803+871C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039051 | ||||||
chr4:49039076
|
A | T | 1 | a0002c0002t0001g0098 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1803+896A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039076 | ||||||
chr4:49039077
|
TTAAA | T | 143 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0008others(140): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1803+917_1803+920d others(6): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039077 | |||||
chr4:49039082
|
T | A | 1 | a0003c0003t0001g0085 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1803+902T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039082 | ||||||
chr4:49039083
|
AAATAAAT others(8): Show |
A | 2 | a0001c0001t0001g0267a0001c0007t0001g0015 | 3 | HG03831.hp2 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1803+918_1803+932d others(17): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039083 | |||||
chr4:49039186
|
C | A | 2 | a0002c0002t0001g0088a0002c0002t0001g0089 | 2 | HG01433.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1803+1006C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039186 | ||||||
chr4:49039306
|
G | GAGATATA others(15): Show |
2 | a0006c0008t0001g0146a0006c0008t0001g0147 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1803+1127_1803+112 others(26): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | |||||
chr4:49039306
|
G | GATATATA others(1): Show |
3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0229 | 3 | HG06807.hp1 NA18968.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1803+1146_1803+115 others(12): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | |||||
chr4:49039306
|
G | GATATATA others(7): Show |
2 | a0001c0001t0001g0170a0001c0001t0001g0225 | 2 | HG03041.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1803+1140_1803+115 others(18): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | |||||
chr4:49039306
|
G | GATATATA others(9): Show |
1 | a0001c0001t0001g0197 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1803+1138_1803+115 others(20): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | |||||
chr4:49039306
|
G | GATATATA others(11): Show |
9 | a0001c0001t0001g0016a0001c0001t0001g0219a0001c0001t0001g0224others(6): Show | 10 | HG00140.hp1 HG00438.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.1803+1136_1803+115 others(22): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | |||||
chr4:49039306
|
G | GATATATA others(13): Show |
9 | a0001c0001t0001g0017a0001c0001t0001g0174a0001c0001t0001g0192others(6): Show | 10 | HG00639.hp1 HG01074.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1803+1134_1803+115 others(24): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | |||||
chr4:49039306
|
G | GATATATA others(15): Show |
21 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0019others(18): Show | 25 | HG01175.hp1 HG01975.hp1 HG01981.hp1 others(22): Show |
intron_variant | MODIFIER | c.1803+1132_1803+115 others(26): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | |||||
chr4:49039306
|
G | GATATATA others(17): Show |
20 | a0001c0001t0001g0162a0001c0001t0001g0171a0001c0001t0001g0173others(17): Show | 20 | HG00423.hp1 HG01167.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1803+1130_1803+115 others(28): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | |||||
chr4:49039306
|
G | GATATATA others(19): Show |
20 | a0001c0001t0001g0040a0001c0001t0001g0136a0001c0001t0001g0149others(17): Show | 21 | HG00609.hp2 HG01099.hp1 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1803+1128_1803+115 others(30): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | |||||
chr4:49039306
|
G | GATATATA others(21): Show |
11 | a0001c0001t0001g0022a0001c0001t0001g0130a0001c0001t0001g0160others(8): Show | 11 | HG00558.hp1 HG02258.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(32): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | |||||
chr4:49039306
|
G | GATATATA others(23): Show |
3 | a0001c0001t0001g0235a0001c0001t0001g0262a0001c0001t0001g0266 | 3 | HG02132.hp1 HG02622.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(34): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | |||||
chr4:49039306
|
G | GATATATA others(25): Show |
2 | a0001c0001t0001g0193a0001c0001t0001g0251 | 2 | HG01255.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(36): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | |||||
chr4:49039306
|
G | GATATATA others(27): Show |
2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG02615.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(38): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | |||||
chr4:49039306
|
G | GATATATA others(31): Show |
1 | a0001c0001t0001g0194 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(42): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | |||||
chr4:49039306
|
G | GATATATA others(35): Show |
1 | a0001c0001t0001g0177 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(46): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | |||||
chr4:49039306
|
GATATATA others(7): Show |
G | 1 | a0001c0001t0001g0215 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1803+1140_1803+115 others(18): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | |||||
chr4:49039311
|
A | ATATATAT others(29): Show |
1 | a0007c0006t0001g0144 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(40): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039311 | |||||
chr4:49039311
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0269 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(32): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039311 | |||||
chr4:49039320
|
T | G | 1 | a0003c0003t0001g0131 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1803+1140T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039320 | ||||||
chr4:49039320
|
T | TATATATA others(7): Show |
1 | a0002c0002t0001g0052 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1803+1151_1803+115 others(18): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | |||||
chr4:49039320
|
T | TATATATA others(9): Show |
3 | a0002c0002t0001g0078a0003c0003t0001g0118a0003c0003t0001g0119 | 3 | HG02004.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1803+1143_1803+115 others(20): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | |||||
chr4:49039320
|
T | TATATATA others(11): Show |
2 | a0002c0002t0001g0099a0003c0003t0001g0190 | 2 | HG03209.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(22): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | |||||
chr4:49039320
|
T | TATATATA others(13): Show |
1 | a0002c0002t0001g0117 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(24): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | |||||
chr4:49039320
|
T | TATATATA others(17): Show |
1 | a0003c0003t0001g0140 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(28): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | |||||
chr4:49039320
|
T | TATATATA others(25): Show |
11 | a0002c0002t0001g0094a0003c0003t0001g0004a0003c0003t0001g0027others(8): Show | 12 | HG00735.hp1 HG01167.hp2 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(36): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | |||||
chr4:49039320
|
T | TATATATA others(27): Show |
16 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0001g0087others(13): Show | 16 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(13): Show |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(38): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | |||||
chr4:49039320
|
T | TATATATA others(33): Show |
1 | a0002c0002t0001g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(44): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | |||||
chr4:49039320
|
T | TATATATA others(29): Show |
13 | a0002c0002t0001g0008a0002c0002t0001g0075a0002c0002t0001g0081others(10): Show | 15 | HG00609.hp1 HG00741.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(40): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | |||||
chr4:49039320
|
T | TATATATA others(31): Show |
20 | a0002c0002t0001g0070a0002c0002t0001g0073a0002c0002t0001g0074others(17): Show | 20 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(42): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | |||||
chr4:49039320
|
T | TATATATA others(69): Show |
1 | a0003c0003t0001g0210 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(80): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | |||||
chr4:49039320
|
T | TATATATA others(33): Show |
26 | a0002c0002t0001g0050a0002c0002t0001g0051a0002c0002t0001g0053others(23): Show | 27 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(44): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | |||||
chr4:49039320
|
T | TATATATA others(65): Show |
1 | a0003c0003t0001g0032 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(76): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | |||||
chr4:49039320
|
T | TATATATA others(35): Show |
29 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0009others(26): Show | 33 | HG00140.hp2 HG00741.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(46): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | |||||
chr4:49039320
|
T | TATATATA others(37): Show |
9 | a0002c0002t0001g0061a0002c0002t0001g0062a0002c0002t0001g0067others(6): Show | 10 | HG01069.hp1 HG01071.hp2 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(48): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | |||||
chr4:49039320
|
T | TATATATA others(39): Show |
2 | a0002c0002t0001g0060a0002c0002t0001g0105 | 2 | HG01192.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(50): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | |||||
chr4:49039320
|
T | TATATATA others(108): Show |
1 | a0001c0001t0001g0271 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(119): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | |||||
chr4:49039320
|
T | TATATATA others(158): Show |
1 | a0001c0001t0001g0273 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(169): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | |||||
chr4:49039322
|
T | A | 1 | a0001c0001t0001g0272 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1803+1142T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039322 | ||||||
chr4:49039322
|
T | TATATATA others(21): Show |
1 | a0004c0004t0001g0155 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1803+1151_1803+115 others(32): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039322 | |||||
chr4:49039322
|
T | TATATATA others(59): Show |
1 | a0003c0003t0001g0141 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(70): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039322 | |||||
chr4:49039322
|
T | TATATATA others(43): Show |
1 | a0004c0004t0001g0150 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(54): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039322 | |||||
chr4:49039322
|
T | TATATATA others(45): Show |
2 | a0001c0001t0001g0208a0004c0004t0001g0151 | 2 | HG03195.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(56): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039322 | |||||
chr4:49039322
|
T | TATATATA others(47): Show |
1 | a0004c0004t0001g0152 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(58): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039322 | |||||
chr4:49039322
|
T | TATATATA others(49): Show |
3 | a0004c0004t0001g0011a0004c0004t0001g0012a0004c0004t0001g0154 | 5 | HG00738.hp2 HG01069.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(60): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039322 | |||||
chr4:49039322
|
T | TATATATA others(41): Show |
1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(52): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039322 | |||||
chr4:49039332
|
T | TATATATA others(17): Show |
1 | a0003c0003t0001g0001 | 3 | HG01070.hp1 HG01071.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(28): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039332 | |||||
chr4:49039332
|
T | TATATATA others(19): Show |
1 | a0003c0003t0001g0024 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(30): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039332 | |||||
chr4:49039332
|
T | TATATATA others(19): Show |
1 | a0001c0001t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(30): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039332 | |||||
chr4:49039332
|
T | TATATATA others(21): Show |
1 | a0001c0001t0001g0253 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(32): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039332 | |||||
chr4:49039332
|
T | TATATATA others(23): Show |
1 | a0003c0003t0001g0058 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(34): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039332 | |||||
chr4:49039333
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(27): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039333 | ||||||
chr4:49039334
|
C | A | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1803+1154C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039334 | ||||||
chr4:49039334
|
C | T | 3 | a0003c0003t0001g0001a0003c0003t0001g0024a0003c0003t0001g0058 | 5 | HG01070.hp1 HG01071.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1803+1154C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039334 | ||||||
chr4:49039337
|
A | ATATATAT others(93): Show |
1 | a0001c0001t0001g0272 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1803+1158_1803+115 others(104): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039337 | |||||
chr4:49039339
|
G | A | 2 | a0001c0001t0001g0272a0003c0003t0001g0116 | 2 | HG00639.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1803+1159G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039339 | ||||||
chr4:49039352
|
G | GAT | 8 | a0001c0001t0001g0021a0001c0001t0001g0271a0001c0001t0001g0272others(5): Show | 8 | HG00639.hp1 HG01884.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1803+1182_1803+118 others(6): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039352 | |||||
chr4:49039369
|
G | A | 1 | a0003c0003t0001g0141 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1803+1189G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039369 | ||||||
chr4:49039382
|
G | GAT | 125 | a0001c0001t0001g0021a0001c0001t0001g0271a0001c0001t0001g0272others(122): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.1803+1212_1803+121 others(6): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039382 | |||||
chr4:49039431
|
T | TTA | 7 | a0001c0001t0001g0233a0001c0001t0001g0246a0001c0001t0001g0266others(4): Show | 7 | HG02132.hp1 HG02258.hp2 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.1803+1268_1803+126 others(6): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039431 | |||||
chr4:49039431
|
T | TTATA | 4 | a0001c0001t0001g0021a0001c0001t0001g0168a0006c0008t0001g0146others(1): Show | 4 | HG01884.hp1 HG02615.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1803+1266_1803+126 others(8): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039431 | |||||
chr4:49039448
|
T | C | 6 | a0002c0002t0001g0084a0002c0002t0001g0088a0002c0002t0001g0089others(3): Show | 6 | HG01070.hp2 HG01433.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1803+1268T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039448 | ||||||
chr4:49039735
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1803+1555G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039735 | ||||||
chr4:49039742
|
T | A | 1 | a0003c0003t0001g0058 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1803+1562T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039742 | ||||||
chr4:49039743
|
T | A | 143 | a0001c0001t0004g0270a0002c0002t0001g0006a0002c0002t0001g0007others(140): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1803+1563T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039743 | ||||||
chr4:49039792
|
T | C | 4 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(1): Show | 4 | HG02145.hp2 HG02486.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1803+1612T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039792 | ||||||
chr4:49040304
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1803+2124T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49040304 | ||||||
chr4:49040393
|
C | T | 5 | a0002c0002t0001g0009a0002c0002t0001g0086a0002c0002t0001g0102others(2): Show | 6 | HG00099.hp2 HG00140.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1803+2213C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49040393 | ||||||
chr4:49040913
|
T | C | 1 | a0001c0001t0001g0272 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1803+2733T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49040913 | ||||||
chr4:49040985
|
A | C | 1 | a0001c0001t0001g0169 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1803+2805A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49040985 | ||||||
chr4:49041055
|
A | G | 152 | a0001c0001t0001g0021a0001c0001t0001g0040a0001c0001t0001g0200others(149): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1803+2875A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49041055 | ||||||
chr4:49041088
|
C | G | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1803+2908C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49041088 | ||||||
chr4:49041183
|
T | G | 1 | a0002c0002t0001g0100 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1803+3003T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49041183 | ||||||
chr4:49041317
|
G | C | 3 | a0001c0001t0001g0160a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG02258.hp1 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1803+3137G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49041317 | ||||||
chr4:49041330
|
T | G | 1 | a0003c0003t0001g0001 | 3 | HG01070.hp1 HG01071.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1803+3150T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49041330 | ||||||
chr4:49041650
|
T | C | 1 | a0002c0002t0001g0025 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1804-3136T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49041650 | ||||||
chr4:49041729
|
A | C | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1804-3057A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49041729 | ||||||
chr4:49041770
|
T | C | 1 | a0002c0002t0001g0104 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1804-3016T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49041770 | ||||||
chr4:49041823
|
G | A | 1 | a0002c0002t0001g0051 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1804-2963G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49041823 | ||||||
chr4:49041908
|
T | C | 151 | a0001c0001t0001g0021a0001c0001t0001g0224a0001c0001t0001g0271others(148): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1804-2878T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49041908 | ||||||
chr4:49042262
|
C | T | 1 | a0003c0003t0001g0118 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1804-2524C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49042262 | ||||||
chr4:49042306
|
C | G | 1 | a0001c0001t0001g0149 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1804-2480C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49042306 | ||||||
chr4:49042311
|
A | G | 144 | a0001c0001t0001g0040a0002c0002t0001g0006a0002c0002t0001g0007others(141): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1804-2475A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49042311 | ||||||
chr4:49042335
|
C | A | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1804-2451C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49042335 | ||||||
chr4:49042481
|
T | C | 151 | a0001c0001t0001g0021a0001c0001t0001g0040a0001c0001t0001g0271others(148): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1804-2305T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49042481 | ||||||
chr4:49042548
|
T | C | 6 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0252others(3): Show | 6 | HG01243.hp1 HG02622.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1804-2238T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49042548 | ||||||
chr4:49042912
|
T | C | 1 | a0002c0002t0001g0050 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1804-1874T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49042912 | ||||||
chr4:49043007
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1804-1779C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49043007 | ||||||
chr4:49043151
|
G | A | 143 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0008others(140): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1804-1635G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49043151 | ||||||
chr4:49043219
|
C | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1804-1567C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49043219 | ||||||
chr4:49043286
|
G | A | 2 | a0002c0002t0001g0056a0002c0002t0001g0057 | 2 | NA19010.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.1804-1500G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49043286 | ||||||
chr4:49043356
|
G | A | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1804-1430G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49043356 | ||||||
chr4:49043585
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1804-1201T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49043585 | ||||||
chr4:49043764
|
C | A | 1 | a0001c0001t0001g0249 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1804-1022C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49043764 | ||||||
chr4:49043879
|
G | T | 1 | a0002c0002t0001g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1804-907G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49043879 | ||||||
chr4:49044089
|
C | A | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1804-697C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49044089 | ||||||
chr4:49044135
|
T | C | 1 | a0002c0002t0001g0106 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1804-651T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49044135 | ||||||
chr4:49044542
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1804-244C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49044542 | ||||||
chr4:49044553
|
C | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0200a0001c0001t0001g0234others(1): Show | 5 | NA18941.hp2 NA18957.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.1804-233C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49044553 | ||||||
chr4:49044592
|
G | T | 2 | a0006c0008t0001g0146a0006c0008t0001g0147 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1804-194G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49044592 | ||||||
chr4:49044658
|
T | C | 1 | a0002c0002t0001g0094 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1804-128T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49044658 | ||||||
chr4:49044739
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1804-47G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49044739 | ||||||
chr4:49044906
|
G | C | 2 | a0003c0003t0001g0027a0003c0003t0001g0028 | 2 | HG02735.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1865+59G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49044906 | ||||||
chr4:49044923
|
A | G | 1 | a0002c0002t0001g0089 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1865+76A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49044923 | ||||||
chr4:49045102
|
G | A | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1865+255G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49045102 | ||||||
chr4:49045354
|
C | T | 150 | a0001c0001t0001g0021a0001c0001t0001g0271a0001c0001t0001g0272others(147): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.1865+507C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49045354 | ||||||
chr4:49045678
|
A | C | 1 | a0003c0003t0001g0031 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1865+831A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49045678 | ||||||
chr4:49045990
|
C | T | 3 | a0001c0001t0001g0160a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG02258.hp1 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1865+1143C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49045990 | ||||||
chr4:49046031
|
T | C | 2 | a0006c0008t0001g0146a0006c0008t0001g0147 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1865+1184T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49046031 | ||||||
chr4:49046033
|
G | C | 1 | a0001c0001t0001g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1865+1186G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49046033 | ||||||
chr4:49046129
|
C | T | 3 | a0002c0002t0001g0078a0003c0003t0001g0121a0003c0003t0001g0127 | 3 | HG00741.hp1 HG01074.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1865+1282C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49046129 | ||||||
chr4:49046144
|
A | T | 4 | a0001c0001t0001g0130a0001c0001t0001g0165a0001c0001t0001g0169others(1): Show | 4 | HG03041.hp1 HG03139.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1865+1297A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49046144 | ||||||
chr4:49046308
|
CCATT | C | 146 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(143): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1865+1490_1865+149 others(8): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr4 | 49046308 | |||||
chr4:49046314
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1865+1467A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49046314 | ||||||
chr4:49046510
|
T | C | 1 | a0002c0002t0001g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1865+1663T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49046510 | ||||||
chr4:49046580
|
T | C | 1 | a0001c0001t0001g0237 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1865+1733T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49046580 | ||||||
chr4:49046688
|
G | A | 6 | a0003c0003t0001g0014a0003c0003t0001g0183a0003c0003t0001g0184others(3): Show | 7 | HG02056.hp2 HG02155.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1865+1841G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49046688 | ||||||
chr4:49046756
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1865+1909A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49046756 | ||||||
chr4:49046993
|
T | A | 170 | a0001c0001t0001g0021a0001c0001t0001g0130a0001c0001t0001g0160others(167): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.1865+2146T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49046993 | ||||||
chr4:49047005
|
G | A | 1 | a0007c0006t0001g0134 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1865+2158G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49047005 | ||||||
chr4:49047084
|
G | A | 143 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0008others(140): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1865+2237G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49047084 | ||||||
chr4:49047152
|
T | G | 1 | a0003c0003t0001g0028 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1865+2305T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49047152 | ||||||
chr4:49047189
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1865+2342C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49047189 | ||||||
chr4:49047285
|
A | G | 143 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0008others(140): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1865+2438A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49047285 | ||||||
chr4:49047481
|
G | T | 3 | a0001c0001t0001g0165a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG03041.hp1 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1865+2634G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49047481 | ||||||
chr4:49047507
|
G | A | 1 | a0003c0003t0001g0188 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1865+2660G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49047507 | ||||||
chr4:49047617
|
C | T | 1 | a0002c0002t0001g0054 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1865+2770C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49047617 | ||||||
chr4:49047793
|
T | C | 1 | a0008c0009t0001g0033 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1866-2901T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49047793 | ||||||
chr4:49048122
|
A | G | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | NA19062.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1866-2572A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49048122 | ||||||
chr4:49048143
|
AG | A | 4 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(1): Show | 4 | HG02258.hp2 HG03540.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1866-2549delG | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr4 | 49048143 | |||||
chr4:49048182
|
G | A | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1866-2512G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49048182 | ||||||
chr4:49048405
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1866-2289T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49048405 | ||||||
chr4:49048425
|
ATATT | A | 7 | a0001c0001t0001g0021a0001c0001t0001g0271a0001c0001t0001g0272others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1866-2261_1866-225 others(8): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr4 | 49048425 | |||||
chr4:49048665
|
G | T | 5 | a0002c0002t0001g0087a0002c0002t0001g0092a0002c0002t0001g0094others(2): Show | 5 | HG01358.hp1 HG01496.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1866-2029G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49048665 | ||||||
chr4:49048957
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1866-1737A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49048957 | ||||||
chr4:49048988
|
T | C | 1 | a0003c0003t0001g0190 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1866-1706T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49048988 | ||||||
chr4:49049108
|
G | T | 143 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0008others(140): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1866-1586G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049108 | ||||||
chr4:49049120
|
C | G | 1 | a0003c0003t0001g0046 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1866-1574C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049120 | ||||||
chr4:49049137
|
C | A | 2 | a0001c0001t0001g0165a0001c0001t0001g0170 | 2 | HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1866-1557C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049137 | ||||||
chr4:49049165
|
C | T | 7 | a0001c0001t0001g0021a0001c0001t0001g0271a0001c0001t0001g0272others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1866-1529C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049165 | ||||||
chr4:49049203
|
T | C | 1 | a0002c0002t0001g0080 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1866-1491T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049203 | ||||||
chr4:49049413
|
T | A | 1 | a0002c0002t0001g0052 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1866-1281T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049413 | ||||||
chr4:49049520
|
T | A | 1 | a0001c0001t0001g0198 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1866-1174T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049520 | ||||||
chr4:49049531
|
A | G | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1866-1163A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049531 | ||||||
chr4:49049534
|
G | A | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1866-1160G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049534 | ||||||
chr4:49049748
|
C | T | 144 | a0001c0001t0001g0272a0002c0002t0001g0006a0002c0002t0001g0007others(141): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1866-946C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049748 | ||||||
chr4:49049910
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1866-784T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049910 | ||||||
chr4:49049920
|
T | A | 1 | a0001c0001t0001g0268 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1866-774T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049920 | ||||||
chr4:49049955
|
A | T | 1 | a0002c0002t0001g0074 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1866-739A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049955 | ||||||
chr4:49050147
|
C | T | 2 | a0002c0002t0001g0143a0003c0003t0001g0031 | 2 | HG00323.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1866-547C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49050147 | ||||||
chr4:49050523
|
G | A | 1 | a0003c0003t0001g0085 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1866-171G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49050523 | ||||||
chr4:49050523
|
G | T | 1 | a0003c0003t0001g0035 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1866-171G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49050523 | ||||||
chr4:49050637
|
C | T | 2 | a0001c0001t0001g0267a0001c0007t0001g0015 | 3 | HG03831.hp2 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1866-57C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49050637 | ||||||
chr4:49050947
|
C | T | 4 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(1): Show | 4 | HG02145.hp2 HG02486.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2021+98C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49050947 | ||||||
chr4:49051195
|
C | G | 1 | a0002c0002t0001g0055 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2021+346C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49051195 | ||||||
chr4:49051370
|
C | T | 2 | a0006c0008t0001g0146a0006c0008t0001g0147 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2021+521C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49051370 | ||||||
chr4:49051505
|
G | A | 143 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0008others(140): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.2021+656G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49051505 | ||||||
chr4:49051782
|
G | A | 1 | a0004c0004t0001g0150 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2021+933G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49051782 | ||||||
chr4:49051796
|
C | T | 1 | a0003c0003t0001g0085 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2021+947C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49051796 | ||||||
chr4:49051840
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2021+991G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49051840 | ||||||
chr4:49052050
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2021+1201A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49052050 | ||||||
chr4:49052069
|
G | T | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2021+1220G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49052069 | ||||||
chr4:49052535
|
A | G | 3 | a0002c0002t0001g0064a0002c0002t0001g0075a0002c0002t0001g0079 | 3 | HG00408.hp2 HG00609.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.2021+1686A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49052535 | ||||||
chr4:49052590
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2021+1741G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49052590 | ||||||
chr4:49052663
|
T | G | 88 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0009others(85): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.2021+1814T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49052663 | ||||||
chr4:49052747
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2021+1898C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49052747 | ||||||
chr4:49053377
|
A | C | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2021+2528A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49053377 | ||||||
chr4:49053458
|
G | A | 4 | a0002c0002t0001g0099a0002c0002t0001g0100a0002c0002t0001g0108others(1): Show | 4 | HG03139.hp1 HG03195.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2021+2609G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49053458 | ||||||
chr4:49054315
|
G | C | 1 | a0001c0001t0001g0229 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2021+3466G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49054315 | ||||||
chr4:49054467
|
T | C | 4 | a0002c0002t0001g0047a0002c0002t0001g0050a0002c0002t0001g0053others(1): Show | 4 | NA18941.hp1 NA18999.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.2021+3618T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49054467 | ||||||
chr4:49054709
|
C | T | 1 | a0003c0003t0001g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2021+3860C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49054709 | ||||||
chr4:49054814
|
C | T | 1 | a0003c0003t0001g0187 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2021+3965C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49054814 | ||||||
chr4:49054864
|
A | C | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2021+4015A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49054864 | ||||||
chr4:49054918
|
G | GAT | 6 | a0001c0001t0001g0021a0001c0001t0001g0161a0001c0001t0001g0271others(3): Show | 6 | HG02145.hp2 HG02615.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2021+4085_2021+408 others(6): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr4 | 49054918 | |||||
chr4:49054994
|
T | G | 1 | a0003c0003t0002g0156 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2021+4145T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49054994 | ||||||
chr4:49055284
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2021+4435C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49055284 | ||||||
chr4:49055385
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2021+4536G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49055385 | ||||||
chr4:49055407
|
A | T | 151 | a0001c0001t0001g0021a0001c0001t0001g0171a0001c0001t0001g0271others(148): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.2021+4558A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49055407 | ||||||
chr4:49055479
|
T | A | 3 | a0001c0001t0001g0171a0006c0008t0001g0146a0006c0008t0001g0147 | 3 | HG01884.hp1 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2021+4630T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49055479 | ||||||
chr4:49055591
|
AT | A | 145 | a0001c0001t0001g0021a0001c0001t0001g0130a0001c0001t0001g0171others(142): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.2021+4757delT | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr4 | 49055591 | |||||
chr4:49055725
|
G | T | 1 | a0001c0001t0001g0225 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2021+4876G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49055725 | ||||||
chr4:49055728
|
T | A | 1 | a0001c0001t0001g0272 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2021+4879T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49055728 | ||||||
chr4:49055876
|
C | T | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2021+5027C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49055876 | ||||||
chr4:49055882
|
C | T | 2 | a0002c0002t0001g0062a0002c0002t0001g0067 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2021+5033C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49055882 | ||||||
chr4:49055895
|
T | C | 151 | a0001c0001t0001g0021a0001c0001t0001g0171a0001c0001t0001g0271others(148): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.2021+5046T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49055895 | ||||||
chr4:49055913
|
CT | C | 129 | a0001c0001t0001g0165a0001c0001t0001g0170a0001c0001t0001g0206others(126): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.2021+5078delT | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr4 | 49055913 | |||||
chr4:49055913
|
CTT | C | 16 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0059others(13): Show | 18 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.2021+5077_2021+507 others(6): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr4 | 49055913 | |||||
chr4:49055914
|
T | C | 1 | a0003c0003t0001g0005 | 2 | HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.2021+5065T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49055914 | ||||||
chr4:49055968
|
G | C | 1 | a0003c0003t0001g0058 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2021+5119G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49055968 | ||||||
chr4:49056004
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2021+5155C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056004 | ||||||
chr4:49056018
|
C | A | 271 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(268): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.2021+5169C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056018 | ||||||
chr4:49056069
|
C | T | 16 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0055others(13): Show | 18 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.2021+5220C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056069 | ||||||
chr4:49056177
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2021+5328G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056177 | ||||||
chr4:49056184
|
C | T | 4 | a0001c0001t0001g0224a0001c0001t0001g0271a0001c0001t0001g0272others(1): Show | 4 | HG00438.hp2 HG03540.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.2021+5335C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056184 | ||||||
chr4:49056230
|
A | G | 1 | a0003c0003t0001g0005 | 2 | HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.2021+5381A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056230 | ||||||
chr4:49056278
|
A | G | 143 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0008others(140): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.2021+5429A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056278 | ||||||
chr4:49056331
|
C | A | 2 | a0006c0008t0001g0146a0006c0008t0001g0147 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2022-5481C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056331 | ||||||
chr4:49056463
|
G | T | 1 | a0001c0001t0003g0220 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2022-5349G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056463 | ||||||
chr4:49056467
|
A | C | 2 | a0001c0001t0001g0269a0007c0006t0001g0144 | 2 | HG00735.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2022-5345A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056467 | ||||||
chr4:49056471
|
T | C | 1 | a0003c0003t0001g0120 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2022-5341T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056471 | ||||||
chr4:49056535
|
T | A | 1 | a0004c0004t0001g0011 | 2 | HG01069.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.2022-5277T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056535 | ||||||
chr4:49056682
|
A | G | 144 | a0001c0001t0001g0021a0002c0002t0001g0006a0002c0002t0001g0007others(141): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.2022-5130A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056682 | ||||||
chr4:49056877
|
A | C | 1 | a0002c0002t0001g0142 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2022-4935A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056877 | ||||||
chr4:49056879
|
A | G | 1 | a0003c0003t0001g0038 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2022-4933A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056879 | ||||||
chr4:49056985
|
T | C | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2022-4827T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056985 | ||||||
chr4:49056997
|
G | T | 4 | a0002c0002t0001g0088a0002c0002t0001g0089a0002c0002t0001g0090others(1): Show | 4 | HG01070.hp2 HG01433.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.2022-4815G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056997 | ||||||
chr4:49057069
|
A | T | 1 | a0003c0003t0001g0039 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2022-4743A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49057069 | ||||||
chr4:49057298
|
C | T | 5 | a0002c0002t0001g0087a0002c0002t0001g0092a0002c0002t0001g0094others(2): Show | 5 | HG01358.hp1 HG01496.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.2022-4514C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49057298 | ||||||
chr4:49057337
|
C | T | 3 | a0002c0002t0001g0078a0003c0003t0001g0121a0003c0003t0001g0127 | 3 | HG00741.hp1 HG01074.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.2022-4475C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49057337 | ||||||
chr4:49057367
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2022-4445G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49057367 | ||||||
chr4:49057480
|
C | G | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2022-4332C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49057480 | ||||||
chr4:49057590
|
C | T | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2022-4222C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49057590 | ||||||
chr4:49057677
|
T | G | 9 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(6): Show | 9 | HG02132.hp1 HG02523.hp2 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.2022-4135T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49057677 | ||||||
chr4:49058027
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2022-3785C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49058027 | ||||||
chr4:49058082
|
A | G | 1 | a0002c0002t0001g0083 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2022-3730A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49058082 | ||||||
chr4:49058136
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2022-3676A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49058136 | ||||||
chr4:49058259
|
A | G | 3 | a0001c0001t0001g0171a0006c0008t0001g0146a0006c0008t0001g0147 | 3 | HG01884.hp1 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2022-3553A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49058259 | ||||||
chr4:49058298
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2022-3514A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49058298 | ||||||
chr4:49058674
|
T | G | 4 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0234others(1): Show | 4 | HG00609.hp2 NA18941.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.2022-3138T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49058674 | ||||||
chr4:49058679
|
T | C | 1 | a0003c0003t0001g0124 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2022-3133T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49058679 | ||||||
chr4:49058884
|
T | C | 1 | a0003c0003t0001g0125 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2022-2928T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49058884 | ||||||
chr4:49059041
|
T | A | 1 | a0009c0010t0001g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2022-2771T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49059041 | ||||||
chr4:49059068
|
T | C | 1 | a0003c0003t0001g0085 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2022-2744T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49059068 | ||||||
chr4:49059124
|
T | C | 101 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(98): Show | 108 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.2022-2688T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49059124 | ||||||
chr4:49059587
|
G | A | 121 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(118): Show | 130 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2022-2225G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49059587 | ||||||
chr4:49059831
|
C | T | 54 | a0002c0002t0001g0008a0002c0002t0001g0064a0002c0002t0001g0075others(51): Show | 60 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.2022-1981C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49059831 | ||||||
chr4:49059855
|
G | T | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2022-1957G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49059855 | ||||||
chr4:49059870
|
C | T | 2 | a0002c0002t0001g0093a0002c0002t0001g0097 | 2 | HG00738.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2022-1942C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49059870 | ||||||
chr4:49059889
|
C | A | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2022-1923C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49059889 | ||||||
chr4:49060134
|
A | G | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2022-1678A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49060134 | ||||||
chr4:49060135
|
T | A | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2022-1677T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49060135 | ||||||
chr4:49060351
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2022-1461G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49060351 | ||||||
chr4:49060359
|
C | A | 1 | a0003c0003t0001g0183 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2022-1453C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49060359 | ||||||
chr4:49060792
|
A | C | 1 | a0001c0001t0001g0162 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2022-1020A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49060792 | ||||||
chr4:49060794
|
T | G | 1 | a0001c0001t0001g0169 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2022-1018T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49060794 | ||||||
chr4:49060875
|
G | A | 2 | a0003c0003t0001g0188a0003c0003t0001g0189 | 2 | HG00099.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.2022-937G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49060875 | ||||||
chr4:49060878
|
T | A | 2 | a0006c0008t0001g0146a0006c0008t0001g0147 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2022-934T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49060878 | ||||||
chr4:49060911
|
T | C | 1 | a0003c0003t0001g0124 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2022-901T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49060911 | ||||||
chr4:49061107
|
G | A | 2 | a0006c0008t0001g0146a0006c0008t0001g0147 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2022-705G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49061107 | ||||||
chr4:49061143
|
T | G | 1 | a0001c0001t0003g0220 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2022-669T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49061143 | ||||||
chr4:49061462
|
C | G | 82 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0009others(79): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.2022-350C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49061462 | ||||||
chr4:49061479
|
T | A | 2 | a0006c0008t0001g0146a0006c0008t0001g0147 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2022-333T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49061479 | ||||||
chr4:49061617
|
G | T | 1 | a0001c0001t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2022-195G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49061617 | ||||||
chr4:49061721
|
T | G | 2 | a0002c0002t0001g0098a0003c0003t0001g0191 | 2 | NA18971.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2022-91T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49061721 |