geneid | 7472 |
---|---|
ensemblid | ENSG00000105989.10 |
hgncid | 12780 |
symbol | WNT2 |
name | Wnt family member 2 |
refseq_nuc | NM_003391.3 |
refseq_prot | NP_003382.1 |
ensembl_nuc | ENST00000265441.8 |
ensembl_prot | ENSP00000265441.3 |
mane_status | MANE Select |
chr | chr7 |
start | 117275451 |
end | 117323058 |
strand | - |
ver | v1.2 |
region | chr7:117275451-117323058 |
region5000 | chr7:117270451-117328058 |
regionname0 | WNT2_chr7_117275451_117323058 |
regionname5000 | WNT2_chr7_117270451_117328058 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 360 | 313 | 76 | 58 | 127 | 12 | 38 | 97 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0002 | 0/0 | 360 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0003 | 0/0 | 360 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1083 | 307 | 74 | 56 | 126 | 11 | 38 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
c0002 | 0/0 | 1083 | 3 | 2 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
c0003 | 0/0 | 1083 | 2 | 2 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
c0004 | 0/0 | 1083 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
c0005 | 0/0 | 1083 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
c0006 | 0/0 | 1083 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
c0007 | 0/0 | 1083 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2775 | 74 | 24 | 13 | 27 | 2 | 8 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0002 | 0/0 | 2774 | 70 | 3 | 12 | 44 | 1 | 10 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0003 | 0/0 | 2774 | 67 | 2 | 9 | 47 | 1 | 8 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0004 | 0/0 | 2774 | 22 | 7 | 10 | 1 | 2 | 2 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0005 | 1/0 | 2774 | 10 | 3 | 2 | 0 | 1 | 3 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0006 | 0/0 | 2775 | 9 | 9 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0007 | 0/1 | 2775 | 6 | 0 | 4 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0008 | 0/0 | 2774 | 4 | 3 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0009 | 0/0 | 2775 | 4 | 4 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0010 | 0/0 | 2775 | 4 | 0 | 0 | 4 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0011 | 0/0 | 2775 | 4 | 1 | 1 | 0 | 0 | 2 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0012 | 0/0 | 2775 | 4 | 4 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0013 | 0/0 | 2775 | 3 | 1 | 0 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0014 | 0/0 | 2775 | 3 | 0 | 1 | 0 | 1 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0015 | 0/0 | 2775 | 3 | 2 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0016 | 0/0 | 2775 | 3 | 3 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0017 | 0/0 | 2774 | 3 | 0 | 1 | 0 | 2 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0018 | 0/0 | 2774 | 2 | 2 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0019 | 0/0 | 2775 | 2 | 0 | 1 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0020 | 0/0 | 2774 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0021 | 0/0 | 2774 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0022 | 0/0 | 2774 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0023 | 0/0 | 2775 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0024 | 0/0 | 2774 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0025 | 0/0 | 2774 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0026 | 0/0 | 2774 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0027 | 0/0 | 2775 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0028 | 0/0 | 2775 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0029 | 0/0 | 2774 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0030 | 0/0 | 2775 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0031 | 0/0 | 2775 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0032 | 0/0 | 2775 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0033 | 0/0 | 2775 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0034 | 0/0 | 2775 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0035 | 0/0 | 2775 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0036 | 0/0 | 2775 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0037 | 0/0 | 2774 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
t0038 | 0/0 | 2775 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0258 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1083 | 307 | 74 | 56 | 126 | 11 | 38 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0002 | 0/0 | 1083 | 3 | 2 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0005 | 0/0 | 1083 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0006 | 0/0 | 1083 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0007 | 0/0 | 1083 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0002c0003 | 0/0 | 1083 | 2 | 2 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0003c0004 | 0/0 | 1083 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3857 | 72 | 23 | 12 | 27 | 2 | 8 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0002 | 0/0 | 3856 | 67 | 2 | 12 | 42 | 1 | 10 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0003 | 0/0 | 3856 | 67 | 2 | 9 | 47 | 1 | 8 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0004 | 0/0 | 3856 | 21 | 7 | 10 | 1 | 1 | 2 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0005 | 1/0 | 3856 | 9 | 2 | 2 | 0 | 1 | 3 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0006 | 0/0 | 3857 | 9 | 9 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0007 | 0/1 | 3857 | 6 | 0 | 4 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0008 | 0/0 | 3856 | 4 | 3 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0009 | 0/0 | 3857 | 4 | 4 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0010 | 0/0 | 3857 | 4 | 0 | 0 | 4 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0011 | 0/0 | 3857 | 4 | 1 | 1 | 0 | 0 | 2 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0012 | 0/0 | 3857 | 4 | 4 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0013 | 0/0 | 3857 | 3 | 1 | 0 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0014 | 0/0 | 3857 | 3 | 0 | 1 | 0 | 1 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0015 | 0/0 | 3857 | 3 | 2 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0016 | 0/0 | 3857 | 3 | 3 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0017 | 0/0 | 3856 | 3 | 0 | 1 | 0 | 2 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0018 | 0/0 | 3856 | 2 | 2 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0019 | 0/0 | 3857 | 2 | 0 | 1 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0020 | 0/0 | 3856 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0021 | 0/0 | 3856 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0022 | 0/0 | 3856 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0024 | 0/0 | 3856 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0025 | 0/0 | 3856 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0026 | 0/0 | 3856 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0027 | 0/0 | 3857 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0028 | 0/0 | 3857 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0029 | 0/0 | 3856 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0030 | 0/0 | 3857 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0032 | 0/0 | 3857 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0033 | 0/0 | 3857 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0034 | 0/0 | 3857 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0035 | 0/0 | 3857 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0036 | 0/0 | 3857 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0037 | 0/0 | 3856 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0001t0038 | 0/0 | 3857 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0002t0005 | 0/0 | 3856 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0002t0023 | 0/0 | 3857 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0002t0031 | 0/0 | 3857 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0005t0002 | 0/0 | 3856 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0006t0004 | 0/0 | 3856 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0001c0007t0001 | 0/0 | 3857 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0002c0003t0001 | 0/0 | 3857 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0002c0003t0002 | 0/0 | 3856 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
a0003c0004t0002 | 0/0 | 3856 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | copy fasta | chr7 | 117270451 | 117328058 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0004g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0005g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0005g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0006g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0006g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0006g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0006g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0007g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0007g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0007g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0007g0258 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0008g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0008g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0008g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0008g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0009g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0009g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0009g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0010g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0010g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0010g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0010g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0011g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0011g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0011g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0012g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0012g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0012g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0012g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0013g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0013g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0013g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0014g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0014g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0014g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0015g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0015g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0015g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0016g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0016g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0016g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0017g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0017g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0017g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0018g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0019g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0019g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0020g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0021g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0022g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0024g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0025g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0026g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0027g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0028g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0029g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0030g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0032g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0033g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0034g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0035g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0036g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0037g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0001t0038g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0002t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0002t0023g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0002t0031g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0005t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0006t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0001c0007t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0002c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0002c0003t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
a0003c0004t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | GBR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG00099 | hp2 | a0001 | c0006 | t0004 | g0197 | EUR | GBR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG00140 | hp1 | a0001 | c0001 | t0005 | g0205 | EUR | GBR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0060 | EUR | GBR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG00323 | hp1 | a0001 | c0001 | t0014 | g0233 | EUR | FIN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0133 | EUR | FIN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | CHS | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | CHS | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG00558 | hp2 | a0001 | c0001 | t0027 | g0091 | EAS | CHS | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | CHS | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | CHS | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG00733 | hp2 | a0001 | c0001 | t0007 | g0247 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0042 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG00741 | hp1 | a0001 | c0001 | t0035 | g0243 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG00741 | hp2 | a0001 | c0001 | t0017 | g0055 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0103 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01069 | hp2 | a0001 | c0001 | t0007 | g0007 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0102 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01071 | hp1 | a0001 | c0001 | t0007 | g0007 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01074 | hp1 | a0001 | c0001 | t0007 | g0007 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01074 | hp2 | a0001 | c0001 | t0004 | g0226 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0114 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01109 | hp1 | a0001 | c0001 | t0014 | g0117 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01175 | hp2 | a0001 | c0001 | t0019 | g0106 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0225 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01243 | hp1 | a0001 | c0001 | t0015 | g0094 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01243 | hp2 | a0001 | c0001 | t0024 | g0260 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01255 | hp1 | a0001 | c0002 | t0031 | g0058 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01256 | hp1 | a0001 | c0001 | t0005 | g0013 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01258 | hp1 | a0001 | c0001 | t0005 | g0013 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0259 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0221 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01346 | hp2 | a0001 | c0001 | t0004 | g0077 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01358 | hp2 | a0001 | c0007 | t0001 | g0154 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0252 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01517 | hp1 | a0001 | c0001 | t0017 | g0056 | EUR | IBS | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01517 | hp2 | a0001 | c0001 | t0008 | g0255 | EUR | IBS | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0217 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01891 | hp2 | a0001 | c0001 | t0018 | g0009 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01943 | hp1 | a0001 | c0001 | t0011 | g0244 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0088 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0057 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0210 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0159 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0194 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0271 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02145 | hp2 | a0001 | c0001 | t0012 | g0219 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0134 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | CDX | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | CDX | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02165 | hp1 | a0001 | c0001 | t0033 | g0075 | EAS | CDX | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02165 | hp2 | a0001 | c0001 | t0010 | g0137 | EAS | CDX | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0095 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0059 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02258 | hp2 | a0001 | c0001 | t0032 | g0262 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02280 | hp1 | a0001 | c0001 | t0012 | g0273 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0254 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0054 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02615 | hp2 | a0001 | c0001 | t0021 | g0235 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02630 | hp1 | a0001 | c0001 | t0008 | g0251 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0282 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02647 | hp1 | a0001 | c0001 | t0006 | g0264 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02647 | hp2 | a0001 | c0001 | t0015 | g0047 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02698 | hp1 | a0001 | c0001 | t0005 | g0043 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02698 | hp2 | a0001 | c0001 | t0007 | g0037 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02717 | hp2 | a0001 | c0001 | t0011 | g0250 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0246 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02738 | hp2 | a0001 | c0001 | t0014 | g0120 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0092 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0236 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02818 | hp1 | a0001 | c0001 | t0016 | g0216 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0272 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02896 | hp1 | a0001 | c0001 | t0006 | g0265 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02922 | hp2 | a0001 | c0001 | t0009 | g0218 | AFR | ESN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02965 | hp1 | a0001 | c0001 | t0028 | g0204 | AFR | ESN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02965 | hp2 | a0001 | c0001 | t0009 | g0274 | AFR | ESN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02976 | hp1 | a0001 | c0001 | t0018 | g0009 | AFR | ESN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02976 | hp2 | a0001 | c0002 | t0005 | g0249 | AFR | ESN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03017 | hp1 | a0001 | c0001 | t0005 | g0046 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0171 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0220 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03041 | hp2 | a0001 | c0001 | t0006 | g0261 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03098 | hp2 | a0001 | c0001 | t0008 | g0206 | AFR | MSL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03130 | hp1 | a0001 | c0001 | t0022 | g0074 | AFR | ESN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03130 | hp2 | a0001 | c0001 | t0025 | g0224 | AFR | ESN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03195 | hp2 | a0001 | c0001 | t0013 | g0156 | AFR | ESN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03209 | hp1 | a0001 | c0001 | t0016 | g0227 | AFR | MSL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03225 | hp1 | a0002 | c0003 | t0001 | g0026 | AFR | MSL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03225 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | MSL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03453 | hp2 | a0001 | c0001 | t0038 | g0028 | AFR | MSL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03490 | hp2 | a0001 | c0001 | t0011 | g0014 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0024 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0196 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03492 | hp1 | a0001 | c0001 | t0011 | g0014 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0024 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0279 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03579 | hp1 | a0001 | c0001 | t0015 | g0229 | AFR | MSL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03579 | hp2 | a0001 | c0002 | t0023 | g0248 | AFR | MSL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03654 | hp2 | a0001 | c0001 | t0037 | g0076 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0135 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0131 | SAS | STU | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | STU | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0267 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0126 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0127 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0253 | SAS | BEB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | BEB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0129 | SAS | BEB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | STU | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | STU | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG04184 | hp1 | a0001 | c0001 | t0029 | g0098 | SAS | BEB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG04184 | hp2 | a0001 | c0001 | t0005 | g0231 | SAS | BEB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | STU | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | STU | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18522 | hp1 | a0001 | c0001 | t0009 | g0023 | AFR | YRI | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0237 | AFR | YRI | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | CHB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | CHB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | CHB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18906 | hp1 | a0001 | c0001 | t0012 | g0215 | AFR | YRI | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18906 | hp2 | a0001 | c0001 | t0036 | g0214 | AFR | YRI | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0151 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18951 | hp2 | a0001 | c0001 | t0013 | g0172 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18963 | hp1 | a0003 | c0004 | t0002 | g0063 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18982 | hp1 | a0001 | c0001 | t0010 | g0033 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18982 | hp2 | a0001 | c0001 | t0010 | g0065 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19002 | hp2 | a0001 | c0001 | t0026 | g0112 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19006 | hp1 | a0001 | c0005 | t0002 | g0207 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19006 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19007 | hp2 | a0001 | c0001 | t0013 | g0052 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19043 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | LWK | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | LWK | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19060 | hp2 | a0001 | c0001 | t0010 | g0034 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19072 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19075 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19089 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19240 | hp1 | a0001 | c0001 | t0012 | g0281 | AFR | YRI | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | YRI | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0228 | AFR | ASW | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA20129 | hp2 | a0001 | c0001 | t0008 | g0239 | AFR | ASW | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0268 | EUR | TSI | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0256 | EUR | TSI | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA20805 | hp1 | a0001 | c0001 | t0019 | g0069 | EUR | TSI | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA20805 | hp2 | a0001 | c0001 | t0017 | g0257 | EUR | TSI | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0238 | SAS | GIH | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA20905 | hp2 | a0001 | c0001 | t0020 | g0115 | SAS | GIH | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0087 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02109 | hp2 | a0002 | c0003 | t0002 | g0027 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02486 | hp1 | a0001 | c0001 | t0034 | g0278 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02559 | hp1 | a0001 | c0001 | t0016 | g0263 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG06807 | hp1 | a0001 | c0001 | t0030 | g0269 | AFR | USA | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
HG06807 | hp2 | a0001 | c0001 | t0009 | g0023 | AFR | USA | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0230 | AFR | LWK | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | LWK | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0007 | g0258 | REF | REF | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0039 | REF | REF | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:117297789
|
C | T | 1 | a0003 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.676G>A | p.Asp226Asn | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/5 | 745/3856 | 676/1083 | 226/360 | chr7 | 117297789 | ||
chr7:117322976
|
A | C | 1 | a0002 | 2 | HG02109.hp2 HG03225.hp1 |
missense_variant | MODERATE | c.14T>G | p.Leu5Arg | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/5 | 83/3856 | 14/1083 | 5/360 | chr7 | 117322976 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:117278179
|
G | A | 1 | a0001c0005 | 1 | NA19006.hp1 | synonymous_variant | LOW | c.1059C>T | p.Asn353Asn | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 1128/3856 | 1059/1083 | 353/360 | chr7 | 117278179 | ||
chr7:117297661
|
G | A | 1 | a0001c0006 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.804C>T | p.Leu268Leu | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/5 | 873/3856 | 804/1083 | 268/360 | chr7 | 117297661 | ||
chr7:117297673
|
C | T | 1 | a0001c0002 | 3 | HG01255.hp1 HG02976.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.792G>A | p.Thr264Thr | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/5 | 861/3856 | 792/1083 | 264/360 | chr7 | 117297673 | ||
chr7:117297838
|
G | A | 1 | a0001c0007 | 1 | HG01358.hp2 | synonymous_variant | LOW | c.627C>T | p.His209His | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/5 | 696/3856 | 627/1083 | 209/360 | chr7 | 117297838 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:117275630
|
G | C | 20 | a0001c0001t0001a0001c0001t0007a0001c0001t0009others(17): Show | 112 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*2525C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 2525 | chr7 | 117275630 | |||||
chr7:117275729
|
T | C | 7 | a0001c0001t0009a0001c0001t0011a0001c0001t0012others(4): Show | 18 | HG01943.hp1 HG02145.hp2 HG02280.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2426A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 2426 | chr7 | 117275729 | |||||
chr7:117275827
|
T | G | 1 | a0001c0001t0024 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2328A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 2328 | chr7 | 117275827 | |||||
chr7:117275830
|
G | A | 3 | a0001c0001t0014a0001c0001t0019a0001c0001t0030 | 6 | HG00323.hp1 HG01109.hp1 HG01175.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2325C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 2325 | chr7 | 117275830 | |||||
chr7:117275845
|
C | A | 1 | a0001c0001t0016 | 3 | HG02559.hp1 HG02818.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2310G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 2310 | chr7 | 117275845 | |||||
chr7:117275852
|
A | G | 1 | a0001c0001t0032 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2303T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 2303 | chr7 | 117275852 | |||||
chr7:117275897
|
C | T | 1 | a0001c0001t0014 | 3 | HG00323.hp1 HG01109.hp1 HG02738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2258G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 2258 | chr7 | 117275897 | |||||
chr7:117275928
|
C | T | 1 | a0001c0001t0037 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2227G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 2227 | chr7 | 117275928 | |||||
chr7:117275958
|
A | C | 36 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(33): Show | 278 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(275): Show |
3_prime_UTR_variant | MODIFIER | c.*2197T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 2197 | chr7 | 117275958 | |||||
chr7:117276060
|
T | A | 1 | a0001c0001t0036 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2095A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 2095 | chr7 | 117276060 | |||||
chr7:117276086
|
G | A | 3 | a0001c0001t0034a0001c0001t0038a0001c0002t0023 | 3 | HG02486.hp1 HG03453.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2069C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 2069 | chr7 | 117276086 | |||||
chr7:117276174
|
A | G | 23 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(20): Show | 125 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*1981T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 1981 | chr7 | 117276174 | |||||
chr7:117276206
|
C | A | 1 | a0001c0001t0012 | 4 | HG02145.hp2 HG02280.hp1 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1949G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 1949 | chr7 | 117276206 | |||||
chr7:117276359
|
T | C | 9 | a0001c0001t0006a0001c0001t0009a0001c0001t0011others(6): Show | 32 | HG01243.hp1 HG01891.hp1 HG01943.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1796A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 1796 | chr7 | 117276359 | |||||
chr7:117276423
|
G | A | 1 | a0001c0001t0036 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1732C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 1732 | chr7 | 117276423 | |||||
chr7:117276606
|
T | C | 1 | a0001c0002t0031 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1549A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 1549 | chr7 | 117276606 | |||||
chr7:117276877
|
A | G | 1 | a0001c0001t0028 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1278T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 1278 | chr7 | 117276877 | |||||
chr7:117276959
|
T | C | 1 | a0001c0001t0029 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1196A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 1196 | chr7 | 117276959 | |||||
chr7:117277064
|
C | T | 9 | a0001c0001t0001a0001c0001t0007a0001c0001t0014others(6): Show | 88 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1091G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 1091 | chr7 | 117277064 | |||||
chr7:117277089
|
G | A | 1 | a0001c0001t0018 | 2 | HG01891.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1066C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 1066 | chr7 | 117277089 | |||||
chr7:117277186
|
C | T | 1 | a0001c0001t0030 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*969G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 969 | chr7 | 117277186 | |||||
chr7:117277191
|
C | CA | 25 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(22): Show | 130 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*963_*964insT | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 963 | chr7 | 117277191 | |||||
chr7:117277373
|
G | A | 31 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(28): Show | 194 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*782C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 782 | chr7 | 117277373 | |||||
chr7:117277613
|
A | C | 1 | a0001c0001t0026 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*542T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 542 | chr7 | 117277613 | |||||
chr7:117278006
|
G | A | 11 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(8): Show | 45 | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*149C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 149 | chr7 | 117278006 | |||||
chr7:117278031
|
C | T | 12 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(9): Show | 52 | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*124G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 124 | chr7 | 117278031 | |||||
chr7:117278070
|
C | T | 1 | a0001c0001t0020 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*85G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 85 | chr7 | 117278070 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:117278432
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.854-48G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117278432 | ||||||
chr7:117278700
|
C | T | 1 | a0001c0001t0008g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.854-316G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117278700 | ||||||
chr7:117278738
|
A | C | 107 | a0001c0001t0001g0032a0001c0001t0001g0062a0001c0001t0001g0071others(104): Show | 117 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.854-354T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117278738 | ||||||
chr7:117278777
|
C | T | 3 | a0001c0001t0002g0067a0001c0001t0003g0083a0001c0001t0026g0112 | 3 | HG00609.hp2 NA18968.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.854-393G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117278777 | ||||||
chr7:117278857
|
A | G | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(85): Show | 103 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.854-473T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117278857 | ||||||
chr7:117279046
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.854-662G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117279046 | ||||||
chr7:117279235
|
C | T | 1 | a0001c0001t0003g0131 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.854-851G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117279235 | ||||||
chr7:117279459
|
G | C | 1 | a0001c0001t0003g0035 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.854-1075C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117279459 | ||||||
chr7:117279474
|
T | C | 2 | a0001c0001t0012g0273a0001c0001t0012g0281 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.854-1090A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117279474 | ||||||
chr7:117279540
|
G | T | 2 | a0001c0001t0001g0276a0001c0001t0032g0262 | 2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.854-1156C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117279540 | ||||||
chr7:117279562
|
A | T | 1 | a0001c0001t0020g0115 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.854-1178T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117279562 | ||||||
chr7:117279599
|
A | C | 3 | a0001c0001t0002g0282a0001c0001t0008g0251a0002c0003t0002g0027 | 3 | HG02109.hp2 HG02630.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.854-1215T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117279599 | ||||||
chr7:117279676
|
C | T | 1 | a0001c0001t0003g0279 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.854-1292G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117279676 | ||||||
chr7:117279924
|
G | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(183): Show | 208 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.854-1540C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117279924 | ||||||
chr7:117279931
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.854-1547G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117279931 | ||||||
chr7:117280081
|
G | A | 2 | a0001c0001t0004g0060a0001c0001t0004g0114 | 2 | HG00140.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.854-1697C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280081 | ||||||
chr7:117280117
|
G | C | 1 | a0001c0001t0004g0077 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.854-1733C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280117 | ||||||
chr7:117280175
|
T | C | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.854-1791A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280175 | ||||||
chr7:117280193
|
C | A | 1 | a0001c0001t0001g0078 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.854-1809G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280193 | ||||||
chr7:117280295
|
A | T | 2 | a0001c0001t0011g0014a0001c0001t0035g0243 | 3 | HG00741.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.854-1911T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280295 | ||||||
chr7:117280532
|
A | G | 1 | a0001c0001t0008g0255 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.854-2148T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280532 | ||||||
chr7:117280554
|
T | C | 23 | a0001c0001t0001g0266a0001c0001t0001g0276a0001c0001t0003g0279others(20): Show | 24 | HG00741.hp2 HG01074.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.854-2170A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280554 | ||||||
chr7:117280591
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.854-2207T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280591 | ||||||
chr7:117280654
|
T | G | 103 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0053others(100): Show | 112 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.854-2270A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280654 | ||||||
chr7:117280663
|
T | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(96): Show | 113 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.854-2279A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280663 | ||||||
chr7:117280696
|
A | C | 1 | a0001c0001t0012g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.854-2312T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280696 | ||||||
chr7:117280709
|
C | T | 2 | a0001c0001t0011g0014a0001c0001t0035g0243 | 3 | HG00741.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.854-2325G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280709 | ||||||
chr7:117280798
|
T | C | 1 | a0001c0001t0007g0258 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.854-2414A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280798 | ||||||
chr7:117280828
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.854-2444G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280828 | ||||||
chr7:117280910
|
A | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(191): Show | 217 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.854-2526T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280910 | ||||||
chr7:117280916
|
T | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(191): Show | 217 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.854-2532A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280916 | ||||||
chr7:117280940
|
A | G | 1 | a0001c0001t0005g0013 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.854-2556T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280940 | ||||||
chr7:117281176
|
C | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(195): Show | 223 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.854-2792G>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117281176 | ||||||
chr7:117281243
|
GTTA | G | 3 | a0001c0001t0004g0246a0001c0001t0004g0272a0001c0001t0006g0261 | 3 | HG02723.hp1 HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.854-2862_854-2860d others(5): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117281243 | ||||||
chr7:117281282
|
G | A | 11 | a0001c0001t0002g0022a0001c0001t0002g0049a0001c0001t0002g0085others(8): Show | 14 | HG02004.hp1 HG02129.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.854-2898C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117281282 | ||||||
chr7:117281342
|
A | C | 1 | a0001c0001t0012g0281 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.854-2958T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117281342 | ||||||
chr7:117281520
|
G | A | 3 | a0001c0001t0001g0093a0001c0001t0001g0122a0001c0001t0015g0094 | 3 | HG01243.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.854-3136C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117281520 | ||||||
chr7:117281701
|
C | T | 1 | a0001c0001t0008g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.854-3317G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117281701 | ||||||
chr7:117281924
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0141 | 2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.854-3540C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117281924 | ||||||
chr7:117281935
|
G | A | 2 | a0001c0001t0017g0055a0001c0001t0017g0056 | 2 | HG00741.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.854-3551C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117281935 | ||||||
chr7:117282003
|
G | A | 2 | a0001c0001t0001g0032a0001c0001t0005g0043 | 2 | HG02698.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.854-3619C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117282003 | ||||||
chr7:117282157
|
T | C | 2 | a0001c0001t0002g0036a0001c0001t0002g0116 | 2 | NA18989.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.854-3773A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117282157 | ||||||
chr7:117282174
|
A | G | 2 | a0001c0001t0002g0080a0001c0001t0002g0081 | 2 | HG00438.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.854-3790T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117282174 | ||||||
chr7:117282263
|
A | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(93): Show | 110 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.854-3879T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117282263 | ||||||
chr7:117282400
|
GAGGAGGA others(8): Show |
G | 1 | a0001c0001t0013g0052 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.854-4031_854-4017d others(17): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117282400 | ||||||
chr7:117282415
|
A | AAAG | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(106): Show | 123 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.854-4032_854-4031i others(5): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117282415 | ||||||
chr7:117282448
|
A | G | 1 | a0001c0001t0017g0055 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.854-4064T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117282448 | ||||||
chr7:117282685
|
C | A | 4 | a0001c0001t0008g0251a0001c0001t0017g0055a0001c0001t0017g0056others(1): Show | 4 | HG00741.hp2 HG01517.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.854-4301G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117282685 | ||||||
chr7:117282888
|
T | G | 1 | a0001c0001t0015g0229 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.854-4504A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117282888 | ||||||
chr7:117282997
|
G | A | 1 | a0001c0001t0012g0281 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.854-4613C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117282997 | ||||||
chr7:117283129
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.854-4745T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117283129 | ||||||
chr7:117283420
|
G | A | 2 | a0001c0001t0001g0266a0001c0001t0002g0282 | 2 | HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.854-5036C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117283420 | ||||||
chr7:117283508
|
T | A | 1 | a0001c0001t0038g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.854-5124A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117283508 | ||||||
chr7:117283952
|
G | T | 1 | a0001c0001t0001g0072 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.854-5568C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117283952 | ||||||
chr7:117284023
|
AG | A | 5 | a0001c0001t0004g0225a0001c0001t0004g0226a0001c0001t0006g0264others(2): Show | 5 | HG01074.hp2 HG01192.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.854-5640delC | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117284023 | ||||||
chr7:117284155
|
C | T | 2 | a0001c0001t0003g0134a0001c0001t0003g0210 | 2 | HG01975.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.854-5771G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117284155 | ||||||
chr7:117284199
|
G | C | 2 | a0001c0001t0002g0128a0001c0001t0002g0140 | 2 | HG00642.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.854-5815C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117284199 | ||||||
chr7:117284619
|
C | G | 2 | a0001c0001t0001g0266a0001c0001t0002g0282 | 2 | HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.854-6235G>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117284619 | ||||||
chr7:117284635
|
T | C | 1 | a0001c0001t0028g0204 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.854-6251A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117284635 | ||||||
chr7:117285059
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.854-6675G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117285059 | ||||||
chr7:117285412
|
C | T | 2 | a0001c0001t0002g0238a0001c0001t0005g0231 | 2 | HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.854-7028G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117285412 | ||||||
chr7:117285424
|
A | C | 2 | a0001c0001t0001g0266a0001c0001t0002g0282 | 2 | HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.854-7040T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117285424 | ||||||
chr7:117285462
|
T | C | 1 | a0001c0001t0001g0110 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.854-7078A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117285462 | ||||||
chr7:117285490
|
C | G | 1 | a0001c0001t0009g0274 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.854-7106G>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117285490 | ||||||
chr7:117285548
|
A | T | 2 | a0001c0001t0013g0052a0001c0001t0015g0047 | 2 | HG02647.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.854-7164T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117285548 | ||||||
chr7:117286093
|
G | T | 2 | a0001c0001t0001g0041a0001c0001t0002g0008 | 3 | HG03239.hp2 HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.854-7709C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117286093 | ||||||
chr7:117286098
|
G | A | 2 | a0001c0001t0018g0009a0002c0003t0001g0026 | 3 | HG01891.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.854-7714C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117286098 | ||||||
chr7:117286359
|
C | T | 1 | a0001c0001t0015g0047 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.854-7975G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117286359 | ||||||
chr7:117286578
|
C | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(107): Show | 124 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.854-8194G>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117286578 | ||||||
chr7:117286770
|
A | AAAGACAA others(13): Show |
94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(91): Show | 108 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.854-8406_854-8387d others(22): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117286770 | ||||||
chr7:117286817
|
G | A | 2 | a0001c0001t0004g0059a0001c0001t0005g0236 | 2 | HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.854-8433C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117286817 | ||||||
chr7:117287119
|
C | T | 2 | a0001c0001t0018g0009a0002c0003t0001g0026 | 3 | HG01891.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.854-8735G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117287119 | ||||||
chr7:117287138
|
T | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(107): Show | 124 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.854-8754A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117287138 | ||||||
chr7:117287192
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.854-8808G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117287192 | ||||||
chr7:117287206
|
G | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(93): Show | 110 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.854-8822C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117287206 | ||||||
chr7:117287306
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(91): Show | 108 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.854-8922G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117287306 | ||||||
chr7:117287458
|
A | G | 1 | a0001c0001t0002g0181 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.854-9074T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117287458 | ||||||
chr7:117287493
|
C | G | 2 | a0001c0001t0008g0251a0002c0003t0002g0027 | 2 | HG02109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.854-9109G>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117287493 | ||||||
chr7:117287506
|
T | A | 2 | a0001c0001t0001g0266a0001c0001t0002g0282 | 2 | HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.854-9122A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117287506 | ||||||
chr7:117287533
|
A | G | 6 | a0001c0001t0002g0067a0001c0001t0002g0082a0001c0001t0002g0188others(3): Show | 6 | HG00609.hp2 NA18968.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.854-9149T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117287533 | ||||||
chr7:117287598
|
GTCTTATG others(6): Show |
G | 6 | a0001c0001t0006g0220a0001c0001t0015g0229a0001c0001t0016g0216others(3): Show | 6 | HG02258.hp2 HG02559.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.854-9227_854-9215d others(15): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117287598 | ||||||
chr7:117287903
|
G | A | 2 | a0001c0001t0003g0024a0001c0001t0003g0253 | 3 | HG03491.hp1 HG03492.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.854-9519C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117287903 | ||||||
chr7:117287918
|
G | A | 1 | a0001c0001t0002g0128 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.854-9534C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117287918 | ||||||
chr7:117288143
|
A | G | 1 | a0001c0001t0003g0213 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.853+9469T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117288143 | ||||||
chr7:117288267
|
T | A | 1 | a0001c0001t0003g0164 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.853+9345A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117288267 | ||||||
chr7:117288317
|
T | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(101): Show | 118 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.853+9295A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117288317 | ||||||
chr7:117288360
|
T | C | 1 | a0001c0001t0032g0262 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.853+9252A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117288360 | ||||||
chr7:117288570
|
A | G | 2 | a0001c0001t0002g0267a0001c0001t0020g0115 | 2 | HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.853+9042T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117288570 | ||||||
chr7:117289011
|
G | A | 74 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0053others(71): Show | 82 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.853+8601C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289011 | ||||||
chr7:117289051
|
C | CT | 96 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0062others(93): Show | 104 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.853+8560dupA | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289051 | ||||||
chr7:117289051
|
C | CTT | 23 | a0001c0001t0002g0124a0001c0001t0002g0140a0001c0001t0002g0177others(20): Show | 24 | HG00323.hp2 HG01123.hp1 HG02129.hp2 others(21): Show |
intron_variant | MODIFIER | c.853+8559_853+8560d others(4): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289051 | ||||||
chr7:117289198
|
C | T | 1 | a0001c0001t0004g0054 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.853+8414G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289198 | ||||||
chr7:117289279
|
T | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(109): Show | 126 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.853+8333A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289279 | ||||||
chr7:117289329
|
A | G | 1 | a0001c0001t0003g0164 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.853+8283T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289329 | ||||||
chr7:117289415
|
T | A | 2 | a0001c0001t0001g0266a0001c0001t0002g0282 | 2 | HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.853+8197A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289415 | ||||||
chr7:117289432
|
C | A | 1 | a0001c0001t0036g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.853+8180G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289432 | ||||||
chr7:117289440
|
T | C | 2 | a0001c0001t0001g0266a0001c0001t0002g0282 | 2 | HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.853+8172A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289440 | ||||||
chr7:117289477
|
G | A | 1 | a0001c0001t0002g0238 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.853+8135C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289477 | ||||||
chr7:117289487
|
A | T | 2 | a0001c0001t0008g0251a0002c0003t0002g0027 | 2 | HG02109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.853+8125T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289487 | ||||||
chr7:117289719
|
C | A | 11 | a0001c0001t0002g0022a0001c0001t0002g0049a0001c0001t0002g0085others(8): Show | 14 | HG02004.hp1 HG02129.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.853+7893G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289719 | ||||||
chr7:117289720
|
G | A | 2 | a0001c0001t0001g0266a0001c0001t0002g0282 | 2 | HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.853+7892C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289720 | ||||||
chr7:117289788
|
A | G | 2 | a0001c0001t0011g0014a0001c0001t0035g0243 | 3 | HG00741.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.853+7824T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289788 | ||||||
chr7:117290075
|
G | T | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.853+7537C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117290075 | ||||||
chr7:117290188
|
G | A | 11 | a0001c0001t0001g0277a0001c0001t0003g0279a0001c0001t0004g0095others(8): Show | 11 | HG00741.hp2 HG01433.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.853+7424C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117290188 | ||||||
chr7:117290335
|
A | G | 8 | a0001c0001t0001g0266a0001c0001t0002g0282a0001c0001t0006g0220others(5): Show | 8 | HG01496.hp2 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.853+7277T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117290335 | ||||||
chr7:117290606
|
T | G | 2 | a0001c0001t0002g0086a0001c0001t0002g0192 | 2 | HG02004.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.853+7006A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117290606 | ||||||
chr7:117290841
|
T | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(103): Show | 120 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.853+6771A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117290841 | ||||||
chr7:117290878
|
C | A | 2 | a0001c0001t0018g0009a0002c0003t0001g0026 | 3 | HG01891.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.853+6734G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117290878 | ||||||
chr7:117290908
|
A | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(108): Show | 125 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.853+6704T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117290908 | ||||||
chr7:117291045
|
T | C | 6 | a0001c0001t0003g0279a0001c0001t0004g0095a0001c0001t0004g0237others(3): Show | 6 | HG02257.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.853+6567A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117291045 | ||||||
chr7:117291076
|
G | C | 1 | a0001c0001t0004g0237 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.853+6536C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117291076 | ||||||
chr7:117291269
|
G | A | 3 | a0001c0001t0007g0007a0001c0001t0007g0247a0001c0001t0007g0258 | 5 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.853+6343C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117291269 | ||||||
chr7:117291516
|
T | A | 1 | a0001c0001t0003g0129 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.853+6096A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117291516 | ||||||
chr7:117291654
|
C | T | 1 | a0001c0001t0002g0267 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.853+5958G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117291654 | ||||||
chr7:117291939
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.853+5673C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117291939 | ||||||
chr7:117291953
|
T | A | 1 | a0001c0001t0003g0020 | 2 | NA18970.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.853+5659A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117291953 | ||||||
chr7:117291975
|
T | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(196): Show | 222 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.853+5637A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117291975 | ||||||
chr7:117292020
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.853+5592C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292020 | ||||||
chr7:117292029
|
G | A | 1 | a0001c0001t0008g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.853+5583C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292029 | ||||||
chr7:117292114
|
G | A | 3 | a0001c0001t0001g0280a0001c0001t0028g0204a0001c0001t0034g0278 | 3 | HG02486.hp1 HG02965.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.853+5498C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292114 | ||||||
chr7:117292132
|
G | C | 1 | a0001c0001t0003g0185 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.853+5480C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292132 | ||||||
chr7:117292141
|
T | C | 3 | a0001c0001t0006g0005a0001c0001t0006g0217a0001c0001t0013g0156 | 5 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.853+5471A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292141 | ||||||
chr7:117292270
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.853+5342T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292270 | ||||||
chr7:117292293
|
T | TCA | 11 | a0001c0001t0001g0268a0001c0001t0001g0280a0001c0001t0003g0150others(8): Show | 11 | HG02258.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.853+5317_853+5318d others(4): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292293 | ||||||
chr7:117292293
|
T | TCACA | 6 | a0001c0001t0003g0279a0001c0001t0004g0095a0001c0001t0004g0237others(3): Show | 6 | HG02257.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.853+5315_853+5318d others(6): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292293 | ||||||
chr7:117292480
|
A | G | 73 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0053others(70): Show | 81 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.853+5132T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292480 | ||||||
chr7:117292493
|
C | A | 1 | a0001c0001t0036g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.853+5119G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292493 | ||||||
chr7:117292501
|
C | T | 1 | a0001c0001t0003g0066 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.853+5111G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292501 | ||||||
chr7:117292503
|
G | T | 1 | a0001c0001t0003g0066 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.853+5109C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292503 | ||||||
chr7:117292731
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.853+4881C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292731 | ||||||
chr7:117292786
|
G | A | 1 | a0002c0003t0002g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.853+4826C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292786 | ||||||
chr7:117292803
|
A | T | 1 | a0001c0001t0005g0013 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.853+4809T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292803 | ||||||
chr7:117292864
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.853+4748A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292864 | ||||||
chr7:117293078
|
T | C | 1 | a0001c0001t0013g0052 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.853+4534A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117293078 | ||||||
chr7:117293130
|
A | T | 15 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0051others(12): Show | 18 | HG01243.hp1 HG01433.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.853+4482T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117293130 | ||||||
chr7:117293210
|
GA | G | 86 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0053others(83): Show | 95 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.853+4401delT | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117293210 | ||||||
chr7:117293519
|
G | C | 1 | a0001c0001t0003g0149 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.853+4093C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117293519 | ||||||
chr7:117293596
|
A | G | 3 | a0001c0001t0012g0215a0001c0001t0012g0219a0001c0001t0036g0214 | 3 | HG02145.hp2 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.853+4016T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117293596 | ||||||
chr7:117293674
|
T | G | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.853+3938A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117293674 | ||||||
chr7:117293752
|
G | A | 4 | a0001c0001t0008g0251a0001c0001t0017g0055a0001c0001t0017g0056others(1): Show | 4 | HG00741.hp2 HG01517.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.853+3860C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117293752 | ||||||
chr7:117293759
|
G | A | 1 | a0001c0001t0002g0232 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.853+3853C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117293759 | ||||||
chr7:117293846
|
T | C | 2 | a0001c0001t0003g0003a0001c0001t0003g0100 | 4 | HG02129.hp1 HG02132.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.853+3766A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117293846 | ||||||
chr7:117294110
|
G | C | 1 | a0001c0001t0002g0180 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.853+3502C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117294110 | ||||||
chr7:117294112
|
T | C | 2 | a0001c0001t0002g0211a0001c0001t0002g0212 | 2 | NA18957.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.853+3500A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117294112 | ||||||
chr7:117294146
|
G | A | 86 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0053others(83): Show | 95 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.853+3466C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117294146 | ||||||
chr7:117294328
|
A | G | 2 | a0001c0001t0006g0264a0001c0001t0006g0265 | 2 | HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.853+3284T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117294328 | ||||||
chr7:117294415
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0002g0008 | 3 | HG03239.hp2 HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.853+3197T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117294415 | ||||||
chr7:117294593
|
TA | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(186): Show | 212 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.853+3018delT | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117294593 | ||||||
chr7:117294593
|
TAA | T | 11 | a0001c0001t0003g0064a0001c0001t0003g0159a0001c0001t0003g0160others(8): Show | 11 | HG00741.hp2 HG01517.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.853+3017_853+3018d others(4): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117294593 | ||||||
chr7:117294667
|
T | A | 2 | a0001c0001t0001g0139a0001c0001t0003g0138 | 2 | NA18963.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.853+2945A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117294667 | ||||||
chr7:117294737
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.853+2875G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117294737 | ||||||
chr7:117294758
|
G | A | 7 | a0001c0001t0004g0225a0001c0001t0004g0226a0001c0001t0006g0264others(4): Show | 8 | HG01074.hp2 HG01192.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.853+2854C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117294758 | ||||||
chr7:117294783
|
A | G | 3 | a0001c0001t0003g0187a0001c0001t0003g0201a0001c0001t0003g0202 | 3 | NA18954.hp1 NA18972.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.853+2829T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117294783 | ||||||
chr7:117294945
|
C | A | 2 | a0001c0001t0004g0230a0001c0001t0004g0252 | 2 | HG01433.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.853+2667G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117294945 | ||||||
chr7:117295024
|
G | T | 1 | a0001c0001t0025g0224 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.853+2588C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117295024 | ||||||
chr7:117295134
|
T | C | 6 | a0001c0001t0003g0279a0001c0001t0004g0095a0001c0001t0004g0237others(3): Show | 6 | HG02257.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.853+2478A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117295134 | ||||||
chr7:117295144
|
C | T | 1 | a0001c0001t0003g0175 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.853+2468G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117295144 | ||||||
chr7:117295149
|
CAAGAT | C | 85 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0053others(82): Show | 94 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.853+2458_853+2462d others(7): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117295149 | ||||||
chr7:117295150
|
A | G | 1 | a0001c0001t0003g0175 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.853+2462T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117295150 | ||||||
chr7:117295154
|
T | C | 1 | a0001c0001t0003g0175 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.853+2458A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117295154 | ||||||
chr7:117295198
|
T | G | 5 | a0001c0001t0004g0095a0001c0001t0004g0237a0001c0001t0005g0236others(2): Show | 5 | HG02257.hp1 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.853+2414A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117295198 | ||||||
chr7:117295403
|
A | G | 1 | a0001c0001t0003g0163 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.853+2209T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117295403 | ||||||
chr7:117295424
|
G | A | 86 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0053others(83): Show | 95 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.853+2188C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117295424 | ||||||
chr7:117295491
|
TA | T | 86 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0053others(83): Show | 95 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.853+2120delT | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117295491 | ||||||
chr7:117295509
|
A | G | 86 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0053others(83): Show | 95 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.853+2103T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117295509 | ||||||
chr7:117295746
|
G | A | 1 | a0001c0001t0002g0275 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.853+1866C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117295746 | ||||||
chr7:117296162
|
A | C | 1 | a0001c0001t0002g0126 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.853+1450T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117296162 | ||||||
chr7:117296201
|
G | A | 3 | a0001c0001t0003g0187a0001c0001t0003g0201a0001c0001t0003g0202 | 3 | NA18954.hp1 NA18972.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.853+1411C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117296201 | ||||||
chr7:117296278
|
G | A | 1 | a0001c0001t0012g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.853+1334C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117296278 | ||||||
chr7:117296610
|
C | T | 1 | a0001c0001t0015g0229 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.853+1002G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117296610 | ||||||
chr7:117296900
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.853+712C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117296900 | ||||||
chr7:117297124
|
C | T | 1 | a0001c0001t0028g0204 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.853+488G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117297124 | ||||||
chr7:117297424
|
C | T | 3 | a0001c0001t0001g0061a0001c0001t0002g0017a0001c0001t0002g0018 | 5 | HG00738.hp1 HG01106.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.853+188G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117297424 | ||||||
chr7:117297461
|
C | T | 1 | a0001c0001t0002g0090 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.853+151G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117297461 | ||||||
chr7:117297466
|
A | G | 102 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0053others(99): Show | 111 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.853+146T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117297466 | ||||||
chr7:117297966
|
T | C | 104 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0053others(101): Show | 113 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.589-90A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117297966 | ||||||
chr7:117298095
|
G | A | 1 | a0001c0001t0002g0116 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.589-219C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117298095 | ||||||
chr7:117298411
|
G | A | 1 | a0001c0001t0019g0106 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.589-535C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117298411 | ||||||
chr7:117298453
|
G | C | 1 | a0001c0001t0005g0046 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.589-577C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117298453 | ||||||
chr7:117298986
|
G | T | 3 | a0001c0001t0001g0266a0001c0001t0002g0282a0001c0001t0015g0047 | 3 | HG01496.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.589-1110C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117298986 | ||||||
chr7:117299035
|
AG | A | 3 | a0001c0001t0001g0266a0001c0001t0002g0282a0001c0001t0015g0047 | 3 | HG01496.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.589-1160delC | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299035 | ||||||
chr7:117299233
|
C | T | 1 | a0001c0001t0015g0047 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.589-1357G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299233 | ||||||
chr7:117299362
|
T | A | 1 | a0001c0001t0002g0238 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.589-1486A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299362 | ||||||
chr7:117299364
|
A | G | 2 | a0001c0001t0001g0032a0001c0001t0005g0043 | 2 | HG02698.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.589-1488T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299364 | ||||||
chr7:117299447
|
T | G | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.589-1571A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299447 | ||||||
chr7:117299494
|
CT | C | 93 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0053others(90): Show | 102 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.589-1619delA | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299494 | ||||||
chr7:117299581
|
C | G | 2 | a0001c0001t0002g0238a0001c0001t0005g0231 | 2 | HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.589-1705G>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299581 | ||||||
chr7:117299707
|
G | C | 1 | a0001c0001t0002g0181 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.589-1831C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299707 | ||||||
chr7:117299736
|
T | C | 1 | a0001c0001t0015g0094 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.589-1860A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299736 | ||||||
chr7:117299841
|
A | G | 1 | a0001c0001t0005g0092 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.589-1965T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299841 | ||||||
chr7:117299847
|
A | T | 1 | a0001c0001t0001g0276 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.589-1971T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299847 | ||||||
chr7:117299874
|
T | C | 1 | a0001c0001t0013g0052 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.589-1998A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299874 | ||||||
chr7:117299994
|
A | G | 109 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0053others(106): Show | 118 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.589-2118T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299994 | ||||||
chr7:117300155
|
T | TA | 6 | a0001c0001t0003g0279a0001c0001t0004g0095a0001c0001t0004g0237others(3): Show | 6 | HG02257.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-2280dupT | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117300155 | ||||||
chr7:117300326
|
A | G | 1 | a0001c0001t0004g0259 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.589-2450T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117300326 | ||||||
chr7:117300432
|
G | A | 1 | a0001c0001t0029g0098 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.589-2556C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117300432 | ||||||
chr7:117300482
|
G | A | 10 | a0001c0001t0001g0266a0001c0001t0002g0282a0001c0001t0008g0251others(7): Show | 10 | HG00741.hp2 HG01496.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.589-2606C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117300482 | ||||||
chr7:117300614
|
T | A | 101 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0053others(98): Show | 109 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.589-2738A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117300614 | ||||||
chr7:117301010
|
G | A | 3 | a0001c0001t0012g0215a0001c0001t0012g0219a0001c0001t0036g0214 | 3 | HG02145.hp2 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.589-3134C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301010 | ||||||
chr7:117301015
|
A | G | 4 | a0001c0001t0002g0022a0001c0001t0002g0190a0001c0001t0003g0189others(1): Show | 5 | NA18612.hp1 NA18954.hp2 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.589-3139T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301015 | ||||||
chr7:117301048
|
C | CT | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(123): Show | 145 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.589-3173dupA | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301048 | ||||||
chr7:117301097
|
A | G | 1 | a0001c0001t0004g0114 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.589-3221T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301097 | ||||||
chr7:117301163
|
G | A | 3 | a0001c0001t0006g0220a0001c0001t0016g0216a0001c0001t0016g0227 | 3 | HG02818.hp1 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.589-3287C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301163 | ||||||
chr7:117301182
|
C | G | 27 | a0001c0001t0001g0029a0001c0001t0001g0168a0001c0001t0001g0234others(24): Show | 29 | HG00738.hp2 HG00741.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.589-3306G>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301182 | ||||||
chr7:117301202
|
G | A | 2 | a0001c0001t0002g0238a0001c0001t0005g0231 | 2 | HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.589-3326C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301202 | ||||||
chr7:117301223
|
C | T | 5 | a0001c0001t0001g0266a0001c0001t0012g0215a0001c0001t0012g0219others(2): Show | 5 | HG01496.hp2 HG02145.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.589-3347G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301223 | ||||||
chr7:117301246
|
T | C | 3 | a0001c0002t0005g0249a0001c0002t0023g0248a0002c0003t0002g0027 | 3 | HG02109.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.589-3370A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301246 | ||||||
chr7:117301289
|
G | A | 6 | a0001c0001t0002g0050a0001c0001t0002g0096a0001c0001t0002g0097others(3): Show | 6 | HG02040.hp1 HG02071.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.589-3413C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301289 | ||||||
chr7:117301293
|
A | T | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.589-3417T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301293 | ||||||
chr7:117301401
|
G | A | 1 | a0001c0001t0008g0239 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.589-3525C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301401 | ||||||
chr7:117301593
|
C | T | 2 | a0001c0001t0002g0036a0001c0001t0002g0116 | 2 | NA18989.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.589-3717G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301593 | ||||||
chr7:117301769
|
G | A | 1 | a0001c0001t0003g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.589-3893C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301769 | ||||||
chr7:117301802
|
C | CT | 24 | a0001c0001t0001g0109a0001c0001t0001g0157a0001c0001t0001g0242others(21): Show | 25 | HG01192.hp2 HG01433.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.589-3927dupA | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301802 | ||||||
chr7:117301802
|
CT | C | 10 | a0001c0001t0001g0032a0001c0001t0001g0145a0001c0001t0001g0146others(7): Show | 11 | HG01070.hp1 HG01261.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.589-3927delA | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301802 | ||||||
chr7:117301915
|
C | T | 9 | a0001c0001t0003g0150a0001c0001t0004g0151a0001c0001t0005g0046others(6): Show | 11 | HG02572.hp2 HG02630.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.589-4039G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301915 | ||||||
chr7:117301961
|
C | T | 12 | a0001c0001t0004g0225a0001c0001t0004g0226a0001c0001t0004g0228others(9): Show | 13 | HG01074.hp2 HG01192.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.589-4085G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301961 | ||||||
chr7:117302061
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(128): Show | 149 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.589-4185C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117302061 | ||||||
chr7:117302124
|
T | C | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG01433.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.589-4248A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117302124 | ||||||
chr7:117302221
|
T | C | 1 | a0001c0001t0003g0208 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.589-4345A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117302221 | ||||||
chr7:117302265
|
C | T | 1 | a0002c0003t0002g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.589-4389G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117302265 | ||||||
chr7:117302303
|
A | C | 1 | a0001c0001t0001g0040 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.589-4427T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117302303 | ||||||
chr7:117302379
|
G | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(118): Show | 139 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.589-4503C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117302379 | ||||||
chr7:117302451
|
A | T | 6 | a0001c0001t0001g0146a0001c0001t0001g0280a0001c0001t0009g0274others(3): Show | 6 | HG02486.hp1 HG02965.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-4575T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117302451 | ||||||
chr7:117302484
|
C | T | 4 | a0001c0001t0006g0217a0001c0001t0006g0220a0001c0001t0016g0216others(1): Show | 4 | HG01891.hp1 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-4608G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117302484 | ||||||
chr7:117302867
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.589-4991C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117302867 | ||||||
chr7:117302960
|
T | C | 1 | a0001c0001t0002g0090 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.589-5084A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117302960 | ||||||
chr7:117303025
|
C | T | 1 | a0001c0001t0004g0246 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.589-5149G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117303025 | ||||||
chr7:117303081
|
C | T | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(126): Show | 147 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.589-5205G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117303081 | ||||||
chr7:117303274
|
G | A | 1 | a0002c0003t0002g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.589-5398C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117303274 | ||||||
chr7:117303283
|
T | C | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.589-5407A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117303283 | ||||||
chr7:117303470
|
A | G | 3 | a0001c0001t0002g0104a0001c0001t0008g0255a0001c0001t0019g0106 | 3 | HG01175.hp2 HG01517.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.589-5594T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117303470 | ||||||
chr7:117303646
|
G | A | 2 | a0001c0001t0002g0183a0001c0001t0002g0198 | 2 | NA19063.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.589-5770C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117303646 | ||||||
chr7:117303651
|
C | T | 1 | a0001c0001t0013g0052 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.589-5775G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117303651 | ||||||
chr7:117303683
|
T | G | 2 | a0001c0001t0011g0014a0001c0001t0035g0243 | 3 | HG00741.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.589-5807A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117303683 | ||||||
chr7:117303739
|
A | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(128): Show | 152 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.589-5863T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117303739 | ||||||
chr7:117304092
|
C | T | 1 | a0001c0001t0028g0204 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.589-6216G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304092 | ||||||
chr7:117304229
|
T | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(107): Show | 128 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.589-6353A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304229 | ||||||
chr7:117304355
|
G | C | 1 | a0001c0001t0001g0110 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.589-6479C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304355 | ||||||
chr7:117304432
|
AT | A | 69 | a0001c0001t0001g0015a0001c0001t0001g0029a0001c0001t0001g0053others(66): Show | 76 | HG00323.hp1 HG00733.hp2 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.589-6557delA | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304432 | ||||||
chr7:117304432
|
ATT | A | 16 | a0001c0001t0002g0096a0001c0001t0004g0228a0001c0001t0004g0252others(13): Show | 17 | HG01433.hp2 HG02145.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.589-6558_589-6557d others(4): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304432 | ||||||
chr7:117304432
|
ATTT | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0038a0001c0001t0001g0040others(91): Show | 106 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.589-6559_589-6557d others(5): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304432 | ||||||
chr7:117304432
|
ATTTT | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0016others(14): Show | 23 | HG00558.hp2 HG01192.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.589-6560_589-6557d others(6): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304432 | ||||||
chr7:117304624
|
C | T | 9 | a0001c0001t0001g0029a0001c0001t0004g0042a0001c0001t0004g0054others(6): Show | 10 | HG00738.hp2 HG00741.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.589-6748G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304624 | ||||||
chr7:117304636
|
A | G | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG01433.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.589-6760T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304636 | ||||||
chr7:117304786
|
A | G | 3 | a0001c0001t0012g0215a0001c0001t0012g0219a0001c0001t0036g0214 | 3 | HG02145.hp2 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.589-6910T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304786 | ||||||
chr7:117304897
|
T | C | 3 | a0001c0001t0012g0215a0001c0001t0012g0219a0001c0001t0036g0214 | 3 | HG02145.hp2 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.589-7021A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304897 | ||||||
chr7:117304963
|
G | T | 3 | a0001c0001t0012g0273a0001c0001t0016g0263a0001c0001t0032g0262 | 3 | HG02258.hp2 HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.589-7087C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304963 | ||||||
chr7:117304967
|
G | C | 1 | a0002c0003t0002g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.589-7091C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304967 | ||||||
chr7:117305128
|
C | T | 3 | a0001c0001t0012g0273a0001c0001t0016g0263a0001c0001t0032g0262 | 3 | HG02258.hp2 HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.589-7252G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117305128 | ||||||
chr7:117305281
|
G | A | 1 | a0001c0001t0002g0282 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.589-7405C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117305281 | ||||||
chr7:117305444
|
T | C | 1 | a0001c0001t0038g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.589-7568A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117305444 | ||||||
chr7:117305529
|
G | T | 13 | a0001c0001t0001g0029a0001c0001t0001g0266a0001c0001t0004g0042others(10): Show | 14 | HG00738.hp2 HG00741.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.589-7653C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117305529 | ||||||
chr7:117305925
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.589-8049C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117305925 | ||||||
chr7:117306321
|
G | A | 6 | a0001c0001t0001g0146a0001c0001t0001g0280a0001c0001t0009g0274others(3): Show | 6 | HG02486.hp1 HG02965.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-8445C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117306321 | ||||||
chr7:117306336
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.589-8460C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117306336 | ||||||
chr7:117306389
|
T | G | 5 | a0001c0001t0001g0093a0001c0001t0001g0122a0001c0001t0004g0095others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.589-8513A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117306389 | ||||||
chr7:117306616
|
A | C | 3 | a0001c0001t0028g0204a0001c0002t0005g0249a0001c0002t0023g0248 | 3 | HG02965.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.588+8455T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117306616 | ||||||
chr7:117306637
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.588+8434G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117306637 | ||||||
chr7:117306759
|
C | T | 1 | a0002c0003t0002g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.588+8312G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117306759 | ||||||
chr7:117306939
|
G | A | 1 | a0002c0003t0002g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.588+8132C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117306939 | ||||||
chr7:117307142
|
A | C | 14 | a0001c0001t0001g0168a0001c0001t0001g0242a0001c0001t0001g0245others(11): Show | 14 | HG00323.hp1 HG01123.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.588+7929T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117307142 | ||||||
chr7:117307145
|
G | C | 3 | a0001c0001t0028g0204a0001c0002t0005g0249a0001c0002t0023g0248 | 3 | HG02965.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.588+7926C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117307145 | ||||||
chr7:117307257
|
T | G | 2 | a0001c0001t0006g0005a0001c0001t0013g0156 | 4 | HG02572.hp2 HG03195.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.588+7814A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117307257 | ||||||
chr7:117307409
|
T | A | 1 | a0001c0001t0034g0278 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.588+7662A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117307409 | ||||||
chr7:117307728
|
G | C | 1 | a0001c0001t0003g0184 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.588+7343C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117307728 | ||||||
chr7:117308117
|
C | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(145): Show | 170 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.588+6954G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117308117 | ||||||
chr7:117308353
|
C | T | 5 | a0001c0001t0001g0038a0001c0001t0004g0059a0001c0001t0004g0060others(2): Show | 5 | HG00099.hp1 HG00140.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.588+6718G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117308353 | ||||||
chr7:117308807
|
T | C | 6 | a0001c0001t0002g0050a0001c0001t0002g0096a0001c0001t0002g0097others(3): Show | 6 | HG02040.hp1 HG02071.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+6264A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117308807 | ||||||
chr7:117308859
|
A | G | 1 | a0001c0001t0013g0172 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.588+6212T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117308859 | ||||||
chr7:117309027
|
T | TA | 8 | a0001c0001t0001g0099a0001c0001t0001g0242a0001c0001t0002g0188others(5): Show | 8 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.588+6043dupT | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309027 | ||||||
chr7:117309053
|
C | A | 12 | a0001c0001t0001g0015a0001c0001t0001g0105a0001c0001t0001g0110others(9): Show | 14 | HG00642.hp2 HG03017.hp2 HG03491.hp1 others(11): Show |
intron_variant | MODIFIER | c.588+6018G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309053 | ||||||
chr7:117309144
|
C | T | 1 | a0001c0001t0002g0022 | 2 | NA18954.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.588+5927G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309144 | ||||||
chr7:117309145
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.588+5926C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309145 | ||||||
chr7:117309184
|
C | CA | 29 | a0001c0001t0001g0168a0001c0001t0001g0234a0001c0001t0001g0240others(26): Show | 29 | HG00323.hp1 HG01123.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.588+5886dupT | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309184 | ||||||
chr7:117309196
|
A | T | 1 | a0001c0001t0036g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.588+5875T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309196 | ||||||
chr7:117309197
|
T | A | 1 | a0001c0001t0001g0053 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.588+5874A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309197 | ||||||
chr7:117309232
|
C | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(111): Show | 134 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.588+5839G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309232 | ||||||
chr7:117309429
|
C | A | 1 | a0001c0001t0006g0217 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.588+5642G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309429 | ||||||
chr7:117309858
|
C | A | 9 | a0001c0001t0001g0268a0001c0001t0002g0025a0001c0001t0002g0256others(6): Show | 12 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.588+5213G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309858 | ||||||
chr7:117309867
|
T | G | 2 | a0001c0001t0001g0113a0001c0001t0001g0121 | 2 | HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.588+5204A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309867 | ||||||
chr7:117309937
|
A | G | 14 | a0001c0001t0001g0125a0001c0001t0001g0141a0001c0001t0002g0126others(11): Show | 14 | HG00642.hp2 HG03017.hp2 HG03654.hp1 others(11): Show |
intron_variant | MODIFIER | c.588+5134T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309937 | ||||||
chr7:117309950
|
ATC | A | 5 | a0001c0001t0006g0217a0001c0001t0006g0220a0001c0001t0012g0273others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.588+5119_588+5120d others(4): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309950 | ||||||
chr7:117310276
|
C | T | 5 | a0001c0001t0006g0217a0001c0001t0006g0220a0001c0001t0012g0273others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.588+4795G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117310276 | ||||||
chr7:117310386
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.588+4685C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117310386 | ||||||
chr7:117310438
|
T | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0105a0001c0001t0001g0110 | 4 | NA18965.hp1 NA18971.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.588+4633A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117310438 | ||||||
chr7:117310582
|
C | CA | 68 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0045others(65): Show | 72 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.588+4488dupT | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117310582 | ||||||
chr7:117310582
|
C | CAA | 14 | a0001c0001t0001g0245a0001c0001t0001g0277a0001c0001t0002g0275others(11): Show | 14 | HG00741.hp1 HG01123.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.588+4487_588+4488d others(4): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117310582 | ||||||
chr7:117310582
|
CA | C | 8 | a0001c0001t0002g0123a0001c0001t0002g0188a0001c0001t0003g0057others(5): Show | 8 | HG01975.hp1 HG01993.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.588+4488delT | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117310582 | ||||||
chr7:117310702
|
C | T | 6 | a0001c0001t0001g0266a0001c0001t0006g0217a0001c0001t0006g0220others(3): Show | 6 | HG01496.hp2 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+4369G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117310702 | ||||||
chr7:117310749
|
T | C | 8 | a0001c0001t0001g0146a0001c0001t0001g0280a0001c0001t0003g0024others(5): Show | 9 | HG02486.hp1 HG02630.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.588+4322A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117310749 | ||||||
chr7:117310777
|
T | G | 1 | a0001c0001t0001g0266 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.588+4294A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117310777 | ||||||
chr7:117311165
|
A | T | 2 | a0001c0001t0017g0055a0001c0001t0017g0056 | 2 | HG00741.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.588+3906T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117311165 | ||||||
chr7:117311337
|
T | C | 1 | a0001c0001t0004g0042 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.588+3734A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117311337 | ||||||
chr7:117311395
|
T | G | 3 | a0001c0001t0028g0204a0001c0002t0005g0249a0001c0002t0023g0248 | 3 | HG02965.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.588+3676A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117311395 | ||||||
chr7:117311431
|
A | G | 2 | a0001c0001t0001g0029a0001c0001t0004g0054 | 2 | HG02559.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.588+3640T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117311431 | ||||||
chr7:117311599
|
G | A | 4 | a0001c0001t0006g0217a0001c0001t0006g0220a0001c0001t0016g0216others(1): Show | 4 | HG01891.hp1 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+3472C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117311599 | ||||||
chr7:117311617
|
G | A | 37 | a0001c0001t0001g0234a0001c0001t0001g0240a0001c0001t0001g0241others(34): Show | 40 | HG00323.hp1 HG00733.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.588+3454C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117311617 | ||||||
chr7:117312010
|
C | T | 3 | a0001c0001t0012g0273a0001c0001t0016g0263a0001c0001t0032g0262 | 3 | HG02258.hp2 HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.588+3061G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117312010 | ||||||
chr7:117312072
|
C | T | 2 | a0001c0001t0006g0005a0001c0001t0013g0156 | 4 | HG02572.hp2 HG03195.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.588+2999G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117312072 | ||||||
chr7:117312250
|
G | A | 49 | a0001c0001t0001g0234a0001c0001t0001g0240a0001c0001t0001g0241others(46): Show | 53 | HG00323.hp1 HG00733.hp2 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.588+2821C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117312250 | ||||||
chr7:117312300
|
G | C | 4 | a0001c0001t0006g0217a0001c0001t0006g0220a0001c0001t0016g0216others(1): Show | 4 | HG01891.hp1 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+2771C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117312300 | ||||||
chr7:117312334
|
G | A | 2 | a0001c0001t0002g0143a0001c0001t0003g0144 | 2 | HG02040.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.588+2737C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117312334 | ||||||
chr7:117312617
|
T | C | 4 | a0001c0001t0006g0217a0001c0001t0006g0220a0001c0001t0016g0216others(1): Show | 4 | HG01891.hp1 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+2454A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117312617 | ||||||
chr7:117312687
|
A | C | 67 | a0001c0001t0001g0146a0001c0001t0001g0234a0001c0001t0001g0240others(64): Show | 72 | HG00323.hp1 HG00733.hp2 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.588+2384T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117312687 | ||||||
chr7:117312701
|
G | T | 2 | a0001c0001t0004g0151a0001c0001t0005g0046 | 2 | HG03017.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.588+2370C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117312701 | ||||||
chr7:117312729
|
T | G | 12 | a0001c0001t0004g0225a0001c0001t0004g0226a0001c0001t0004g0228others(9): Show | 13 | HG01074.hp2 HG01192.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.588+2342A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117312729 | ||||||
chr7:117312878
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.588+2193A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117312878 | ||||||
chr7:117313106
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.588+1965G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117313106 | ||||||
chr7:117313247
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.588+1824A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117313247 | ||||||
chr7:117313582
|
A | G | 1 | a0001c0001t0002g0169 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.588+1489T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117313582 | ||||||
chr7:117313848
|
T | C | 1 | a0001c0001t0002g0282 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.588+1223A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117313848 | ||||||
chr7:117314063
|
T | G | 60 | a0001c0001t0001g0146a0001c0001t0001g0234a0001c0001t0001g0240others(57): Show | 64 | HG00323.hp1 HG00733.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.588+1008A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117314063 | ||||||
chr7:117314497
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.588+574C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117314497 | ||||||
chr7:117314691
|
GTCTAA | G | 45 | a0001c0001t0001g0234a0001c0001t0001g0240a0001c0001t0001g0241others(42): Show | 48 | HG00323.hp1 HG00733.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.588+375_588+379del others(5): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117314691 | ||||||
chr7:117314702
|
A | T | 2 | a0002c0003t0001g0026a0002c0003t0002g0027 | 2 | HG02109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.588+369T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117314702 | ||||||
chr7:117314731
|
A | C | 138 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0045others(135): Show | 147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.588+340T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117314731 | ||||||
chr7:117314926
|
G | A | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG01433.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.588+145C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117314926 | ||||||
chr7:117315400
|
T | G | 1 | a0001c0001t0001g0155 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.311-52A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117315400 | ||||||
chr7:117315585
|
T | C | 1 | a0001c0001t0003g0208 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.311-237A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117315585 | ||||||
chr7:117315604
|
A | G | 1 | a0001c0001t0010g0033 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.311-256T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117315604 | ||||||
chr7:117315645
|
C | T | 65 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0045others(62): Show | 70 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.311-297G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117315645 | ||||||
chr7:117315739
|
C | T | 7 | a0001c0001t0006g0217a0001c0001t0006g0220a0001c0001t0012g0215others(4): Show | 7 | HG01891.hp1 HG02145.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.311-391G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117315739 | ||||||
chr7:117316034
|
T | G | 1 | a0001c0001t0001g0016 | 2 | HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.311-686A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117316034 | ||||||
chr7:117316210
|
C | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0155a0001c0001t0001g0167others(2): Show | 7 | HG01192.hp1 HG01255.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.311-862G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117316210 | ||||||
chr7:117316516
|
T | C | 1 | a0001c0001t0003g0213 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.311-1168A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117316516 | ||||||
chr7:117316863
|
A | G | 2 | a0001c0001t0006g0005a0001c0001t0013g0156 | 4 | HG02572.hp2 HG03195.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.311-1515T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117316863 | ||||||
chr7:117317509
|
TA | T | 141 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0045others(138): Show | 153 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.311-2162delT | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117317509 | ||||||
chr7:117317714
|
G | A | 1 | a0001c0001t0016g0227 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.311-2366C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117317714 | ||||||
chr7:117317912
|
G | T | 1 | a0001c0001t0001g0125 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.311-2564C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117317912 | ||||||
chr7:117317973
|
G | A | 7 | a0001c0001t0006g0217a0001c0001t0006g0220a0001c0001t0012g0215others(4): Show | 7 | HG01891.hp1 HG02145.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.310+2594C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117317973 | ||||||
chr7:117318014
|
C | A | 1 | a0001c0001t0036g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.310+2553G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117318014 | ||||||
chr7:117318117
|
A | G | 1 | a0001c0001t0002g0124 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.310+2450T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117318117 | ||||||
chr7:117318363
|
C | T | 4 | a0001c0001t0012g0273a0001c0001t0016g0263a0001c0001t0032g0262others(1): Show | 4 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.310+2204G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117318363 | ||||||
chr7:117319062
|
G | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0051a0001c0001t0018g0009 | 6 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.310+1505C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319062 | ||||||
chr7:117319094
|
T | C | 4 | a0001c0001t0004g0230a0001c0001t0004g0252a0001c0001t0006g0264others(1): Show | 4 | HG01433.hp2 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.310+1473A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319094 | ||||||
chr7:117319158
|
C | T | 2 | a0001c0001t0004g0151a0001c0001t0005g0046 | 2 | HG03017.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.310+1409G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319158 | ||||||
chr7:117319214
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.310+1353C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319214 | ||||||
chr7:117319398
|
G | A | 1 | a0001c0001t0026g0112 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.310+1169C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319398 | ||||||
chr7:117319521
|
T | G | 1 | a0001c0001t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.310+1046A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319521 | ||||||
chr7:117319522
|
T | TG | 22 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0121others(19): Show | 25 | HG00738.hp1 HG00738.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.310+1044dupC | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319522 | ||||||
chr7:117319522
|
TG | T | 57 | a0001c0001t0001g0004a0001c0001t0001g0048a0001c0001t0001g0152others(54): Show | 63 | HG00323.hp1 HG00733.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.310+1044delC | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319522 | ||||||
chr7:117319524
|
G | C | 1 | a0001c0001t0005g0231 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.310+1043C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319524 | ||||||
chr7:117319525
|
G | C | 25 | a0001c0001t0001g0234a0001c0001t0001g0240a0001c0001t0001g0241others(22): Show | 25 | HG00323.hp1 HG00741.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.310+1042C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319525 | ||||||
chr7:117319529
|
G | C | 1 | a0001c0001t0002g0123 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.310+1038C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319529 | ||||||
chr7:117319530
|
G | C | 70 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0045others(67): Show | 75 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.310+1037C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319530 | ||||||
chr7:117319532
|
G | C | 1 | a0001c0001t0006g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.310+1035C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319532 | ||||||
chr7:117319771
|
G | A | 1 | a0001c0001t0003g0150 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.310+796C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319771 | ||||||
chr7:117319791
|
G | A | 5 | a0001c0001t0004g0225a0001c0001t0004g0226a0001c0001t0009g0023others(2): Show | 6 | HG01074.hp2 HG01192.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.310+776C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319791 | ||||||
chr7:117319791
|
G | T | 15 | a0001c0001t0001g0268a0001c0001t0001g0276a0001c0001t0001g0277others(12): Show | 18 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.310+776C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319791 | ||||||
chr7:117320050
|
C | A | 46 | a0001c0001t0001g0234a0001c0001t0001g0240a0001c0001t0001g0241others(43): Show | 50 | HG00323.hp1 HG00733.hp2 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.310+517G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117320050 | ||||||
chr7:117320141
|
C | G | 2 | a0001c0001t0007g0007a0001c0001t0007g0247 | 4 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.310+426G>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117320141 | ||||||
chr7:117320442
|
G | A | 1 | a0001c0001t0008g0206 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.310+125C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117320442 | ||||||
chr7:117320524
|
A | T | 1 | a0001c0001t0001g0152 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.310+43T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117320524 | ||||||
chr7:117321354
|
A | T | 3 | a0001c0001t0003g0035a0001c0001t0010g0033a0001c0001t0010g0034 | 3 | NA18982.hp1 NA18993.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.84-561T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117321354 | ||||||
chr7:117321694
|
TTAAG | T | 3 | a0001c0001t0012g0215a0001c0001t0012g0219a0001c0001t0036g0214 | 3 | HG02145.hp2 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.84-905_84-902delCT others(2): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117321694 | ||||||
chr7:117321737
|
T | C | 2 | a0002c0003t0001g0026a0002c0003t0002g0027 | 2 | HG02109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.84-944A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117321737 | ||||||
chr7:117321836
|
G | A | 1 | a0001c0001t0004g0151 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.84-1043C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117321836 | ||||||
chr7:117321960
|
T | C | 1 | a0001c0001t0016g0227 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.83+947A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117321960 | ||||||
chr7:117322409
|
A | G | 3 | a0001c0001t0004g0246a0001c0001t0004g0272a0001c0001t0006g0261 | 3 | HG02723.hp1 HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.83+498T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322409 | ||||||
chr7:117322419
|
A | T | 3 | a0001c0001t0004g0246a0001c0001t0004g0272a0001c0001t0006g0261 | 3 | HG02723.hp1 HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.83+488T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322419 | ||||||
chr7:117322536
|
T | TAC | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(124): Show | 147 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.83+369_83+370dupGT | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322536 | ||||||
chr7:117322536
|
T | TACAC | 52 | a0001c0001t0001g0004a0001c0001t0001g0152a0001c0001t0001g0153others(49): Show | 60 | HG00609.hp1 HG00642.hp1 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.83+367_83+370dupGT others(2): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322536 | ||||||
chr7:117322536
|
T | TACACAC | 33 | a0001c0001t0001g0191a0001c0001t0001g0234a0001c0001t0001g0240others(30): Show | 33 | HG00099.hp2 HG00323.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.83+365_83+370dupGT others(4): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322536 | ||||||
chr7:117322536
|
T | TACACACA others(1): Show |
20 | a0001c0001t0001g0203a0001c0001t0002g0256a0001c0001t0003g0253others(17): Show | 22 | HG00140.hp1 HG00733.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.83+363_83+370dupGT others(6): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322536 | ||||||
chr7:117322536
|
T | TACACACA others(3): Show |
18 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0270others(15): Show | 21 | HG01496.hp2 HG01975.hp2 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.83+361_83+370dupGT others(8): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322536 | ||||||
chr7:117322536
|
T | TACACACA others(5): Show |
6 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0002g0275others(3): Show | 6 | HG01358.hp1 HG01433.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.83+359_83+370dupGT others(10): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322536 | ||||||
chr7:117322536
|
T | TACACACA others(7): Show |
4 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0003g0279others(1): Show | 4 | HG02486.hp1 HG03540.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+357_83+370dupGT others(12): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322536 | ||||||
chr7:117322536
|
T | TACACACA others(9): Show |
2 | a0001c0001t0001g0280a0001c0001t0012g0281 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.83+355_83+370dupGT others(14): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322536 | ||||||
chr7:117322536
|
T | TACACACA others(11): Show |
1 | a0001c0001t0002g0282 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.83+353_83+370dupGT others(16): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322536 | ||||||
chr7:117322536
|
TAC | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0002g0030others(1): Show | 4 | HG02559.hp2 HG03239.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+369_83+370delGT | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322536 | ||||||
chr7:117322771
|
G | T | 1 | a0001c0001t0038g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.83+136C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322771 | ||||||
chr7:117322817
|
C | A | 1 | a0001c0001t0003g0213 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.83+90G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322817 | ||||||
chr7:117322879
|
T | TC | 73 | a0001c0001t0001g0234a0001c0001t0001g0240a0001c0001t0001g0241others(70): Show | 78 | HG00323.hp1 HG00733.hp2 HG00741.hp1 others(75): Show |
intron_variant | MODIFIER | c.83+27dupG | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322879 |