geneid | 8976 |
---|---|
ensemblid | ENSG00000106299.8 |
hgncid | 12735 |
symbol | WASL |
name | WASP like actin nucleation promoting factor |
refseq_nuc | NM_003941.4 |
refseq_prot | NP_003932.3 |
ensembl_nuc | ENST00000223023.5 |
ensembl_prot | ENSP00000223023.4 |
mane_status | MANE Select |
chr | chr7 |
start | 123681943 |
end | 123749003 |
strand | - |
ver | v1.2 |
region | chr7:123681943-123749003 |
region5000 | chr7:123676943-123754003 |
regionname0 | WASL_chr7_123681943_123749003 |
regionname5000 | WASL_chr7_123676943_123754003 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 505 | 355 | 88 | 60 | 151 | 14 | 40 | 117 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0002 | 0/0 | 505 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1518 | 189 | 59 | 34 | 73 | 7 | 14 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
c0002 | 0/0 | 1518 | 150 | 29 | 24 | 64 | 7 | 26 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
c0003 | 0/0 | 1518 | 15 | 0 | 1 | 14 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
c0004 | 0/0 | 1518 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
c0005 | 0/0 | 1518 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2844 | 145 | 29 | 23 | 63 | 6 | 24 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
t0002 | 1/0 | 2846 | 89 | 32 | 13 | 32 | 3 | 8 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
t0003 | 0/1 | 2846 | 59 | 15 | 12 | 28 | 1 | 2 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
t0004 | 0/0 | 2846 | 33 | 3 | 4 | 19 | 3 | 4 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
t0005 | 0/0 | 2846 | 4 | 0 | 0 | 4 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
t0006 | 0/0 | 2844 | 3 | 3 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
t0007 | 0/0 | 2846 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
t0008 | 0/0 | 2846 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
t0009 | 0/0 | 2846 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
t0010 | 0/0 | 2844 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
t0011 | 0/0 | 2846 | 2 | 0 | 2 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
t0012 | 0/0 | 2846 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
t0013 | 0/0 | 2846 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
t0014 | 0/0 | 2846 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
t0015 | 0/0 | 2846 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
t0016 | 0/0 | 2846 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
t0017 | 0/0 | 2844 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
t0018 | 0/0 | 2844 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
t0019 | 0/0 | 2844 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
t0020 | 0/0 | 2844 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
t0021 | 0/0 | 2844 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
t0022 | 0/0 | 2844 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
t0023 | 0/0 | 2844 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
t0024 | 0/0 | 2844 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0003 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0004 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0006 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0056 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1518 | 189 | 59 | 34 | 73 | 7 | 14 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0002 | 0/0 | 1518 | 150 | 29 | 24 | 64 | 7 | 26 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0003 | 0/0 | 1518 | 15 | 0 | 1 | 14 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0005 | 0/0 | 1518 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0002c0004 | 0/0 | 1518 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4361 | 3 | 3 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0001t0002 | 1/0 | 4363 | 88 | 32 | 13 | 31 | 3 | 8 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0001t0003 | 0/1 | 4363 | 47 | 13 | 11 | 19 | 1 | 2 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0001t0004 | 0/0 | 4363 | 33 | 3 | 4 | 19 | 3 | 4 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0001t0006 | 0/0 | 4361 | 3 | 3 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0001t0007 | 0/0 | 4363 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0001t0008 | 0/0 | 4363 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0001t0009 | 0/0 | 4363 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0001t0010 | 0/0 | 4361 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0001t0011 | 0/0 | 4363 | 2 | 0 | 2 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0001t0012 | 0/0 | 4363 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0001t0013 | 0/0 | 4363 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0001t0014 | 0/0 | 4363 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0001t0015 | 0/0 | 4363 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0001t0016 | 0/0 | 4363 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0002t0001 | 0/0 | 4361 | 141 | 26 | 22 | 63 | 6 | 24 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0002t0003 | 0/0 | 4363 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0002t0017 | 0/0 | 4361 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0002t0018 | 0/0 | 4361 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0002t0019 | 0/0 | 4361 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0002t0021 | 0/0 | 4361 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0002t0022 | 0/0 | 4361 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0002t0023 | 0/0 | 4361 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0002t0024 | 0/0 | 4361 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0003t0003 | 0/0 | 4363 | 10 | 0 | 1 | 9 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0003t0005 | 0/0 | 4363 | 4 | 0 | 0 | 4 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0003t0020 | 0/0 | 4361 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0001c0005t0001 | 0/0 | 4361 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
a0002c0004t0002 | 0/0 | 4363 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | copy fasta | chr7 | 123676943 | 123754003 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0056 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0006 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0007g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0008g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0008g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0009g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0009g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0010g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0010g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0011g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0012g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0013g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0014g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0015g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0001t0016g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0003 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0004 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0017g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0018g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0019g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0021g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0022g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0023g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0002t0024g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0003t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0003t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0003t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0003t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0003t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0003t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0003t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0003t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0003t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0003t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0003t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0003t0005g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0003t0005g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0003t0020g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0001c0005t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
a0002c0004t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0099 | EUR | GBR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00099 | hp2 | a0001 | c0002 | t0021 | g0262 | EUR | GBR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0247 | EUR | GBR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0214 | EUR | GBR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0154 | EUR | FIN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0293 | EUR | FIN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00323 | hp1 | a0001 | c0001 | t0004 | g0151 | EUR | FIN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0241 | EUR | FIN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00408 | hp1 | a0001 | c0001 | t0008 | g0159 | EAS | CHS | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | CHS | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | CHS | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | CHS | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00544 | hp1 | a0001 | c0003 | t0003 | g0124 | EAS | CHS | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | CHS | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | CHS | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00621 | hp2 | a0001 | c0001 | t0004 | g0172 | EAS | CHS | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0294 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00639 | hp2 | a0001 | c0001 | t0015 | g0060 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0302 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00673 | hp1 | a0001 | c0003 | t0005 | g0131 | EAS | CHS | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00673 | hp2 | a0001 | c0001 | t0004 | g0167 | EAS | CHS | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0196 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00735 | hp1 | a0001 | c0002 | t0018 | g0207 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0155 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0297 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0229 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0275 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0231 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0289 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0230 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0176 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0158 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01109 | hp2 | a0001 | c0005 | t0001 | g0244 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01167 | hp1 | a0001 | c0001 | t0011 | g0034 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0217 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01169 | hp1 | a0001 | c0001 | t0011 | g0034 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0150 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0291 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0186 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0220 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0300 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0198 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0025 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0185 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0184 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01361 | hp2 | a0001 | c0001 | t0016 | g0134 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0135 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0157 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0003 | EUR | IBS | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01516 | hp2 | a0001 | c0001 | t0004 | g0156 | EUR | IBS | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0256 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01943 | hp2 | a0001 | c0003 | t0003 | g0133 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0301 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0311 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01981 | hp2 | a0001 | c0001 | t0012 | g0049 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0303 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0116 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0279 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02015 | hp2 | a0001 | c0001 | t0004 | g0170 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0259 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02056 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02071 | hp2 | a0001 | c0003 | t0005 | g0140 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0309 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02083 | hp1 | a0001 | c0001 | t0004 | g0162 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0251 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02145 | hp1 | a0001 | c0001 | t0006 | g0043 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0218 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02148 | hp1 | a0001 | c0001 | t0013 | g0078 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0182 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | CDX | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | CDX | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0226 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0188 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02273 | hp2 | a0001 | c0002 | t0022 | g0299 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0132 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02280 | hp2 | a0001 | c0002 | t0001 | g0298 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02451 | hp2 | a0001 | c0001 | t0009 | g0121 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0280 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0227 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0165 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0232 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02683 | hp2 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0032 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0312 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0177 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0029 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0118 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0215 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0137 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0178 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0200 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02922 | hp1 | a0001 | c0001 | t0010 | g0039 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0179 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02970 | hp1 | a0001 | c0002 | t0003 | g0306 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0264 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0024 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03098 | hp1 | a0001 | c0001 | t0014 | g0190 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03130 | hp2 | a0001 | c0002 | t0003 | g0307 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0212 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03195 | hp1 | a0001 | c0001 | t0010 | g0040 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0138 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03209 | hp1 | a0001 | c0001 | t0006 | g0041 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0209 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0290 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0032 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0265 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0304 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0204 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03491 | hp1 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0205 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03492 | hp2 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03579 | hp2 | a0001 | c0001 | t0009 | g0120 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0011 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0310 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03688 | hp1 | a0001 | c0002 | t0023 | g0236 | SAS | STU | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0222 | SAS | STU | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0295 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0201 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0245 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0271 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0292 | SAS | BEB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0221 | SAS | BEB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0153 | SAS | BEB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03942 | hp2 | a0001 | c0002 | t0024 | g0216 | SAS | BEB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0257 | SAS | STU | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0234 | SAS | STU | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0206 | SAS | STU | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | STU | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0024 | SAS | STU | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0202 | SAS | STU | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0203 | SAS | STU | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | STU | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0225 | AFR | YRI | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0281 | AFR | YRI | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18747 | hp1 | a0001 | c0002 | t0019 | g0308 | EAS | CHB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | CHB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0213 | AFR | YRI | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | YRI | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18939 | hp1 | a0001 | c0001 | t0004 | g0168 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18941 | hp1 | a0002 | c0004 | t0002 | g0065 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18948 | hp2 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18949 | hp1 | a0001 | c0003 | t0003 | g0189 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18949 | hp2 | a0001 | c0001 | t0008 | g0160 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18952 | hp2 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18964 | hp1 | a0001 | c0003 | t0005 | g0129 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18967 | hp1 | a0001 | c0003 | t0005 | g0136 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18972 | hp1 | a0001 | c0003 | t0003 | g0125 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18986 | hp1 | a0001 | c0003 | t0003 | g0122 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18989 | hp2 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18993 | hp1 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18993 | hp2 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18998 | hp1 | a0001 | c0003 | t0003 | g0126 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0173 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19001 | hp2 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0296 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | LWK | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | LWK | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | LWK | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0152 | AFR | LWK | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19055 | hp1 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19058 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19062 | hp2 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19063 | hp1 | a0001 | c0003 | t0020 | g0130 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19063 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19070 | hp2 | a0001 | c0003 | t0003 | g0142 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19074 | hp2 | a0001 | c0003 | t0003 | g0013 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19084 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19084 | hp2 | a0001 | c0003 | t0003 | g0013 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19087 | hp1 | a0001 | c0003 | t0003 | g0123 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19091 | hp2 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0228 | AFR | YRI | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA19240 | hp2 | a0001 | c0002 | t0017 | g0305 | AFR | YRI | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0197 | AFR | ASW | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | ASW | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0106 | EUR | TSI | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0096 | EUR | TSI | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0208 | EUR | TSI | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0074 | EUR | TSI | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0242 | SAS | GIH | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | GIH | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0223 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02559 | hp1 | a0001 | c0001 | t0006 | g0042 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0219 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0148 | AFR | USA | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | USA | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | USA | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0288 | AFR | USA | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | LWK | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0224 | AFR | LWK | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0105 | REF | REF | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0056 | REF | REF | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:123692700
|
C | T | 1 | a0002 | 1 | NA18941.hp1 | missense_variant | MODERATE | c.994G>A | p.Val332Ile | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/11 | 1263/4363 | 994/1518 | 332/505 | chr7 | 123692700 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:123696668
|
G | A | 1 | a0001c0003 | 15 | HG00544.hp1 HG00673.hp1 HG01943.hp2 others(12): Show |
synonymous_variant | LOW | c.540C>T | p.Asn180Asn | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 6/11 | 809/4363 | 540/1518 | 180/505 | chr7 | 123696668 | ||
chr7:123709197
|
T | C | 1 | a0001c0005 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.144A>G | p.Leu48Leu | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/11 | 413/4363 | 144/1518 | 48/505 | chr7 | 123709197 | ||
chr7:123748678
|
G | A | 2 | a0001c0002a0001c0005 | 151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
synonymous_variant | LOW | c.57C>T | p.Ser19Ser | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/11 | 326/4363 | 57/1518 | 19/505 | chr7 | 123748678 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:123681982
|
G | T | 1 | a0001c0002t0021 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2537C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 2537 | chr7 | 123681982 | |||||
chr7:123682134
|
G | A | 1 | a0001c0001t0006 | 3 | HG02145.hp1 HG02559.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2385C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 2385 | chr7 | 123682134 | |||||
chr7:123682209
|
A | C | 1 | a0001c0001t0014 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2310T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 2310 | chr7 | 123682209 | |||||
chr7:123682329
|
G | A | 1 | a0001c0002t0022 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2190C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 2190 | chr7 | 123682329 | |||||
chr7:123682622
|
G | A | 1 | a0001c0003t0005 | 4 | HG00673.hp1 HG02071.hp2 NA18964.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1897C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 1897 | chr7 | 123682622 | |||||
chr7:123682662
|
T | A | 12 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(9): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*1857A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 1857 | chr7 | 123682662 | |||||
chr7:123682725
|
G | C | 2 | a0001c0001t0004a0001c0001t0008 | 35 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1794C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 1794 | chr7 | 123682725 | |||||
chr7:123683030
|
C | G | 1 | a0001c0001t0013 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1489G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 1489 | chr7 | 123683030 | |||||
chr7:123683197
|
T | G | 2 | a0001c0001t0004a0001c0001t0008 | 35 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1322A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 1322 | chr7 | 123683197 | |||||
chr7:123683248
|
T | C | 1 | a0001c0002t0023 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1271A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 1271 | chr7 | 123683248 | |||||
chr7:123683374
|
T | A | 6 | a0001c0001t0003a0001c0001t0016a0001c0002t0003others(3): Show | 65 | HG00544.hp1 HG00673.hp1 HG01099.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1145A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 1145 | chr7 | 123683374 | |||||
chr7:123683512
|
G | A | 1 | a0001c0001t0008 | 2 | HG00408.hp1 NA18949.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1007C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 1007 | chr7 | 123683512 | |||||
chr7:123683610
|
C | T | 1 | a0001c0003t0020 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*909G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 909 | chr7 | 123683610 | |||||
chr7:123683624
|
T | C | 1 | a0001c0001t0010 | 2 | HG02922.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*895A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 895 | chr7 | 123683624 | |||||
chr7:123683687
|
A | G | 1 | a0001c0001t0012 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*832T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 832 | chr7 | 123683687 | |||||
chr7:123683700
|
T | C | 1 | a0001c0002t0024 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*819A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 819 | chr7 | 123683700 | |||||
chr7:123683771
|
T | A | 1 | a0001c0001t0009 | 2 | HG02451.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*748A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 748 | chr7 | 123683771 | |||||
chr7:123683928
|
C | T | 1 | a0001c0002t0019 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*591G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 591 | chr7 | 123683928 | |||||
chr7:123684016
|
G | T | 1 | a0001c0001t0007 | 2 | NA18993.hp1 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*503C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 503 | chr7 | 123684016 | |||||
chr7:123684019
|
C | A | 1 | a0001c0001t0015 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*500G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 500 | chr7 | 123684019 | |||||
chr7:123684107
|
A | T | 1 | a0001c0002t0018 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*412T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 412 | chr7 | 123684107 | |||||
chr7:123684113
|
G | T | 1 | a0001c0002t0017 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*406C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 406 | chr7 | 123684113 | |||||
chr7:123684332
|
T | C | 1 | a0001c0001t0016 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*187A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 187 | chr7 | 123684332 | |||||
chr7:123684492
|
AAT | A | 13 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(10): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*25_*26delAT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 25 | chr7 | 123684492 | |||||
chr7:123749001
|
T | G | 1 | a0001c0001t0011 | 2 | HG01167.hp1 HG01169.hp1 |
5_prime_UTR_variant | MODIFIER | c.-267A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/11 | 267 | chr7 | 123749001 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:123684691
|
CCAG | C | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1457-114_1457-112d others(5): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123684691 | ||||||
chr7:123684770
|
T | C | 1 | a0001c0002t0001g0252 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1457-190A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123684770 | ||||||
chr7:123684809
|
A | G | 1 | a0001c0001t0002g0074 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1457-229T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123684809 | ||||||
chr7:123684903
|
T | C | 2 | a0001c0001t0010g0039a0001c0001t0010g0040 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1457-323A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123684903 | ||||||
chr7:123685285
|
A | G | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1457-705T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685285 | ||||||
chr7:123685297
|
A | T | 3 | a0001c0001t0004g0006a0001c0001t0004g0150a0001c0001t0004g0151 | 5 | HG00323.hp1 HG01175.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.1457-717T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685297 | ||||||
chr7:123685333
|
A | G | 1 | a0001c0002t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1457-753T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685333 | ||||||
chr7:123685337
|
C | T | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1457-757G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685337 | ||||||
chr7:123685405
|
C | T | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1457-825G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685405 | ||||||
chr7:123685611
|
T | C | 1 | a0001c0001t0003g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1457-1031A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685611 | ||||||
chr7:123685642
|
A | G | 2 | a0001c0001t0003g0019a0001c0001t0003g0175 | 3 | NA18941.hp2 NA18984.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1457-1062T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685642 | ||||||
chr7:123685654
|
T | C | 2 | a0001c0002t0001g0273a0001c0002t0001g0278 | 2 | HG00423.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1457-1074A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685654 | ||||||
chr7:123685682
|
C | G | 1 | a0001c0001t0008g0160 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1457-1102G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685682 | ||||||
chr7:123685781
|
C | T | 1 | a0001c0001t0003g0177 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1457-1201G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685781 | ||||||
chr7:123685783
|
T | A | 2 | a0001c0001t0010g0039a0001c0001t0010g0040 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1457-1203A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685783 | ||||||
chr7:123685805
|
A | G | 3 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0043 | 3 | HG02145.hp1 HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1457-1225T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685805 | ||||||
chr7:123685859
|
TATATATA others(1): Show |
T | 6 | a0001c0002t0001g0223a0001c0002t0001g0224a0001c0002t0001g0225others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1457-1287_1457-128 others(12): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685859 | ||||||
chr7:123685871
|
TATAA | T | 54 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0019others(51): Show | 61 | HG00544.hp1 HG00673.hp1 HG01099.hp1 others(58): Show |
intron_variant | MODIFIER | c.1457-1295_1457-129 others(8): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685871 | ||||||
chr7:123685905
|
T | C | 2 | a0001c0001t0010g0039a0001c0001t0010g0040 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1457-1325A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685905 | ||||||
chr7:123685990
|
G | T | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1457-1410C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685990 | ||||||
chr7:123686001
|
T | C | 3 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0043 | 3 | HG02145.hp1 HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1457-1421A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123686001 | ||||||
chr7:123686183
|
A | T | 1 | a0001c0002t0001g0274 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1457-1603T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123686183 | ||||||
chr7:123686281
|
T | C | 2 | a0001c0001t0003g0011a0001c0001t0003g0106 | 3 | HG01168.hp2 HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1457-1701A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123686281 | ||||||
chr7:123686302
|
C | T | 1 | a0001c0002t0001g0295 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1457-1722G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123686302 | ||||||
chr7:123686926
|
A | G | 2 | a0001c0001t0002g0111a0001c0001t0002g0112 | 2 | NA19001.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1456+2116T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123686926 | ||||||
chr7:123686939
|
A | G | 1 | a0001c0003t0005g0129 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1456+2103T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123686939 | ||||||
chr7:123686969
|
A | G | 2 | a0001c0002t0001g0210a0001c0002t0001g0211 | 2 | NA18945.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1456+2073T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123686969 | ||||||
chr7:123687109
|
T | C | 2 | a0001c0001t0004g0148a0001c0001t0004g0154 | 2 | HG00280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1456+1933A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123687109 | ||||||
chr7:123687346
|
A | G | 1 | a0001c0002t0001g0312 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1456+1696T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123687346 | ||||||
chr7:123687426
|
A | G | 1 | a0001c0001t0002g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1456+1616T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123687426 | ||||||
chr7:123687618
|
C | T | 1 | a0001c0002t0001g0200 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1456+1424G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123687618 | ||||||
chr7:123687756
|
C | CTT | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1456+1284_1456+128 others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123687756 | ||||||
chr7:123687806
|
T | C | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1456+1236A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123687806 | ||||||
chr7:123687882
|
G | C | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1456+1160C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123687882 | ||||||
chr7:123688256
|
A | C | 1 | a0001c0001t0002g0014 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1456+786T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123688256 | ||||||
chr7:123688321
|
T | A | 1 | a0001c0002t0001g0251 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1456+721A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123688321 | ||||||
chr7:123688371
|
T | A | 1 | a0001c0001t0002g0103 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1456+671A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123688371 | ||||||
chr7:123688382
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1456+660G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123688382 | ||||||
chr7:123688485
|
C | T | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1456+557G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123688485 | ||||||
chr7:123688992
|
C | T | 3 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0001g0247 | 3 | HG00140.hp1 HG00323.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1456+50G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123688992 | ||||||
chr7:123689006
|
G | GTC | 10 | a0001c0001t0002g0045a0001c0001t0002g0098a0001c0001t0002g0149others(7): Show | 10 | HG01256.hp2 HG02258.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.1456+34_1456+35dup others(2): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123689006 | ||||||
chr7:123689006
|
GTC | G | 213 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(210): Show | 248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.1456+34_1456+35del others(2): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123689006 | ||||||
chr7:123689006
|
GTCTC | G | 4 | a0001c0001t0002g0067a0001c0001t0002g0090a0001c0001t0002g0094others(1): Show | 4 | HG01243.hp2 HG02970.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.1456+32_1456+35del others(4): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123689006 | ||||||
chr7:123689006
|
GTCTCTCT others(3): Show |
G | 1 | a0001c0001t0015g0060 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1456+26_1456+35del others(10): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123689006 | ||||||
chr7:123689006
|
GTCTCTCT others(9): Show |
G | 3 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0043 | 3 | HG02145.hp1 HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1456+20_1456+35del others(16): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123689006 | ||||||
chr7:123689032
|
C | T | 6 | a0001c0002t0001g0223a0001c0002t0001g0224a0001c0002t0001g0225others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1456+10G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123689032 | ||||||
chr7:123689213
|
A | G | 4 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(1): Show | 4 | HG00738.hp1 HG01099.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.1348-63T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123689213 | ||||||
chr7:123689313
|
C | A | 2 | a0001c0002t0001g0002a0001c0002t0001g0235 | 5 | NA18942.hp1 NA18962.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1348-163G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123689313 | ||||||
chr7:123689427
|
T | A | 1 | a0001c0002t0001g0206 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1348-277A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123689427 | ||||||
chr7:123689528
|
C | T | 311 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(308): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.1348-378G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123689528 | ||||||
chr7:123689549
|
G | A | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1348-399C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123689549 | ||||||
chr7:123689700
|
T | G | 239 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(236): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.1348-550A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123689700 | ||||||
chr7:123689793
|
ATT | A | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1348-645_1348-644d others(4): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123689793 | ||||||
chr7:123689798
|
A | T | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1348-648T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123689798 | ||||||
chr7:123689799
|
AT | A | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1348-650delA | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123689799 | ||||||
chr7:123689825
|
T | C | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1348-675A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123689825 | ||||||
chr7:123689900
|
A | AATT | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1348-753_1348-751d others(5): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123689900 | ||||||
chr7:123690071
|
T | C | 8 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(5): Show | 8 | HG02145.hp1 HG02559.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1348-921A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123690071 | ||||||
chr7:123690212
|
A | C | 2 | a0001c0002t0001g0210a0001c0002t0001g0211 | 2 | NA18945.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1348-1062T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123690212 | ||||||
chr7:123690421
|
C | A | 1 | a0001c0001t0002g0062 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1348-1271G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123690421 | ||||||
chr7:123690453
|
C | A | 1 | a0001c0001t0002g0062 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1348-1303G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123690453 | ||||||
chr7:123690579
|
A | ATCCAACA others(36): Show |
138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1348-1430_1348-142 others(47): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123690579 | ||||||
chr7:123690585
|
A | C | 99 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0035others(96): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1348-1435T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123690585 | ||||||
chr7:123690612
|
T | G | 1 | a0001c0002t0001g0245 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1348-1462A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123690612 | ||||||
chr7:123690613
|
C | CT | 8 | a0001c0001t0002g0045a0001c0001t0002g0070a0001c0001t0002g0072others(5): Show | 9 | HG00673.hp2 HG02015.hp2 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.1348-1464dupA | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123690613 | ||||||
chr7:123690613
|
C | T | 1 | a0001c0001t0002g0117 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1348-1463G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123690613 | ||||||
chr7:123690762
|
G | A | 1 | a0001c0001t0002g0014 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1347+1585C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123690762 | ||||||
chr7:123690902
|
T | C | 1 | a0001c0003t0003g0125 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1347+1445A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123690902 | ||||||
chr7:123690921
|
C | T | 1 | a0001c0002t0001g0300 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1347+1426G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123690921 | ||||||
chr7:123691108
|
T | C | 1 | a0001c0001t0016g0134 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1347+1239A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123691108 | ||||||
chr7:123691156
|
C | G | 3 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0001g0247 | 3 | HG00140.hp1 HG00323.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1347+1191G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123691156 | ||||||
chr7:123691193
|
A | C | 2 | a0001c0002t0003g0306a0001c0002t0003g0307 | 2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1347+1154T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123691193 | ||||||
chr7:123691340
|
T | C | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1347+1007A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123691340 | ||||||
chr7:123691359
|
G | A | 1 | a0001c0002t0001g0221 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1347+988C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123691359 | ||||||
chr7:123691399
|
A | T | 2 | a0001c0001t0010g0039a0001c0001t0010g0040 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1347+948T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123691399 | ||||||
chr7:123691823
|
T | C | 1 | a0001c0002t0001g0025 | 2 | HG00642.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1347+524A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123691823 | ||||||
chr7:123691882
|
T | C | 2 | a0001c0001t0003g0127a0001c0001t0003g0128 | 2 | NA18991.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1347+465A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123691882 | ||||||
chr7:123691914
|
C | G | 2 | a0001c0001t0010g0039a0001c0001t0010g0040 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1347+433G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123691914 | ||||||
chr7:123692094
|
A | G | 4 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0178others(1): Show | 6 | HG01884.hp2 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1347+253T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123692094 | ||||||
chr7:123692255
|
GAA | G | 4 | a0001c0001t0002g0008a0001c0001t0002g0077a0001c0001t0002g0082others(1): Show | 5 | HG01891.hp2 HG03130.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1347+90_1347+91del others(2): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123692255 | ||||||
chr7:123692874
|
T | C | 1 | a0001c0001t0003g0137 | 1 | HG02886.hp2 | splice_region_variant&intron_variant | LOW | c.827-7A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123692874 | ||||||
chr7:123693074
|
T | C | 3 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0043 | 3 | HG02145.hp1 HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.827-207A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123693074 | ||||||
chr7:123693079
|
C | T | 2 | a0001c0001t0010g0039a0001c0001t0010g0040 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.827-212G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123693079 | ||||||
chr7:123693235
|
A | G | 1 | a0001c0001t0002g0014 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.827-368T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123693235 | ||||||
chr7:123693336
|
T | C | 3 | a0001c0002t0001g0263a0001c0002t0001g0266a0001c0002t0001g0282 | 3 | NA18983.hp1 NA19002.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.827-469A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123693336 | ||||||
chr7:123693676
|
A | G | 1 | a0001c0002t0001g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.827-809T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123693676 | ||||||
chr7:123693753
|
G | A | 2 | a0001c0002t0003g0306a0001c0002t0003g0307 | 2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.827-886C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123693753 | ||||||
chr7:123694190
|
T | A | 2 | a0001c0001t0003g0118a0001c0001t0003g0119 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.826+525A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123694190 | ||||||
chr7:123694208
|
A | G | 3 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0147 | 5 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.826+507T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123694208 | ||||||
chr7:123694209
|
C | T | 3 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0043 | 3 | HG02145.hp1 HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.826+506G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123694209 | ||||||
chr7:123694278
|
T | G | 31 | a0001c0001t0003g0001a0001c0001t0004g0006a0001c0001t0004g0016others(28): Show | 39 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.826+437A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123694278 | ||||||
chr7:123694642
|
GT | G | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.826+72delA | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123694642 | ||||||
chr7:123694693
|
G | A | 2 | a0001c0001t0010g0039a0001c0001t0010g0040 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.826+22C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123694693 | ||||||
chr7:123694911
|
T | C | 36 | a0001c0001t0003g0001a0001c0001t0003g0011a0001c0001t0003g0012others(33): Show | 43 | HG00544.hp1 HG00673.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.673-43A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 7/10 | chr7 | 123694911 | ||||||
chr7:123695024
|
T | G | 99 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0035others(96): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.673-156A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 7/10 | chr7 | 123695024 | ||||||
chr7:123695296
|
A | G | 130 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(127): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.673-428T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 7/10 | chr7 | 123695296 | ||||||
chr7:123695429
|
T | G | 5 | a0001c0002t0001g0206a0001c0002t0001g0220a0001c0002t0001g0221others(2): Show | 5 | HG01256.hp1 HG02572.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.672+394A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 7/10 | chr7 | 123695429 | ||||||
chr7:123695544
|
G | A | 1 | a0001c0002t0001g0268 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.672+279C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 7/10 | chr7 | 123695544 | ||||||
chr7:123695630
|
C | T | 1 | a0001c0002t0018g0207 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.672+193G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 7/10 | chr7 | 123695630 | ||||||
chr7:123695879
|
T | C | 1 | a0001c0001t0009g0120 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.630-14A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 6/10 | chr7 | 123695879 | ||||||
chr7:123696115
|
T | C | 1 | a0001c0001t0002g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.630-250A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 6/10 | chr7 | 123696115 | ||||||
chr7:123696412
|
T | TA | 6 | a0001c0002t0001g0209a0001c0002t0001g0212a0001c0002t0001g0213others(3): Show | 6 | HG02071.hp2 HG02886.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.629+166dupT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 6/10 | chr7 | 123696412 | ||||||
chr7:123696750
|
G | A | 99 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0035others(96): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(113): Show |
splice_region_variant&intron_variant | LOW | c.461-3C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123696750 | ||||||
chr7:123696967
|
C | T | 1 | a0001c0001t0008g0160 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.461-220G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123696967 | ||||||
chr7:123697060
|
C | A | 39 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0031others(36): Show | 43 | HG00099.hp2 HG00423.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.461-313G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123697060 | ||||||
chr7:123697067
|
T | A | 1 | a0001c0001t0003g0187 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.461-320A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123697067 | ||||||
chr7:123697098
|
A | G | 3 | a0001c0001t0004g0006a0001c0001t0004g0150a0001c0001t0004g0151 | 5 | HG00323.hp1 HG01175.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.461-351T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123697098 | ||||||
chr7:123697119
|
GAAAGT | G | 31 | a0001c0001t0002g0149a0001c0001t0004g0006a0001c0001t0004g0016others(28): Show | 36 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.461-377_461-373del others(5): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123697119 | ||||||
chr7:123697132
|
C | T | 1 | a0001c0001t0003g0108 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.461-385G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123697132 | ||||||
chr7:123697348
|
T | C | 2 | a0001c0001t0003g0118a0001c0001t0003g0119 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.461-601A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123697348 | ||||||
chr7:123697680
|
G | C | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.461-933C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123697680 | ||||||
chr7:123697772
|
A | G | 1 | a0001c0002t0001g0202 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.461-1025T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123697772 | ||||||
chr7:123697809
|
T | C | 1 | a0001c0001t0002g0055 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.461-1062A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123697809 | ||||||
chr7:123697819
|
C | T | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.461-1072G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123697819 | ||||||
chr7:123698058
|
G | GT | 6 | a0001c0001t0002g0044a0001c0002t0001g0028a0001c0002t0001g0197others(3): Show | 7 | HG02280.hp2 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.461-1312dupA | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123698058 | ||||||
chr7:123698058
|
GT | G | 6 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(3): Show | 6 | HG02145.hp1 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.461-1312delA | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123698058 | ||||||
chr7:123698103
|
T | C | 1 | a0001c0002t0001g0234 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.461-1356A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123698103 | ||||||
chr7:123698234
|
A | G | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG02965.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.461-1487T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123698234 | ||||||
chr7:123698351
|
G | GA | 13 | a0001c0002t0001g0026a0001c0002t0001g0206a0001c0002t0001g0219others(10): Show | 14 | HG01256.hp1 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.461-1605dupT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123698351 | ||||||
chr7:123698659
|
G | C | 130 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(127): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.461-1912C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123698659 | ||||||
chr7:123698818
|
A | G | 311 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(308): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.461-2071T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123698818 | ||||||
chr7:123698881
|
G | A | 1 | a0001c0001t0002g0083 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.461-2134C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123698881 | ||||||
chr7:123699123
|
C | T | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.461-2376G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123699123 | ||||||
chr7:123699223
|
C | T | 2 | a0001c0001t0010g0039a0001c0001t0010g0040 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.461-2476G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123699223 | ||||||
chr7:123699239
|
G | A | 1 | a0001c0001t0002g0044 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.461-2492C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123699239 | ||||||
chr7:123699663
|
C | G | 1 | a0001c0001t0002g0101 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.461-2916G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123699663 | ||||||
chr7:123699867
|
C | T | 99 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0035others(96): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.461-3120G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123699867 | ||||||
chr7:123699888
|
T | A | 1 | a0001c0002t0001g0241 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.461-3141A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123699888 | ||||||
chr7:123699942
|
C | T | 1 | a0001c0001t0002g0096 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.461-3195G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123699942 | ||||||
chr7:123699951
|
C | T | 1 | a0001c0002t0001g0233 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.461-3204G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123699951 | ||||||
chr7:123699959
|
G | A | 1 | a0001c0001t0003g0186 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.461-3212C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123699959 | ||||||
chr7:123699993
|
G | A | 1 | a0001c0002t0001g0295 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.461-3246C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123699993 | ||||||
chr7:123700133
|
G | A | 2 | a0001c0002t0001g0267a0001c0002t0001g0268 | 2 | NA18948.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.461-3386C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700133 | ||||||
chr7:123700175
|
CA | C | 29 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0023others(26): Show | 34 | HG00408.hp2 HG00621.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.461-3429delT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700175 | ||||||
chr7:123700175
|
CAA | C | 22 | a0001c0001t0002g0009a0001c0001t0002g0045a0001c0001t0002g0047others(19): Show | 24 | HG00099.hp1 HG00733.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.461-3430_461-3429d others(4): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700175 | ||||||
chr7:123700175
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0002g0149a0001c0001t0004g0153 | 2 | HG02258.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.461-3439_461-3429d others(13): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700175 | ||||||
chr7:123700175
|
CAAAAAAA others(5): Show |
C | 37 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0147others(34): Show | 48 | HG00280.hp1 HG00621.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.461-3440_461-3429d others(14): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700175 | ||||||
chr7:123700175
|
CAAAAAAA others(6): Show |
C | 57 | a0001c0001t0002g0010a0001c0001t0002g0086a0001c0001t0002g0089others(54): Show | 64 | HG00408.hp1 HG00544.hp1 HG01099.hp1 others(61): Show |
intron_variant | MODIFIER | c.461-3441_461-3429d others(15): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700175 | ||||||
chr7:123700175
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0004g0151 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.461-3442_461-3429d others(16): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700175 | ||||||
chr7:123700175
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0002g0071 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.461-3445_461-3429d others(19): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700175 | ||||||
chr7:123700183
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0002g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.461-3437_461-3436i others(15): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700183 | ||||||
chr7:123700198
|
AAAAAAAA others(3): Show |
A | 2 | a0001c0001t0010g0039a0001c0001t0010g0040 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.461-3461_461-3452d others(12): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700198 | ||||||
chr7:123700200
|
AAAAAAAA others(1): Show |
A | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0026others(65): Show | 79 | HG00099.hp2 HG00738.hp2 HG01071.hp1 others(76): Show |
intron_variant | MODIFIER | c.461-3461_461-3454d others(10): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700200 | ||||||
chr7:123700201
|
AAAAAAAC | A | 50 | a0001c0001t0006g0041a0001c0002t0001g0004a0001c0002t0001g0024others(47): Show | 57 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.461-3461_461-3455d others(9): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700201 | ||||||
chr7:123700202
|
AAAAAAC | A | 13 | a0001c0001t0006g0043a0001c0002t0001g0025a0001c0002t0001g0211others(10): Show | 14 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.461-3461_461-3456d others(8): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700202 | ||||||
chr7:123700203
|
A | AAAAAAAA others(20): Show |
1 | a0001c0001t0002g0035 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.461-3457_461-3456i others(29): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700203 | ||||||
chr7:123700203
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0002g0038 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.461-3457_461-3456i others(23): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700203 | ||||||
chr7:123700203
|
A | AAAAAAAA others(6): Show |
2 | a0001c0001t0002g0037a0001c0001t0014g0190 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.461-3457_461-3456i others(15): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700203 | ||||||
chr7:123700203
|
A | C | 1 | a0001c0001t0002g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.461-3456T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700203 | ||||||
chr7:123700446
|
CT | C | 239 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(236): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.461-3700delA | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700446 | ||||||
chr7:123700533
|
G | T | 3 | a0001c0001t0004g0006a0001c0001t0004g0150a0001c0001t0004g0151 | 5 | HG00323.hp1 HG01175.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.461-3786C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700533 | ||||||
chr7:123700795
|
C | T | 130 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(127): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.460+3839G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700795 | ||||||
chr7:123701068
|
A | G | 3 | a0001c0002t0001g0225a0001c0002t0001g0304a0001c0002t0017g0305 | 3 | HG03486.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.460+3566T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123701068 | ||||||
chr7:123701069
|
G | C | 99 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0035others(96): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.460+3565C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123701069 | ||||||
chr7:123701129
|
T | C | 3 | a0001c0002t0001g0301a0001c0002t0001g0302a0001c0002t0001g0303 | 3 | HG00642.hp1 HG01978.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.460+3505A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123701129 | ||||||
chr7:123701162
|
G | A | 1 | a0001c0001t0003g0184 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.460+3472C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123701162 | ||||||
chr7:123701270
|
A | C | 5 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.460+3364T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123701270 | ||||||
chr7:123701456
|
A | C | 2 | a0001c0001t0003g0118a0001c0001t0003g0119 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.460+3178T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123701456 | ||||||
chr7:123701692
|
C | A | 2 | a0001c0002t0001g0240a0001c0002t0001g0246 | 2 | NA18986.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.460+2942G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123701692 | ||||||
chr7:123701884
|
T | G | 31 | a0001c0001t0003g0001a0001c0001t0004g0006a0001c0001t0004g0016others(28): Show | 39 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.460+2750A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123701884 | ||||||
chr7:123701892
|
T | A | 1 | a0001c0002t0001g0245 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.460+2742A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123701892 | ||||||
chr7:123701945
|
T | TA | 231 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(228): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.460+2688dupT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123701945 | ||||||
chr7:123701945
|
T | TAA | 6 | a0001c0002t0001g0213a0001c0002t0001g0217a0001c0003t0003g0124others(3): Show | 6 | HG00544.hp1 HG00673.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.460+2687_460+2688d others(4): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123701945 | ||||||
chr7:123702111
|
A | G | 2 | a0001c0001t0004g0167a0001c0001t0004g0170 | 2 | HG00673.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.460+2523T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123702111 | ||||||
chr7:123702230
|
A | G | 1 | a0001c0001t0002g0087 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.460+2404T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123702230 | ||||||
chr7:123702231
|
C | T | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.460+2403G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123702231 | ||||||
chr7:123702389
|
G | A | 2 | a0001c0002t0001g0312a0001c0002t0023g0236 | 2 | HG02698.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.460+2245C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123702389 | ||||||
chr7:123702466
|
C | A | 2 | a0001c0002t0001g0304a0001c0002t0017g0305 | 2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.460+2168G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123702466 | ||||||
chr7:123702691
|
G | A | 1 | a0001c0001t0004g0155 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.460+1943C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123702691 | ||||||
chr7:123702713
|
T | C | 9 | a0001c0002t0001g0030a0001c0002t0001g0258a0001c0002t0001g0270others(6): Show | 10 | HG01081.hp1 HG02080.hp2 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.460+1921A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123702713 | ||||||
chr7:123702812
|
C | A | 2 | a0001c0002t0001g0253a0001c0002t0001g0255 | 2 | HG02155.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.460+1822G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123702812 | ||||||
chr7:123703034
|
T | C | 2 | a0001c0001t0002g0091a0001c0001t0002g0092 | 2 | HG01943.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.460+1600A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123703034 | ||||||
chr7:123703268
|
C | T | 1 | a0001c0001t0002g0044 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.460+1366G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123703268 | ||||||
chr7:123703425
|
G | C | 4 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.460+1209C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123703425 | ||||||
chr7:123703494
|
G | T | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG02965.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.460+1140C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123703494 | ||||||
chr7:123703665
|
A | G | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.460+969T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123703665 | ||||||
chr7:123703705
|
G | T | 2 | a0001c0002t0001g0198a0001c0002t0001g0199 | 2 | HG01261.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.460+929C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123703705 | ||||||
chr7:123703893
|
A | G | 39 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0031others(36): Show | 43 | HG00099.hp2 HG00423.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.460+741T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123703893 | ||||||
chr7:123704760
|
G | A | 1 | a0001c0001t0002g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.437-103C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 4/10 | chr7 | 123704760 | ||||||
chr7:123704975
|
A | C | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.437-318T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 4/10 | chr7 | 123704975 | ||||||
chr7:123705070
|
G | T | 2 | a0001c0001t0002g0055a0001c0001t0002g0117 | 2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.437-413C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 4/10 | chr7 | 123705070 | ||||||
chr7:123705080
|
T | C | 1 | a0001c0001t0010g0040 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.437-423A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 4/10 | chr7 | 123705080 | ||||||
chr7:123705796
|
C | G | 1 | a0001c0001t0002g0089 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.436+481G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 4/10 | chr7 | 123705796 | ||||||
chr7:123705835
|
T | C | 59 | a0001c0001t0002g0143a0001c0001t0002g0144a0001c0001t0002g0145others(56): Show | 69 | HG00544.hp1 HG00673.hp1 HG01099.hp1 others(66): Show |
intron_variant | MODIFIER | c.436+442A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 4/10 | chr7 | 123705835 | ||||||
chr7:123705843
|
T | C | 2 | a0001c0001t0002g0091a0001c0001t0002g0092 | 2 | HG01943.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.436+434A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 4/10 | chr7 | 123705843 | ||||||
chr7:123706139
|
T | C | 4 | a0001c0002t0001g0209a0001c0002t0001g0212a0001c0002t0001g0213others(1): Show | 4 | HG02886.hp1 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+138A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 4/10 | chr7 | 123706139 | ||||||
chr7:123706244
|
C | T | 1 | a0001c0002t0001g0298 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.436+33G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 4/10 | chr7 | 123706244 | ||||||
chr7:123706539
|
A | G | 1 | a0001c0001t0002g0044 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.340-166T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 3/10 | chr7 | 123706539 | ||||||
chr7:123706595
|
T | C | 1 | a0001c0002t0001g0200 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.339+145A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 3/10 | chr7 | 123706595 | ||||||
chr7:123706708
|
T | C | 10 | a0001c0002t0001g0031a0001c0002t0001g0256a0001c0002t0001g0260others(7): Show | 11 | HG00423.hp2 HG01934.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.339+32A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 3/10 | chr7 | 123706708 | ||||||
chr7:123706943
|
C | T | 2 | a0001c0001t0002g0045a0001c0001t0002g0070 | 2 | HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.253-117G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123706943 | ||||||
chr7:123706965
|
T | C | 1 | a0001c0001t0002g0096 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.253-139A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123706965 | ||||||
chr7:123707009
|
A | C | 237 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(234): Show | 273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.253-183T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123707009 | ||||||
chr7:123707126
|
T | C | 1 | a0001c0001t0003g0183 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.253-300A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123707126 | ||||||
chr7:123707179
|
T | C | 8 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(5): Show | 8 | HG02145.hp1 HG02559.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.253-353A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123707179 | ||||||
chr7:123707214
|
C | T | 6 | a0001c0001t0002g0053a0001c0001t0002g0061a0001c0001t0002g0063others(3): Show | 6 | HG01884.hp1 HG02148.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.253-388G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123707214 | ||||||
chr7:123707383
|
T | C | 1 | a0001c0001t0003g0182 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.253-557A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123707383 | ||||||
chr7:123707439
|
T | C | 1 | a0001c0001t0014g0190 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.253-613A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123707439 | ||||||
chr7:123707574
|
C | T | 11 | a0001c0001t0003g0021a0001c0001t0003g0116a0001c0001t0003g0180others(8): Show | 12 | HG01192.hp2 HG01346.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.253-748G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123707574 | ||||||
chr7:123707910
|
G | A | 1 | a0001c0002t0001g0259 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.253-1084C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123707910 | ||||||
chr7:123708152
|
T | C | 1 | a0001c0002t0001g0260 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.252+937A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123708152 | ||||||
chr7:123708181
|
AAAC | A | 130 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(127): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.252+905_252+907del others(3): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123708181 | ||||||
chr7:123708261
|
C | T | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.252+828G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123708261 | ||||||
chr7:123708302
|
G | T | 43 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0019others(40): Show | 50 | HG00544.hp1 HG00673.hp1 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.252+787C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123708302 | ||||||
chr7:123708569
|
A | G | 137 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(134): Show | 156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.252+520T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123708569 | ||||||
chr7:123708690
|
C | T | 239 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(236): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.252+399G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123708690 | ||||||
chr7:123708935
|
G | A | 2 | a0001c0002t0001g0297a0001c0005t0001g0244 | 2 | HG00738.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.252+154C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123708935 | ||||||
chr7:123709460
|
T | G | 4 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0104others(1): Show | 4 | HG01192.hp1 HG01255.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-237A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123709460 | ||||||
chr7:123709523
|
A | T | 13 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0064others(10): Show | 14 | HG00423.hp1 HG01192.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.118-300T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123709523 | ||||||
chr7:123709572
|
G | T | 6 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(3): Show | 6 | HG02145.hp1 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-349C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123709572 | ||||||
chr7:123709573
|
T | G | 239 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(236): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.118-350A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123709573 | ||||||
chr7:123709605
|
A | G | 1 | a0001c0001t0002g0143 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.118-382T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123709605 | ||||||
chr7:123709732
|
T | A | 2 | a0001c0002t0001g0249a0001c0002t0001g0254 | 2 | HG00544.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.118-509A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123709732 | ||||||
chr7:123709733
|
G | C | 2 | a0001c0002t0001g0249a0001c0002t0001g0254 | 2 | HG00544.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.118-510C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123709733 | ||||||
chr7:123709734
|
T | A | 2 | a0001c0002t0001g0249a0001c0002t0001g0254 | 2 | HG00544.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.118-511A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123709734 | ||||||
chr7:123709784
|
G | A | 1 | a0001c0002t0001g0301 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.118-561C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123709784 | ||||||
chr7:123709839
|
A | T | 1 | a0001c0001t0002g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.118-616T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123709839 | ||||||
chr7:123709865
|
G | T | 1 | a0001c0001t0003g0175 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.118-642C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123709865 | ||||||
chr7:123709870
|
G | A | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.118-647C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123709870 | ||||||
chr7:123710006
|
C | T | 137 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(134): Show | 156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.118-783G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123710006 | ||||||
chr7:123710164
|
T | C | 2 | a0001c0002t0001g0273a0001c0002t0001g0278 | 2 | HG00423.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.118-941A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123710164 | ||||||
chr7:123710364
|
AAGTAATT others(5): Show |
A | 1 | a0001c0002t0001g0237 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.118-1153_118-1142d others(14): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123710364 | ||||||
chr7:123710481
|
T | C | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.118-1258A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123710481 | ||||||
chr7:123710513
|
T | C | 1 | a0001c0001t0003g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.118-1290A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123710513 | ||||||
chr7:123711005
|
A | G | 1 | a0001c0002t0001g0250 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.118-1782T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123711005 | ||||||
chr7:123711141
|
C | A | 4 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0002t0001g0273others(1): Show | 4 | HG00423.hp2 HG02647.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-1918G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123711141 | ||||||
chr7:123711165
|
G | C | 2 | a0001c0001t0010g0039a0001c0001t0010g0040 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.118-1942C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123711165 | ||||||
chr7:123711298
|
A | C | 1 | a0001c0001t0002g0047 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.118-2075T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123711298 | ||||||
chr7:123711341
|
A | T | 2 | a0001c0002t0001g0267a0001c0002t0001g0268 | 2 | NA18948.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.118-2118T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123711341 | ||||||
chr7:123711468
|
A | G | 3 | a0001c0001t0002g0053a0001c0001t0002g0061a0001c0001t0002g0066 | 3 | HG03490.hp2 HG03492.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.118-2245T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123711468 | ||||||
chr7:123711498
|
T | C | 1 | a0001c0001t0003g0179 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.118-2275A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123711498 | ||||||
chr7:123711525
|
T | C | 2 | a0001c0001t0010g0039a0001c0001t0010g0040 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.118-2302A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123711525 | ||||||
chr7:123711554
|
C | A | 5 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-2331G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123711554 | ||||||
chr7:123711766
|
C | T | 3 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0043 | 3 | HG02145.hp1 HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.118-2543G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123711766 | ||||||
chr7:123711818
|
G | A | 8 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(5): Show | 8 | HG02145.hp1 HG02559.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-2595C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123711818 | ||||||
chr7:123711843
|
A | G | 1 | a0001c0001t0003g0106 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.118-2620T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123711843 | ||||||
chr7:123712159
|
G | T | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG02965.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.118-2936C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123712159 | ||||||
chr7:123712253
|
T | C | 32 | a0001c0001t0002g0149a0001c0001t0003g0001a0001c0001t0004g0006others(29): Show | 40 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.118-3030A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123712253 | ||||||
chr7:123712319
|
A | G | 1 | a0001c0003t0003g0133 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.118-3096T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123712319 | ||||||
chr7:123712729
|
C | T | 1 | a0001c0001t0003g0118 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.118-3506G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123712729 | ||||||
chr7:123712802
|
T | C | 2 | a0001c0001t0002g0192a0001c0001t0002g0193 | 2 | NA18952.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.118-3579A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123712802 | ||||||
chr7:123713093
|
CTA | C | 2 | a0001c0001t0002g0015a0001c0001t0002g0147 | 3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.118-3872_118-3871d others(4): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123713093 | ||||||
chr7:123713360
|
G | A | 130 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(127): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.118-4137C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123713360 | ||||||
chr7:123713432
|
T | C | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG02965.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.118-4209A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123713432 | ||||||
chr7:123713567
|
C | T | 1 | a0001c0002t0001g0200 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.118-4344G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123713567 | ||||||
chr7:123713643
|
C | T | 2 | a0001c0001t0003g0011a0001c0001t0003g0106 | 3 | HG01168.hp2 HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.118-4420G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123713643 | ||||||
chr7:123713654
|
G | C | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.118-4431C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123713654 | ||||||
chr7:123713780
|
G | A | 1 | a0001c0002t0001g0238 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.118-4557C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123713780 | ||||||
chr7:123713783
|
G | A | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG02965.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.118-4560C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123713783 | ||||||
chr7:123713964
|
T | C | 1 | a0001c0001t0004g0170 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.118-4741A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123713964 | ||||||
chr7:123714296
|
G | A | 4 | a0001c0002t0001g0239a0001c0002t0001g0240a0001c0002t0001g0246others(1): Show | 4 | NA18986.hp2 NA19005.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-5073C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123714296 | ||||||
chr7:123714482
|
A | G | 239 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(236): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.118-5259T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123714482 | ||||||
chr7:123714746
|
G | C | 1 | a0001c0001t0002g0044 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.118-5523C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123714746 | ||||||
chr7:123714753
|
T | C | 130 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(127): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.118-5530A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123714753 | ||||||
chr7:123714784
|
G | C | 1 | a0001c0002t0001g0222 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.118-5561C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123714784 | ||||||
chr7:123714849
|
T | C | 3 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0147 | 5 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-5626A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123714849 | ||||||
chr7:123715077
|
A | G | 1 | a0001c0001t0004g0155 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.118-5854T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123715077 | ||||||
chr7:123715224
|
A | C | 1 | a0001c0001t0002g0059 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.118-6001T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123715224 | ||||||
chr7:123715325
|
G | T | 2 | a0001c0001t0010g0039a0001c0001t0010g0040 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.118-6102C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123715325 | ||||||
chr7:123715350
|
T | C | 1 | a0001c0002t0001g0292 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.118-6127A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123715350 | ||||||
chr7:123715429
|
T | C | 239 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(236): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.118-6206A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123715429 | ||||||
chr7:123715475
|
C | A | 1 | a0001c0001t0002g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.118-6252G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123715475 | ||||||
chr7:123715640
|
C | G | 2 | a0001c0002t0001g0301a0001c0002t0001g0302 | 2 | HG00642.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.118-6417G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123715640 | ||||||
chr7:123715665
|
A | C | 1 | a0001c0002t0001g0200 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.118-6442T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123715665 | ||||||
chr7:123715709
|
A | G | 1 | a0001c0002t0001g0256 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.118-6486T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123715709 | ||||||
chr7:123715723
|
G | C | 1 | a0001c0001t0002g0014 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.118-6500C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123715723 | ||||||
chr7:123715920
|
A | G | 8 | a0001c0001t0003g0132a0001c0001t0003g0135a0001c0001t0003g0137others(5): Show | 8 | HG01433.hp1 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.118-6697T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123715920 | ||||||
chr7:123716008
|
C | T | 239 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(236): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.118-6785G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123716008 | ||||||
chr7:123716292
|
T | C | 1 | a0001c0002t0001g0222 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.118-7069A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123716292 | ||||||
chr7:123716457
|
A | C | 130 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(127): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.118-7234T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123716457 | ||||||
chr7:123716586
|
A | G | 3 | a0001c0001t0003g0011a0001c0001t0003g0105a0001c0001t0003g0106 | 4 | HG01168.hp2 HG03654.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-7363T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123716586 | ||||||
chr7:123716588
|
C | G | 130 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(127): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.118-7365G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123716588 | ||||||
chr7:123716635
|
G | GGGAGAGA others(5): Show |
3 | a0001c0002t0001g0263a0001c0002t0001g0266a0001c0002t0001g0282 | 3 | NA18983.hp1 NA19002.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.118-7424_118-7413d others(14): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123716635 | ||||||
chr7:123716673
|
G | A | 2 | a0001c0001t0010g0039a0001c0001t0010g0040 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.118-7450C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123716673 | ||||||
chr7:123716841
|
A | G | 2 | a0001c0002t0001g0297a0001c0005t0001g0244 | 2 | HG00738.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.118-7618T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123716841 | ||||||
chr7:123716846
|
A | G | 1 | a0001c0003t0003g0124 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.118-7623T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123716846 | ||||||
chr7:123716867
|
A | C | 239 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(236): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.118-7644T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123716867 | ||||||
chr7:123717114
|
T | C | 1 | a0001c0002t0001g0198 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.118-7891A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123717114 | ||||||
chr7:123717224
|
C | A | 8 | a0001c0001t0003g0132a0001c0001t0003g0135a0001c0001t0003g0137others(5): Show | 8 | HG01433.hp1 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.118-8001G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123717224 | ||||||
chr7:123717456
|
G | A | 1 | a0001c0001t0002g0044 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.118-8233C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123717456 | ||||||
chr7:123717525
|
C | T | 1 | a0001c0001t0002g0054 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.118-8302G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123717525 | ||||||
chr7:123717574
|
T | C | 1 | a0001c0002t0001g0219 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.118-8351A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123717574 | ||||||
chr7:123717592
|
A | G | 237 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(234): Show | 273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.118-8369T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123717592 | ||||||
chr7:123717931
|
C | T | 1 | a0002c0004t0002g0065 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.118-8708G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123717931 | ||||||
chr7:123718093
|
GTTAA | G | 130 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(127): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.118-8874_118-8871d others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123718093 | ||||||
chr7:123718295
|
G | C | 2 | a0001c0001t0003g0118a0001c0001t0003g0119 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.118-9072C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123718295 | ||||||
chr7:123718302
|
G | T | 1 | a0001c0001t0002g0095 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.118-9079C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123718302 | ||||||
chr7:123718331
|
T | C | 2 | a0001c0002t0001g0241a0001c0002t0001g0242 | 2 | HG00323.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.118-9108A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123718331 | ||||||
chr7:123718393
|
C | G | 1 | a0001c0001t0003g0110 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.118-9170G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123718393 | ||||||
chr7:123718484
|
AAGAT | A | 3 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0043 | 3 | HG02145.hp1 HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.118-9265_118-9262d others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123718484 | ||||||
chr7:123718700
|
T | C | 31 | a0001c0001t0003g0001a0001c0001t0004g0006a0001c0001t0004g0016others(28): Show | 39 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.118-9477A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123718700 | ||||||
chr7:123719011
|
T | G | 66 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0028others(63): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.118-9788A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123719011 | ||||||
chr7:123719144
|
C | G | 3 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0147 | 5 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-9921G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123719144 | ||||||
chr7:123719218
|
A | G | 8 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(5): Show | 8 | HG02145.hp1 HG02559.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-9995T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123719218 | ||||||
chr7:123719225
|
T | C | 1 | a0001c0001t0002g0083 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.118-10002A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123719225 | ||||||
chr7:123719654
|
A | G | 1 | a0001c0001t0003g0176 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.118-10431T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123719654 | ||||||
chr7:123719953
|
A | C | 99 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0035others(96): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.118-10730T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123719953 | ||||||
chr7:123720123
|
A | C | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG02965.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.118-10900T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720123 | ||||||
chr7:123720139
|
G | A | 1 | a0001c0002t0001g0245 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.118-10916C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720139 | ||||||
chr7:123720298
|
T | C | 39 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0035others(36): Show | 46 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.118-11075A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720298 | ||||||
chr7:123720335
|
A | C | 2 | a0001c0002t0001g0288a0001c0002t0001g0289 | 2 | HG01081.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.118-11112T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720335 | ||||||
chr7:123720344
|
C | CA | 70 | a0001c0001t0002g0055a0001c0001t0002g0077a0001c0001t0002g0085others(67): Show | 81 | HG00423.hp2 HG00544.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.118-11122dupT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720344 | ||||||
chr7:123720344
|
CA | C | 42 | a0001c0001t0002g0046a0001c0001t0002g0064a0001c0001t0002g0074others(39): Show | 47 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.118-11122delT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720344 | ||||||
chr7:123720344
|
CAA | C | 6 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(3): Show | 6 | HG01496.hp1 HG02922.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-11123_118-1112 others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720344 | ||||||
chr7:123720369
|
T | A | 1 | a0001c0001t0001g0114 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.118-11146A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720369 | ||||||
chr7:123720627
|
T | A | 1 | a0001c0001t0003g0141 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.118-11404A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720627 | ||||||
chr7:123720650
|
A | AT | 32 | a0001c0001t0003g0012a0001c0001t0003g0107a0001c0001t0003g0108others(29): Show | 36 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.118-11428dupA | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720650 | ||||||
chr7:123720650
|
A | T | 1 | a0001c0001t0002g0046 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.118-11427T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720650 | ||||||
chr7:123720650
|
AT | A | 10 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(7): Show | 10 | HG02145.hp1 HG02258.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.118-11428delA | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720650 | ||||||
chr7:123720673
|
T | C | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.118-11450A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720673 | ||||||
chr7:123720681
|
C | G | 1 | a0001c0001t0002g0099 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.118-11458G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720681 | ||||||
chr7:123720689
|
C | G | 1 | a0001c0002t0001g0301 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.118-11466G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720689 | ||||||
chr7:123720793
|
G | C | 2 | a0001c0002t0001g0301a0001c0002t0001g0302 | 2 | HG00642.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.118-11570C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720793 | ||||||
chr7:123720810
|
G | A | 1 | a0001c0001t0002g0046 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.118-11587C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720810 | ||||||
chr7:123720811
|
A | T | 1 | a0001c0001t0002g0046 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.118-11588T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720811 | ||||||
chr7:123720827
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.118-11604C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720827 | ||||||
chr7:123720855
|
T | A | 1 | a0001c0002t0001g0279 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.118-11632A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720855 | ||||||
chr7:123720868
|
T | C | 2 | a0001c0001t0004g0017a0001c0001t0004g0163 | 3 | HG02040.hp2 NA18952.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.118-11645A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720868 | ||||||
chr7:123720872
|
C | T | 2 | a0001c0002t0001g0223a0001c0002t0001g0226 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.118-11649G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720872 | ||||||
chr7:123721051
|
G | A | 1 | a0001c0002t0001g0296 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.118-11828C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721051 | ||||||
chr7:123721226
|
T | C | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.118-12003A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721226 | ||||||
chr7:123721231
|
A | G | 2 | a0001c0001t0003g0019a0001c0001t0003g0175 | 3 | NA18941.hp2 NA18984.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.118-12008T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721231 | ||||||
chr7:123721318
|
C | CTT | 304 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(301): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.118-12096_118-1209 others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721318 | ||||||
chr7:123721337
|
T | A | 1 | a0001c0002t0001g0201 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.118-12114A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721337 | ||||||
chr7:123721366
|
C | T | 1 | a0001c0002t0001g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.118-12143G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721366 | ||||||
chr7:123721391
|
T | C | 3 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0043 | 3 | HG02145.hp1 HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.118-12168A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721391 | ||||||
chr7:123721510
|
A | T | 2 | a0001c0001t0010g0039a0001c0001t0010g0040 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.118-12287T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721510 | ||||||
chr7:123721625
|
C | CACAATTT others(26): Show |
1 | a0001c0001t0002g0046 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.118-12435_118-1240 others(37): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721625 | ||||||
chr7:123721712
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.118-12489C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721712 | ||||||
chr7:123721717
|
A | G | 2 | a0001c0001t0003g0118a0001c0001t0003g0119 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.118-12494T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721717 | ||||||
chr7:123721719
|
C | T | 130 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(127): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.118-12496G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721719 | ||||||
chr7:123721856
|
C | T | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.118-12633G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721856 | ||||||
chr7:123721882
|
A | ATAACT | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.118-12660_118-1265 others(9): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721882 | ||||||
chr7:123721942
|
C | T | 2 | a0001c0001t0002g0051a0001c0001t0002g0052 | 2 | NA18968.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.118-12719G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721942 | ||||||
chr7:123722016
|
G | A | 130 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(127): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.118-12793C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123722016 | ||||||
chr7:123722092
|
T | A | 1 | a0001c0001t0008g0160 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.118-12869A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123722092 | ||||||
chr7:123722365
|
A | T | 3 | a0001c0002t0001g0220a0001c0002t0001g0221a0001c0002t0001g0310 | 3 | HG01256.hp1 HG03669.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.118-13142T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123722365 | ||||||
chr7:123722638
|
C | T | 2 | a0001c0001t0003g0118a0001c0001t0003g0119 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.118-13415G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123722638 | ||||||
chr7:123722818
|
A | C | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.118-13595T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123722818 | ||||||
chr7:123723032
|
T | C | 8 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0001t0004g0161others(5): Show | 10 | HG00408.hp1 HG02040.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.118-13809A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123723032 | ||||||
chr7:123723058
|
T | C | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.118-13835A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123723058 | ||||||
chr7:123723105
|
T | C | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.118-13882A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123723105 | ||||||
chr7:123723145
|
G | A | 1 | a0001c0002t0001g0203 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.118-13922C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123723145 | ||||||
chr7:123723194
|
T | A | 1 | a0001c0001t0002g0059 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.118-13971A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123723194 | ||||||
chr7:123723604
|
A | G | 239 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(236): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.118-14381T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123723604 | ||||||
chr7:123723643
|
T | C | 5 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-14420A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123723643 | ||||||
chr7:123723920
|
T | C | 1 | a0001c0002t0001g0233 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.118-14697A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123723920 | ||||||
chr7:123724003
|
T | C | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG02965.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.118-14780A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123724003 | ||||||
chr7:123724073
|
T | C | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.118-14850A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123724073 | ||||||
chr7:123724318
|
C | T | 9 | a0001c0001t0003g0132a0001c0001t0003g0135a0001c0001t0003g0137others(6): Show | 9 | HG01361.hp2 HG01433.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.118-15095G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123724318 | ||||||
chr7:123724372
|
T | C | 4 | a0001c0001t0002g0143a0001c0001t0002g0144a0001c0001t0002g0145others(1): Show | 4 | HG02647.hp2 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-15149A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123724372 | ||||||
chr7:123724693
|
G | A | 130 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(127): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.118-15470C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123724693 | ||||||
chr7:123724879
|
A | G | 1 | a0001c0001t0003g0127 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.118-15656T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123724879 | ||||||
chr7:123724936
|
G | A | 2 | a0001c0001t0003g0138a0001c0001t0003g0139 | 2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.118-15713C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123724936 | ||||||
chr7:123725016
|
T | C | 3 | a0001c0001t0002g0098a0001c0001t0002g0100a0001c0001t0002g0102 | 3 | HG01074.hp2 HG01256.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.118-15793A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123725016 | ||||||
chr7:123725068
|
G | A | 239 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(236): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.118-15845C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123725068 | ||||||
chr7:123725417
|
A | G | 1 | a0001c0002t0001g0260 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.118-16194T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123725417 | ||||||
chr7:123725508
|
T | TA | 5 | a0001c0001t0002g0052a0001c0002t0001g0205a0001c0002t0001g0208others(2): Show | 5 | HG00280.hp2 HG00735.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-16286dupT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123725508 | ||||||
chr7:123725652
|
C | T | 3 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0043 | 3 | HG02145.hp1 HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.118-16429G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123725652 | ||||||
chr7:123725728
|
T | C | 1 | a0001c0002t0001g0258 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.118-16505A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123725728 | ||||||
chr7:123725734
|
C | T | 130 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(127): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.118-16511G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123725734 | ||||||
chr7:123725747
|
G | T | 1 | a0001c0002t0022g0299 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.118-16524C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123725747 | ||||||
chr7:123726343
|
A | G | 3 | a0001c0001t0002g0035a0001c0001t0002g0037a0001c0001t0002g0038 | 3 | HG01243.hp1 HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.118-17120T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123726343 | ||||||
chr7:123726550
|
C | T | 1 | a0001c0003t0005g0129 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.118-17327G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123726550 | ||||||
chr7:123726787
|
A | G | 1 | a0001c0001t0003g0188 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.118-17564T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123726787 | ||||||
chr7:123726803
|
T | C | 5 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-17580A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123726803 | ||||||
chr7:123726866
|
A | AAAT | 56 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0023others(53): Show | 62 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.118-17646_118-1764 others(7): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123726866 | ||||||
chr7:123726988
|
G | A | 1 | a0001c0001t0002g0059 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.118-17765C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123726988 | ||||||
chr7:123727130
|
A | G | 2 | a0001c0001t0002g0063a0001c0001t0002g0074 | 2 | HG01884.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.118-17907T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727130 | ||||||
chr7:123727349
|
T | C | 2 | a0001c0001t0010g0039a0001c0001t0010g0040 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.118-18126A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727349 | ||||||
chr7:123727352
|
G | GTC | 2 | a0001c0002t0001g0002a0001c0002t0001g0235 | 5 | NA18942.hp1 NA18962.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-18131_118-1813 others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727352 | ||||||
chr7:123727353
|
T | TCA | 49 | a0001c0001t0002g0023a0001c0001t0002g0050a0001c0001t0002g0074others(46): Show | 58 | HG00544.hp2 HG00639.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.118-18132_118-1813 others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727353 | ||||||
chr7:123727353
|
T | TCACA | 22 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(19): Show | 24 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.118-18134_118-1813 others(8): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727353 | ||||||
chr7:123727353
|
T | TCACACA | 60 | a0001c0001t0002g0044a0001c0002t0001g0026a0001c0002t0001g0029others(57): Show | 65 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.118-18136_118-1813 others(10): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727353 | ||||||
chr7:123727353
|
T | TCACACAC others(1): Show |
12 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(9): Show | 13 | HG01167.hp2 HG01243.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.118-18138_118-1813 others(12): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727353 | ||||||
chr7:123727353
|
T | TCACACAC others(3): Show |
50 | a0001c0001t0002g0143a0001c0001t0002g0144a0001c0001t0003g0012others(47): Show | 58 | HG00544.hp1 HG00673.hp1 HG01192.hp2 others(55): Show |
intron_variant | MODIFIER | c.118-18140_118-1813 others(14): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727353 | ||||||
chr7:123727353
|
T | TCACACAC others(5): Show |
12 | a0001c0001t0003g0011a0001c0001t0003g0106a0001c0001t0003g0118others(9): Show | 15 | HG00280.hp1 HG00621.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.118-18142_118-1813 others(16): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727353 | ||||||
chr7:123727353
|
T | TCACACAC others(7): Show |
7 | a0001c0001t0003g0001a0001c0001t0004g0155a0001c0001t0004g0156others(4): Show | 10 | HG00738.hp1 HG01516.hp2 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.118-18144_118-1813 others(18): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727353 | ||||||
chr7:123727353
|
T | TCACACAC others(9): Show |
12 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0004g0018others(9): Show | 13 | HG00323.hp1 HG00408.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.118-18146_118-1813 others(20): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727353 | ||||||
chr7:123727353
|
T | TCACACAC others(11): Show |
6 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0004g0161others(3): Show | 6 | HG03942.hp1 NA18945.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-18148_118-1813 others(22): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727353 | ||||||
chr7:123727353
|
T | TCACACAC others(13): Show |
1 | a0001c0001t0004g0167 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.118-18150_118-1813 others(24): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727353 | ||||||
chr7:123727353
|
T | TCGCACAC others(7): Show |
1 | a0001c0001t0002g0014 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.118-18131_118-1813 others(18): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727353 | ||||||
chr7:123727353
|
T | TCGCACAC others(9): Show |
2 | a0001c0001t0002g0015a0001c0001t0002g0147 | 3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.118-18131_118-1813 others(20): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727353 | ||||||
chr7:123727383
|
A | ACACACAC others(4): Show |
1 | a0001c0003t0003g0126 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.118-18161_118-1816 others(15): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727383 | ||||||
chr7:123727383
|
A | ACACACAC others(6): Show |
1 | a0001c0002t0003g0307 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.118-18161_118-1816 others(17): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727383 | ||||||
chr7:123727384
|
A | C | 1 | a0001c0001t0003g0001 | 4 | NA18960.hp2 NA18970.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-18161T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727384 | ||||||
chr7:123727429
|
G | A | 1 | a0001c0002t0001g0243 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.118-18206C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727429 | ||||||
chr7:123727639
|
C | T | 51 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0019others(48): Show | 57 | HG00544.hp1 HG00673.hp1 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.118-18416G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727639 | ||||||
chr7:123727651
|
A | C | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.118-18428T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727651 | ||||||
chr7:123728023
|
G | A | 2 | a0001c0001t0004g0167a0001c0001t0004g0170 | 2 | HG00673.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.118-18800C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123728023 | ||||||
chr7:123728227
|
T | C | 1 | a0001c0002t0001g0221 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.118-19004A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123728227 | ||||||
chr7:123728434
|
G | A | 130 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(127): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.118-19211C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123728434 | ||||||
chr7:123728567
|
C | T | 1 | a0001c0002t0001g0033 | 2 | NA18955.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.118-19344G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123728567 | ||||||
chr7:123728685
|
C | T | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.118-19462G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123728685 | ||||||
chr7:123728778
|
G | A | 64 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(61): Show | 76 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.118-19555C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123728778 | ||||||
chr7:123728778
|
GTGAGC | G | 3 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0147 | 5 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-19560_118-1955 others(9): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123728778 | ||||||
chr7:123728807
|
G | C | 2 | a0001c0001t0004g0167a0001c0001t0004g0170 | 2 | HG00673.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.118-19584C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123728807 | ||||||
chr7:123728990
|
T | C | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.117+19628A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123728990 | ||||||
chr7:123729106
|
G | C | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG02965.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.117+19512C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123729106 | ||||||
chr7:123729420
|
A | G | 8 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(5): Show | 8 | HG02145.hp1 HG02559.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+19198T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123729420 | ||||||
chr7:123729458
|
G | A | 2 | a0001c0002t0001g0297a0001c0005t0001g0244 | 2 | HG00738.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.117+19160C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123729458 | ||||||
chr7:123729485
|
T | C | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.117+19133A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123729485 | ||||||
chr7:123729638
|
A | G | 1 | a0001c0002t0003g0306 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.117+18980T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123729638 | ||||||
chr7:123729802
|
C | T | 239 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(236): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.117+18816G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123729802 | ||||||
chr7:123729820
|
A | C | 4 | a0001c0003t0005g0129a0001c0003t0005g0131a0001c0003t0005g0136others(1): Show | 4 | HG00673.hp1 HG02071.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+18798T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123729820 | ||||||
chr7:123730024
|
T | C | 2 | a0001c0001t0010g0039a0001c0001t0010g0040 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.117+18594A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123730024 | ||||||
chr7:123730178
|
T | C | 1 | a0001c0001t0002g0062 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.117+18440A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123730178 | ||||||
chr7:123730349
|
C | T | 54 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0023others(51): Show | 60 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.117+18269G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123730349 | ||||||
chr7:123730401
|
G | C | 2 | a0001c0002t0001g0253a0001c0002t0001g0255 | 2 | HG02155.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.117+18217C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123730401 | ||||||
chr7:123730468
|
A | G | 1 | a0001c0001t0015g0060 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.117+18150T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123730468 | ||||||
chr7:123730496
|
T | A | 1 | a0001c0001t0004g0171 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.117+18122A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123730496 | ||||||
chr7:123730656
|
A | G | 130 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(127): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.117+17962T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123730656 | ||||||
chr7:123730718
|
C | G | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.117+17900G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123730718 | ||||||
chr7:123730849
|
C | T | 140 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(137): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.117+17769G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123730849 | ||||||
chr7:123730972
|
C | A | 130 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(127): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.117+17646G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123730972 | ||||||
chr7:123731387
|
A | G | 2 | a0001c0001t0010g0039a0001c0001t0010g0040 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.117+17231T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123731387 | ||||||
chr7:123731448
|
T | C | 6 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(3): Show | 6 | HG02145.hp1 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.117+17170A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123731448 | ||||||
chr7:123731524
|
G | A | 8 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0001t0004g0161others(5): Show | 10 | HG00408.hp1 HG02040.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.117+17094C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123731524 | ||||||
chr7:123731560
|
A | G | 1 | a0001c0002t0001g0295 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.117+17058T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123731560 | ||||||
chr7:123731709
|
C | T | 2 | a0001c0001t0002g0051a0001c0001t0002g0052 | 2 | NA18968.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.117+16909G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123731709 | ||||||
chr7:123731833
|
A | G | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.117+16785T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123731833 | ||||||
chr7:123732046
|
G | A | 1 | a0001c0002t0001g0026 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.117+16572C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123732046 | ||||||
chr7:123732199
|
G | A | 4 | a0001c0002t0001g0025a0001c0002t0001g0196a0001c0002t0001g0214others(1): Show | 5 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+16419C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123732199 | ||||||
chr7:123732246
|
C | T | 1 | a0001c0002t0021g0262 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.117+16372G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123732246 | ||||||
chr7:123732330
|
G | A | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.117+16288C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123732330 | ||||||
chr7:123732436
|
T | G | 1 | a0001c0002t0001g0224 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.117+16182A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123732436 | ||||||
chr7:123732482
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.117+16136G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123732482 | ||||||
chr7:123732899
|
T | C | 1 | a0001c0001t0009g0121 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.117+15719A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123732899 | ||||||
chr7:123733008
|
C | T | 1 | a0001c0001t0002g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.117+15610G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123733008 | ||||||
chr7:123733139
|
C | T | 1 | a0001c0001t0002g0062 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.117+15479G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123733139 | ||||||
chr7:123733362
|
A | T | 3 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0204 | 3 | HG03490.hp1 HG04204.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.117+15256T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123733362 | ||||||
chr7:123733568
|
T | C | 130 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(127): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.117+15050A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123733568 | ||||||
chr7:123733913
|
CA | C | 102 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(99): Show | 117 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.117+14704delT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123733913 | ||||||
chr7:123733913
|
CAA | C | 124 | a0001c0001t0002g0044a0001c0001t0006g0041a0001c0001t0006g0042others(121): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.117+14703_117+1470 others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123733913 | ||||||
chr7:123734016
|
G | A | 1 | a0001c0001t0003g0105 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.117+14602C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123734016 | ||||||
chr7:123734070
|
G | A | 6 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(3): Show | 6 | HG02145.hp1 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.117+14548C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123734070 | ||||||
chr7:123734358
|
A | G | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.117+14260T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123734358 | ||||||
chr7:123734591
|
T | TA | 127 | a0001c0001t0002g0009a0001c0001t0002g0057a0001c0001t0002g0088others(124): Show | 145 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.117+14026dupT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123734591 | ||||||
chr7:123734591
|
T | TAA | 67 | a0001c0001t0002g0079a0001c0001t0003g0119a0001c0001t0003g0128others(64): Show | 79 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.117+14025_117+1402 others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123734591 | ||||||
chr7:123734613
|
A | T | 3 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0147 | 5 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+14005T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123734613 | ||||||
chr7:123734666
|
G | T | 3 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0043 | 3 | HG02145.hp1 HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.117+13952C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123734666 | ||||||
chr7:123734712
|
A | G | 130 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(127): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.117+13906T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123734712 | ||||||
chr7:123734785
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.117+13833G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123734785 | ||||||
chr7:123734786
|
G | A | 99 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0035others(96): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.117+13832C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123734786 | ||||||
chr7:123735019
|
C | CAGTCCTT others(29): Show |
1 | a0001c0002t0001g0281 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.117+13563_117+1359 others(40): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123735019 | ||||||
chr7:123735131
|
CA | C | 135 | a0001c0001t0002g0111a0001c0001t0003g0178a0001c0001t0004g0168others(132): Show | 154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.117+13486delT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123735131 | ||||||
chr7:123735162
|
A | T | 1 | a0001c0001t0015g0060 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.117+13456T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123735162 | ||||||
chr7:123735337
|
T | C | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.117+13281A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123735337 | ||||||
chr7:123735381
|
G | GA | 134 | a0001c0001t0002g0080a0001c0001t0002g0090a0001c0001t0004g0174others(131): Show | 153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.117+13236dupT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123735381 | ||||||
chr7:123735451
|
G | C | 140 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(137): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.117+13167C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123735451 | ||||||
chr7:123735775
|
C | T | 4 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0178others(1): Show | 6 | HG01884.hp2 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.117+12843G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123735775 | ||||||
chr7:123735853
|
G | A | 105 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0035others(102): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.117+12765C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123735853 | ||||||
chr7:123735942
|
T | C | 1 | a0001c0002t0001g0218 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.117+12676A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123735942 | ||||||
chr7:123735994
|
T | C | 1 | a0001c0002t0001g0247 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.117+12624A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123735994 | ||||||
chr7:123736006
|
G | A | 3 | a0001c0001t0002g0023a0001c0001t0002g0192a0001c0001t0002g0193 | 4 | NA18952.hp1 NA18962.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+12612C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123736006 | ||||||
chr7:123736240
|
A | G | 4 | a0001c0001t0002g0010a0001c0001t0002g0086a0001c0001t0002g0089others(1): Show | 5 | HG02922.hp2 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+12378T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123736240 | ||||||
chr7:123736298
|
TCTC | T | 11 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0096others(8): Show | 12 | HG00099.hp1 HG00733.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+12317_117+1231 others(7): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123736298 | ||||||
chr7:123736393
|
T | C | 1 | a0001c0002t0001g0219 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+12225A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123736393 | ||||||
chr7:123736402
|
T | C | 3 | a0001c0002t0001g0248a0001c0002t0001g0249a0001c0002t0001g0254 | 3 | HG00544.hp2 NA18970.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.117+12216A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123736402 | ||||||
chr7:123736436
|
C | G | 3 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0147 | 5 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+12182G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123736436 | ||||||
chr7:123736506
|
G | A | 130 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(127): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.117+12112C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123736506 | ||||||
chr7:123736801
|
A | T | 239 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(236): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.117+11817T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123736801 | ||||||
chr7:123737012
|
G | A | 129 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(126): Show | 148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.117+11606C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123737012 | ||||||
chr7:123737052
|
A | G | 1 | a0001c0001t0002g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.117+11566T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123737052 | ||||||
chr7:123737159
|
A | G | 130 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(127): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.117+11459T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123737159 | ||||||
chr7:123737466
|
C | T | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.117+11152G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123737466 | ||||||
chr7:123737596
|
C | CA | 30 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0002g0058others(27): Show | 30 | HG00621.hp1 HG00621.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.117+11021dupT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123737596 | ||||||
chr7:123737596
|
C | CAAAA | 104 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(101): Show | 122 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.117+11018_117+1102 others(8): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123737596 | ||||||
chr7:123737596
|
C | CAAAAA | 23 | a0001c0002t0001g0027a0001c0002t0001g0194a0001c0002t0001g0195others(20): Show | 24 | HG00544.hp2 HG01167.hp2 HG01978.hp2 others(21): Show |
intron_variant | MODIFIER | c.117+11017_117+1102 others(9): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123737596 | ||||||
chr7:123737990
|
A | C | 1 | a0001c0001t0002g0083 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.117+10628T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123737990 | ||||||
chr7:123738050
|
T | C | 1 | a0001c0001t0002g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.117+10568A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123738050 | ||||||
chr7:123738158
|
C | A | 1 | a0001c0001t0003g0119 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.117+10460G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123738158 | ||||||
chr7:123738170
|
G | GTTAA | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.117+10444_117+1044 others(8): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123738170 | ||||||
chr7:123738417
|
C | A | 129 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(126): Show | 148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.117+10201G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123738417 | ||||||
chr7:123738424
|
T | C | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG02965.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.117+10194A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123738424 | ||||||
chr7:123738640
|
T | A | 1 | a0001c0001t0002g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.117+9978A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123738640 | ||||||
chr7:123738723
|
G | T | 4 | a0001c0002t0001g0205a0001c0002t0001g0208a0001c0002t0001g0293others(1): Show | 4 | HG00280.hp2 HG00735.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+9895C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123738723 | ||||||
chr7:123738757
|
C | CT | 11 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0096others(8): Show | 12 | HG00099.hp1 HG00733.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+9860dupA | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123738757 | ||||||
chr7:123738835
|
G | A | 1 | a0001c0002t0001g0255 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.117+9783C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123738835 | ||||||
chr7:123738952
|
G | T | 1 | a0001c0001t0002g0104 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.117+9666C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123738952 | ||||||
chr7:123738977
|
C | T | 2 | a0001c0002t0001g0301a0001c0002t0001g0302 | 2 | HG00642.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.117+9641G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123738977 | ||||||
chr7:123738979
|
G | A | 1 | a0001c0002t0001g0227 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.117+9639C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123738979 | ||||||
chr7:123739073
|
C | T | 1 | a0001c0002t0001g0258 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.117+9545G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739073 | ||||||
chr7:123739138
|
T | G | 2 | a0001c0001t0010g0039a0001c0001t0010g0040 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.117+9480A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739138 | ||||||
chr7:123739463
|
A | C | 4 | a0001c0002t0001g0228a0001c0002t0001g0229a0001c0002t0001g0230others(1): Show | 4 | HG01071.hp1 HG01074.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+9155T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739463 | ||||||
chr7:123739512
|
TCAGTA | T | 5 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+9101_117+9105d others(7): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739512 | ||||||
chr7:123739557
|
T | C | 100 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0035others(97): Show | 117 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.117+9061A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739557 | ||||||
chr7:123739603
|
T | C | 2 | a0001c0002t0001g0285a0001c0002t0001g0286 | 2 | NA18955.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.117+9015A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739603 | ||||||
chr7:123739623
|
T | C | 1 | a0001c0002t0001g0026 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.117+8995A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739623 | ||||||
chr7:123739631
|
A | C | 1 | a0001c0001t0002g0044 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.117+8987T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739631 | ||||||
chr7:123739637
|
G | A | 1 | a0001c0002t0001g0203 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.117+8981C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739637 | ||||||
chr7:123739876
|
ATG | A | 42 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(39): Show | 48 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.117+8740_117+8741d others(4): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739876 | ||||||
chr7:123739876
|
ATGTG | A | 3 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0085 | 3 | HG00621.hp1 HG04199.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.117+8738_117+8741d others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739876 | ||||||
chr7:123739890
|
GTGTGTGT others(19): Show |
G | 6 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(3): Show | 6 | HG02145.hp1 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.117+8702_117+8727d others(28): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739890 | ||||||
chr7:123739894
|
GTGTGTGT others(15): Show |
G | 2 | a0001c0001t0010g0039a0001c0001t0010g0040 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.117+8702_117+8723d others(24): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739894 | ||||||
chr7:123739896
|
GTGTGTGT others(13): Show |
G | 2 | a0001c0002t0001g0194a0001c0002t0001g0195 | 2 | NA19070.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.117+8702_117+8721d others(22): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739896 | ||||||
chr7:123739902
|
GTGTGTGT others(7): Show |
G | 51 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0147others(48): Show | 64 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.117+8702_117+8715d others(16): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739902 | ||||||
chr7:123739902
|
GTGTGTGT others(9): Show |
G | 1 | a0001c0002t0001g0287 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.117+8700_117+8715d others(18): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739902 | ||||||
chr7:123739904
|
GTGTGTGT others(5): Show |
G | 16 | a0001c0002t0001g0026a0001c0002t0001g0219a0001c0002t0001g0220others(13): Show | 17 | HG01175.hp2 HG01256.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.117+8702_117+8713d others(14): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739904 | ||||||
chr7:123739904
|
GTGTGTGT others(7): Show |
G | 59 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0028others(56): Show | 66 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.117+8700_117+8713d others(16): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739904 | ||||||
chr7:123739904
|
GTGTGTGT others(9): Show |
G | 1 | a0001c0001t0003g0116 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.117+8698_117+8713d others(18): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739904 | ||||||
chr7:123739906
|
GTGTGTGT others(5): Show |
G | 2 | a0001c0001t0002g0146a0001c0001t0003g0141 | 2 | HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.117+8700_117+8711d others(14): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739906 | ||||||
chr7:123739906
|
GTGTGTGT others(7): Show |
G | 1 | a0001c0002t0001g0256 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.117+8698_117+8711d others(16): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739906 | ||||||
chr7:123739906
|
GTGTGTGT others(9): Show |
G | 1 | a0001c0002t0001g0205 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.117+8696_117+8711d others(18): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739906 | ||||||
chr7:123739908
|
GTGTGTGT others(3): Show |
G | 9 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0138others(6): Show | 9 | HG02071.hp2 HG02451.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.117+8700_117+8709d others(12): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739908 | ||||||
chr7:123739910
|
GTGTGTAT others(1): Show |
G | 39 | a0001c0001t0002g0044a0001c0001t0002g0149a0001c0001t0003g0011others(36): Show | 46 | HG00323.hp1 HG00544.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.117+8700_117+8707d others(10): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739910 | ||||||
chr7:123739912
|
G | A | 1 | a0001c0001t0002g0092 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.117+8706C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739912 | ||||||
chr7:123739912
|
GTGTA | G | 6 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0050others(3): Show | 7 | HG01167.hp1 HG01169.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+8702_117+8705d others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739912 | ||||||
chr7:123739912
|
GTGTATA | G | 26 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(23): Show | 29 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.117+8700_117+8705d others(8): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739912 | ||||||
chr7:123739914
|
G | A | 10 | a0001c0001t0002g0010a0001c0001t0002g0086a0001c0001t0002g0087others(7): Show | 11 | HG01255.hp2 HG01943.hp1 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.117+8704C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739914 | ||||||
chr7:123739914
|
GTA | G | 5 | a0001c0001t0002g0046a0001c0001t0002g0095a0001c0001t0002g0096others(2): Show | 5 | HG00733.hp1 HG00735.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+8702_117+8703d others(4): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739914 | ||||||
chr7:123739914
|
GTATA | G | 18 | a0001c0001t0002g0035a0001c0001t0002g0143a0001c0001t0002g0144others(15): Show | 19 | HG00673.hp2 HG01192.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.117+8700_117+8703d others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739914 | ||||||
chr7:123739914
|
GTATATA | G | 2 | a0001c0001t0003g0001a0001c0001t0003g0175 | 5 | NA18960.hp2 NA18970.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+8698_117+8703d others(8): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739914 | ||||||
chr7:123739916
|
A | G | 1 | a0001c0001t0002g0094 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.117+8702T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739916 | ||||||
chr7:123739918
|
A | G | 1 | a0001c0001t0003g0181 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.117+8700T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739918 | ||||||
chr7:123740017
|
T | C | 1 | a0001c0002t0001g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.117+8601A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740017 | ||||||
chr7:123740135
|
A | C | 2 | a0001c0001t0010g0039a0001c0001t0010g0040 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.117+8483T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740135 | ||||||
chr7:123740174
|
A | G | 3 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0043 | 3 | HG02145.hp1 HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.117+8444T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740174 | ||||||
chr7:123740259
|
GC | G | 11 | a0001c0001t0003g0021a0001c0001t0003g0116a0001c0001t0003g0180others(8): Show | 12 | HG01192.hp2 HG01346.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.117+8358delG | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740259 | ||||||
chr7:123740351
|
T | A | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.117+8267A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740351 | ||||||
chr7:123740454
|
GATTT | G | 46 | a0001c0002t0001g0028a0001c0002t0001g0029a0001c0002t0001g0030others(43): Show | 51 | HG00099.hp2 HG00423.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.117+8160_117+8163d others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740454 | ||||||
chr7:123740490
|
T | G | 1 | a0001c0001t0014g0190 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.117+8128A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740490 | ||||||
chr7:123740627
|
C | G | 138 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.117+7991G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740627 | ||||||
chr7:123740696
|
A | G | 3 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0204 | 3 | HG03490.hp1 HG04204.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.117+7922T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740696 | ||||||
chr7:123740705
|
C | A | 1 | a0001c0003t0003g0142 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.117+7913G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740705 | ||||||
chr7:123740767
|
T | C | 130 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(127): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.117+7851A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740767 | ||||||
chr7:123740877
|
C | T | 6 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(3): Show | 6 | HG02145.hp1 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.117+7741G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740877 | ||||||
chr7:123740949
|
T | C | 3 | a0001c0002t0001g0290a0001c0002t0001g0291a0001c0002t0001g0292 | 3 | HG01175.hp2 HG03239.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.117+7669A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740949 | ||||||
chr7:123741149
|
T | C | 2 | a0001c0001t0002g0015a0001c0001t0002g0147 | 3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.117+7469A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123741149 | ||||||
chr7:123741262
|
T | C | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG02965.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.117+7356A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123741262 | ||||||
chr7:123741269
|
A | G | 1 | a0001c0001t0002g0045 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.117+7349T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123741269 | ||||||
chr7:123741333
|
T | C | 10 | a0001c0001t0004g0018a0001c0001t0004g0166a0001c0001t0004g0167others(7): Show | 11 | HG00621.hp2 HG00673.hp2 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.117+7285A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123741333 | ||||||
chr7:123741416
|
C | T | 1 | a0001c0002t0001g0201 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.117+7202G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123741416 | ||||||
chr7:123741476
|
G | C | 100 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0035others(97): Show | 117 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.117+7142C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123741476 | ||||||
chr7:123741730
|
A | C | 3 | a0001c0001t0003g0011a0001c0001t0003g0105a0001c0001t0003g0106 | 4 | HG01168.hp2 HG03654.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+6888T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123741730 | ||||||
chr7:123741901
|
C | T | 1 | a0001c0001t0011g0034 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.117+6717G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123741901 | ||||||
chr7:123741960
|
C | T | 1 | a0001c0003t0003g0189 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.117+6658G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123741960 | ||||||
chr7:123742075
|
T | C | 1 | a0001c0002t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.117+6543A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742075 | ||||||
chr7:123742098
|
A | C | 130 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(127): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.117+6520T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742098 | ||||||
chr7:123742136
|
C | T | 1 | a0001c0002t0001g0200 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.117+6482G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742136 | ||||||
chr7:123742174
|
G | T | 1 | a0001c0003t0003g0126 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.117+6444C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742174 | ||||||
chr7:123742203
|
T | A | 1 | a0001c0001t0003g0177 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.117+6415A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742203 | ||||||
chr7:123742236
|
C | T | 130 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(127): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.117+6382G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742236 | ||||||
chr7:123742264
|
A | G | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.117+6354T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742264 | ||||||
chr7:123742375
|
A | T | 6 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(3): Show | 6 | HG02145.hp1 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.117+6243T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742375 | ||||||
chr7:123742387
|
C | T | 1 | a0001c0002t0001g0312 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.117+6231G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742387 | ||||||
chr7:123742455
|
C | T | 58 | a0001c0001t0002g0143a0001c0001t0002g0144a0001c0001t0002g0145others(55): Show | 65 | HG00544.hp1 HG00673.hp1 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.117+6163G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742455 | ||||||
chr7:123742645
|
A | G | 1 | a0001c0002t0001g0024 | 2 | HG03017.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.117+5973T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742645 | ||||||
chr7:123742867
|
A | G | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.117+5751T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742867 | ||||||
chr7:123742878
|
G | A | 1 | a0001c0002t0001g0311 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.117+5740C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742878 | ||||||
chr7:123743091
|
C | T | 2 | a0001c0002t0001g0198a0001c0002t0001g0199 | 2 | HG01261.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.117+5527G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123743091 | ||||||
chr7:123743336
|
C | CA | 100 | a0001c0001t0001g0115a0001c0001t0002g0014a0001c0001t0002g0015others(97): Show | 117 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.117+5281dupT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123743336 | ||||||
chr7:123743374
|
A | G | 1 | a0001c0001t0002g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.117+5244T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123743374 | ||||||
chr7:123743407
|
G | A | 11 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0096others(8): Show | 12 | HG00099.hp1 HG00733.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+5211C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123743407 | ||||||
chr7:123743427
|
C | A | 4 | a0001c0001t0002g0143a0001c0001t0002g0144a0001c0001t0002g0145others(1): Show | 4 | HG02647.hp2 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+5191G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123743427 | ||||||
chr7:123743430
|
G | C | 1 | a0001c0001t0002g0104 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.117+5188C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123743430 | ||||||
chr7:123743461
|
G | C | 99 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0035others(96): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.117+5157C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123743461 | ||||||
chr7:123743487
|
C | A | 1 | a0001c0001t0003g0188 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.117+5131G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123743487 | ||||||
chr7:123743835
|
T | G | 2 | a0001c0001t0010g0039a0001c0001t0010g0040 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.117+4783A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123743835 | ||||||
chr7:123743877
|
T | C | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.117+4741A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123743877 | ||||||
chr7:123743922
|
G | A | 3 | a0001c0002t0001g0301a0001c0002t0001g0302a0001c0002t0001g0303 | 3 | HG00642.hp1 HG01978.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.117+4696C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123743922 | ||||||
chr7:123744244
|
G | A | 1 | a0001c0001t0009g0121 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.117+4374C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123744244 | ||||||
chr7:123744262
|
A | G | 1 | a0001c0001t0004g0148 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.117+4356T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123744262 | ||||||
chr7:123744282
|
A | C | 2 | a0001c0001t0010g0039a0001c0001t0010g0040 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.117+4336T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123744282 | ||||||
chr7:123744290
|
C | T | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.117+4328G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123744290 | ||||||
chr7:123744352
|
C | G | 1 | a0001c0002t0001g0197 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.117+4266G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123744352 | ||||||
chr7:123744392
|
T | C | 3 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0147 | 5 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+4226A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123744392 | ||||||
chr7:123744513
|
G | A | 2 | a0001c0002t0001g0304a0001c0002t0017g0305 | 2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.117+4105C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123744513 | ||||||
chr7:123744727
|
T | C | 99 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0035others(96): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.117+3891A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123744727 | ||||||
chr7:123745111
|
G | A | 1 | a0001c0002t0001g0032 | 2 | HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.117+3507C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123745111 | ||||||
chr7:123745163
|
A | G | 1 | a0001c0002t0001g0196 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.117+3455T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123745163 | ||||||
chr7:123745445
|
G | C | 31 | a0001c0001t0002g0149a0001c0001t0004g0006a0001c0001t0004g0016others(28): Show | 36 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.117+3173C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123745445 | ||||||
chr7:123745862
|
G | A | 4 | a0001c0001t0003g0019a0001c0001t0003g0175a0001c0001t0003g0176others(1): Show | 5 | HG01099.hp1 HG02735.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+2756C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123745862 | ||||||
chr7:123746177
|
T | A | 2 | a0001c0001t0002g0111a0001c0001t0002g0112 | 2 | NA19001.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.117+2441A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123746177 | ||||||
chr7:123746184
|
T | A | 4 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0178others(1): Show | 6 | HG01884.hp2 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.117+2434A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123746184 | ||||||
chr7:123746423
|
C | A | 1 | a0001c0002t0019g0308 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.117+2195G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123746423 | ||||||
chr7:123746428
|
T | C | 8 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(5): Show | 8 | HG02145.hp1 HG02559.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+2190A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123746428 | ||||||
chr7:123746652
|
G | A | 2 | a0001c0002t0001g0033a0001c0002t0001g0309 | 3 | HG02080.hp1 NA18955.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.117+1966C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123746652 | ||||||
chr7:123746799
|
T | C | 11 | a0001c0001t0003g0021a0001c0001t0003g0116a0001c0001t0003g0180others(8): Show | 12 | HG01192.hp2 HG01346.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.117+1819A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123746799 | ||||||
chr7:123747090
|
C | T | 2 | a0001c0002t0001g0194a0001c0002t0001g0195 | 2 | NA19070.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.117+1528G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123747090 | ||||||
chr7:123747615
|
G | A | 1 | a0001c0001t0002g0117 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.117+1003C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123747615 | ||||||
chr7:123747739
|
G | A | 1 | a0001c0003t0003g0189 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.117+879C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123747739 | ||||||
chr7:123747900
|
C | G | 2 | a0001c0001t0003g0118a0001c0001t0003g0119 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.117+718G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123747900 | ||||||
chr7:123747982
|
G | A | 227 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0035others(224): Show | 261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.117+636C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123747982 | ||||||
chr7:123748003
|
G | A | 1 | a0001c0002t0001g0310 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.117+615C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123748003 | ||||||
chr7:123748123
|
T | C | 1 | a0001c0002t0001g0311 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.117+495A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123748123 | ||||||
chr7:123748261
|
C | G | 1 | a0001c0001t0002g0045 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.117+357G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123748261 | ||||||
chr7:123748420
|
A | G | 138 | a0001c0001t0002g0044a0001c0001t0006g0041a0001c0001t0006g0042others(135): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.117+198T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123748420 | ||||||
chr7:123748458
|
C | T | 5 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0043others(2): Show | 5 | HG02145.hp1 HG02559.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+160G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123748458 | ||||||
chr7:123748477
|
AGGGGCCG others(5): Show |
A | 2 | a0001c0001t0003g0022a0001c0001t0014g0190 | 3 | HG02647.hp1 HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.117+129_117+140del others(12): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123748477 | ||||||
chr7:123748478
|
GGGGCCGG others(4): Show |
G | 4 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+129_117+139del others(11): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123748478 | ||||||
chr7:123748505
|
G | A | 1 | a0001c0002t0001g0312 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.117+113C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123748505 | ||||||
chr7:123748599
|
G | A | 1 | a0001c0001t0002g0191 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.117+19C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123748599 | ||||||
chr7:123748600
|
C | A | 1 | a0001c0001t0002g0191 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.117+18G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123748600 | ||||||
chr7:123748604
|
T | A | 3 | a0001c0001t0002g0023a0001c0001t0002g0192a0001c0001t0002g0193 | 4 | NA18952.hp1 NA18962.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+14A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123748604 |