geneid | 10163 |
---|---|
ensemblid | ENSG00000158195.11 |
hgncid | 12733 |
symbol | WASF2 |
name | WASP family member 2 |
refseq_nuc | NM_006990.5 |
refseq_prot | NP_008921.1 |
ensembl_nuc | ENST00000618852.5 |
ensembl_prot | ENSP00000483313.1 |
mane_status | MANE Select |
chr | chr1 |
start | 27404230 |
end | 27490167 |
strand | - |
ver | v1.2 |
region | chr1:27404230-27490167 |
region5000 | chr1:27399230-27495167 |
regionname0 | WASF2_chr1_27404230_27490167 |
regionname5000 | WASF2_chr1_27399230_27495167 |
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 | 498 | 257 | 81 | 42 | 96 | 8 | 28 | 64 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0002 | 0/0 | 498 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
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 | 1497 | 198 | 72 | 39 | 56 | 8 | 21 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
c0002 | 0/0 | 1497 | 56 | 7 | 2 | 40 | 0 | 7 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
c0003 | 0/0 | 1497 | 3 | 3 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
c0004 | 0/0 | 1497 | 2 | 2 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
c0005 | 0/0 | 1497 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
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 | 4175 | 59 | 12 | 16 | 21 | 4 | 6 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0002 | 0/0 | 4176 | 25 | 3 | 4 | 14 | 0 | 4 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0003 | 1/0 | 4185 | 21 | 11 | 3 | 6 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0004 | 0/1 | 4175 | 21 | 8 | 4 | 0 | 3 | 5 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0005 | 0/0 | 4191 | 18 | 2 | 0 | 15 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0006 | 0/0 | 4192 | 17 | 1 | 0 | 11 | 0 | 5 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0007 | 0/0 | 4181 | 11 | 8 | 3 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0008 | 0/0 | 4176 | 7 | 0 | 7 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0009 | 0/0 | 4176 | 6 | 0 | 1 | 4 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0010 | 0/0 | 4187 | 5 | 2 | 1 | 1 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0011 | 0/0 | 4180 | 5 | 3 | 1 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0012 | 0/0 | 4180 | 4 | 4 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0013 | 0/0 | 4182 | 4 | 4 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0014 | 0/0 | 4181 | 3 | 3 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0015 | 0/0 | 4177 | 3 | 0 | 0 | 3 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0016 | 0/0 | 4177 | 3 | 0 | 0 | 3 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0017 | 0/0 | 4176 | 3 | 0 | 0 | 3 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0018 | 0/0 | 4181 | 2 | 2 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0019 | 0/0 | 4200 | 2 | 1 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0020 | 0/0 | 4199 | 2 | 0 | 0 | 2 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0021 | 0/0 | 4174 | 2 | 1 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0022 | 0/0 | 4171 | 2 | 2 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0023 | 0/0 | 4171 | 2 | 2 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0024 | 0/0 | 4192 | 2 | 2 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0025 | 0/0 | 4175 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0026 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0027 | 0/0 | 4180 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0028 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0029 | 0/0 | 4181 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0030 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0031 | 0/0 | 4187 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0032 | 0/0 | 4187 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0033 | 0/0 | 4185 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0034 | 0/0 | 4185 | 1 | 0 | 0 | 0 | 1 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0035 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0036 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0037 | 0/0 | 4205 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0038 | 0/0 | 4202 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0039 | 0/0 | 4197 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0040 | 0/0 | 4196 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0041 | 0/0 | 4195 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0042 | 0/0 | 4192 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0043 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0044 | 0/0 | 4176 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0045 | 0/0 | 4176 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0046 | 0/0 | 4163 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0047 | 0/0 | 4172 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0048 | 0/0 | 4185 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0049 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0050 | 0/0 | 4176 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0051 | 0/0 | 4185 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0052 | 0/0 | 4192 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0053 | 0/0 | 4175 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0054 | 0/0 | 4203 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
t0055 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
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 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0106 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0162 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
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 | 1497 | 198 | 72 | 39 | 56 | 8 | 21 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0002 | 0/0 | 1497 | 56 | 7 | 2 | 40 | 0 | 7 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0004 | 0/0 | 1497 | 2 | 2 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0005 | 0/0 | 1497 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0002c0003 | 0/0 | 1497 | 3 | 3 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5671 | 57 | 12 | 16 | 19 | 4 | 6 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0002 | 0/0 | 5672 | 25 | 3 | 4 | 14 | 0 | 4 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0003 | 1/0 | 5681 | 14 | 11 | 1 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0004 | 0/1 | 5671 | 21 | 8 | 4 | 0 | 3 | 5 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0007 | 0/0 | 5677 | 11 | 8 | 3 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0008 | 0/0 | 5672 | 6 | 0 | 6 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0009 | 0/0 | 5672 | 6 | 0 | 1 | 4 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0010 | 0/0 | 5683 | 4 | 2 | 1 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0011 | 0/0 | 5676 | 4 | 3 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0012 | 0/0 | 5676 | 3 | 3 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0013 | 0/0 | 5678 | 3 | 3 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0014 | 0/0 | 5677 | 3 | 3 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0015 | 0/0 | 5673 | 3 | 0 | 0 | 3 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0016 | 0/0 | 5673 | 3 | 0 | 0 | 3 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0017 | 0/0 | 5672 | 3 | 0 | 0 | 3 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0018 | 0/0 | 5677 | 2 | 2 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0019 | 0/0 | 5696 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0020 | 0/0 | 5695 | 2 | 0 | 0 | 2 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0021 | 0/0 | 5670 | 2 | 1 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0022 | 0/0 | 5667 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0023 | 0/0 | 5667 | 2 | 2 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0025 | 0/0 | 5671 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0026 | 0/0 | 5678 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0027 | 0/0 | 5676 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0028 | 0/0 | 5678 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0029 | 0/0 | 5677 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0031 | 0/0 | 5683 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0032 | 0/0 | 5683 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0033 | 0/0 | 5681 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0034 | 0/0 | 5681 | 1 | 0 | 0 | 0 | 1 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0036 | 0/0 | 5678 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0037 | 0/0 | 5701 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0040 | 0/0 | 5692 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0043 | 0/0 | 5672 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0044 | 0/0 | 5672 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0045 | 0/0 | 5672 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0046 | 0/0 | 5659 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0047 | 0/0 | 5668 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0049 | 0/0 | 5678 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0050 | 0/0 | 5672 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0051 | 0/0 | 5681 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0053 | 0/0 | 5671 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0001t0055 | 0/0 | 5669 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0002t0001 | 0/0 | 5671 | 2 | 0 | 0 | 2 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0002t0003 | 0/0 | 5681 | 7 | 0 | 2 | 5 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0002t0005 | 0/0 | 5687 | 18 | 2 | 0 | 15 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0002t0006 | 0/0 | 5688 | 17 | 1 | 0 | 11 | 0 | 5 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0002t0010 | 0/0 | 5683 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0002t0011 | 0/0 | 5676 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0002t0019 | 0/0 | 5696 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0002t0024 | 0/0 | 5688 | 2 | 2 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0002t0038 | 0/0 | 5698 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0002t0039 | 0/0 | 5693 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0002t0041 | 0/0 | 5691 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0002t0042 | 0/0 | 5688 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0002t0048 | 0/0 | 5681 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0002t0052 | 0/0 | 5688 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0002t0054 | 0/0 | 5699 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0004t0012 | 0/0 | 5676 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0004t0030 | 0/0 | 5678 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0001c0005t0008 | 0/0 | 5672 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0002c0003t0013 | 0/0 | 5678 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0002c0003t0022 | 0/0 | 5667 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
a0002c0003t0035 | 0/0 | 5678 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | copy fasta | chr1 | 27399230 | 27495167 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0003g0106 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0004g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0004g0162 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0004g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0007g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0007g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0007g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0007g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0007g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0007g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0007g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0007g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0008g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0008g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0008g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0008g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0008g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0008g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0009g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0009g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0009g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0009g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0009g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0009g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0010g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0010g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0010g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0010g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0011g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0011g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0011g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0011g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0012g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0012g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0012g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0013g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0013g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0013g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0014g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0014g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0014g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0015g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0015g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0015g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0016g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0016g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0016g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0017g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0017g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0017g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0018g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0018g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0019g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0020g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0020g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0021g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0021g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0022g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0023g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0023g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0025g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0026g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0027g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0028g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0029g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0031g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0032g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0033g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0034g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0036g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0037g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0040g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0043g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0044g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0045g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0046g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0047g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0049g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0050g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0051g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0053g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0001t0055g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0005g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0006g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0006g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0006g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0006g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0006g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0006g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0006g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0006g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0006g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0006g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0006g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0006g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0010g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0011g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0019g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0024g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0024g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0038g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0039g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0041g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0042g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0048g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0052g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0002t0054g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0004t0012g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0004t0030g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0001c0005t0008g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0002c0003t0013g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0002c0003t0022g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
a0002c0003t0035g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0034 | g0067 | EUR | GBR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | GBR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG00323 | hp1 | a0001 | c0001 | t0004 | g0105 | EUR | FIN | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | FIN | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | CHS | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG00408 | hp2 | a0001 | c0002 | t0039 | g0027 | EAS | CHS | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG00438 | hp1 | a0001 | c0001 | t0009 | g0163 | EAS | CHS | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG00438 | hp2 | a0001 | c0002 | t0006 | g0005 | EAS | CHS | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG00597 | hp1 | a0001 | c0002 | t0006 | g0076 | EAS | CHS | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | CHS | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG00609 | hp1 | a0001 | c0002 | t0006 | g0033 | EAS | CHS | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG00621 | hp1 | a0001 | c0002 | t0005 | g0054 | EAS | CHS | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | CHS | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0069 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG00673 | hp2 | a0001 | c0002 | t0003 | g0021 | EAS | CHS | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG00741 | hp1 | a0001 | c0001 | t0009 | g0136 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG00741 | hp2 | a0001 | c0001 | t0045 | g0153 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01069 | hp1 | a0001 | c0002 | t0003 | g0017 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01070 | hp1 | a0001 | c0001 | t0011 | g0191 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01071 | hp2 | a0001 | c0001 | t0007 | g0192 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01074 | hp1 | a0001 | c0001 | t0032 | g0080 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01074 | hp2 | a0001 | c0001 | t0004 | g0137 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01081 | hp1 | a0001 | c0001 | t0008 | g0242 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01106 | hp1 | a0001 | c0002 | t0003 | g0045 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01109 | hp1 | a0001 | c0001 | t0007 | g0093 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0138 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0099 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01192 | hp2 | a0001 | c0001 | t0010 | g0066 | AMR | PUR | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01255 | hp1 | a0001 | c0001 | t0007 | g0125 | AMR | CLM | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01261 | hp2 | a0001 | c0001 | t0008 | g0141 | AMR | CLM | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01358 | hp2 | a0001 | c0001 | t0008 | g0245 | AMR | CLM | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01433 | hp1 | a0001 | c0001 | t0008 | g0247 | AMR | CLM | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0171 | AMR | CLM | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01496 | hp2 | a0001 | c0001 | t0008 | g0252 | AMR | CLM | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01884 | hp1 | a0001 | c0001 | t0023 | g0063 | AFR | ACB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01884 | hp2 | a0001 | c0004 | t0030 | g0224 | AFR | ACB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02015 | hp1 | a0001 | c0002 | t0041 | g0007 | EAS | KHV | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02015 | hp2 | a0001 | c0001 | t0053 | g0236 | EAS | KHV | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02055 | hp2 | a0001 | c0001 | t0007 | g0165 | AFR | ACB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02056 | hp1 | a0001 | c0002 | t0003 | g0040 | EAS | KHV | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02071 | hp2 | a0001 | c0002 | t0006 | g0009 | EAS | KHV | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02074 | hp1 | a0001 | c0002 | t0011 | g0041 | EAS | KHV | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02132 | hp1 | a0001 | c0001 | t0009 | g0172 | EAS | KHV | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02132 | hp2 | a0001 | c0002 | t0006 | g0008 | EAS | KHV | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02135 | hp2 | a0001 | c0002 | t0042 | g0032 | EAS | KHV | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02145 | hp1 | a0001 | c0001 | t0046 | g0181 | AFR | ACB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02145 | hp2 | a0001 | c0002 | t0005 | g0016 | AFR | ACB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02155 | hp1 | a0001 | c0002 | t0003 | g0006 | EAS | CDX | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | CDX | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02257 | hp2 | a0001 | c0001 | t0049 | g0166 | AFR | ACB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0103 | AFR | ACB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0073 | AFR | ACB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0102 | AFR | ACB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02280 | hp2 | a0001 | c0002 | t0019 | g0012 | AFR | ACB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02293 | hp1 | a0001 | c0005 | t0008 | g0246 | AMR | PEL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | PEL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02300 | hp1 | a0001 | c0001 | t0008 | g0110 | AMR | PEL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02451 | hp1 | a0001 | c0001 | t0012 | g0222 | AFR | ACB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02523 | hp2 | a0001 | c0002 | t0005 | g0048 | EAS | KHV | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02572 | hp1 | a0001 | c0001 | t0022 | g0087 | AFR | GWD | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02572 | hp2 | a0001 | c0001 | t0026 | g0002 | AFR | GWD | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02602 | hp1 | a0001 | c0002 | t0005 | g0049 | SAS | PJL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02615 | hp2 | a0002 | c0003 | t0013 | g0089 | AFR | GWD | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | GWD | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02647 | hp1 | a0002 | c0003 | t0022 | g0091 | AFR | GWD | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | GWD | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02738 | hp1 | a0001 | c0001 | t0033 | g0079 | SAS | PJL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02738 | hp2 | a0001 | c0001 | t0050 | g0148 | SAS | PJL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02809 | hp1 | a0001 | c0001 | t0018 | g0216 | AFR | GWD | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02809 | hp2 | a0001 | c0002 | t0054 | g0010 | AFR | GWD | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02818 | hp1 | a0001 | c0001 | t0021 | g0107 | AFR | GWD | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0117 | AFR | GWD | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02886 | hp1 | a0001 | c0001 | t0014 | g0220 | AFR | GWD | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02886 | hp2 | a0001 | c0002 | t0005 | g0053 | AFR | GWD | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02895 | hp1 | a0001 | c0001 | t0011 | g0095 | AFR | GWD | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02895 | hp2 | a0001 | c0001 | t0007 | g0129 | AFR | GWD | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02896 | hp1 | a0001 | c0001 | t0031 | g0062 | AFR | GWD | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02896 | hp2 | a0001 | c0002 | t0024 | g0015 | AFR | GWD | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0128 | AFR | GWD | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02897 | hp2 | a0001 | c0002 | t0024 | g0014 | AFR | GWD | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02970 | hp1 | a0001 | c0001 | t0013 | g0082 | AFR | ESN | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | ESN | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0101 | AFR | ESN | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02976 | hp2 | a0001 | c0001 | t0027 | g0050 | AFR | ESN | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0230 | SAS | PJL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0133 | SAS | PJL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03041 | hp2 | a0001 | c0001 | t0007 | g0059 | AFR | GWD | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03098 | hp1 | a0001 | c0001 | t0012 | g0225 | AFR | MSL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | MSL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03130 | hp1 | a0001 | c0004 | t0012 | g0223 | AFR | ESN | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03130 | hp2 | a0001 | c0001 | t0011 | g0097 | AFR | ESN | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03139 | hp1 | a0001 | c0001 | t0013 | g0212 | AFR | ESN | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03195 | hp1 | a0001 | c0001 | t0012 | g0218 | AFR | ESN | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0086 | AFR | ESN | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03209 | hp1 | a0001 | c0002 | t0006 | g0044 | AFR | MSL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0104 | AFR | MSL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03225 | hp2 | a0001 | c0001 | t0023 | g0064 | AFR | MSL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03239 | hp1 | a0001 | c0002 | t0006 | g0068 | SAS | PJL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03453 | hp1 | a0001 | c0001 | t0010 | g0071 | AFR | MSL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03453 | hp2 | a0001 | c0001 | t0007 | g0094 | AFR | MSL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03491 | hp1 | a0001 | c0002 | t0048 | g0038 | SAS | PJL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0114 | SAS | PJL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0113 | SAS | PJL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03516 | hp1 | a0001 | c0001 | t0014 | g0219 | AFR | ESN | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03516 | hp2 | a0001 | c0001 | t0010 | g0072 | AFR | ESN | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03540 | hp1 | a0001 | c0001 | t0013 | g0186 | AFR | GWD | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03540 | hp2 | a0002 | c0003 | t0035 | g0092 | AFR | GWD | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03579 | hp1 | a0001 | c0001 | t0028 | g0003 | AFR | MSL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0078 | AFR | MSL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03704 | hp1 | a0001 | c0001 | t0004 | g0182 | SAS | PJL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03704 | hp2 | a0001 | c0002 | t0006 | g0022 | SAS | PJL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03710 | hp1 | a0001 | c0001 | t0010 | g0061 | SAS | PJL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0170 | SAS | PJL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03831 | hp1 | a0001 | c0002 | t0006 | g0034 | SAS | BEB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0237 | SAS | BEB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0238 | SAS | BEB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03834 | hp2 | a0001 | c0002 | t0006 | g0013 | SAS | BEB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG04115 | hp1 | a0001 | c0001 | t0025 | g0001 | SAS | STU | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | STU | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG04184 | hp2 | a0001 | c0001 | t0009 | g0149 | SAS | BEB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0232 | SAS | STU | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG04228 | hp2 | a0001 | c0002 | t0006 | g0077 | SAS | STU | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18522 | hp1 | a0001 | c0001 | t0029 | g0088 | AFR | YRI | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0084 | AFR | YRI | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | CHB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18612 | hp2 | a0001 | c0002 | t0005 | g0028 | EAS | CHB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18747 | hp1 | a0001 | c0002 | t0038 | g0035 | EAS | CHB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | CHB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18906 | hp1 | a0001 | c0001 | t0014 | g0221 | AFR | YRI | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18906 | hp2 | a0001 | c0001 | t0007 | g0130 | AFR | YRI | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18939 | hp2 | a0001 | c0002 | t0005 | g0031 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18940 | hp1 | a0001 | c0001 | t0043 | g0168 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18940 | hp2 | a0001 | c0002 | t0010 | g0039 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18951 | hp2 | a0001 | c0002 | t0005 | g0029 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18952 | hp1 | a0001 | c0002 | t0005 | g0058 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18952 | hp2 | a0001 | c0001 | t0009 | g0158 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18954 | hp1 | a0001 | c0002 | t0003 | g0019 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18954 | hp2 | a0001 | c0001 | t0009 | g0135 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18957 | hp1 | a0001 | c0002 | t0005 | g0057 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18957 | hp2 | a0001 | c0001 | t0016 | g0254 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18960 | hp2 | a0001 | c0002 | t0006 | g0030 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18962 | hp1 | a0001 | c0001 | t0037 | g0255 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18962 | hp2 | a0001 | c0002 | t0005 | g0023 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18966 | hp1 | a0001 | c0001 | t0020 | g0257 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18971 | hp1 | a0001 | c0002 | t0006 | g0075 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18977 | hp1 | a0001 | c0001 | t0015 | g0173 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18977 | hp2 | a0001 | c0001 | t0016 | g0231 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18978 | hp1 | a0001 | c0002 | t0006 | g0043 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18980 | hp1 | a0001 | c0001 | t0017 | g0233 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18980 | hp2 | a0001 | c0002 | t0005 | g0056 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18981 | hp2 | a0001 | c0002 | t0005 | g0037 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18991 | hp1 | a0001 | c0001 | t0021 | g0164 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18991 | hp2 | a0001 | c0001 | t0051 | g0226 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18993 | hp2 | a0001 | c0002 | t0005 | g0046 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19000 | hp2 | a0001 | c0001 | t0015 | g0157 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19003 | hp1 | a0001 | c0002 | t0005 | g0052 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19007 | hp2 | a0001 | c0001 | t0040 | g0026 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19009 | hp1 | a0001 | c0002 | t0005 | g0036 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19011 | hp2 | a0001 | c0001 | t0017 | g0174 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | LWK | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | LWK | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19055 | hp1 | a0001 | c0002 | t0005 | g0051 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19064 | hp1 | a0001 | c0002 | t0006 | g0060 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19074 | hp1 | a0001 | c0001 | t0020 | g0256 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19074 | hp2 | a0001 | c0001 | t0016 | g0199 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19079 | hp1 | a0001 | c0001 | t0017 | g0259 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19084 | hp1 | a0001 | c0001 | t0015 | g0159 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19084 | hp2 | a0001 | c0002 | t0003 | g0047 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19086 | hp1 | a0001 | c0002 | t0005 | g0042 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19088 | hp1 | a0001 | c0002 | t0052 | g0018 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19088 | hp2 | a0001 | c0001 | t0019 | g0025 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19090 | hp1 | a0001 | c0002 | t0006 | g0055 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0217 | AFR | YRI | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA19240 | hp2 | a0001 | c0001 | t0007 | g0207 | AFR | YRI | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | ASW | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ASW | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0100 | EUR | TSI | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | TSI | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0142 | EUR | TSI | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | TSI | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | GIH | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA20905 | hp2 | a0001 | c0001 | t0044 | g0258 | SAS | GIH | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0127 | AFR | ACB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | ACB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG02559 | hp2 | a0001 | c0001 | t0018 | g0208 | AFR | ACB | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0070 | AFR | MSL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0161 | AFR | MSL | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG06807 | hp1 | a0001 | c0001 | t0055 | g0260 | AFR | USA | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | USA | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA18955 | hp2 | a0001 | c0002 | t0006 | g0024 | EAS | JPT | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA20300 | hp1 | a0001 | c0001 | t0047 | g0065 | AFR | USA | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA20300 | hp2 | a0001 | c0001 | t0011 | g0096 | AFR | USA | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA21309 | hp1 | a0001 | c0001 | t0036 | g0124 | AFR | LWK | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | LWK | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0162 | REF | REF | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0106 | REF | REF | WASF2_chr1_27399230_27495167 | WASF2 | chr1 | 27399230 | 27495167 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:27409994
|
G | A | 1 | a0002 | 3 | HG02615.hp2 HG02647.hp1 HG03540.hp2 |
missense_variant | MODERATE | c.1037C>T | p.Thr346Met | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 8/9 | 1262/5681 | 1037/1497 | 346/498 | chr1 | 27409994 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:27409729
|
G | A | 1 | a0001c0004 | 2 | HG01884.hp2 HG03130.hp1 |
synonymous_variant | LOW | c.1302C>T | p.Ser434Ser | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 8/9 | 1527/5681 | 1302/1497 | 434/498 | chr1 | 27409729 | ||
chr1:27409984
|
T | C | 1 | a0001c0002 | 56 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(53): Show |
synonymous_variant | LOW | c.1047A>G | p.Pro349Pro | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 8/9 | 1272/5681 | 1047/1497 | 349/498 | chr1 | 27409984 | ||
chr1:27419012
|
A | G | 1 | a0001c0005 | 1 | HG02293.hp1 | synonymous_variant | LOW | c.207T>C | p.Ala69Ala | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 3/9 | 432/5681 | 207/1497 | 69/498 | chr1 | 27419012 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:27404270
|
G | A | 1 | a0001c0001t0045 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3919C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 3919 | chr1 | 27404270 | |||||
chr1:27404382
|
A | G | 2 | a0001c0001t0018a0001c0001t0026 | 3 | HG02559.hp2 HG02572.hp2 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3807T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 3807 | chr1 | 27404382 | |||||
chr1:27404561
|
T | C | 1 | a0001c0001t0027 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3628A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 3628 | chr1 | 27404561 | |||||
chr1:27404736
|
T | C | 4 | a0001c0001t0012a0001c0001t0014a0001c0004t0012others(1): Show | 8 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3453A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 3453 | chr1 | 27404736 | |||||
chr1:27404814
|
TAGGAGGC others(5): Show |
T | 2 | a0001c0001t0046a0001c0001t0055 | 2 | HG02145.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3363_*3374delTCTG others(8): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 3363 | chr1 | 27404814 | |||||
chr1:27405147
|
C | T | 4 | a0001c0001t0004a0001c0001t0009a0001c0001t0015others(1): Show | 31 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*3042G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 3042 | chr1 | 27405147 | |||||
chr1:27405191
|
G | A | 2 | a0001c0001t0023a0001c0001t0047 | 3 | HG01884.hp1 HG03225.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2998C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2998 | chr1 | 27405191 | |||||
chr1:27405245
|
G | A | 1 | a0001c0002t0042 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2944C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2944 | chr1 | 27405245 | |||||
chr1:27405261
|
G | A | 2 | a0001c0001t0032a0001c0001t0034 | 2 | HG00140.hp1 HG01074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2928C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2928 | chr1 | 27405261 | |||||
chr1:27405307
|
A | G | 1 | a0001c0001t0044 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2882T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2882 | chr1 | 27405307 | |||||
chr1:27405405
|
G | T | 1 | a0001c0002t0048 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2784C>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2784 | chr1 | 27405405 | |||||
chr1:27405480
|
TAGCTTAG others(4): Show |
T | 1 | a0001c0001t0043 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2698_*2708delGGGC others(7): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2698 | chr1 | 27405480 | |||||
chr1:27405599
|
C | CTT | 5 | a0001c0001t0010a0001c0001t0031a0001c0001t0032others(2): Show | 8 | HG01074.hp1 HG01192.hp2 HG02896.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2588_*2589dupAA | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2589 | chr1 | 27405599 | |||||
chr1:27405599
|
C | CTTTTTT | 1 | a0001c0002t0005 | 18 | HG00621.hp1 HG02145.hp2 HG02523.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2584_*2589dupAAAA others(2): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2589 | chr1 | 27405599 | |||||
chr1:27405599
|
C | CTTTTTTT | 4 | a0001c0002t0006a0001c0002t0024a0001c0002t0042others(1): Show | 21 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2583_*2589dupAAAA others(3): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2589 | chr1 | 27405599 | |||||
chr1:27405599
|
C | CTTTTTTT others(3): Show |
1 | a0001c0002t0041 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2580_*2589dupAAAA others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2589 | chr1 | 27405599 | |||||
chr1:27405599
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0040 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2579_*2589dupAAAA others(7): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2589 | chr1 | 27405599 | |||||
chr1:27405599
|
C | CTTTTTTT others(5): Show |
1 | a0001c0002t0039 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2578_*2589dupAAAA others(8): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2589 | chr1 | 27405599 | |||||
chr1:27405599
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0020 | 2 | NA18966.hp1 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2576_*2589dupAAAA others(10): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2589 | chr1 | 27405599 | |||||
chr1:27405599
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0019a0001c0002t0019 | 2 | HG02280.hp2 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2575_*2589dupAAAA others(11): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2589 | chr1 | 27405599 | |||||
chr1:27405599
|
C | CTTTTTTT others(10): Show |
1 | a0001c0002t0038 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2573_*2589dupAAAA others(13): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2589 | chr1 | 27405599 | |||||
chr1:27405599
|
C | CTTTTTTT others(11): Show |
1 | a0001c0002t0054 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2572_*2589dupAAAA others(14): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2589 | chr1 | 27405599 | |||||
chr1:27405599
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0037 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2570_*2589dupAAAA others(16): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2589 | chr1 | 27405599 | |||||
chr1:27405599
|
CTTT | C | 8 | a0001c0001t0013a0001c0001t0026a0001c0001t0028others(5): Show | 10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2587_*2589delAAA | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2587 | chr1 | 27405599 | |||||
chr1:27405599
|
CTTTT | C | 4 | a0001c0001t0007a0001c0001t0014a0001c0001t0018others(1): Show | 17 | HG01071.hp2 HG01109.hp1 HG01255.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2586_*2589delAAAA | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2586 | chr1 | 27405599 | |||||
chr1:27405599
|
CTTTTT | C | 5 | a0001c0001t0011a0001c0001t0012a0001c0001t0027others(2): Show | 10 | HG01070.hp1 HG02074.hp1 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2585_*2589delAAAA others(1): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2585 | chr1 | 27405599 | |||||
chr1:27405599
|
CTTTTTTT others(1): Show |
C | 2 | a0001c0001t0015a0001c0001t0016 | 6 | NA18957.hp2 NA18977.hp1 NA18977.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2582_*2589delAAAA others(4): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2582 | chr1 | 27405599 | |||||
chr1:27405599
|
CTTTTTTT others(2): Show |
C | 8 | a0001c0001t0002a0001c0001t0008a0001c0001t0009others(5): Show | 44 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*2581_*2589delAAAA others(5): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2581 | chr1 | 27405599 | |||||
chr1:27405599
|
CTTTTTTT others(3): Show |
C | 6 | a0001c0001t0001a0001c0001t0004a0001c0001t0025others(3): Show | 83 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*2580_*2589delAAAA others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2580 | chr1 | 27405599 | |||||
chr1:27405599
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0021 | 2 | HG02818.hp1 NA18991.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2579_*2589delAAAA others(7): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2579 | chr1 | 27405599 | |||||
chr1:27405599
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0047 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2577_*2589delAAAA others(9): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2577 | chr1 | 27405599 | |||||
chr1:27405599
|
CTTTTTTT others(7): Show |
C | 3 | a0001c0001t0022a0001c0001t0023a0002c0003t0022 | 4 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2576_*2589delAAAA others(10): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2576 | chr1 | 27405599 | |||||
chr1:27405689
|
C | T | 1 | a0001c0001t0029 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2500G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2500 | chr1 | 27405689 | |||||
chr1:27405692
|
G | A | 5 | a0001c0001t0012a0001c0001t0014a0001c0001t0029others(2): Show | 9 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2497C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2497 | chr1 | 27405692 | |||||
chr1:27405707
|
C | T | 1 | a0001c0001t0036 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2482G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2482 | chr1 | 27405707 | |||||
chr1:27406105
|
T | C | 2 | a0001c0001t0008a0001c0005t0008 | 7 | HG01081.hp1 HG01261.hp2 HG01358.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2084A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2084 | chr1 | 27406105 | |||||
chr1:27406166
|
C | A | 1 | a0001c0002t0048 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2023G>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 2023 | chr1 | 27406166 | |||||
chr1:27406349
|
C | T | 1 | a0002c0003t0035 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1840G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 1840 | chr1 | 27406349 | |||||
chr1:27406416
|
C | T | 4 | a0001c0001t0031a0001c0001t0032a0001c0001t0033others(1): Show | 4 | HG00140.hp1 HG01074.hp1 HG02738.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1773G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 1773 | chr1 | 27406416 | |||||
chr1:27406703
|
G | T | 6 | a0001c0001t0012a0001c0001t0014a0001c0001t0028others(3): Show | 10 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1486C>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 1486 | chr1 | 27406703 | |||||
chr1:27407153
|
T | C | 1 | a0001c0001t0049 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1036A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 1036 | chr1 | 27407153 | |||||
chr1:27407189
|
G | C | 1 | a0001c0002t0024 | 2 | HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1000C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 1000 | chr1 | 27407189 | |||||
chr1:27407422
|
T | C | 1 | a0001c0001t0050 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*767A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 767 | chr1 | 27407422 | |||||
chr1:27407440
|
T | C | 2 | a0001c0001t0017a0001c0001t0051 | 4 | NA18980.hp1 NA18991.hp2 NA19011.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*749A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 749 | chr1 | 27407440 | |||||
chr1:27407542
|
A | C | 1 | a0001c0001t0027 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*647T>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 647 | chr1 | 27407542 | |||||
chr1:27407741
|
G | C | 1 | a0001c0002t0052 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*448C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 448 | chr1 | 27407741 | |||||
chr1:27407777
|
G | A | 1 | a0001c0001t0053 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*412C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 412 | chr1 | 27407777 | |||||
chr1:27407877
|
C | T | 2 | a0001c0001t0018a0001c0001t0026 | 3 | HG02559.hp2 HG02572.hp2 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*312G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 312 | chr1 | 27407877 | |||||
chr1:27408004
|
G | A | 1 | a0001c0002t0054 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*185C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 9/9 | 185 | chr1 | 27408004 | |||||
chr1:27490029
|
G | A | 1 | a0001c0001t0055 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-87C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/9 | 61139 | chr1 | 27490029 | |||||
chr1:27490095
|
C | T | 1 | a0001c0001t0025 | 1 | HG04115.hp1 | 5_prime_UTR_variant | MODIFIER | c.-153G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/9 | 61205 | chr1 | 27490095 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:27408380
|
G | A | 1 | a0002c0003t0035g0092 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1340-34C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 8/8 | chr1 | 27408380 | ||||||
chr1:27408491
|
G | C | 1 | a0002c0003t0035g0092 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1340-145C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 8/8 | chr1 | 27408491 | ||||||
chr1:27408563
|
G | T | 2 | a0001c0001t0007g0192a0001c0001t0011g0191 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1340-217C>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 8/8 | chr1 | 27408563 | ||||||
chr1:27408804
|
G | C | 1 | a0001c0001t0012g0222 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1340-458C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 8/8 | chr1 | 27408804 | ||||||
chr1:27409009
|
G | A | 1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1340-663C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 8/8 | chr1 | 27409009 | ||||||
chr1:27409141
|
T | TTGGCCGG others(119): Show |
1 | a0001c0001t0045g0153 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1339+550_1339+551i others(128): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 8/8 | chr1 | 27409141 | ||||||
chr1:27409147
|
G | A | 9 | a0001c0001t0007g0207a0001c0001t0012g0218a0001c0001t0012g0222others(6): Show | 9 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1339+545C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 8/8 | chr1 | 27409147 | ||||||
chr1:27409163
|
G | T | 5 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0011g0095others(2): Show | 5 | HG01109.hp1 HG02895.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1339+529C>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 8/8 | chr1 | 27409163 | ||||||
chr1:27409195
|
C | T | 1 | a0001c0001t0045g0153 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1339+497G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 8/8 | chr1 | 27409195 | ||||||
chr1:27409200
|
G | A | 1 | a0002c0003t0022g0091 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1339+492C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 8/8 | chr1 | 27409200 | ||||||
chr1:27409396
|
G | A | 5 | a0001c0001t0019g0025a0001c0001t0020g0256a0001c0001t0020g0257others(2): Show | 5 | NA18962.hp1 NA18966.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.1339+296C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 8/8 | chr1 | 27409396 | ||||||
chr1:27409428
|
C | CA | 40 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0126others(37): Show | 40 | HG00639.hp1 HG00738.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.1339+263dupT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 8/8 | chr1 | 27409428 | ||||||
chr1:27409428
|
C | CAA | 7 | a0001c0001t0001g0196a0001c0001t0010g0061a0001c0001t0010g0066others(4): Show | 7 | HG00140.hp1 HG01074.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.1339+262_1339+263d others(4): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 8/8 | chr1 | 27409428 | ||||||
chr1:27409428
|
CA | C | 10 | a0001c0001t0001g0154a0001c0001t0002g0237a0001c0001t0004g0101others(7): Show | 10 | HG01081.hp2 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1339+263delT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 8/8 | chr1 | 27409428 | ||||||
chr1:27409428
|
CAA | C | 22 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0007g0125others(19): Show | 22 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1339+262_1339+263d others(4): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 8/8 | chr1 | 27409428 | ||||||
chr1:27409428
|
CAAAAAA | C | 7 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0012g0225others(4): Show | 7 | HG01884.hp2 HG02451.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1339+258_1339+263d others(8): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 8/8 | chr1 | 27409428 | ||||||
chr1:27409428
|
CAAAAAAA others(3): Show |
C | 3 | a0001c0002t0005g0042a0001c0002t0005g0046a0001c0002t0006g0043 | 3 | NA18978.hp1 NA18993.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1339+254_1339+263d others(12): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 8/8 | chr1 | 27409428 | ||||||
chr1:27409428
|
CAAAAAAA others(4): Show |
C | 54 | a0001c0001t0004g0170a0001c0001t0009g0136a0001c0002t0001g0004others(51): Show | 54 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.1339+253_1339+263d others(13): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 8/8 | chr1 | 27409428 | ||||||
chr1:27409447
|
A | G | 16 | a0001c0001t0007g0125a0001c0001t0007g0127a0001c0001t0007g0128others(13): Show | 16 | HG01070.hp1 HG01071.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.1339+245T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 8/8 | chr1 | 27409447 | ||||||
chr1:27409452
|
A | G | 22 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0007g0125others(19): Show | 22 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1339+240T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 8/8 | chr1 | 27409452 | ||||||
chr1:27410299
|
G | A | 2 | a0001c0001t0003g0081a0001c0001t0003g0090 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.825-93C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 7/8 | chr1 | 27410299 | ||||||
chr1:27410359
|
C | G | 1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.825-153G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 7/8 | chr1 | 27410359 | ||||||
chr1:27410841
|
C | T | 12 | a0001c0001t0007g0125a0001c0001t0007g0127a0001c0001t0007g0128others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.825-635G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 7/8 | chr1 | 27410841 | ||||||
chr1:27411101
|
A | G | 2 | a0001c0001t0023g0063a0001c0001t0023g0064 | 2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.825-895T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 7/8 | chr1 | 27411101 | ||||||
chr1:27411589
|
C | T | 5 | a0001c0001t0019g0025a0001c0001t0020g0256a0001c0001t0020g0257others(2): Show | 5 | NA18962.hp1 NA18966.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.824+983G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 7/8 | chr1 | 27411589 | ||||||
chr1:27411601
|
T | C | 5 | a0001c0001t0019g0025a0001c0001t0020g0256a0001c0001t0020g0257others(2): Show | 5 | NA18962.hp1 NA18966.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.824+971A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 7/8 | chr1 | 27411601 | ||||||
chr1:27411645
|
T | C | 169 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(166): Show | 169 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.824+927A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 7/8 | chr1 | 27411645 | ||||||
chr1:27411740
|
G | A | 1 | a0001c0001t0004g0162 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.824+832C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 7/8 | chr1 | 27411740 | ||||||
chr1:27411752
|
A | C | 1 | a0001c0001t0001g0201 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.824+820T>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 7/8 | chr1 | 27411752 | ||||||
chr1:27411755
|
C | A | 1 | a0001c0002t0019g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.824+817G>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 7/8 | chr1 | 27411755 | ||||||
chr1:27412077
|
G | A | 1 | a0001c0001t0034g0067 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.824+495C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 7/8 | chr1 | 27412077 | ||||||
chr1:27412122
|
A | T | 1 | a0001c0002t0005g0051 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.824+450T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 7/8 | chr1 | 27412122 | ||||||
chr1:27412352
|
G | A | 6 | a0001c0001t0001g0196a0001c0001t0001g0198a0001c0001t0001g0201others(3): Show | 6 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.824+220C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 7/8 | chr1 | 27412352 | ||||||
chr1:27412490
|
C | T | 1 | a0001c0001t0002g0232 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.824+82G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 7/8 | chr1 | 27412490 | ||||||
chr1:27412543
|
T | C | 1 | a0001c0001t0012g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.824+29A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 7/8 | chr1 | 27412543 | ||||||
chr1:27412874
|
C | G | 1 | a0001c0001t0055g0260 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.669-147G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 6/8 | chr1 | 27412874 | ||||||
chr1:27412975
|
C | T | 21 | a0001c0002t0003g0021a0001c0002t0005g0023a0001c0002t0005g0029others(18): Show | 21 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.669-248G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 6/8 | chr1 | 27412975 | ||||||
chr1:27413018
|
G | A | 21 | a0001c0002t0003g0021a0001c0002t0005g0023a0001c0002t0005g0029others(18): Show | 21 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.669-291C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 6/8 | chr1 | 27413018 | ||||||
chr1:27413170
|
A | C | 1 | a0001c0001t0018g0208 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.669-443T>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 6/8 | chr1 | 27413170 | ||||||
chr1:27413181
|
G | A | 1 | a0001c0001t0013g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.669-454C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 6/8 | chr1 | 27413181 | ||||||
chr1:27413241
|
G | T | 2 | a0001c0001t0003g0081a0001c0001t0003g0090 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.669-514C>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 6/8 | chr1 | 27413241 | ||||||
chr1:27413290
|
G | A | 1 | a0001c0001t0021g0107 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.669-563C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 6/8 | chr1 | 27413290 | ||||||
chr1:27413575
|
C | T | 1 | a0001c0001t0004g0171 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.669-848G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 6/8 | chr1 | 27413575 | ||||||
chr1:27413711
|
A | T | 1 | a0001c0001t0019g0025 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.669-984T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 6/8 | chr1 | 27413711 | ||||||
chr1:27413918
|
T | G | 2 | a0001c0001t0003g0085a0001c0001t0003g0086 | 2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.668+915A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 6/8 | chr1 | 27413918 | ||||||
chr1:27413931
|
T | G | 136 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(133): Show | 136 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.668+902A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 6/8 | chr1 | 27413931 | ||||||
chr1:27414228
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.668+605G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 6/8 | chr1 | 27414228 | ||||||
chr1:27414251
|
G | C | 2 | a0001c0001t0007g0128a0001c0001t0007g0129 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.668+582C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 6/8 | chr1 | 27414251 | ||||||
chr1:27414351
|
A | C | 1 | a0001c0001t0002g0243 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.668+482T>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 6/8 | chr1 | 27414351 | ||||||
chr1:27414577
|
T | G | 5 | a0001c0001t0001g0111a0001c0001t0001g0123a0001c0001t0001g0154others(2): Show | 5 | HG01081.hp2 HG01167.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.668+256A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 6/8 | chr1 | 27414577 | ||||||
chr1:27414637
|
T | C | 136 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(133): Show | 136 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.668+196A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 6/8 | chr1 | 27414637 | ||||||
chr1:27414644
|
T | A | 1 | a0001c0001t0003g0074 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.668+189A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 6/8 | chr1 | 27414644 | ||||||
chr1:27414999
|
C | A | 1 | a0001c0001t0004g0171 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.538-36G>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 5/8 | chr1 | 27414999 | ||||||
chr1:27415147
|
C | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0193a0001c0001t0001g0194others(1): Show | 4 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.538-184G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 5/8 | chr1 | 27415147 | ||||||
chr1:27415160
|
T | A | 1 | a0001c0001t0029g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.538-197A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 5/8 | chr1 | 27415160 | ||||||
chr1:27415193
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.538-230C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 5/8 | chr1 | 27415193 | ||||||
chr1:27415396
|
T | C | 1 | a0001c0001t0029g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.538-433A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 5/8 | chr1 | 27415396 | ||||||
chr1:27415545
|
C | G | 2 | a0001c0001t0004g0113a0001c0001t0004g0114 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.537+440G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 5/8 | chr1 | 27415545 | ||||||
chr1:27415558
|
C | T | 5 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0011g0095others(2): Show | 5 | HG01109.hp1 HG02895.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.537+427G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 5/8 | chr1 | 27415558 | ||||||
chr1:27415712
|
A | G | 1 | a0001c0001t0002g0253 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.537+273T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 5/8 | chr1 | 27415712 | ||||||
chr1:27415814
|
A | G | 136 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(133): Show | 136 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.537+171T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 5/8 | chr1 | 27415814 | ||||||
chr1:27416135
|
T | C | 1 | a0001c0001t0003g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.420-33A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 4/8 | chr1 | 27416135 | ||||||
chr1:27416337
|
T | G | 158 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(155): Show | 158 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.420-235A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 4/8 | chr1 | 27416337 | ||||||
chr1:27416530
|
T | C | 248 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(245): Show | 248 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.420-428A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 4/8 | chr1 | 27416530 | ||||||
chr1:27416532
|
G | C | 1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.420-430C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 4/8 | chr1 | 27416532 | ||||||
chr1:27416713
|
C | A | 8 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0012g0225others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.420-611G>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 4/8 | chr1 | 27416713 | ||||||
chr1:27417063
|
C | A | 1 | a0001c0001t0004g0100 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.420-961G>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 4/8 | chr1 | 27417063 | ||||||
chr1:27417120
|
C | T | 5 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0011g0095others(2): Show | 5 | HG01109.hp1 HG02895.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.420-1018G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 4/8 | chr1 | 27417120 | ||||||
chr1:27417185
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.420-1083T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 4/8 | chr1 | 27417185 | ||||||
chr1:27417324
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.419+945G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 4/8 | chr1 | 27417324 | ||||||
chr1:27417327
|
T | C | 11 | a0001c0002t0003g0021a0001c0002t0005g0029a0001c0002t0005g0031others(8): Show | 11 | HG00438.hp2 HG00673.hp2 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.419+942A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 4/8 | chr1 | 27417327 | ||||||
chr1:27417456
|
T | TAC | 5 | a0001c0001t0001g0196a0001c0001t0001g0198a0001c0001t0001g0201others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.419+811_419+812dup others(2): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 4/8 | chr1 | 27417456 | ||||||
chr1:27417697
|
T | C | 4 | a0001c0001t0001g0187a0001c0001t0001g0193a0001c0001t0001g0194others(1): Show | 4 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.419+572A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 4/8 | chr1 | 27417697 | ||||||
chr1:27417774
|
C | T | 1 | a0001c0001t0004g0171 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.419+495G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 4/8 | chr1 | 27417774 | ||||||
chr1:27417881
|
G | A | 9 | a0001c0001t0001g0098a0001c0001t0001g0134a0001c0001t0001g0146others(6): Show | 9 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.419+388C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 4/8 | chr1 | 27417881 | ||||||
chr1:27417908
|
G | GGATCCAT | 136 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(133): Show | 136 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.419+354_419+360dup others(7): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 4/8 | chr1 | 27417908 | ||||||
chr1:27418012
|
C | T | 136 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(133): Show | 136 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.419+257G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 4/8 | chr1 | 27418012 | ||||||
chr1:27418222
|
G | A | 1 | a0001c0001t0002g0239 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.419+47C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 4/8 | chr1 | 27418222 | ||||||
chr1:27418600
|
T | C | 22 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0007g0125others(19): Show | 22 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.266-178A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 3/8 | chr1 | 27418600 | ||||||
chr1:27418613
|
C | T | 5 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0011g0095others(2): Show | 5 | HG01109.hp1 HG02895.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.266-191G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 3/8 | chr1 | 27418613 | ||||||
chr1:27418641
|
T | C | 2 | a0001c0002t0003g0047a0001c0002t0006g0033 | 2 | HG00609.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.266-219A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 3/8 | chr1 | 27418641 | ||||||
chr1:27418665
|
C | T | 1 | a0001c0001t0029g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.266-243G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 3/8 | chr1 | 27418665 | ||||||
chr1:27418759
|
G | C | 1 | a0001c0001t0029g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.265+195C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 3/8 | chr1 | 27418759 | ||||||
chr1:27418881
|
A | T | 1 | a0001c0001t0001g0132 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.265+73T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 3/8 | chr1 | 27418881 | ||||||
chr1:27418929
|
C | A | 1 | a0001c0001t0009g0149 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.265+25G>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 3/8 | chr1 | 27418929 | ||||||
chr1:27418946
|
T | C | 1 | a0001c0001t0016g0231 | 1 | NA18977.hp2 | splice_region_variant&intron_variant | LOW | c.265+8A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 3/8 | chr1 | 27418946 | ||||||
chr1:27419132
|
C | T | 1 | a0001c0001t0003g0244 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.131-44G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27419132 | ||||||
chr1:27419404
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.131-316A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27419404 | ||||||
chr1:27419408
|
T | C | 2 | a0001c0001t0019g0025a0001c0001t0040g0026 | 2 | NA19007.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.131-320A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27419408 | ||||||
chr1:27419680
|
A | G | 23 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0007g0125others(20): Show | 23 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.131-592T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27419680 | ||||||
chr1:27419812
|
T | C | 1 | a0001c0001t0002g0243 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.131-724A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27419812 | ||||||
chr1:27419951
|
C | T | 1 | a0001c0005t0008g0246 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.131-863G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27419951 | ||||||
chr1:27420119
|
G | C | 1 | a0001c0001t0001g0131 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.131-1031C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27420119 | ||||||
chr1:27420514
|
C | CT | 123 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(120): Show | 123 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.131-1427dupA | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27420514 | ||||||
chr1:27420514
|
C | CTT | 44 | a0001c0001t0001g0116a0001c0001t0001g0126a0001c0001t0001g0144others(41): Show | 44 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.131-1428_131-1427d others(4): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27420514 | ||||||
chr1:27420514
|
CT | C | 8 | a0001c0001t0007g0094a0001c0001t0011g0095a0001c0001t0011g0096others(5): Show | 8 | HG02559.hp2 HG02572.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.131-1427delA | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27420514 | ||||||
chr1:27420614
|
C | T | 1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.131-1526G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27420614 | ||||||
chr1:27420867
|
T | C | 7 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0014g0219others(4): Show | 7 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.131-1779A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27420867 | ||||||
chr1:27420966
|
G | A | 136 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(133): Show | 136 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.131-1878C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27420966 | ||||||
chr1:27421136
|
T | G | 136 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(133): Show | 136 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.131-2048A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27421136 | ||||||
chr1:27421321
|
C | T | 248 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(245): Show | 248 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.131-2233G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27421321 | ||||||
chr1:27421377
|
T | A | 1 | a0001c0001t0002g0238 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.131-2289A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27421377 | ||||||
chr1:27421432
|
C | G | 3 | a0001c0002t0005g0049a0001c0002t0006g0022a0001c0002t0006g0034 | 3 | HG02602.hp1 HG03704.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.131-2344G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27421432 | ||||||
chr1:27421439
|
A | T | 1 | a0001c0001t0027g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.131-2351T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27421439 | ||||||
chr1:27421514
|
A | T | 136 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(133): Show | 136 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.131-2426T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27421514 | ||||||
chr1:27421844
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.131-2756G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27421844 | ||||||
chr1:27422017
|
C | T | 1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.131-2929G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27422017 | ||||||
chr1:27422111
|
G | A | 1 | a0001c0001t0027g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.131-3023C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27422111 | ||||||
chr1:27422351
|
G | A | 1 | a0001c0001t0013g0212 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.131-3263C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27422351 | ||||||
chr1:27422361
|
T | C | 1 | a0001c0001t0004g0170 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.131-3273A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27422361 | ||||||
chr1:27422476
|
A | G | 169 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(166): Show | 169 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.131-3388T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27422476 | ||||||
chr1:27422480
|
G | A | 2 | a0001c0001t0003g0069a0001c0001t0003g0073 | 2 | HG00639.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.131-3392C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27422480 | ||||||
chr1:27422614
|
G | A | 158 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(155): Show | 158 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.131-3526C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27422614 | ||||||
chr1:27422618
|
C | CA | 159 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(156): Show | 159 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.131-3531dupT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27422618 | ||||||
chr1:27422618
|
C | CAA | 9 | a0001c0001t0001g0200a0001c0001t0002g0118a0001c0001t0004g0171others(6): Show | 9 | HG01109.hp1 HG01433.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.131-3532_131-3531d others(4): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27422618 | ||||||
chr1:27422618
|
CA | C | 9 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0012g0225others(6): Show | 9 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.131-3531delT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27422618 | ||||||
chr1:27422637
|
G | A | 1 | a0001c0001t0043g0168 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.131-3549C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27422637 | ||||||
chr1:27422910
|
G | A | 1 | a0001c0001t0013g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.131-3822C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27422910 | ||||||
chr1:27423140
|
C | CA | 5 | a0001c0001t0003g0081a0001c0001t0003g0090a0001c0001t0028g0003others(2): Show | 5 | HG03579.hp1 NA18964.hp2 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.131-4053dupT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27423140 | ||||||
chr1:27423140
|
CA | C | 135 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(132): Show | 135 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.131-4053delT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27423140 | ||||||
chr1:27423203
|
T | A | 1 | a0001c0002t0005g0016 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.131-4115A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27423203 | ||||||
chr1:27423338
|
C | T | 3 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0014g0221 | 3 | NA18906.hp1 NA18993.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.131-4250G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27423338 | ||||||
chr1:27423396
|
G | C | 55 | a0001c0002t0001g0004a0001c0002t0001g0020a0001c0002t0003g0006others(52): Show | 55 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.131-4308C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27423396 | ||||||
chr1:27423619
|
C | T | 3 | a0001c0001t0018g0208a0001c0001t0018g0216a0001c0001t0026g0002 | 3 | HG02559.hp2 HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.131-4531G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27423619 | ||||||
chr1:27423654
|
C | T | 1 | a0001c0001t0013g0212 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.131-4566G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27423654 | ||||||
chr1:27423675
|
A | G | 1 | a0001c0002t0006g0068 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.131-4587T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27423675 | ||||||
chr1:27423775
|
T | TGA | 45 | a0001c0001t0001g0098a0001c0001t0001g0112a0001c0001t0001g0115others(42): Show | 45 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.131-4689_131-4688d others(4): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27423775 | ||||||
chr1:27423816
|
A | T | 1 | a0001c0001t0029g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.131-4728T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27423816 | ||||||
chr1:27423898
|
T | C | 136 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(133): Show | 136 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.131-4810A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27423898 | ||||||
chr1:27424084
|
T | C | 1 | a0001c0002t0054g0010 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.130+4677A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27424084 | ||||||
chr1:27424244
|
C | T | 1 | a0001c0001t0018g0216 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.130+4517G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27424244 | ||||||
chr1:27424530
|
A | AT | 124 | a0001c0001t0001g0098a0001c0001t0001g0112a0001c0001t0001g0115others(121): Show | 124 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.130+4230dupA | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27424530 | ||||||
chr1:27424530
|
A | ATT | 11 | a0001c0001t0001g0111a0001c0001t0001g0123a0001c0001t0001g0154others(8): Show | 11 | HG00741.hp2 HG01081.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.130+4229_130+4230d others(4): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27424530 | ||||||
chr1:27424872
|
G | C | 10 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0012g0225others(7): Show | 10 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.130+3889C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27424872 | ||||||
chr1:27424944
|
C | T | 1 | a0001c0001t0002g0227 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.130+3817G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27424944 | ||||||
chr1:27425172
|
T | C | 1 | a0001c0001t0004g0171 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.130+3589A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27425172 | ||||||
chr1:27425192
|
G | A | 1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.130+3569C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27425192 | ||||||
chr1:27425385
|
G | A | 5 | a0001c0001t0019g0025a0001c0001t0020g0256a0001c0001t0020g0257others(2): Show | 5 | NA18962.hp1 NA18966.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+3376C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27425385 | ||||||
chr1:27425565
|
G | A | 6 | a0001c0001t0019g0025a0001c0001t0020g0256a0001c0001t0020g0257others(3): Show | 6 | HG02647.hp1 NA18962.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.130+3196C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27425565 | ||||||
chr1:27425725
|
G | A | 1 | a0001c0001t0027g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.130+3036C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27425725 | ||||||
chr1:27425825
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.130+2936A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27425825 | ||||||
chr1:27425838
|
C | CA | 22 | a0001c0001t0003g0074a0001c0001t0003g0083a0001c0001t0003g0084others(19): Show | 22 | HG00438.hp2 HG01106.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.130+2922dupT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27425838 | ||||||
chr1:27425838
|
C | CAA | 125 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(122): Show | 125 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.130+2921_130+2922d others(4): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27425838 | ||||||
chr1:27425838
|
C | CAAA | 42 | a0001c0001t0001g0116a0001c0001t0001g0132a0001c0001t0001g0160others(39): Show | 42 | HG00438.hp1 HG00741.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.130+2920_130+2922d others(5): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27425838 | ||||||
chr1:27425838
|
C | CAAAA | 6 | a0001c0001t0002g0234a0001c0001t0014g0219a0001c0001t0014g0220others(3): Show | 6 | HG00738.hp1 HG01884.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.130+2919_130+2922d others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27425838 | ||||||
chr1:27425935
|
C | T | 1 | a0001c0001t0013g0212 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.130+2826G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27425935 | ||||||
chr1:27426072
|
T | C | 12 | a0001c0001t0007g0125a0001c0001t0007g0127a0001c0001t0007g0128others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.130+2689A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27426072 | ||||||
chr1:27426232
|
C | G | 168 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(165): Show | 168 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.130+2529G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27426232 | ||||||
chr1:27426356
|
T | C | 1 | a0001c0001t0045g0153 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.130+2405A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27426356 | ||||||
chr1:27426374
|
A | G | 1 | a0001c0002t0019g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.130+2387T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27426374 | ||||||
chr1:27426415
|
A | G | 1 | a0001c0002t0005g0036 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.130+2346T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27426415 | ||||||
chr1:27426513
|
A | AT | 157 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(154): Show | 157 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.130+2247dupA | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27426513 | ||||||
chr1:27426513
|
AT | A | 7 | a0001c0001t0019g0025a0001c0001t0020g0256a0001c0001t0020g0257others(4): Show | 7 | HG02976.hp2 NA18962.hp1 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.130+2247delA | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27426513 | ||||||
chr1:27426725
|
G | A | 12 | a0001c0001t0007g0125a0001c0001t0007g0127a0001c0001t0007g0128others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.130+2036C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27426725 | ||||||
chr1:27427056
|
T | C | 1 | a0001c0002t0041g0007 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.130+1705A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27427056 | ||||||
chr1:27427074
|
T | C | 2 | a0001c0001t0003g0081a0001c0001t0003g0090 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.130+1687A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27427074 | ||||||
chr1:27427087
|
A | G | 136 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(133): Show | 136 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.130+1674T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27427087 | ||||||
chr1:27427227
|
T | C | 1 | a0001c0001t0004g0117 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.130+1534A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27427227 | ||||||
chr1:27427512
|
T | C | 1 | a0001c0001t0001g0250 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.130+1249A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27427512 | ||||||
chr1:27427546
|
C | T | 63 | a0001c0001t0003g0011a0001c0001t0007g0059a0001c0001t0019g0025others(60): Show | 63 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.130+1215G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27427546 | ||||||
chr1:27427556
|
C | G | 1 | a0001c0001t0003g0244 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.130+1205G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27427556 | ||||||
chr1:27427566
|
T | C | 136 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(133): Show | 136 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.130+1195A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27427566 | ||||||
chr1:27427713
|
G | C | 1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.130+1048C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27427713 | ||||||
chr1:27427775
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.130+986A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27427775 | ||||||
chr1:27428046
|
G | A | 2 | a0001c0001t0003g0081a0001c0001t0003g0090 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.130+715C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27428046 | ||||||
chr1:27428469
|
C | T | 1 | a0001c0001t0003g0090 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.130+292G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27428469 | ||||||
chr1:27428750
|
G | A | 5 | a0001c0001t0019g0025a0001c0001t0020g0256a0001c0001t0020g0257others(2): Show | 5 | NA18962.hp1 NA18966.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+11C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 2/8 | chr1 | 27428750 | ||||||
chr1:27428997
|
G | C | 1 | a0001c0002t0003g0021 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-43-64C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27428997 | ||||||
chr1:27429001
|
C | CT | 20 | a0001c0001t0001g0131a0001c0001t0001g0155a0001c0001t0001g0167others(17): Show | 20 | HG00735.hp1 HG01123.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-43-69dupA | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27429001 | ||||||
chr1:27429029
|
C | G | 1 | a0001c0002t0006g0077 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-43-96G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27429029 | ||||||
chr1:27429047
|
A | T | 13 | a0001c0001t0003g0081a0001c0001t0003g0090a0001c0001t0010g0061others(10): Show | 13 | HG00140.hp1 HG01074.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.-43-114T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27429047 | ||||||
chr1:27429048
|
A | T | 1 | a0001c0001t0023g0063 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-43-115T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27429048 | ||||||
chr1:27429159
|
C | A | 157 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(154): Show | 157 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.-43-226G>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27429159 | ||||||
chr1:27429164
|
CT | C | 248 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(245): Show | 248 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.-43-232delA | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27429164 | ||||||
chr1:27429189
|
T | C | 1 | a0001c0001t0027g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-43-256A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27429189 | ||||||
chr1:27429198
|
T | C | 1 | a0001c0001t0009g0135 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-43-265A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27429198 | ||||||
chr1:27429400
|
C | T | 232 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(229): Show | 232 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.-43-467G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27429400 | ||||||
chr1:27429484
|
C | G | 1 | a0001c0002t0005g0028 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-43-551G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27429484 | ||||||
chr1:27429552
|
G | C | 10 | a0001c0001t0010g0061a0001c0001t0010g0066a0001c0001t0022g0087others(7): Show | 10 | HG00140.hp1 HG01074.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.-43-619C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27429552 | ||||||
chr1:27429584
|
T | C | 2 | a0001c0004t0012g0223a0001c0004t0030g0224 | 2 | HG01884.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-43-651A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27429584 | ||||||
chr1:27429776
|
C | CA | 68 | a0001c0001t0001g0143a0001c0001t0002g0243a0001c0001t0003g0011others(65): Show | 68 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.-43-844dupT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27429776 | ||||||
chr1:27430006
|
A | T | 2 | a0001c0001t0003g0083a0001c0001t0003g0084 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-43-1073T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27430006 | ||||||
chr1:27430395
|
C | T | 2 | a0001c0001t0002g0119a0001c0001t0025g0001 | 2 | HG00738.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-43-1462G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27430395 | ||||||
chr1:27430766
|
T | C | 1 | a0001c0001t0029g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-43-1833A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27430766 | ||||||
chr1:27430774
|
C | T | 1 | a0001c0001t0010g0066 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-43-1841G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27430774 | ||||||
chr1:27430782
|
C | G | 33 | a0001c0001t0001g0145a0001c0001t0001g0249a0001c0001t0002g0227others(30): Show | 33 | HG00408.hp1 HG00597.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-43-1849G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27430782 | ||||||
chr1:27430807
|
T | C | 1 | a0001c0001t0004g0182 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-43-1874A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27430807 | ||||||
chr1:27430811
|
TA | T | 8 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0012g0225others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-1879delT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27430811 | ||||||
chr1:27430973
|
G | C | 1 | a0001c0001t0013g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-43-2040C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27430973 | ||||||
chr1:27431444
|
C | G | 1 | a0001c0001t0017g0233 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-43-2511G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27431444 | ||||||
chr1:27431522
|
A | G | 1 | a0001c0001t0008g0110 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-43-2589T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27431522 | ||||||
chr1:27431547
|
C | T | 63 | a0001c0001t0003g0011a0001c0001t0007g0059a0001c0001t0019g0025others(60): Show | 63 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.-43-2614G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27431547 | ||||||
chr1:27431835
|
T | C | 3 | a0001c0001t0004g0113a0001c0001t0004g0114a0001c0001t0004g0133 | 3 | HG03017.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-43-2902A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27431835 | ||||||
chr1:27431941
|
G | C | 1 | a0001c0001t0004g0100 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-43-3008C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27431941 | ||||||
chr1:27432229
|
G | A | 1 | a0001c0001t0009g0135 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-43-3296C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27432229 | ||||||
chr1:27432230
|
A | G | 1 | a0001c0001t0009g0135 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-43-3297T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27432230 | ||||||
chr1:27432254
|
C | T | 6 | a0001c0001t0010g0061a0001c0001t0010g0066a0001c0001t0031g0062others(3): Show | 6 | HG00140.hp1 HG01074.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43-3321G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27432254 | ||||||
chr1:27432405
|
T | C | 1 | a0001c0001t0003g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-43-3472A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27432405 | ||||||
chr1:27432435
|
T | G | 5 | a0001c0001t0019g0025a0001c0001t0020g0256a0001c0001t0020g0257others(2): Show | 5 | NA18962.hp1 NA18966.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-3502A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27432435 | ||||||
chr1:27432450
|
C | A | 55 | a0001c0002t0001g0004a0001c0002t0001g0020a0001c0002t0003g0006others(52): Show | 55 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.-43-3517G>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27432450 | ||||||
chr1:27432541
|
G | A | 136 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(133): Show | 136 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.-43-3608C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27432541 | ||||||
chr1:27432627
|
G | A | 55 | a0001c0002t0001g0004a0001c0002t0001g0020a0001c0002t0003g0006others(52): Show | 55 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.-43-3694C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27432627 | ||||||
chr1:27432647
|
C | CA | 9 | a0001c0001t0003g0011a0001c0001t0007g0125a0001c0001t0010g0072others(6): Show | 9 | HG01255.hp1 HG02056.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-43-3715dupT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27432647 | ||||||
chr1:27432647
|
C | CAA | 27 | a0001c0001t0001g0215a0001c0001t0002g0189a0001c0001t0007g0127others(24): Show | 27 | HG01070.hp1 HG01071.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.-43-3716_-43-3715d others(4): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27432647 | ||||||
chr1:27432647
|
C | CAAA | 117 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(114): Show | 117 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.-43-3717_-43-3715d others(5): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27432647 | ||||||
chr1:27432647
|
C | CAAAA | 21 | a0001c0001t0001g0151a0001c0001t0001g0196a0001c0001t0001g0198others(18): Show | 21 | HG00597.hp2 HG00738.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.-43-3718_-43-3715d others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27432647 | ||||||
chr1:27432647
|
CA | C | 6 | a0001c0001t0037g0255a0001c0001t0055g0260a0001c0002t0003g0017others(3): Show | 6 | HG01069.hp1 HG02897.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-3715delT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27432647 | ||||||
chr1:27432704
|
G | A | 1 | a0001c0002t0006g0022 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-43-3771C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27432704 | ||||||
chr1:27433078
|
A | T | 1 | a0001c0001t0001g0154 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-43-4145T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27433078 | ||||||
chr1:27433133
|
T | C | 158 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(155): Show | 158 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.-43-4200A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27433133 | ||||||
chr1:27433139
|
G | A | 252 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(249): Show | 252 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.-43-4206C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27433139 | ||||||
chr1:27433175
|
G | A | 1 | a0002c0003t0022g0091 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-43-4242C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27433175 | ||||||
chr1:27433255
|
T | G | 1 | a0001c0001t0003g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-43-4322A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27433255 | ||||||
chr1:27433257
|
A | G | 1 | a0001c0001t0013g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-43-4324T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27433257 | ||||||
chr1:27433294
|
G | C | 8 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0012g0225others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-4361C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27433294 | ||||||
chr1:27433359
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-43-4426C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27433359 | ||||||
chr1:27433473
|
T | C | 10 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0012g0225others(7): Show | 10 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-43-4540A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27433473 | ||||||
chr1:27433533
|
T | C | 1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-43-4600A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27433533 | ||||||
chr1:27433644
|
C | G | 232 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(229): Show | 232 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.-43-4711G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27433644 | ||||||
chr1:27433649
|
G | A | 2 | a0001c0001t0004g0104a0001c0001t0004g0117 | 2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-43-4716C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27433649 | ||||||
chr1:27433740
|
C | T | 1 | a0001c0001t0022g0087 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-43-4807G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27433740 | ||||||
chr1:27433745
|
G | T | 63 | a0001c0001t0003g0011a0001c0001t0007g0059a0001c0001t0019g0025others(60): Show | 63 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.-43-4812C>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27433745 | ||||||
chr1:27433929
|
G | A | 58 | a0001c0001t0003g0011a0001c0001t0007g0059a0001c0002t0001g0004others(55): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.-43-4996C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27433929 | ||||||
chr1:27434230
|
G | C | 1 | a0001c0001t0004g0182 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-43-5297C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27434230 | ||||||
chr1:27434491
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-43-5558C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27434491 | ||||||
chr1:27434607
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-43-5674G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27434607 | ||||||
chr1:27434630
|
G | A | 10 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0012g0225others(7): Show | 10 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-43-5697C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27434630 | ||||||
chr1:27434790
|
T | C | 1 | a0001c0001t0029g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-43-5857A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27434790 | ||||||
chr1:27434823
|
G | A | 2 | a0001c0002t0005g0037a0001c0002t0005g0042 | 2 | NA18981.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-43-5890C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27434823 | ||||||
chr1:27434982
|
T | C | 1 | a0001c0001t0008g0252 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-43-6049A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27434982 | ||||||
chr1:27435033
|
G | A | 1 | a0001c0001t0001g0206 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-43-6100C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27435033 | ||||||
chr1:27435302
|
C | CTG | 252 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(249): Show | 252 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.-43-6370_-43-6369i others(4): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27435302 | ||||||
chr1:27435321
|
C | T | 5 | a0001c0001t0019g0025a0001c0001t0020g0256a0001c0001t0020g0257others(2): Show | 5 | NA18962.hp1 NA18966.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-6388G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27435321 | ||||||
chr1:27435375
|
A | G | 1 | a0001c0001t0013g0212 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-43-6442T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27435375 | ||||||
chr1:27435570
|
G | A | 1 | a0001c0001t0004g0101 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-43-6637C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27435570 | ||||||
chr1:27435756
|
T | C | 9 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0012g0225others(6): Show | 9 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-43-6823A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27435756 | ||||||
chr1:27435792
|
G | T | 6 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0011g0095others(3): Show | 6 | HG01109.hp1 HG02895.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43-6859C>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27435792 | ||||||
chr1:27435904
|
G | A | 7 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0014g0219others(4): Show | 7 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-6971C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27435904 | ||||||
chr1:27435910
|
T | C | 1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-43-6977A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27435910 | ||||||
chr1:27436100
|
T | C | 1 | a0001c0001t0012g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-43-7167A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27436100 | ||||||
chr1:27436153
|
T | G | 1 | a0001c0001t0029g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-43-7220A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27436153 | ||||||
chr1:27436329
|
C | T | 1 | a0001c0001t0013g0212 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-43-7396G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27436329 | ||||||
chr1:27436354
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-43-7421C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27436354 | ||||||
chr1:27436454
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-43-7521G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27436454 | ||||||
chr1:27436522
|
A | G | 58 | a0001c0001t0003g0011a0001c0001t0007g0059a0001c0002t0001g0004others(55): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.-43-7589T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27436522 | ||||||
chr1:27436876
|
C | T | 1 | a0001c0001t0003g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-43-7943G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27436876 | ||||||
chr1:27437391
|
C | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0193a0001c0001t0001g0194others(1): Show | 4 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-8458G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27437391 | ||||||
chr1:27437732
|
A | G | 1 | a0001c0001t0055g0260 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-43-8799T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27437732 | ||||||
chr1:27437742
|
T | C | 1 | a0001c0002t0005g0048 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-43-8809A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27437742 | ||||||
chr1:27437787
|
A | C | 1 | a0001c0001t0003g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-43-8854T>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27437787 | ||||||
chr1:27438005
|
C | T | 1 | a0001c0001t0002g0188 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-43-9072G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27438005 | ||||||
chr1:27438072
|
T | C | 12 | a0001c0001t0007g0125a0001c0001t0007g0127a0001c0001t0007g0128others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.-43-9139A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27438072 | ||||||
chr1:27438426
|
C | T | 255 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(252): Show | 255 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.-43-9493G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27438426 | ||||||
chr1:27438673
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-43-9740G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27438673 | ||||||
chr1:27438763
|
G | A | 1 | a0001c0001t0025g0001 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-43-9830C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27438763 | ||||||
chr1:27439024
|
A | C | 1 | a0001c0001t0001g0120 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-43-10091T>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27439024 | ||||||
chr1:27439047
|
C | A | 4 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0179others(1): Show | 4 | HG00609.hp2 NA19007.hp1 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-10114G>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27439047 | ||||||
chr1:27439047
|
C | T | 31 | a0001c0001t0001g0145a0001c0001t0001g0249a0001c0001t0002g0227others(28): Show | 31 | HG00408.hp1 HG00597.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.-43-10114G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27439047 | ||||||
chr1:27439342
|
A | G | 1 | a0001c0001t0029g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-43-10409T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27439342 | ||||||
chr1:27439464
|
T | C | 10 | a0001c0001t0010g0061a0001c0001t0010g0066a0001c0001t0022g0087others(7): Show | 10 | HG00140.hp1 HG01074.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.-43-10531A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27439464 | ||||||
chr1:27439714
|
C | G | 1 | a0001c0001t0003g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-43-10781G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27439714 | ||||||
chr1:27439867
|
GTA | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0012g0225others(2): Show | 5 | HG02451.hp1 HG02886.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-10936_-43-1093 others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27439867 | ||||||
chr1:27439922
|
C | T | 1 | a0001c0001t0013g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-43-10989G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27439922 | ||||||
chr1:27440079
|
G | T | 1 | a0001c0002t0019g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-43-11146C>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27440079 | ||||||
chr1:27440126
|
C | T | 1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-43-11193G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27440126 | ||||||
chr1:27440261
|
T | G | 1 | a0001c0001t0002g0248 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-43-11328A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27440261 | ||||||
chr1:27440303
|
C | T | 14 | a0001c0001t0003g0081a0001c0001t0003g0090a0001c0001t0010g0061others(11): Show | 14 | HG00140.hp1 HG01074.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.-43-11370G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27440303 | ||||||
chr1:27440315
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-43-11382G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27440315 | ||||||
chr1:27440339
|
T | C | 1 | a0001c0002t0010g0039 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-43-11406A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27440339 | ||||||
chr1:27440824
|
A | G | 1 | a0001c0002t0005g0052 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-43-11891T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27440824 | ||||||
chr1:27440979
|
G | A | 1 | a0001c0001t0046g0181 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-43-12046C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27440979 | ||||||
chr1:27441069
|
T | C | 3 | a0001c0001t0012g0218a0001c0001t0014g0219a0001c0001t0014g0220 | 3 | HG02886.hp1 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-43-12136A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27441069 | ||||||
chr1:27441106
|
G | A | 2 | a0001c0002t0024g0014a0001c0002t0024g0015 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-43-12173C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27441106 | ||||||
chr1:27441110
|
T | C | 2 | a0001c0001t0001g0155a0001c0001t0001g0180 | 2 | HG00735.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.-43-12177A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27441110 | ||||||
chr1:27441321
|
T | G | 2 | a0001c0001t0001g0249a0001c0001t0008g0252 | 2 | HG01496.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.-43-12388A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27441321 | ||||||
chr1:27441347
|
G | C | 1 | a0001c0001t0004g0100 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-43-12414C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27441347 | ||||||
chr1:27441579
|
C | T | 167 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(164): Show | 167 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.-43-12646G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27441579 | ||||||
chr1:27441611
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-43-12678C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27441611 | ||||||
chr1:27441693
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-43-12760C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27441693 | ||||||
chr1:27441732
|
T | C | 2 | a0001c0001t0003g0081a0001c0001t0003g0090 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-43-12799A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27441732 | ||||||
chr1:27441740
|
C | T | 1 | a0001c0001t0029g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-43-12807G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27441740 | ||||||
chr1:27441741
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-43-12808C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27441741 | ||||||
chr1:27441753
|
C | CA | 118 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(115): Show | 118 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.-43-12821dupT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27441753 | ||||||
chr1:27441753
|
C | CAA | 33 | a0001c0001t0001g0115a0001c0001t0001g0151a0001c0001t0001g0167others(30): Show | 33 | HG00597.hp2 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.-43-12822_-43-1282 others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27441753 | ||||||
chr1:27441753
|
CA | C | 6 | a0001c0001t0002g0241a0001c0001t0003g0069a0001c0001t0034g0067others(3): Show | 6 | HG00140.hp1 HG00639.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-12821delT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27441753 | ||||||
chr1:27441753
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0183 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-43-12831_-43-1282 others(15): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27441753 | ||||||
chr1:27441762
|
A | AAG | 5 | a0001c0001t0001g0196a0001c0001t0001g0198a0001c0001t0001g0201others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-12830_-43-1282 others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27441762 | ||||||
chr1:27441924
|
C | CA | 16 | a0001c0001t0001g0176a0001c0001t0001g0205a0001c0001t0002g0227others(13): Show | 16 | HG00408.hp1 HG00738.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.-43-12992dupT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27441924 | ||||||
chr1:27441924
|
CA | C | 6 | a0001c0001t0001g0154a0001c0001t0007g0125a0001c0002t0003g0006others(3): Show | 6 | HG01081.hp2 HG01255.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-12992delT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27441924 | ||||||
chr1:27441938
|
A | G | 1 | a0001c0001t0016g0231 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-43-13005T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27441938 | ||||||
chr1:27441950
|
G | A | 2 | a0001c0001t0001g0152a0001c0001t0002g0109 | 2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-43-13017C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27441950 | ||||||
chr1:27442745
|
A | G | 235 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(232): Show | 235 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.-43-13812T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27442745 | ||||||
chr1:27442990
|
C | CA | 63 | a0001c0001t0003g0011a0001c0001t0004g0171a0001c0001t0007g0059others(60): Show | 63 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.-43-14058dupT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27442990 | ||||||
chr1:27442990
|
C | CAA | 10 | a0001c0001t0019g0025a0001c0001t0020g0256a0001c0001t0020g0257others(7): Show | 10 | HG01106.hp1 HG02145.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.-43-14059_-43-1405 others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27442990 | ||||||
chr1:27442990
|
CA | C | 134 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0115others(131): Show | 134 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.-43-14058delT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27442990 | ||||||
chr1:27442990
|
CAA | C | 7 | a0001c0001t0001g0112a0001c0001t0001g0156a0001c0001t0001g0169others(4): Show | 7 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-14059_-43-1405 others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27442990 | ||||||
chr1:27443250
|
C | T | 1 | a0001c0002t0006g0022 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-43-14317G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27443250 | ||||||
chr1:27443301
|
G | A | 1 | a0001c0002t0006g0068 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-43-14368C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27443301 | ||||||
chr1:27443307
|
TA | T | 140 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(137): Show | 140 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.-43-14375delT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27443307 | ||||||
chr1:27443307
|
TAA | T | 16 | a0001c0001t0012g0222a0001c0001t0019g0025a0001c0001t0020g0256others(13): Show | 16 | HG00597.hp1 HG00621.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.-43-14376_-43-1437 others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27443307 | ||||||
chr1:27443307
|
TAAA | T | 47 | a0001c0001t0003g0011a0001c0001t0007g0059a0001c0002t0001g0004others(44): Show | 47 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-43-14377_-43-1437 others(7): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27443307 | ||||||
chr1:27443574
|
T | C | 1 | a0001c0002t0019g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-43-14641A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27443574 | ||||||
chr1:27443739
|
A | G | 248 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(245): Show | 248 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.-43-14806T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27443739 | ||||||
chr1:27443746
|
A | G | 167 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(164): Show | 167 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.-43-14813T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27443746 | ||||||
chr1:27443823
|
G | A | 1 | a0002c0003t0035g0092 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-43-14890C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27443823 | ||||||
chr1:27443840
|
G | C | 1 | a0001c0001t0018g0208 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-43-14907C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27443840 | ||||||
chr1:27443958
|
T | G | 1 | a0001c0001t0007g0130 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-43-15025A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27443958 | ||||||
chr1:27443969
|
T | C | 225 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(222): Show | 225 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.-43-15036A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27443969 | ||||||
chr1:27443970
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-43-15037C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27443970 | ||||||
chr1:27444001
|
G | A | 2 | a0001c0001t0027g0050a0001c0001t0028g0003 | 2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-43-15068C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27444001 | ||||||
chr1:27444002
|
A | C | 1 | a0001c0001t0016g0199 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-43-15069T>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27444002 | ||||||
chr1:27444147
|
C | T | 252 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(249): Show | 252 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.-43-15214G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27444147 | ||||||
chr1:27444157
|
G | A | 1 | a0001c0001t0015g0159 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-43-15224C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27444157 | ||||||
chr1:27444432
|
G | A | 1 | a0001c0001t0013g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-43-15499C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27444432 | ||||||
chr1:27444596
|
C | A | 3 | a0002c0003t0013g0089a0002c0003t0022g0091a0002c0003t0035g0092 | 3 | HG02615.hp2 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-43-15663G>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27444596 | ||||||
chr1:27444743
|
G | A | 5 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0011g0095others(2): Show | 5 | HG01109.hp1 HG02895.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-15810C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27444743 | ||||||
chr1:27444809
|
A | C | 3 | a0002c0003t0013g0089a0002c0003t0022g0091a0002c0003t0035g0092 | 3 | HG02615.hp2 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-43-15876T>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27444809 | ||||||
chr1:27445227
|
T | C | 7 | a0001c0001t0001g0151a0001c0001t0002g0188a0001c0001t0009g0158others(4): Show | 7 | HG02132.hp1 HG02155.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-16294A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27445227 | ||||||
chr1:27445496
|
T | C | 10 | a0001c0001t0010g0061a0001c0001t0010g0066a0001c0001t0022g0087others(7): Show | 10 | HG00140.hp1 HG01074.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.-43-16563A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27445496 | ||||||
chr1:27445498
|
G | GA | 3 | a0001c0001t0001g0249a0001c0001t0002g0248a0001c0001t0008g0252 | 3 | HG01496.hp2 HG02293.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.-43-16566dupT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27445498 | ||||||
chr1:27445575
|
A | G | 1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-43-16642T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27445575 | ||||||
chr1:27445840
|
C | CT | 7 | a0001c0001t0001g0111a0001c0001t0001g0184a0001c0001t0001g0205others(4): Show | 7 | HG00741.hp2 HG01167.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.-43-16908dupA | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27445840 | ||||||
chr1:27445849
|
T | G | 2 | a0001c0001t0004g0217a0001c0001t0013g0082 | 2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-43-16916A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27445849 | ||||||
chr1:27445881
|
T | C | 3 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0248 | 3 | HG00738.hp1 HG01106.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.-43-16948A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27445881 | ||||||
chr1:27446569
|
C | T | 1 | a0001c0001t0004g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-43-17636G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27446569 | ||||||
chr1:27446781
|
C | CA | 5 | a0001c0001t0010g0066a0001c0001t0023g0063a0002c0003t0013g0089others(2): Show | 5 | HG01192.hp2 HG01884.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-17849dupT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27446781 | ||||||
chr1:27446781
|
CA | C | 230 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(227): Show | 230 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.-43-17849delT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27446781 | ||||||
chr1:27446896
|
T | A | 63 | a0001c0001t0003g0011a0001c0001t0007g0059a0001c0001t0019g0025others(60): Show | 63 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.-43-17963A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27446896 | ||||||
chr1:27447119
|
G | A | 1 | a0001c0002t0003g0017 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-43-18186C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27447119 | ||||||
chr1:27447161
|
T | G | 1 | a0001c0001t0043g0168 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-43-18228A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27447161 | ||||||
chr1:27447162
|
TTAAGATA | T | 4 | a0001c0001t0012g0222a0001c0001t0014g0221a0001c0004t0012g0223others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-18236_-43-1823 others(11): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27447162 | ||||||
chr1:27447164
|
A | T | 1 | a0001c0001t0043g0168 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-43-18231T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27447164 | ||||||
chr1:27447171
|
G | A | 1 | a0001c0001t0043g0168 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-43-18238C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27447171 | ||||||
chr1:27447172
|
A | G | 1 | a0001c0001t0043g0168 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-43-18239T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27447172 | ||||||
chr1:27447390
|
G | A | 136 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(133): Show | 136 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.-43-18457C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27447390 | ||||||
chr1:27447588
|
T | G | 1 | a0001c0001t0043g0168 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-43-18655A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27447588 | ||||||
chr1:27447589
|
G | T | 1 | a0001c0001t0043g0168 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-43-18656C>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27447589 | ||||||
chr1:27447590
|
T | G | 1 | a0001c0001t0043g0168 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-43-18657A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27447590 | ||||||
chr1:27447785
|
A | C | 1 | a0001c0001t0043g0168 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-43-18852T>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27447785 | ||||||
chr1:27447802
|
A | C | 1 | a0001c0001t0043g0168 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-43-18869T>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27447802 | ||||||
chr1:27447804
|
T | A | 1 | a0001c0001t0043g0168 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-43-18871A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27447804 | ||||||
chr1:27447807
|
A | T | 1 | a0001c0001t0043g0168 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-43-18874T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27447807 | ||||||
chr1:27447899
|
A | C | 1 | a0001c0001t0043g0168 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-43-18966T>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27447899 | ||||||
chr1:27447921
|
C | T | 1 | a0001c0001t0029g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-43-18988G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27447921 | ||||||
chr1:27448271
|
C | G | 248 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(245): Show | 248 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.-43-19338G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27448271 | ||||||
chr1:27448399
|
G | A | 1 | a0001c0001t0004g0217 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-43-19466C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27448399 | ||||||
chr1:27448588
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-43-19655G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27448588 | ||||||
chr1:27448640
|
C | A | 8 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0012g0225others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-19707G>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27448640 | ||||||
chr1:27448684
|
T | C | 232 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(229): Show | 232 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.-43-19751A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27448684 | ||||||
chr1:27448741
|
C | G | 165 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(162): Show | 165 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-43-19808G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27448741 | ||||||
chr1:27448841
|
C | CA | 86 | a0001c0001t0001g0198a0001c0001t0001g0202a0001c0001t0003g0011others(83): Show | 86 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.-43-19909dupT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27448841 | ||||||
chr1:27448929
|
C | T | 3 | a0002c0003t0013g0089a0002c0003t0022g0091a0002c0003t0035g0092 | 3 | HG02615.hp2 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-43-19996G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27448929 | ||||||
chr1:27448984
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-43-20051A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27448984 | ||||||
chr1:27449126
|
C | T | 1 | a0001c0001t0029g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-43-20193G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27449126 | ||||||
chr1:27449127
|
A | G | 1 | a0001c0001t0029g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-43-20194T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27449127 | ||||||
chr1:27449163
|
T | C | 1 | a0001c0001t0013g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-43-20230A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27449163 | ||||||
chr1:27449498
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-43-20565A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27449498 | ||||||
chr1:27449554
|
G | C | 1 | a0001c0001t0029g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-43-20621C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27449554 | ||||||
chr1:27449704
|
C | G | 5 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0011g0095others(2): Show | 5 | HG01109.hp1 HG02895.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-20771G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27449704 | ||||||
chr1:27449877
|
C | T | 3 | a0001c0001t0018g0208a0001c0001t0018g0216a0001c0001t0026g0002 | 3 | HG02559.hp2 HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-43-20944G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27449877 | ||||||
chr1:27449908
|
C | G | 1 | a0001c0002t0005g0029 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-43-20975G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27449908 | ||||||
chr1:27449924
|
G | A | 2 | a0001c0001t0004g0137a0001c0001t0004g0138 | 2 | HG01074.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.-43-20991C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27449924 | ||||||
chr1:27449956
|
C | A | 1 | a0001c0001t0043g0168 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-43-21023G>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27449956 | ||||||
chr1:27449957
|
A | T | 1 | a0001c0001t0043g0168 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-43-21024T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27449957 | ||||||
chr1:27449958
|
G | A | 1 | a0001c0001t0043g0168 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-43-21025C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27449958 | ||||||
chr1:27449962
|
G | A | 1 | a0001c0001t0043g0168 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-43-21029C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27449962 | ||||||
chr1:27449967
|
A | T | 1 | a0001c0001t0043g0168 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-43-21034T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27449967 | ||||||
chr1:27449968
|
A | G | 1 | a0001c0001t0043g0168 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-43-21035T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27449968 | ||||||
chr1:27449969
|
TCCCATCT others(42): Show |
T | 1 | a0001c0001t0043g0168 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-43-21085_-43-2103 others(53): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27449969 | ||||||
chr1:27450019
|
C | T | 1 | a0001c0001t0043g0168 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-43-21086G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27450019 | ||||||
chr1:27450068
|
C | T | 1 | a0001c0001t0012g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-43-21135G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27450068 | ||||||
chr1:27450090
|
G | C | 2 | a0001c0002t0006g0068a0001c0002t0006g0077 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-43-21157C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27450090 | ||||||
chr1:27450100
|
C | T | 58 | a0001c0001t0027g0050a0001c0001t0028g0003a0001c0002t0001g0004others(55): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.-43-21167G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27450100 | ||||||
chr1:27450138
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-43-21205G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27450138 | ||||||
chr1:27450192
|
GC | G | 165 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(162): Show | 165 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-43-21260delG | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27450192 | ||||||
chr1:27450274
|
C | G | 1 | a0001c0001t0001g0209 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-43-21341G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27450274 | ||||||
chr1:27450341
|
A | G | 9 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0012g0225others(6): Show | 9 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-43-21408T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27450341 | ||||||
chr1:27450445
|
T | C | 1 | a0001c0001t0013g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-43-21512A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27450445 | ||||||
chr1:27450577
|
C | T | 1 | a0001c0001t0004g0142 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-43-21644G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27450577 | ||||||
chr1:27450712
|
T | A | 2 | a0001c0001t0027g0050a0001c0001t0028g0003 | 2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-43-21779A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27450712 | ||||||
chr1:27450831
|
C | T | 1 | a0001c0001t0016g0254 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-43-21898G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27450831 | ||||||
chr1:27450996
|
G | A | 169 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(166): Show | 169 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.-43-22063C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27450996 | ||||||
chr1:27451149
|
A | G | 1 | a0001c0001t0004g0150 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-43-22216T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27451149 | ||||||
chr1:27451194
|
C | G | 1 | a0001c0001t0004g0099 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-43-22261G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27451194 | ||||||
chr1:27451323
|
G | T | 1 | a0002c0003t0022g0091 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-43-22390C>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27451323 | ||||||
chr1:27451499
|
T | C | 1 | a0001c0001t0001g0206 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-43-22566A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27451499 | ||||||
chr1:27451735
|
T | C | 2 | a0001c0001t0004g0117a0001c0001t0021g0107 | 2 | HG02818.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-43-22802A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27451735 | ||||||
chr1:27451754
|
G | C | 1 | a0001c0002t0006g0044 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-43-22821C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27451754 | ||||||
chr1:27451788
|
T | C | 2 | a0001c0001t0004g0117a0001c0001t0021g0107 | 2 | HG02818.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-43-22855A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27451788 | ||||||
chr1:27451835
|
G | A | 1 | a0001c0001t0004g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-43-22902C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27451835 | ||||||
chr1:27451936
|
T | A | 1 | a0001c0001t0023g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-43-23003A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27451936 | ||||||
chr1:27451938
|
G | A | 1 | a0001c0001t0023g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-43-23005C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27451938 | ||||||
chr1:27452008
|
C | T | 3 | a0001c0001t0001g0116a0001c0001t0001g0132a0001c0001t0001g0185 | 3 | HG01109.hp2 HG01358.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-43-23075G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27452008 | ||||||
chr1:27452042
|
C | T | 247 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(244): Show | 247 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.-43-23109G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27452042 | ||||||
chr1:27452058
|
C | G | 3 | a0001c0001t0001g0112a0001c0001t0001g0126a0001c0001t0021g0164 | 3 | HG02071.hp1 NA18964.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.-43-23125G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27452058 | ||||||
chr1:27452239
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-43-23306C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27452239 | ||||||
chr1:27452285
|
C | A | 157 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(154): Show | 157 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.-43-23352G>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27452285 | ||||||
chr1:27452373
|
C | T | 1 | a0001c0001t0003g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-43-23440G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27452373 | ||||||
chr1:27452470
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-43-23537C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27452470 | ||||||
chr1:27452531
|
A | T | 2 | a0001c0002t0003g0045a0001c0002t0006g0044 | 2 | HG01106.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-43-23598T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27452531 | ||||||
chr1:27452553
|
G | A | 7 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0014g0219others(4): Show | 7 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-23620C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27452553 | ||||||
chr1:27452734
|
C | T | 3 | a0001c0001t0018g0208a0001c0001t0018g0216a0001c0001t0026g0002 | 3 | HG02559.hp2 HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-43-23801G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27452734 | ||||||
chr1:27452797
|
T | G | 2 | a0001c0002t0005g0056a0001c0002t0005g0057 | 2 | NA18957.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-43-23864A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27452797 | ||||||
chr1:27453001
|
C | T | 248 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(245): Show | 248 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.-43-24068G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27453001 | ||||||
chr1:27453002
|
T | C | 2 | a0001c0001t0003g0081a0001c0001t0003g0090 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-43-24069A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27453002 | ||||||
chr1:27453114
|
G | T | 1 | a0001c0001t0004g0100 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-43-24181C>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27453114 | ||||||
chr1:27453140
|
G | C | 12 | a0001c0001t0007g0125a0001c0001t0007g0127a0001c0001t0007g0128others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.-43-24207C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27453140 | ||||||
chr1:27453158
|
T | C | 2 | a0001c0001t0007g0128a0001c0001t0007g0129 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-43-24225A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27453158 | ||||||
chr1:27453176
|
G | T | 1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-43-24243C>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27453176 | ||||||
chr1:27453516
|
C | T | 1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-43-24583G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27453516 | ||||||
chr1:27453522
|
G | A | 5 | a0001c0001t0019g0025a0001c0001t0020g0256a0001c0001t0020g0257others(2): Show | 5 | NA18962.hp1 NA18966.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-24589C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27453522 | ||||||
chr1:27453564
|
C | T | 5 | a0001c0001t0004g0101a0001c0001t0004g0102a0001c0001t0004g0103others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-24631G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27453564 | ||||||
chr1:27453591
|
CA | C | 223 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(220): Show | 223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.-43-24659delT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27453591 | ||||||
chr1:27453591
|
CAA | C | 14 | a0001c0001t0004g0161a0001c0001t0007g0125a0001c0001t0007g0127others(11): Show | 14 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.-43-24660_-43-2465 others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27453591 | ||||||
chr1:27453609
|
A | G | 1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-43-24676T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27453609 | ||||||
chr1:27453613
|
C | T | 10 | a0001c0001t0010g0061a0001c0001t0010g0066a0001c0001t0022g0087others(7): Show | 10 | HG00140.hp1 HG01074.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.-43-24680G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27453613 | ||||||
chr1:27453616
|
A | G | 167 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(164): Show | 167 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.-43-24683T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27453616 | ||||||
chr1:27453653
|
G | C | 1 | a0001c0001t0004g0217 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-43-24720C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27453653 | ||||||
chr1:27453658
|
C | G | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG00735.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-43-24725G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27453658 | ||||||
chr1:27453846
|
G | A | 1 | a0001c0002t0003g0040 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-43-24913C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27453846 | ||||||
chr1:27453930
|
C | T | 1 | a0001c0001t0055g0260 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-43-24997G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27453930 | ||||||
chr1:27453965
|
C | A | 1 | a0001c0001t0001g0140 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-43-25032G>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27453965 | ||||||
chr1:27453985
|
C | T | 248 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(245): Show | 248 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.-43-25052G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27453985 | ||||||
chr1:27454037
|
A | C | 1 | a0001c0001t0029g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-43-25104T>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454037 | ||||||
chr1:27454044
|
A | C | 21 | a0001c0001t0001g0098a0001c0001t0001g0134a0001c0001t0001g0151others(18): Show | 21 | HG00323.hp2 HG00438.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-43-25111T>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454044 | ||||||
chr1:27454119
|
ATGTGTGT others(15): Show |
A | 3 | a0001c0001t0001g0115a0001c0001t0001g0176a0001c0001t0002g0108 | 3 | HG02056.hp2 NA18978.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.-43-25208_-43-2518 others(26): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454119 | ||||||
chr1:27454125
|
G | A | 1 | a0001c0001t0027g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-43-25192C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454125 | ||||||
chr1:27454125
|
G | GTA | 35 | a0001c0001t0003g0083a0001c0001t0003g0084a0001c0001t0003g0085others(32): Show | 35 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.-43-25194_-43-2519 others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454125 | ||||||
chr1:27454135
|
A | ATATG | 7 | a0001c0001t0003g0086a0001c0001t0020g0256a0001c0002t0005g0031others(4): Show | 7 | HG02074.hp1 HG03195.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.-43-25203_-43-2520 others(8): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454135 | ||||||
chr1:27454137
|
G | A | 197 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(194): Show | 197 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.-43-25204C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454137 | ||||||
chr1:27454147
|
GTGTGTGT others(15): Show |
G | 2 | a0001c0001t0002g0227a0001c0001t0002g0241 | 2 | HG00408.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.-43-25236_-43-2521 others(26): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454147 | ||||||
chr1:27454149
|
GTGTGTAT others(3): Show |
G | 6 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0011g0095others(3): Show | 6 | HG01109.hp1 HG02809.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-25226_-43-2521 others(14): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454149 | ||||||
chr1:27454149
|
GTGTGTAT others(5): Show |
G | 4 | a0001c0001t0007g0125a0001c0001t0007g0192a0001c0001t0011g0191others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-25228_-43-2521 others(16): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454149 | ||||||
chr1:27454149
|
GTGTGTAT others(7): Show |
G | 14 | a0001c0001t0001g0155a0001c0001t0001g0180a0001c0001t0003g0244others(11): Show | 14 | HG00735.hp1 HG01123.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-43-25230_-43-2521 others(18): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454149 | ||||||
chr1:27454149
|
GTGTGTAT others(9): Show |
G | 31 | a0001c0001t0001g0112a0001c0001t0001g0116a0001c0001t0001g0126others(28): Show | 31 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.-43-25232_-43-2521 others(20): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454149 | ||||||
chr1:27454149
|
GTGTGTAT others(11): Show |
G | 62 | a0001c0001t0001g0098a0001c0001t0001g0120a0001c0001t0001g0123others(59): Show | 62 | HG00323.hp2 HG00673.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.-43-25234_-43-2521 others(22): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454149 | ||||||
chr1:27454149
|
GTGTGTAT others(13): Show |
G | 23 | a0001c0001t0001g0193a0001c0001t0001g0249a0001c0001t0002g0121others(20): Show | 23 | HG00621.hp2 HG01069.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.-43-25236_-43-2521 others(24): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454149 | ||||||
chr1:27454149
|
GTGTGTAT others(15): Show |
G | 10 | a0001c0001t0001g0156a0001c0001t0001g0187a0001c0001t0001g0194others(7): Show | 10 | HG00639.hp1 HG00741.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.-43-25238_-43-2521 others(26): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454149 | ||||||
chr1:27454149
|
GTGTGTAT others(17): Show |
G | 1 | a0001c0001t0009g0149 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-43-25240_-43-2521 others(28): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454149 | ||||||
chr1:27454149
|
GTGTGTAT others(21): Show |
G | 1 | a0001c0001t0001g0111 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-43-25244_-43-2521 others(32): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454149 | ||||||
chr1:27454150
|
T | C | 1 | a0001c0001t0029g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-43-25217A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454150 | ||||||
chr1:27454151
|
G | A | 2 | a0001c0001t0013g0082a0001c0001t0029g0088 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-43-25218C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454151 | ||||||
chr1:27454153
|
G | A | 9 | a0001c0001t0012g0218a0001c0001t0014g0219a0001c0001t0014g0220others(6): Show | 9 | HG01884.hp2 HG02647.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-43-25220C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454153 | ||||||
chr1:27454153
|
GTATATAT others(3): Show |
G | 1 | a0001c0001t0003g0090 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-43-25230_-43-2522 others(14): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454153 | ||||||
chr1:27454155
|
A | G | 22 | a0001c0001t0003g0011a0001c0001t0007g0059a0001c0001t0013g0082others(19): Show | 22 | HG00597.hp1 HG00621.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.-43-25222T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454155 | ||||||
chr1:27454157
|
A | G | 5 | a0001c0001t0007g0059a0001c0001t0020g0257a0001c0001t0028g0003others(2): Show | 5 | HG02135.hp2 HG03041.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-25224T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454157 | ||||||
chr1:27454170
|
TATATATA others(8): Show |
T | 13 | a0001c0002t0005g0023a0001c0002t0005g0036a0001c0002t0005g0037others(10): Show | 13 | HG00597.hp1 HG00621.hp1 HG03491.hp1 others(10): Show |
intron_variant | MODIFIER | c.-43-25252_-43-2523 others(19): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454170 | ||||||
chr1:27454173
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0115 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-43-25257_-43-2524 others(21): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454173 | ||||||
chr1:27454173
|
ATATATAT others(11): Show |
A | 2 | a0001c0001t0001g0176a0001c0001t0002g0108 | 2 | HG02056.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.-43-25258_-43-2524 others(22): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454173 | ||||||
chr1:27454175
|
ATATATAT others(9): Show |
A | 1 | a0001c0001t0012g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-43-25258_-43-2524 others(20): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454175 | ||||||
chr1:27454175
|
ATATATAT others(11): Show |
A | 1 | a0001c0001t0013g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-43-25260_-43-2524 others(22): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454175 | ||||||
chr1:27454177
|
ATATATAT others(8): Show |
A | 2 | a0001c0004t0012g0223a0001c0004t0030g0224 | 2 | HG01884.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-43-25259_-43-2524 others(19): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454177 | ||||||
chr1:27454177
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0014g0221 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-43-25261_-43-2524 others(21): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454177 | ||||||
chr1:27454179
|
ATATATAT others(8): Show |
A | 1 | a0001c0001t0012g0222 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-43-25261_-43-2524 others(19): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454179 | ||||||
chr1:27454181
|
A | T | 2 | a0001c0001t0003g0011a0001c0001t0029g0088 | 2 | NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-43-25248T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454181 | ||||||
chr1:27454181
|
ATATATAT others(7): Show |
A | 2 | a0001c0001t0012g0218a0001c0001t0014g0219 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-43-25262_-43-2524 others(18): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454181 | ||||||
chr1:27454183
|
A | T | 3 | a0001c0001t0003g0011a0001c0001t0027g0050a0001c0001t0029g0088 | 3 | HG02976.hp2 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-43-25250T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454183 | ||||||
chr1:27454183
|
ATATATT | A | 5 | a0001c0001t0003g0081a0001c0001t0010g0061a0001c0001t0023g0063others(2): Show | 5 | HG01884.hp1 HG03225.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-25256_-43-2525 others(10): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454183 | ||||||
chr1:27454183
|
ATATATTT others(7): Show |
A | 1 | a0001c0001t0014g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-43-25264_-43-2525 others(18): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454183 | ||||||
chr1:27454185
|
A | T | 7 | a0001c0001t0003g0011a0001c0001t0007g0059a0001c0001t0027g0050others(4): Show | 7 | HG01069.hp1 HG02976.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-43-25252T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454185 | ||||||
chr1:27454187
|
A | ATATATAT others(10): Show |
1 | a0001c0002t0052g0018 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-43-25255_-43-2525 others(21): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454187 | ||||||
chr1:27454187
|
A | ATATATAT others(30): Show |
1 | a0001c0002t0006g0055 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-43-25255_-43-2525 others(41): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454187 | ||||||
chr1:27454187
|
A | ATATATAT others(9): Show |
2 | a0001c0002t0005g0046a0001c0002t0006g0030 | 2 | NA18960.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.-43-25255_-43-2525 others(20): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454187 | ||||||
chr1:27454187
|
A | ATATATAT others(10): Show |
1 | a0001c0002t0005g0048 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-43-25255_-43-2525 others(21): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454187 | ||||||
chr1:27454187
|
A | ATATATAT others(15): Show |
1 | a0001c0002t0006g0043 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-43-25255_-43-2525 others(26): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454187 | ||||||
chr1:27454187
|
A | ATATATAT others(7): Show |
1 | a0001c0002t0005g0031 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-43-25255_-43-2525 others(18): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454187 | ||||||
chr1:27454187
|
A | ATATATAT others(8): Show |
1 | a0001c0002t0003g0021 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-43-25255_-43-2525 others(19): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454187 | ||||||
chr1:27454187
|
A | ATATATAT others(10): Show |
1 | a0001c0002t0005g0058 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-43-25255_-43-2525 others(21): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454187 | ||||||
chr1:27454187
|
A | ATATATAT others(12): Show |
1 | a0001c0002t0006g0068 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-43-25255_-43-2525 others(23): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454187 | ||||||
chr1:27454187
|
A | ATATATAT others(4): Show |
1 | a0001c0002t0006g0009 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-43-25255_-43-2525 others(15): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454187 | ||||||
chr1:27454187
|
A | ATATATAT others(6): Show |
2 | a0001c0002t0003g0047a0001c0002t0006g0033 | 2 | HG00609.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-43-25255_-43-2525 others(17): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454187 | ||||||
chr1:27454187
|
A | ATATATAT others(18): Show |
1 | a0001c0002t0024g0015 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-43-25255_-43-2525 others(29): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454187 | ||||||
chr1:27454187
|
A | ATATATAT others(19): Show |
1 | a0001c0002t0024g0014 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-43-25255_-43-2525 others(30): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454187 | ||||||
chr1:27454187
|
A | ATATATAT others(2): Show |
7 | a0001c0002t0005g0049a0001c0002t0005g0056a0001c0002t0006g0005others(4): Show | 7 | HG00408.hp2 HG00438.hp2 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-25255_-43-2525 others(13): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454187 | ||||||
chr1:27454187
|
A | ATATATAT others(3): Show |
1 | a0001c0002t0005g0028 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-43-25255_-43-2525 others(14): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454187 | ||||||
chr1:27454187
|
A | ATATATAT others(4): Show |
1 | a0001c0002t0005g0029 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-43-25255_-43-2525 others(15): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454187 | ||||||
chr1:27454187
|
A | ATATATTT others(3): Show |
1 | a0001c0002t0006g0034 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-43-25255_-43-2525 others(14): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454187 | ||||||
chr1:27454187
|
A | ATATATTT others(4): Show |
1 | a0001c0002t0003g0045 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-43-25255_-43-2525 others(15): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454187 | ||||||
chr1:27454187
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-43-25264_-43-2525 others(14): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454187 | ||||||
chr1:27454187
|
A | T | 27 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0073others(24): Show | 27 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.-43-25254T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454187 | ||||||
chr1:27454187
|
ATTT | A | 11 | a0001c0001t0001g0193a0001c0001t0001g0213a0001c0001t0001g0250others(8): Show | 11 | HG00597.hp2 HG01069.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.-43-25257_-43-2525 others(7): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454187 | ||||||
chr1:27454187
|
ATTTT | A | 60 | a0001c0001t0001g0098a0001c0001t0001g0120a0001c0001t0001g0123others(57): Show | 60 | HG00323.hp2 HG00438.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.-43-25258_-43-2525 others(8): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454187 | ||||||
chr1:27454187
|
ATTTTT | A | 14 | a0001c0001t0001g0140a0001c0001t0001g0147a0001c0001t0001g0175others(11): Show | 14 | HG00609.hp2 HG00735.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.-43-25259_-43-2525 others(9): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454187 | ||||||
chr1:27454187
|
ATTTTTT | A | 19 | a0001c0001t0001g0112a0001c0001t0001g0116a0001c0001t0001g0126others(16): Show | 19 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.-43-25260_-43-2525 others(10): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454187 | ||||||
chr1:27454187
|
ATTTTTTT | A | 10 | a0001c0001t0007g0127a0001c0001t0007g0128a0001c0001t0007g0129others(7): Show | 10 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-43-25261_-43-2525 others(11): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454187 | ||||||
chr1:27454189
|
T | A | 35 | a0001c0001t0001g0111a0001c0001t0001g0156a0001c0001t0001g0187others(32): Show | 35 | HG00408.hp1 HG00621.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.-43-25256A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454189 | ||||||
chr1:27454191
|
T | A | 2 | a0001c0001t0001g0111a0001c0001t0009g0149 | 2 | HG01167.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-43-25258A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454191 | ||||||
chr1:27454265
|
T | A | 1 | a0001c0001t0001g0190 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-43-25332A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454265 | ||||||
chr1:27454394
|
C | T | 1 | a0001c0001t0027g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-43-25461G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454394 | ||||||
chr1:27454565
|
T | C | 1 | a0001c0001t0027g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-43-25632A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454565 | ||||||
chr1:27454821
|
CAT | C | 8 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0012g0225others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-25890_-43-2588 others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454821 | ||||||
chr1:27454824
|
A | T | 8 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0012g0225others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-25891T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454824 | ||||||
chr1:27454942
|
T | C | 2 | a0001c0001t0004g0137a0001c0001t0004g0138 | 2 | HG01074.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.-43-26009A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27454942 | ||||||
chr1:27455200
|
G | A | 1 | a0001c0001t0003g0083 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-43-26267C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27455200 | ||||||
chr1:27455430
|
C | G | 1 | a0001c0001t0055g0260 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-43-26497G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27455430 | ||||||
chr1:27455678
|
C | T | 2 | a0001c0001t0001g0249a0001c0001t0008g0252 | 2 | HG01496.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.-43-26745G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27455678 | ||||||
chr1:27455879
|
C | T | 165 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(162): Show | 165 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-43-26946G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27455879 | ||||||
chr1:27456098
|
G | T | 1 | a0001c0001t0010g0061 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-43-27165C>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27456098 | ||||||
chr1:27456105
|
G | A | 1 | a0001c0001t0004g0100 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-43-27172C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27456105 | ||||||
chr1:27456316
|
TA | T | 72 | a0001c0001t0001g0196a0001c0001t0003g0011a0001c0001t0004g0100others(69): Show | 72 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-43-27384delT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27456316 | ||||||
chr1:27456316
|
TAA | T | 78 | a0001c0001t0001g0098a0001c0001t0001g0116a0001c0001t0001g0134others(75): Show | 78 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.-43-27385_-43-2738 others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27456316 | ||||||
chr1:27456316
|
TAAA | T | 83 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0115others(80): Show | 83 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.-43-27386_-43-2738 others(7): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27456316 | ||||||
chr1:27456317
|
A | G | 6 | a0001c0001t0010g0066a0001c0001t0022g0087a0001c0001t0023g0063others(3): Show | 6 | HG00140.hp1 HG01192.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-27384T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27456317 | ||||||
chr1:27456318
|
A | G | 4 | a0001c0001t0010g0061a0001c0001t0031g0062a0001c0001t0032g0080others(1): Show | 4 | HG01074.hp1 HG02738.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-27385T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27456318 | ||||||
chr1:27456355
|
C | A | 1 | a0001c0001t0004g0171 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-43-27422G>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27456355 | ||||||
chr1:27456395
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-43-27462T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27456395 | ||||||
chr1:27456475
|
A | G | 1 | a0001c0001t0003g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-43-27542T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27456475 | ||||||
chr1:27456733
|
C | CT | 7 | a0001c0001t0001g0176a0001c0001t0001g0206a0001c0001t0001g0251others(4): Show | 7 | HG01255.hp1 HG01261.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.-43-27801dupA | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27456733 | ||||||
chr1:27456782
|
T | A | 3 | a0001c0001t0018g0208a0001c0001t0018g0216a0001c0001t0026g0002 | 3 | HG02559.hp2 HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-43-27849A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27456782 | ||||||
chr1:27456896
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-43-27963G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27456896 | ||||||
chr1:27456898
|
C | T | 5 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0011g0095others(2): Show | 5 | HG01109.hp1 HG02895.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-27965G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27456898 | ||||||
chr1:27456903
|
C | G | 2 | a0001c0004t0012g0223a0001c0004t0030g0224 | 2 | HG01884.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-43-27970G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27456903 | ||||||
chr1:27457012
|
G | T | 1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-43-28079C>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27457012 | ||||||
chr1:27457022
|
C | T | 1 | a0001c0001t0003g0078 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-43-28089G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27457022 | ||||||
chr1:27457034
|
G | T | 169 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(166): Show | 169 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.-43-28101C>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27457034 | ||||||
chr1:27457141
|
G | A | 136 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(133): Show | 136 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.-43-28208C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27457141 | ||||||
chr1:27457169
|
C | T | 1 | a0001c0001t0013g0212 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-43-28236G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27457169 | ||||||
chr1:27457171
|
T | C | 248 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(245): Show | 248 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.-43-28238A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27457171 | ||||||
chr1:27457657
|
G | A | 1 | a0001c0001t0013g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-43-28724C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27457657 | ||||||
chr1:27457878
|
C | T | 165 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(162): Show | 165 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-43-28945G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27457878 | ||||||
chr1:27457880
|
C | T | 1 | a0002c0003t0022g0091 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-43-28947G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27457880 | ||||||
chr1:27458031
|
T | C | 169 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(166): Show | 169 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.-43-29098A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27458031 | ||||||
chr1:27458038
|
G | A | 3 | a0001c0001t0001g0115a0001c0001t0001g0176a0001c0001t0002g0108 | 3 | HG02056.hp2 NA18978.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.-43-29105C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27458038 | ||||||
chr1:27458075
|
C | T | 10 | a0001c0001t0003g0244a0001c0001t0012g0218a0001c0001t0012g0222others(7): Show | 10 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-43-29142G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27458075 | ||||||
chr1:27458230
|
T | A | 1 | a0001c0001t0018g0216 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-43-29297A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27458230 | ||||||
chr1:27458243
|
G | T | 1 | a0001c0001t0007g0059 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-43-29310C>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27458243 | ||||||
chr1:27458275
|
T | C | 1 | a0001c0001t0013g0186 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-43-29342A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27458275 | ||||||
chr1:27458308
|
T | TA | 6 | a0001c0001t0003g0074a0001c0001t0003g0081a0001c0001t0004g0217others(3): Show | 6 | HG00140.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43-29376dupT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27458308 | ||||||
chr1:27458308
|
TA | T | 195 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(192): Show | 195 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.-43-29376delT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27458308 | ||||||
chr1:27458308
|
TAA | T | 10 | a0001c0001t0001g0145a0001c0001t0001g0193a0001c0001t0002g0188others(7): Show | 10 | HG00323.hp1 HG01069.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.-43-29377_-43-2937 others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27458308 | ||||||
chr1:27458308
|
TAAAAAAA others(7): Show |
T | 1 | a0001c0001t0013g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-43-29389_-43-2937 others(18): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27458308 | ||||||
chr1:27458519
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-43-29586G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27458519 | ||||||
chr1:27458639
|
A | G | 1 | a0001c0001t0001g0184 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-43-29706T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27458639 | ||||||
chr1:27458749
|
C | T | 1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-43-29816G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27458749 | ||||||
chr1:27458779
|
C | T | 1 | a0001c0001t0013g0212 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-43-29846G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27458779 | ||||||
chr1:27458815
|
A | T | 1 | a0001c0001t0012g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-43-29882T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27458815 | ||||||
chr1:27458823
|
T | A | 2 | a0001c0001t0003g0085a0001c0001t0003g0086 | 2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-43-29890A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27458823 | ||||||
chr1:27458824
|
A | T | 4 | a0001c0001t0002g0248a0001c0001t0050g0148a0002c0003t0022g0091others(1): Show | 4 | HG02293.hp2 HG02647.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-29891T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27458824 | ||||||
chr1:27458848
|
G | A | 1 | a0001c0001t0009g0149 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-43-29915C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27458848 | ||||||
chr1:27459066
|
C | T | 1 | a0001c0001t0029g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-43-30133G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27459066 | ||||||
chr1:27459533
|
C | G | 1 | a0001c0002t0003g0047 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-44+30453G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27459533 | ||||||
chr1:27459673
|
C | G | 10 | a0001c0001t0010g0061a0001c0001t0010g0066a0001c0001t0022g0087others(7): Show | 10 | HG00140.hp1 HG01074.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.-44+30313G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27459673 | ||||||
chr1:27459724
|
T | C | 1 | a0001c0001t0013g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-44+30262A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27459724 | ||||||
chr1:27459823
|
T | C | 7 | a0001c0001t0001g0116a0001c0001t0001g0120a0001c0001t0001g0132others(4): Show | 7 | HG00140.hp2 HG01070.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-44+30163A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27459823 | ||||||
chr1:27459874
|
C | A | 136 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(133): Show | 136 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.-44+30112G>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27459874 | ||||||
chr1:27459901
|
G | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0126a0001c0001t0021g0164 | 3 | HG02071.hp1 NA18964.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.-44+30085C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27459901 | ||||||
chr1:27460091
|
C | G | 1 | a0001c0001t0001g0131 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-44+29895G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27460091 | ||||||
chr1:27460181
|
C | A | 169 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(166): Show | 169 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.-44+29805G>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27460181 | ||||||
chr1:27460302
|
G | A | 157 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(154): Show | 157 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.-44+29684C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27460302 | ||||||
chr1:27460412
|
C | T | 136 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(133): Show | 136 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.-44+29574G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27460412 | ||||||
chr1:27460456
|
T | C | 1 | a0001c0001t0029g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-44+29530A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27460456 | ||||||
chr1:27460486
|
T | C | 1 | a0001c0001t0002g0188 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-44+29500A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27460486 | ||||||
chr1:27460974
|
G | A | 5 | a0001c0001t0001g0196a0001c0001t0001g0198a0001c0001t0001g0201others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+29012C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27460974 | ||||||
chr1:27460992
|
A | C | 1 | a0001c0002t0048g0038 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-44+28994T>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27460992 | ||||||
chr1:27461014
|
T | G | 1 | a0001c0001t0010g0066 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-44+28972A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27461014 | ||||||
chr1:27461163
|
A | G | 10 | a0001c0001t0010g0061a0001c0001t0010g0066a0001c0001t0022g0087others(7): Show | 10 | HG00140.hp1 HG01074.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.-44+28823T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27461163 | ||||||
chr1:27461180
|
T | C | 1 | a0001c0001t0029g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-44+28806A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27461180 | ||||||
chr1:27461430
|
C | A | 1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-44+28556G>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27461430 | ||||||
chr1:27461460
|
A | AT | 103 | a0001c0001t0001g0116a0001c0001t0001g0132a0001c0001t0001g0140others(100): Show | 103 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.-44+28525dupA | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27461460 | ||||||
chr1:27461460
|
A | ATT | 6 | a0001c0001t0033g0079a0001c0001t0055g0260a0001c0002t0001g0020others(3): Show | 6 | HG02135.hp2 HG02738.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44+28524_-44+2852 others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27461460 | ||||||
chr1:27461505
|
G | A | 8 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0012g0225others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+28481C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27461505 | ||||||
chr1:27461587
|
C | T | 3 | a0001c0001t0004g0113a0001c0001t0004g0114a0001c0001t0004g0133 | 3 | HG03017.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-44+28399G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27461587 | ||||||
chr1:27461600
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-44+28386G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27461600 | ||||||
chr1:27461608
|
G | A | 1 | a0001c0001t0004g0162 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-44+28378C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27461608 | ||||||
chr1:27461640
|
T | A | 1 | a0001c0001t0013g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-44+28346A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27461640 | ||||||
chr1:27461641
|
A | T | 14 | a0001c0001t0009g0158a0001c0001t0010g0061a0001c0001t0010g0066others(11): Show | 14 | HG00140.hp1 HG01074.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.-44+28345T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27461641 | ||||||
chr1:27461676
|
G | A | 7 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0073others(4): Show | 7 | HG00639.hp2 HG02258.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-44+28310C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27461676 | ||||||
chr1:27461764
|
G | A | 1 | a0001c0001t0013g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-44+28222C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27461764 | ||||||
chr1:27461978
|
C | CT | 92 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(89): Show | 92 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.-44+28007dupA | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27461978 | ||||||
chr1:27462004
|
G | A | 1 | a0001c0001t0017g0259 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-44+27982C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27462004 | ||||||
chr1:27462432
|
G | A | 1 | a0001c0001t0022g0087 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-44+27554C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27462432 | ||||||
chr1:27462712
|
T | C | 4 | a0001c0001t0001g0187a0001c0001t0001g0193a0001c0001t0001g0194others(1): Show | 4 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+27274A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27462712 | ||||||
chr1:27462876
|
A | G | 102 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(99): Show | 102 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-44+27110T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27462876 | ||||||
chr1:27462967
|
G | A | 11 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0073others(8): Show | 11 | HG00639.hp2 HG02258.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-44+27019C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27462967 | ||||||
chr1:27462968
|
C | T | 8 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0012g0225others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+27018G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27462968 | ||||||
chr1:27463063
|
G | A | 1 | a0002c0003t0022g0091 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-44+26923C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27463063 | ||||||
chr1:27463269
|
T | C | 2 | a0001c0001t0003g0081a0001c0001t0003g0090 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-44+26717A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27463269 | ||||||
chr1:27463422
|
G | A | 1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-44+26564C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27463422 | ||||||
chr1:27463542
|
T | G | 95 | a0001c0001t0001g0200a0001c0001t0003g0011a0001c0001t0003g0069others(92): Show | 95 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.-44+26444A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27463542 | ||||||
chr1:27463622
|
C | CA | 55 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0126others(52): Show | 55 | HG00597.hp1 HG00639.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.-44+26363dupT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27463622 | ||||||
chr1:27463622
|
C | CAA | 6 | a0001c0001t0001g0176a0001c0001t0003g0081a0001c0001t0003g0083others(3): Show | 6 | HG02056.hp2 HG06807.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44+26362_-44+2636 others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27463622 | ||||||
chr1:27463622
|
CA | C | 6 | a0001c0001t0002g0230a0001c0001t0002g0232a0001c0001t0016g0254others(3): Show | 6 | HG02976.hp2 HG03017.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44+26363delT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27463622 | ||||||
chr1:27463648
|
A | G | 2 | a0001c0001t0001g0210a0001c0001t0001g0215 | 2 | HG02602.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-44+26338T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27463648 | ||||||
chr1:27463696
|
T | C | 1 | a0001c0001t0053g0236 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-44+26290A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27463696 | ||||||
chr1:27463765
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-44+26221A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27463765 | ||||||
chr1:27463804
|
A | T | 51 | a0001c0001t0001g0098a0001c0001t0001g0134a0001c0001t0001g0151others(48): Show | 51 | HG00323.hp2 HG00438.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-44+26182T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27463804 | ||||||
chr1:27463804
|
AT | A | 11 | a0001c0001t0001g0195a0001c0001t0012g0218a0001c0001t0012g0222others(8): Show | 11 | HG00597.hp1 HG00639.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.-44+26181delA | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27463804 | ||||||
chr1:27463805
|
T | A | 31 | a0001c0001t0001g0098a0001c0001t0001g0134a0001c0001t0001g0151others(28): Show | 31 | HG00323.hp2 HG00438.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.-44+26181A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27463805 | ||||||
chr1:27463807
|
T | A | 21 | a0001c0001t0001g0126a0001c0001t0001g0140a0001c0001t0001g0155others(18): Show | 21 | HG00735.hp1 HG01109.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.-44+26179A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27463807 | ||||||
chr1:27463808
|
T | A | 7 | a0001c0001t0004g0217a0001c0001t0012g0218a0001c0001t0012g0222others(4): Show | 7 | HG01884.hp2 HG02451.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44+26178A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27463808 | ||||||
chr1:27463973
|
G | C | 1 | a0001c0002t0019g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-44+26013C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27463973 | ||||||
chr1:27464013
|
C | T | 1 | a0002c0003t0022g0091 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-44+25973G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27464013 | ||||||
chr1:27464208
|
C | T | 1 | a0001c0001t0013g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-44+25778G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27464208 | ||||||
chr1:27464378
|
G | T | 102 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(99): Show | 102 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-44+25608C>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27464378 | ||||||
chr1:27464563
|
G | A | 1 | a0001c0002t0054g0010 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-44+25423C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27464563 | ||||||
chr1:27464566
|
C | A | 1 | a0001c0002t0054g0010 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-44+25420G>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27464566 | ||||||
chr1:27464597
|
T | G | 1 | a0001c0001t0016g0254 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-44+25389A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27464597 | ||||||
chr1:27464661
|
C | T | 1 | a0001c0001t0027g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-44+25325G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27464661 | ||||||
chr1:27464759
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-44+25227G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27464759 | ||||||
chr1:27464873
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-44+25113G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27464873 | ||||||
chr1:27464941
|
C | A | 1 | a0001c0001t0001g0215 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-44+25045G>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27464941 | ||||||
chr1:27464954
|
C | T | 1 | a0001c0001t0027g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-44+25032G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27464954 | ||||||
chr1:27465131
|
T | A | 1 | a0001c0001t0029g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-44+24855A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27465131 | ||||||
chr1:27465360
|
C | T | 123 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(120): Show | 123 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.-44+24626G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27465360 | ||||||
chr1:27465695
|
T | G | 90 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(87): Show | 90 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.-44+24291A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27465695 | ||||||
chr1:27465698
|
G | A | 2 | a0001c0001t0031g0062a0001c0001t0033g0079 | 2 | HG02738.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-44+24288C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27465698 | ||||||
chr1:27465834
|
A | G | 3 | a0001c0001t0001g0145a0001c0001t0002g0121a0001c0001t0002g0122 | 3 | HG00621.hp2 NA18951.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.-44+24152T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27465834 | ||||||
chr1:27466048
|
T | C | 27 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0073others(24): Show | 27 | HG00140.hp1 HG00639.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-44+23938A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27466048 | ||||||
chr1:27466130
|
G | A | 93 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(90): Show | 93 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-44+23856C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27466130 | ||||||
chr1:27466190
|
A | G | 1 | a0001c0001t0007g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-44+23796T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27466190 | ||||||
chr1:27466244
|
T | C | 123 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(120): Show | 123 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.-44+23742A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27466244 | ||||||
chr1:27466270
|
T | C | 1 | a0001c0001t0027g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-44+23716A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27466270 | ||||||
chr1:27466408
|
T | A | 3 | a0002c0003t0013g0089a0002c0003t0022g0091a0002c0003t0035g0092 | 3 | HG02615.hp2 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-44+23578A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27466408 | ||||||
chr1:27466426
|
A | T | 1 | a0001c0001t0022g0087 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-44+23560T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27466426 | ||||||
chr1:27466435
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-44+23551C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27466435 | ||||||
chr1:27466566
|
T | C | 2 | a0001c0001t0002g0228a0001c0001t0002g0229 | 2 | NA18993.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-44+23420A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27466566 | ||||||
chr1:27466647
|
G | A | 1 | a0001c0001t0012g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-44+23339C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27466647 | ||||||
chr1:27466732
|
T | C | 10 | a0001c0001t0010g0061a0001c0001t0010g0066a0001c0001t0022g0087others(7): Show | 10 | HG00140.hp1 HG01074.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.-44+23254A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27466732 | ||||||
chr1:27466747
|
G | C | 2 | a0001c0001t0027g0050a0001c0001t0028g0003 | 2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-44+23239C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27466747 | ||||||
chr1:27467042
|
C | T | 1 | a0001c0002t0019g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-44+22944G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27467042 | ||||||
chr1:27467194
|
T | C | 1 | a0001c0001t0009g0135 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-44+22792A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27467194 | ||||||
chr1:27467215
|
C | CA | 16 | a0001c0001t0001g0116a0001c0001t0001g0131a0001c0001t0001g0132others(13): Show | 16 | HG00735.hp1 HG01109.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.-44+22770dupT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27467215 | ||||||
chr1:27467215
|
CA | C | 96 | a0001c0001t0003g0011a0001c0001t0003g0081a0001c0001t0003g0090others(93): Show | 96 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.-44+22770delT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27467215 | ||||||
chr1:27467215
|
CAA | C | 12 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0073others(9): Show | 12 | HG00639.hp2 HG02258.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+22769_-44+2277 others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27467215 | ||||||
chr1:27467232
|
A | C | 1 | a0001c0001t0013g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-44+22754T>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27467232 | ||||||
chr1:27467234
|
C | A | 1 | a0001c0001t0013g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-44+22752G>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27467234 | ||||||
chr1:27467240
|
A | C | 3 | a0001c0001t0018g0208a0001c0001t0018g0216a0001c0001t0026g0002 | 3 | HG02559.hp2 HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-44+22746T>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27467240 | ||||||
chr1:27467319
|
G | GT | 17 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0073others(14): Show | 17 | HG00639.hp2 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.-44+22666dupA | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27467319 | ||||||
chr1:27467320
|
T | G | 1 | a0001c0001t0001g0154 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-44+22666A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27467320 | ||||||
chr1:27467490
|
A | G | 1 | a0001c0001t0013g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-44+22496T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27467490 | ||||||
chr1:27467503
|
G | A | 1 | a0001c0001t0003g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-44+22483C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27467503 | ||||||
chr1:27467544
|
G | A | 2 | a0001c0002t0024g0014a0001c0002t0024g0015 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-44+22442C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27467544 | ||||||
chr1:27467614
|
T | C | 1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-44+22372A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27467614 | ||||||
chr1:27467684
|
G | C | 26 | a0001c0001t0001g0098a0001c0001t0001g0134a0001c0001t0001g0151others(23): Show | 26 | HG00323.hp2 HG00438.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.-44+22302C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27467684 | ||||||
chr1:27467736
|
C | T | 1 | a0001c0002t0003g0017 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-44+22250G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27467736 | ||||||
chr1:27467738
|
C | T | 14 | a0001c0001t0001g0115a0001c0001t0001g0139a0001c0001t0001g0175others(11): Show | 14 | HG00609.hp2 HG00673.hp1 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.-44+22248G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27467738 | ||||||
chr1:27467925
|
A | C | 1 | a0001c0001t0002g0119 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-44+22061T>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27467925 | ||||||
chr1:27467973
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-44+22013C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27467973 | ||||||
chr1:27468270
|
G | C | 1 | a0001c0001t0029g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-44+21716C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27468270 | ||||||
chr1:27468432
|
G | A | 12 | a0001c0001t0007g0125a0001c0001t0007g0127a0001c0001t0007g0128others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.-44+21554C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27468432 | ||||||
chr1:27468437
|
T | TA | 11 | a0001c0001t0010g0061a0001c0001t0010g0066a0001c0001t0022g0087others(8): Show | 11 | HG00140.hp1 HG01074.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.-44+21548dupT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27468437 | ||||||
chr1:27468489
|
A | G | 5 | a0001c0001t0019g0025a0001c0001t0020g0256a0001c0001t0020g0257others(2): Show | 5 | NA18962.hp1 NA18966.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+21497T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27468489 | ||||||
chr1:27468532
|
T | C | 1 | a0001c0002t0006g0013 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-44+21454A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27468532 | ||||||
chr1:27468647
|
A | G | 2 | a0001c0001t0001g0115a0001c0002t0038g0035 | 2 | NA18747.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.-44+21339T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27468647 | ||||||
chr1:27468816
|
C | T | 6 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0011g0095others(3): Show | 6 | HG01109.hp1 HG02895.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44+21170G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27468816 | ||||||
chr1:27468921
|
CA | C | 98 | a0001c0001t0001g0115a0001c0001t0001g0178a0001c0001t0003g0011others(95): Show | 98 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.-44+21064delT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27468921 | ||||||
chr1:27468984
|
G | C | 3 | a0001c0001t0001g0098a0001c0001t0004g0099a0001c0001t0004g0100 | 3 | HG00323.hp2 HG01192.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-44+21002C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27468984 | ||||||
chr1:27469036
|
G | GA | 3 | a0001c0001t0001g0145a0001c0001t0002g0121a0001c0001t0002g0122 | 3 | HG00621.hp2 NA18951.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.-44+20949dupT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27469036 | ||||||
chr1:27469218
|
T | C | 1 | a0001c0001t0002g0253 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-44+20768A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27469218 | ||||||
chr1:27469352
|
G | A | 2 | a0001c0001t0021g0164a0001c0001t0051g0226 | 2 | NA18991.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.-44+20634C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27469352 | ||||||
chr1:27469457
|
C | T | 90 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(87): Show | 90 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.-44+20529G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27469457 | ||||||
chr1:27469584
|
T | C | 8 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0012g0225others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+20402A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27469584 | ||||||
chr1:27469643
|
T | TAAAAAGT others(316): Show |
1 | a0001c0001t0017g0233 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-44+20342_-44+2034 others(327): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27469643 | ||||||
chr1:27469693
|
G | A | 1 | a0001c0001t0027g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-44+20293C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27469693 | ||||||
chr1:27469857
|
A | G | 123 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(120): Show | 123 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.-44+20129T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27469857 | ||||||
chr1:27470174
|
G | A | 4 | a0001c0001t0003g0083a0001c0001t0003g0084a0001c0001t0003g0085others(1): Show | 4 | HG03195.hp2 HG06807.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+19812C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27470174 | ||||||
chr1:27470499
|
A | C | 1 | a0001c0002t0019g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-44+19487T>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27470499 | ||||||
chr1:27470540
|
C | T | 1 | a0001c0001t0004g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-44+19446G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27470540 | ||||||
chr1:27470586
|
TC | T | 63 | a0001c0001t0003g0011a0001c0001t0007g0059a0001c0001t0019g0025others(60): Show | 63 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.-44+19399delG | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27470586 | ||||||
chr1:27470744
|
A | G | 1 | a0001c0001t0013g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-44+19242T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27470744 | ||||||
chr1:27470948
|
A | T | 1 | a0001c0001t0002g0237 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-44+19038T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27470948 | ||||||
chr1:27471119
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-44+18867G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27471119 | ||||||
chr1:27471162
|
A | G | 94 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(91): Show | 94 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.-44+18824T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27471162 | ||||||
chr1:27471201
|
C | T | 1 | a0001c0001t0003g0069 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-44+18785G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27471201 | ||||||
chr1:27471294
|
G | C | 4 | a0001c0001t0002g0227a0001c0001t0002g0238a0001c0001t0002g0240others(1): Show | 4 | HG00408.hp1 HG03834.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+18692C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27471294 | ||||||
chr1:27471344
|
C | CA | 63 | a0001c0001t0001g0152a0001c0001t0001g0196a0001c0001t0002g0108others(60): Show | 63 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.-44+18641dupT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27471344 | ||||||
chr1:27471344
|
C | CAA | 34 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0073others(31): Show | 34 | HG00140.hp1 HG00609.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.-44+18640_-44+1864 others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27471344 | ||||||
chr1:27471344
|
CA | C | 5 | a0001c0001t0001g0187a0001c0001t0001g0193a0001c0001t0001g0194others(2): Show | 5 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+18641delT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27471344 | ||||||
chr1:27471423
|
C | T | 12 | a0001c0001t0007g0125a0001c0001t0007g0127a0001c0001t0007g0128others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.-44+18563G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27471423 | ||||||
chr1:27471474
|
T | C | 1 | a0001c0001t0003g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-44+18512A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27471474 | ||||||
chr1:27471565
|
C | T | 2 | a0001c0001t0027g0050a0001c0001t0028g0003 | 2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-44+18421G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27471565 | ||||||
chr1:27471613
|
G | A | 1 | a0001c0002t0019g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-44+18373C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27471613 | ||||||
chr1:27471708
|
G | A | 94 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(91): Show | 94 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.-44+18278C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27471708 | ||||||
chr1:27471851
|
C | T | 1 | a0001c0001t0008g0245 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-44+18135G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27471851 | ||||||
chr1:27471877
|
T | C | 1 | a0001c0001t0055g0260 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-44+18109A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27471877 | ||||||
chr1:27471948
|
G | A | 2 | a0001c0001t0027g0050a0001c0001t0028g0003 | 2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-44+18038C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27471948 | ||||||
chr1:27472106
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-44+17880C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27472106 | ||||||
chr1:27472188
|
G | A | 63 | a0001c0001t0003g0011a0001c0001t0007g0059a0001c0001t0019g0025others(60): Show | 63 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.-44+17798C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27472188 | ||||||
chr1:27472192
|
A | G | 123 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(120): Show | 123 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.-44+17794T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27472192 | ||||||
chr1:27472281
|
C | T | 8 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0012g0225others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+17705G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27472281 | ||||||
chr1:27472301
|
T | G | 1 | a0001c0002t0054g0010 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-44+17685A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27472301 | ||||||
chr1:27472324
|
C | CA | 12 | a0001c0001t0001g0183a0001c0001t0001g0211a0001c0001t0001g0214others(9): Show | 12 | HG00673.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+17661dupT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27472324 | ||||||
chr1:27472324
|
CA | C | 7 | a0001c0001t0001g0187a0001c0001t0001g0193a0001c0001t0001g0194others(4): Show | 7 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44+17661delT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27472324 | ||||||
chr1:27472341
|
A | T | 1 | a0002c0003t0022g0091 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-44+17645T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27472341 | ||||||
chr1:27472429
|
T | C | 55 | a0001c0002t0001g0004a0001c0002t0001g0020a0001c0002t0003g0006others(52): Show | 55 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.-44+17557A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27472429 | ||||||
chr1:27472444
|
G | C | 4 | a0001c0002t0003g0045a0001c0002t0005g0016a0001c0002t0005g0053others(1): Show | 4 | HG01106.hp1 HG02145.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+17542C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27472444 | ||||||
chr1:27472451
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-44+17535A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27472451 | ||||||
chr1:27472596
|
TGCACTCC others(1): Show |
T | 8 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0012g0225others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+17382_-44+1738 others(12): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27472596 | ||||||
chr1:27472650
|
C | CA | 16 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0001g0176others(13): Show | 16 | HG00741.hp1 HG02056.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-44+17335dupT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27472650 | ||||||
chr1:27472665
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0002t0054g0010 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-44+17311_-44+1732 others(14): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27472665 | ||||||
chr1:27472673
|
AAG | A | 57 | a0001c0001t0003g0011a0001c0001t0019g0025a0001c0001t0020g0256others(54): Show | 57 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.-44+17311_-44+1731 others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27472673 | ||||||
chr1:27472674
|
AG | A | 47 | a0001c0001t0001g0156a0001c0001t0001g0187a0001c0001t0001g0193others(44): Show | 47 | HG00140.hp1 HG00621.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.-44+17311delC | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27472674 | ||||||
chr1:27472675
|
G | A | 63 | a0001c0001t0001g0098a0001c0001t0001g0134a0001c0001t0001g0151others(60): Show | 63 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.-44+17311C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27472675 | ||||||
chr1:27472684
|
A | AGG | 10 | a0001c0001t0010g0061a0001c0001t0010g0066a0001c0001t0022g0087others(7): Show | 10 | HG00140.hp1 HG01074.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.-44+17300_-44+1730 others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27472684 | ||||||
chr1:27472786
|
C | T | 12 | a0001c0001t0007g0125a0001c0001t0007g0127a0001c0001t0007g0128others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.-44+17200G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27472786 | ||||||
chr1:27472798
|
CA | C | 111 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(108): Show | 111 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.-44+17187delT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27472798 | ||||||
chr1:27472811
|
A | G | 1 | a0001c0001t0046g0181 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-44+17175T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27472811 | ||||||
chr1:27472841
|
G | A | 1 | a0001c0001t0004g0182 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-44+17145C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27472841 | ||||||
chr1:27472971
|
C | CA | 34 | a0001c0001t0001g0156a0001c0001t0001g0204a0001c0001t0001g0214others(31): Show | 34 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.-44+17014dupT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27472971 | ||||||
chr1:27472971
|
C | CAA | 88 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(85): Show | 88 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.-44+17013_-44+1701 others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27472971 | ||||||
chr1:27472971
|
C | CAAA | 5 | a0001c0001t0013g0082a0001c0002t0001g0004a0001c0002t0005g0051others(2): Show | 5 | HG02135.hp2 HG02970.hp1 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+17012_-44+1701 others(7): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27472971 | ||||||
chr1:27473034
|
T | G | 2 | a0001c0001t0003g0081a0001c0001t0003g0090 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-44+16952A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27473034 | ||||||
chr1:27473141
|
A | T | 1 | a0001c0002t0005g0028 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-44+16845T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27473141 | ||||||
chr1:27473340
|
C | T | 3 | a0001c0001t0020g0256a0001c0001t0020g0257a0001c0001t0037g0255 | 3 | NA18962.hp1 NA18966.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-44+16646G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27473340 | ||||||
chr1:27473439
|
C | T | 1 | a0001c0001t0002g0230 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-44+16547G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27473439 | ||||||
chr1:27473455
|
C | CA | 12 | a0001c0001t0004g0133a0001c0001t0004g0217a0001c0001t0007g0165others(9): Show | 12 | HG00609.hp1 HG02055.hp2 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.-44+16530dupT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27473455 | ||||||
chr1:27473471
|
A | G | 4 | a0001c0001t0001g0152a0001c0001t0002g0109a0001c0002t0006g0013others(1): Show | 4 | HG02257.hp1 HG02622.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+16515T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27473471 | ||||||
chr1:27473786
|
A | G | 1 | a0001c0001t0012g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-44+16200T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27473786 | ||||||
chr1:27473856
|
A | G | 102 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(99): Show | 102 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-44+16130T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27473856 | ||||||
chr1:27473971
|
C | T | 123 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(120): Show | 123 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.-44+16015G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27473971 | ||||||
chr1:27473999
|
C | T | 4 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0179others(1): Show | 4 | HG00609.hp2 NA19007.hp1 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+15987G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27473999 | ||||||
chr1:27474003
|
G | C | 1 | a0001c0002t0006g0034 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-44+15983C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27474003 | ||||||
chr1:27474174
|
G | A | 63 | a0001c0001t0003g0011a0001c0001t0007g0059a0001c0001t0019g0025others(60): Show | 63 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.-44+15812C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27474174 | ||||||
chr1:27474215
|
T | G | 1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-44+15771A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27474215 | ||||||
chr1:27474269
|
AG | A | 8 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0012g0225others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+15716delC | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27474269 | ||||||
chr1:27474293
|
A | G | 1 | a0001c0001t0029g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-44+15693T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27474293 | ||||||
chr1:27474937
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-44+15049C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27474937 | ||||||
chr1:27475024
|
C | T | 102 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(99): Show | 102 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-44+14962G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27475024 | ||||||
chr1:27475048
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-44+14938C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27475048 | ||||||
chr1:27475167
|
C | T | 90 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(87): Show | 90 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.-44+14819G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27475167 | ||||||
chr1:27475232
|
C | T | 92 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(89): Show | 92 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.-44+14754G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27475232 | ||||||
chr1:27475607
|
T | G | 1 | a0001c0001t0029g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-44+14379A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27475607 | ||||||
chr1:27475608
|
T | C | 1 | a0001c0001t0055g0260 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-44+14378A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27475608 | ||||||
chr1:27475774
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-44+14212G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27475774 | ||||||
chr1:27475803
|
T | C | 1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-44+14183A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27475803 | ||||||
chr1:27476161
|
A | G | 1 | a0001c0001t0004g0138 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-44+13825T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27476161 | ||||||
chr1:27476192
|
G | A | 1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-44+13794C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27476192 | ||||||
chr1:27476345
|
G | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG00735.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-44+13641C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27476345 | ||||||
chr1:27476871
|
A | G | 1 | a0001c0001t0013g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-44+13115T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27476871 | ||||||
chr1:27476950
|
G | A | 3 | a0002c0003t0013g0089a0002c0003t0022g0091a0002c0003t0035g0092 | 3 | HG02615.hp2 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-44+13036C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27476950 | ||||||
chr1:27477235
|
AT | A | 4 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0179others(1): Show | 4 | HG00609.hp2 NA19007.hp1 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+12750delA | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27477235 | ||||||
chr1:27477361
|
G | A | 1 | a0001c0001t0008g0110 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-44+12625C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27477361 | ||||||
chr1:27477414
|
C | T | 1 | a0001c0002t0006g0076 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-44+12572G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27477414 | ||||||
chr1:27477435
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0014g0219a0001c0001t0014g0220others(2): Show | 5 | HG02886.hp1 HG03195.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+12551A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27477435 | ||||||
chr1:27477601
|
TTAAAAAT others(322): Show |
T | 102 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(99): Show | 102 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-44+12056_-44+1238 others(4): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27477601 | ||||||
chr1:27477673
|
G | C | 1 | a0001c0001t0001g0180 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-44+12313C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27477673 | ||||||
chr1:27477696
|
G | A | 1 | a0001c0001t0002g0239 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-44+12290C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27477696 | ||||||
chr1:27477706
|
C | T | 1 | a0001c0001t0004g0150 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-44+12280G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27477706 | ||||||
chr1:27477755
|
C | T | 1 | a0001c0001t0002g0237 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-44+12231G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27477755 | ||||||
chr1:27477875
|
G | C | 1 | a0001c0001t0004g0138 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-44+12111C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27477875 | ||||||
chr1:27477898
|
C | CA | 5 | a0001c0001t0001g0187a0001c0001t0001g0193a0001c0001t0001g0194others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+12087dupT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27477898 | ||||||
chr1:27477906
|
AAAAATAA others(6): Show |
A | 1 | a0001c0001t0013g0212 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-44+12067_-44+1207 others(17): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27477906 | ||||||
chr1:27477909
|
AAT | A | 5 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0011g0095others(2): Show | 5 | HG01109.hp1 HG02895.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+12075_-44+1207 others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27477909 | ||||||
chr1:27477910
|
A | T | 8 | a0001c0001t0001g0196a0001c0001t0001g0198a0001c0001t0001g0201others(5): Show | 8 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+12076T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27477910 | ||||||
chr1:27477910
|
AT | A | 14 | a0001c0001t0007g0125a0001c0001t0007g0127a0001c0001t0007g0128others(11): Show | 14 | HG01070.hp1 HG01071.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.-44+12075delA | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27477910 | ||||||
chr1:27477911
|
T | A | 42 | a0001c0001t0001g0098a0001c0001t0001g0134a0001c0001t0001g0151others(39): Show | 42 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.-44+12075A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27477911 | ||||||
chr1:27477915
|
T | A | 9 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0007g0130others(6): Show | 9 | HG01109.hp1 HG02257.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44+12071A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27477915 | ||||||
chr1:27477918
|
A | T | 5 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0011g0095others(2): Show | 5 | HG01109.hp1 HG02895.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+12068T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27477918 | ||||||
chr1:27477919
|
T | A | 8 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0011g0095others(5): Show | 8 | HG01109.hp1 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-44+12067A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27477919 | ||||||
chr1:27477920
|
A | T | 3 | a0001c0001t0018g0208a0001c0001t0018g0216a0001c0001t0026g0002 | 3 | HG02559.hp2 HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-44+12066T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27477920 | ||||||
chr1:27477923
|
A | T | 15 | a0001c0001t0001g0139a0001c0001t0001g0160a0001c0001t0001g0175others(12): Show | 15 | HG00408.hp1 HG00609.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.-44+12063T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27477923 | ||||||
chr1:27477925
|
A | AT | 12 | a0001c0001t0007g0125a0001c0001t0007g0127a0001c0001t0007g0128others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.-44+12060_-44+1206 others(5): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27477925 | ||||||
chr1:27477925
|
A | T | 3 | a0001c0001t0018g0208a0001c0001t0018g0216a0001c0001t0026g0002 | 3 | HG02559.hp2 HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-44+12061T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27477925 | ||||||
chr1:27477927
|
A | T | 1 | a0001c0001t0013g0212 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-44+12059T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27477927 | ||||||
chr1:27477928
|
A | T | 1 | a0001c0001t0002g0243 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-44+12058T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27477928 | ||||||
chr1:27478181
|
A | G | 93 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(90): Show | 93 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-44+11805T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27478181 | ||||||
chr1:27478189
|
G | A | 1 | a0001c0002t0005g0046 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-44+11797C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27478189 | ||||||
chr1:27478275
|
C | CA | 6 | a0001c0001t0001g0185a0001c0001t0002g0108a0001c0001t0002g0232others(3): Show | 6 | HG02071.hp2 HG03710.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44+11710dupT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27478275 | ||||||
chr1:27478344
|
C | G | 1 | a0001c0001t0010g0066 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-44+11642G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27478344 | ||||||
chr1:27478503
|
G | A | 1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-44+11483C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27478503 | ||||||
chr1:27478613
|
A | G | 123 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(120): Show | 123 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.-44+11373T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27478613 | ||||||
chr1:27478651
|
C | T | 1 | a0001c0001t0012g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-44+11335G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27478651 | ||||||
chr1:27478828
|
C | T | 5 | a0001c0001t0001g0196a0001c0001t0001g0198a0001c0001t0001g0201others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+11158G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27478828 | ||||||
chr1:27478944
|
C | T | 2 | a0001c0001t0001g0214a0001c0001t0002g0189 | 2 | NA19009.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-44+11042G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27478944 | ||||||
chr1:27478945
|
G | T | 5 | a0001c0001t0019g0025a0001c0001t0020g0256a0001c0001t0020g0257others(2): Show | 5 | NA18962.hp1 NA18966.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+11041C>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27478945 | ||||||
chr1:27478951
|
T | C | 2 | a0001c0001t0004g0104a0001c0001t0004g0117 | 2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-44+11035A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27478951 | ||||||
chr1:27478975
|
A | G | 1 | a0001c0001t0008g0252 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-44+11011T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27478975 | ||||||
chr1:27478983
|
T | C | 5 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0011g0095others(2): Show | 5 | HG01109.hp1 HG02895.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+11003A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27478983 | ||||||
chr1:27479024
|
C | T | 1 | a0001c0001t0029g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-44+10962G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27479024 | ||||||
chr1:27479040
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-44+10946C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27479040 | ||||||
chr1:27479285
|
CA | C | 98 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(95): Show | 98 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.-44+10700delT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27479285 | ||||||
chr1:27479306
|
C | T | 1 | a0001c0001t0050g0148 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-44+10680G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27479306 | ||||||
chr1:27479329
|
T | C | 1 | a0001c0001t0055g0260 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-44+10657A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27479329 | ||||||
chr1:27479330
|
A | C | 2 | a0001c0001t0027g0050a0001c0001t0028g0003 | 2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-44+10656T>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27479330 | ||||||
chr1:27479518
|
A | G | 1 | a0001c0001t0027g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-44+10468T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27479518 | ||||||
chr1:27479603
|
G | A | 1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-44+10383C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27479603 | ||||||
chr1:27479606
|
T | G | 1 | a0001c0001t0050g0148 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-44+10380A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27479606 | ||||||
chr1:27479704
|
A | C | 1 | a0002c0003t0022g0091 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-44+10282T>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27479704 | ||||||
chr1:27479739
|
C | T | 1 | a0001c0001t0055g0260 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-44+10247G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27479739 | ||||||
chr1:27479981
|
C | T | 2 | a0001c0001t0019g0025a0001c0001t0040g0026 | 2 | NA19007.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-44+10005G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27479981 | ||||||
chr1:27480051
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-44+9935A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27480051 | ||||||
chr1:27480224
|
T | C | 5 | a0001c0001t0019g0025a0001c0001t0020g0256a0001c0001t0020g0257others(2): Show | 5 | NA18962.hp1 NA18966.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+9762A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27480224 | ||||||
chr1:27480283
|
G | T | 1 | a0001c0001t0003g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-44+9703C>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27480283 | ||||||
chr1:27480385
|
C | A | 3 | a0001c0001t0018g0208a0001c0001t0018g0216a0001c0001t0026g0002 | 3 | HG02559.hp2 HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-44+9601G>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27480385 | ||||||
chr1:27480490
|
C | T | 5 | a0001c0001t0001g0196a0001c0001t0001g0198a0001c0001t0001g0201others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+9496G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27480490 | ||||||
chr1:27480514
|
TA | T | 8 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0012g0225others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+9471delT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27480514 | ||||||
chr1:27480619
|
G | A | 1 | a0001c0001t0012g0218 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-44+9367C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27480619 | ||||||
chr1:27480742
|
C | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0193a0001c0001t0001g0194others(1): Show | 4 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+9244G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27480742 | ||||||
chr1:27480757
|
G | A | 1 | a0002c0003t0013g0089 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-44+9229C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27480757 | ||||||
chr1:27480824
|
C | T | 2 | a0001c0001t0004g0137a0001c0001t0004g0138 | 2 | HG01074.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.-44+9162G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27480824 | ||||||
chr1:27480825
|
G | A | 1 | a0001c0001t0050g0148 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-44+9161C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27480825 | ||||||
chr1:27480866
|
G | A | 8 | a0001c0001t0004g0101a0001c0001t0004g0102a0001c0001t0004g0103others(5): Show | 8 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+9120C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27480866 | ||||||
chr1:27481253
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-44+8733C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27481253 | ||||||
chr1:27481295
|
C | G | 27 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0073others(24): Show | 27 | HG00140.hp1 HG00639.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-44+8691G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27481295 | ||||||
chr1:27481482
|
T | A | 1 | a0001c0001t0009g0149 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-44+8504A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27481482 | ||||||
chr1:27481582
|
G | A | 55 | a0001c0002t0001g0004a0001c0002t0001g0020a0001c0002t0003g0006others(52): Show | 55 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.-44+8404C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27481582 | ||||||
chr1:27481930
|
C | T | 1 | a0001c0002t0006g0022 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-44+8056G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27481930 | ||||||
chr1:27482250
|
C | T | 1 | a0001c0001t0004g0170 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-44+7736G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27482250 | ||||||
chr1:27482467
|
AGCAATGC others(10): Show |
A | 1 | a0001c0001t0026g0002 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-44+7502_-44+7518d others(19): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27482467 | ||||||
chr1:27482517
|
C | A | 1 | a0001c0001t0012g0222 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-44+7469G>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27482517 | ||||||
chr1:27482605
|
T | A | 9 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0012g0225others(6): Show | 9 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44+7381A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27482605 | ||||||
chr1:27482831
|
T | C | 12 | a0001c0001t0007g0125a0001c0001t0007g0127a0001c0001t0007g0128others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.-44+7155A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27482831 | ||||||
chr1:27482872
|
A | T | 5 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0011g0095others(2): Show | 5 | HG01109.hp1 HG02895.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+7114T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27482872 | ||||||
chr1:27483058
|
G | T | 102 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(99): Show | 102 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-44+6928C>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27483058 | ||||||
chr1:27483073
|
G | A | 27 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0073others(24): Show | 27 | HG00140.hp1 HG00639.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-44+6913C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27483073 | ||||||
chr1:27483076
|
T | C | 1 | a0001c0001t0027g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-44+6910A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27483076 | ||||||
chr1:27483210
|
C | G | 21 | a0001c0001t0001g0098a0001c0001t0001g0134a0001c0001t0001g0151others(18): Show | 21 | HG00323.hp2 HG00438.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-44+6776G>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27483210 | ||||||
chr1:27483285
|
C | T | 1 | a0001c0001t0019g0025 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-44+6701G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27483285 | ||||||
chr1:27483287
|
C | T | 1 | a0001c0002t0005g0054 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-44+6699G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27483287 | ||||||
chr1:27483307
|
T | C | 1 | a0001c0001t0003g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-44+6679A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27483307 | ||||||
chr1:27483525
|
G | A | 1 | a0001c0001t0022g0087 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-44+6461C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27483525 | ||||||
chr1:27483806
|
G | A | 93 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(90): Show | 93 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-44+6180C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27483806 | ||||||
chr1:27484043
|
T | C | 1 | a0001c0001t0029g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-44+5943A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27484043 | ||||||
chr1:27484426
|
C | T | 1 | a0001c0001t0003g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-44+5560G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27484426 | ||||||
chr1:27484661
|
A | C | 2 | a0001c0002t0006g0013a0001c0002t0048g0038 | 2 | HG03491.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-44+5325T>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27484661 | ||||||
chr1:27484799
|
G | A | 1 | a0001c0002t0005g0049 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-44+5187C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27484799 | ||||||
chr1:27484806
|
T | C | 1 | a0001c0001t0002g0237 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-44+5180A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27484806 | ||||||
chr1:27484811
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0003g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-44+5174_-44+5175i others(14): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27484811 | ||||||
chr1:27484811
|
C | CAAAAAAA others(6): Show |
2 | a0001c0001t0003g0090a0001c0001t0027g0050 | 2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-44+5174_-44+5175i others(15): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27484811 | ||||||
chr1:27484811
|
C | CAAAAAAA others(7): Show |
56 | a0001c0001t0003g0011a0001c0001t0007g0059a0001c0001t0019g0025others(53): Show | 56 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.-44+5174_-44+5175i others(16): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27484811 | ||||||
chr1:27484811
|
C | CAAAAAAA others(8): Show |
25 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0073others(22): Show | 25 | HG00140.hp1 HG00597.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.-44+5174_-44+5175i others(17): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27484811 | ||||||
chr1:27484811
|
C | CAAAAAAA others(9): Show |
5 | a0001c0001t0003g0074a0001c0001t0003g0078a0001c0001t0003g0085others(2): Show | 5 | HG02647.hp2 HG02738.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+5174_-44+5175i others(18): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27484811 | ||||||
chr1:27484811
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0013g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-44+5174_-44+5175i others(22): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27484811 | ||||||
chr1:27484814
|
A | AAAAAAAA others(8): Show |
4 | a0001c0001t0022g0087a0001c0001t0023g0063a0001c0001t0023g0064others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+5171_-44+5172i others(17): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27484814 | ||||||
chr1:27484851
|
T | C | 2 | a0001c0001t0027g0050a0001c0001t0028g0003 | 2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-44+5135A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27484851 | ||||||
chr1:27484872
|
G | A | 1 | a0001c0001t0045g0153 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-44+5114C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27484872 | ||||||
chr1:27484936
|
G | A | 1 | a0001c0001t0012g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-44+5050C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27484936 | ||||||
chr1:27484967
|
T | C | 3 | a0001c0001t0018g0208a0001c0001t0018g0216a0001c0001t0026g0002 | 3 | HG02559.hp2 HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-44+5019A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27484967 | ||||||
chr1:27485163
|
T | C | 1 | a0001c0002t0006g0022 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-44+4823A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27485163 | ||||||
chr1:27485371
|
G | A | 2 | a0001c0002t0003g0017a0001c0002t0019g0012 | 2 | HG01069.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-44+4615C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27485371 | ||||||
chr1:27485642
|
T | C | 1 | a0001c0001t0013g0212 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-44+4344A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27485642 | ||||||
chr1:27485932
|
G | A | 1 | a0002c0003t0035g0092 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-44+4054C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27485932 | ||||||
chr1:27485952
|
T | C | 1 | a0001c0001t0003g0244 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-44+4034A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27485952 | ||||||
chr1:27485961
|
C | T | 2 | a0001c0001t0027g0050a0001c0001t0028g0003 | 2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-44+4025G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27485961 | ||||||
chr1:27486002
|
A | G | 102 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(99): Show | 102 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-44+3984T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27486002 | ||||||
chr1:27486150
|
G | GTATT | 124 | a0001c0001t0001g0196a0001c0001t0003g0011a0001c0001t0003g0069others(121): Show | 124 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.-44+3832_-44+3835d others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27486150 | ||||||
chr1:27486177
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0169 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-44+3809G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27486177 | ||||||
chr1:27486299
|
T | A | 1 | a0001c0001t0026g0002 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-44+3687A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27486299 | ||||||
chr1:27486649
|
C | T | 3 | a0001c0001t0018g0208a0001c0001t0018g0216a0001c0001t0026g0002 | 3 | HG02559.hp2 HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-44+3337G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27486649 | ||||||
chr1:27486710
|
G | A | 1 | a0001c0001t0003g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-44+3276C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27486710 | ||||||
chr1:27486924
|
T | C | 91 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(88): Show | 91 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.-44+3062A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27486924 | ||||||
chr1:27486947
|
C | T | 1 | a0001c0001t0027g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-44+3039G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27486947 | ||||||
chr1:27486984
|
A | C | 1 | a0001c0001t0043g0168 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-44+3002T>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27486984 | ||||||
chr1:27487029
|
A | T | 91 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(88): Show | 91 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.-44+2957T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487029 | ||||||
chr1:27487048
|
TATTA | T | 93 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(90): Show | 93 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-44+2934_-44+2937d others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487048 | ||||||
chr1:27487057
|
T | A | 1 | a0001c0001t0026g0002 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-44+2929A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487057 | ||||||
chr1:27487186
|
C | T | 2 | a0001c0002t0003g0017a0001c0002t0019g0012 | 2 | HG01069.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-44+2800G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487186 | ||||||
chr1:27487195
|
G | A | 1 | a0001c0001t0009g0149 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-44+2791C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487195 | ||||||
chr1:27487378
|
C | T | 2 | a0001c0001t0027g0050a0001c0001t0028g0003 | 2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-44+2608G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487378 | ||||||
chr1:27487406
|
T | C | 5 | a0001c0001t0019g0025a0001c0001t0020g0256a0001c0001t0020g0257others(2): Show | 5 | NA18962.hp1 NA18966.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+2580A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487406 | ||||||
chr1:27487464
|
T | TA | 24 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0073others(21): Show | 24 | HG00140.hp1 HG00639.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.-44+2521dupT | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487464 | ||||||
chr1:27487492
|
TATA | T | 14 | a0001c0001t0001g0131a0001c0001t0004g0101a0001c0001t0004g0102others(11): Show | 14 | HG00140.hp1 HG01074.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.-44+2491_-44+2493d others(5): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487492 | ||||||
chr1:27487499
|
T | C | 11 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0073others(8): Show | 11 | HG00639.hp2 HG02258.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-44+2487A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487499 | ||||||
chr1:27487511
|
T | TTATATTA others(25): Show |
4 | a0001c0001t0004g0150a0001c0001t0004g0182a0001c0001t0012g0225others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+2443_-44+2474d others(34): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487511 | ||||||
chr1:27487511
|
T | TTATATTA others(89): Show |
5 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0011g0095others(2): Show | 5 | HG01109.hp1 HG02895.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+2474_-44+2475i others(98): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487511 | ||||||
chr1:27487511
|
TTATATTA others(25): Show |
T | 6 | a0001c0001t0001g0155a0001c0001t0001g0167a0001c0001t0018g0208others(3): Show | 6 | HG00735.hp1 HG00741.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44+2443_-44+2474d others(34): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487511 | ||||||
chr1:27487513
|
ATATTATA others(28): Show |
A | 1 | a0001c0001t0014g0221 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-44+2438_-44+2472d others(37): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487513 | ||||||
chr1:27487548
|
TTATATAT others(27): Show |
T | 1 | a0001c0001t0001g0151 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-44+2404_-44+2437d others(36): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487548 | ||||||
chr1:27487563
|
A | G | 1 | a0001c0001t0027g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-44+2423T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487563 | ||||||
chr1:27487564
|
CAATATAT others(25): Show |
C | 11 | a0001c0001t0001g0131a0001c0001t0001g0152a0001c0001t0002g0109others(8): Show | 11 | HG01123.hp1 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-44+2390_-44+2421d others(34): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487564 | ||||||
chr1:27487566
|
ATATATAA others(18): Show |
A | 1 | a0001c0001t0001g0215 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-44+2395_-44+2419d others(27): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487566 | ||||||
chr1:27487591
|
T | G | 1 | a0001c0001t0027g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-44+2395A>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487591 | ||||||
chr1:27487596
|
T | C | 94 | a0001c0001t0001g0151a0001c0001t0001g0200a0001c0001t0003g0011others(91): Show | 94 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.-44+2390A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487596 | ||||||
chr1:27487596
|
T | TAATATAT others(25): Show |
1 | a0001c0001t0001g0210 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-44+2358_-44+2389d others(34): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487596 | ||||||
chr1:27487628
|
C | T | 64 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(61): Show | 64 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.-44+2358G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487628 | ||||||
chr1:27487630
|
A | ATATATAA others(14): Show |
1 | a0001c0001t0001g0154 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-44+2335_-44+2355d others(23): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487630 | ||||||
chr1:27487632
|
ATATAATA others(5): Show |
A | 16 | a0001c0001t0003g0081a0001c0001t0003g0083a0001c0001t0003g0084others(13): Show | 16 | HG02056.hp1 HG02074.hp1 HG02602.hp1 others(13): Show |
intron_variant | MODIFIER | c.-44+2342_-44+2353d others(14): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487632 | ||||||
chr1:27487636
|
A | AATATATA others(122): Show |
1 | a0001c0001t0013g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-44+2349_-44+2350i others(131): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487636 | ||||||
chr1:27487636
|
A | ATAATATA others(56): Show |
1 | a0001c0001t0028g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-44+2349_-44+2350i others(65): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487636 | ||||||
chr1:27487636
|
A | ATAATATA others(70): Show |
1 | a0001c0001t0027g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-44+2349_-44+2350i others(79): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487636 | ||||||
chr1:27487644
|
T | TTA | 4 | a0001c0001t0001g0250a0001c0001t0017g0233a0001c0001t0017g0259others(1): Show | 4 | NA18980.hp1 NA18991.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+2340_-44+2341d others(4): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487644 | ||||||
chr1:27487644
|
T | TTATATAT others(13): Show |
65 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(62): Show | 65 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.-44+2341_-44+2342i others(22): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487644 | ||||||
chr1:27487644
|
T | TTATATAT others(43): Show |
1 | a0001c0001t0034g0067 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-44+2341_-44+2342i others(52): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487644 | ||||||
chr1:27487644
|
T | TTATATAT others(45): Show |
8 | a0001c0001t0010g0061a0001c0001t0010g0066a0001c0001t0023g0063others(5): Show | 8 | HG01074.hp1 HG01192.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+2341_-44+2342i others(54): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487644 | ||||||
chr1:27487651
|
T | TATTTTAT others(4): Show |
1 | a0001c0001t0022g0087 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-44+2334_-44+2335i others(13): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487651 | ||||||
chr1:27487653
|
A | G | 1 | a0001c0001t0013g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-44+2333T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487653 | ||||||
chr1:27487658
|
A | T | 3 | a0001c0001t0004g0113a0001c0001t0004g0114a0001c0001t0045g0153 | 3 | HG00741.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-44+2328T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487658 | ||||||
chr1:27487665
|
T | A | 1 | a0001c0001t0001g0185 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-44+2321A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487665 | ||||||
chr1:27487666
|
T | A | 2 | a0001c0001t0004g0162a0001c0002t0005g0051 | 2 | NA19055.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-44+2320A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487666 | ||||||
chr1:27487667
|
A | T | 1 | a0001c0002t0005g0051 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+2319T>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487667 | ||||||
chr1:27487675
|
T | A | 58 | a0001c0001t0002g0227a0001c0001t0002g0241a0001c0001t0029g0088others(55): Show | 58 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.-44+2311A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487675 | ||||||
chr1:27487681
|
T | C | 6 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0011g0095others(3): Show | 6 | HG01109.hp1 HG02572.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44+2305A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487681 | ||||||
chr1:27487689
|
A | ATATTATA others(11): Show |
1 | a0001c0001t0022g0087 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-44+2296_-44+2297i others(20): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487689 | ||||||
chr1:27487704
|
C | T | 2 | a0001c0001t0002g0228a0001c0001t0002g0229 | 2 | NA18993.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-44+2282G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487704 | ||||||
chr1:27487718
|
TATC | T | 8 | a0001c0001t0012g0218a0001c0001t0012g0222a0001c0001t0012g0225others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+2265_-44+2267d others(5): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487718 | ||||||
chr1:27487723
|
T | A | 1 | a0001c0001t0026g0002 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-44+2263A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487723 | ||||||
chr1:27487740
|
TATC | T | 12 | a0001c0002t0005g0023a0001c0002t0005g0036a0001c0002t0005g0037others(9): Show | 12 | HG00597.hp1 HG00621.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+2243_-44+2245d others(5): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487740 | ||||||
chr1:27487743
|
C | A | 51 | a0001c0001t0003g0011a0001c0001t0007g0059a0001c0001t0019g0025others(48): Show | 51 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-44+2243G>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487743 | ||||||
chr1:27487747
|
T | A | 12 | a0001c0002t0005g0023a0001c0002t0005g0036a0001c0002t0005g0037others(9): Show | 12 | HG00597.hp1 HG00621.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+2239A>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27487747 | ||||||
chr1:27488523
|
C | T | 1 | a0001c0001t0018g0216 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-44+1463G>A | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27488523 | ||||||
chr1:27489043
|
G | A | 1 | a0001c0001t0018g0208 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-44+943C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489043 | ||||||
chr1:27489054
|
G | A | 1 | a0001c0001t0027g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-44+932C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489054 | ||||||
chr1:27489107
|
T | C | 1 | a0001c0001t0003g0090 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-44+879A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489107 | ||||||
chr1:27489175
|
G | C | 9 | a0001c0001t0002g0227a0001c0001t0002g0234a0001c0001t0002g0235others(6): Show | 9 | HG00408.hp1 HG00738.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.-44+811C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489175 | ||||||
chr1:27489246
|
ACG | A | 9 | a0001c0002t0001g0004a0001c0002t0001g0020a0001c0002t0003g0019others(6): Show | 9 | HG00597.hp1 HG02056.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44+738_-44+739del others(2): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489246 | ||||||
chr1:27489250
|
GCGCA | G | 33 | a0001c0001t0018g0208a0001c0001t0018g0216a0001c0001t0026g0002others(30): Show | 33 | HG00609.hp1 HG00621.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.-44+732_-44+735del others(4): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489250 | ||||||
chr1:27489250
|
GCGCACA | G | 11 | a0001c0001t0003g0081a0001c0002t0003g0045a0001c0002t0005g0016others(8): Show | 11 | HG00438.hp2 HG01106.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-44+730_-44+735del others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489250 | ||||||
chr1:27489250
|
GCGCACAC others(1): Show |
G | 28 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(25): Show | 28 | HG00408.hp2 HG00639.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-44+728_-44+735del others(8): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489250 | ||||||
chr1:27489250
|
GCGCACAC others(3): Show |
G | 19 | a0001c0001t0007g0125a0001c0001t0010g0061a0001c0001t0010g0066others(16): Show | 19 | HG00140.hp1 HG01074.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.-44+726_-44+735del others(10): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489250 | ||||||
chr1:27489250
|
GCGCACAC others(5): Show |
G | 2 | a0001c0001t0028g0003a0001c0001t0055g0260 | 2 | HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-44+724_-44+735del others(12): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489250 | ||||||
chr1:27489252
|
G | A | 5 | a0001c0001t0013g0212a0001c0002t0005g0051a0001c0002t0005g0052others(2): Show | 5 | HG03139.hp1 NA18952.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+734C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489252 | ||||||
chr1:27489252
|
G | GCA | 31 | a0001c0001t0001g0098a0001c0001t0001g0120a0001c0001t0001g0154others(28): Show | 31 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.-44+732_-44+733dup others(2): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489252 | ||||||
chr1:27489252
|
G | GCACA | 6 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0002g0239others(3): Show | 6 | HG00438.hp1 HG04115.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44+730_-44+733dup others(4): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489252 | ||||||
chr1:27489252
|
GCA | G | 16 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0132others(13): Show | 16 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-44+732_-44+733del others(2): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489252 | ||||||
chr1:27489252
|
GCACA | G | 7 | a0001c0001t0001g0131a0001c0001t0007g0093a0001c0001t0007g0094others(4): Show | 7 | HG01109.hp1 HG01123.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44+730_-44+733del others(4): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489252 | ||||||
chr1:27489252
|
GCACACA | G | 8 | a0001c0001t0001g0112a0001c0001t0001g0126a0001c0001t0001g0206others(5): Show | 8 | HG01884.hp2 HG02071.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+728_-44+733del others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489252 | ||||||
chr1:27489252
|
GCACACAC others(1): Show |
G | 7 | a0001c0001t0001g0111a0001c0001t0001g0123a0001c0001t0001g0213others(4): Show | 7 | HG01167.hp1 HG02451.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44+726_-44+733del others(8): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489252 | ||||||
chr1:27489252
|
GCACACAC others(3): Show |
G | 3 | a0001c0001t0008g0110a0001c0001t0012g0218a0002c0003t0022g0091 | 3 | HG02300.hp1 HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-44+724_-44+733del others(10): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489252 | ||||||
chr1:27489348
|
T | TAC | 35 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0115others(32): Show | 35 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.-44+636_-44+637dup others(2): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489348 | ||||||
chr1:27489348
|
T | TACAC | 89 | a0001c0001t0001g0123a0001c0001t0001g0126a0001c0001t0001g0131others(86): Show | 89 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.-44+634_-44+637dup others(4): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489348 | ||||||
chr1:27489348
|
T | TACACAC | 37 | a0001c0001t0001g0167a0001c0001t0001g0169a0001c0001t0001g0175others(34): Show | 37 | HG00609.hp2 HG00673.hp1 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.-44+632_-44+637dup others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489348 | ||||||
chr1:27489348
|
T | TACACACA others(1): Show |
7 | a0001c0001t0001g0187a0001c0001t0001g0190a0001c0001t0002g0188others(4): Show | 7 | HG01496.hp1 HG02155.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44+630_-44+637dup others(8): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489348 | ||||||
chr1:27489348
|
T | TACACACA others(3): Show |
14 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(11): Show | 14 | HG00639.hp1 HG01069.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-44+628_-44+637dup others(10): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489348 | ||||||
chr1:27489348
|
T | TACACACA others(5): Show |
2 | a0001c0001t0001g0203a0001c0001t0003g0078 | 2 | HG03579.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-44+626_-44+637dup others(12): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489348 | ||||||
chr1:27489348
|
T | TACACACA others(7): Show |
1 | a0001c0001t0001g0204 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-44+624_-44+637dup others(14): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489348 | ||||||
chr1:27489348
|
TAC | T | 17 | a0001c0001t0001g0098a0001c0001t0002g0227a0001c0001t0003g0090others(14): Show | 17 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(14): Show |
intron_variant | MODIFIER | c.-44+636_-44+637del others(2): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489348 | ||||||
chr1:27489348
|
TACAC | T | 6 | a0001c0001t0001g0205a0001c0001t0003g0084a0001c0001t0003g0085others(3): Show | 6 | HG02074.hp2 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44+634_-44+637del others(4): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489348 | ||||||
chr1:27489348
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TACACACA others(3): Show |
T | 1 | a0001c0001t0003g0083 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-44+628_-44+637del others(10): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489348 | ||||||
chr1:27489348
|
TACACACA others(5): Show |
T | 5 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0011g0095others(2): Show | 5 | HG01109.hp1 HG02895.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+626_-44+637del others(12): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489348 | ||||||
chr1:27489348
|
TACACACA others(15): Show |
T | 1 | a0001c0001t0027g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-44+616_-44+637del others(22): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489348 | ||||||
chr1:27489356
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CACACACA others(90): Show |
C | 2 | a0001c0002t0005g0051a0001c0002t0005g0052 | 2 | NA19003.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.-44+533_-44+629del others(97): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489356 | ||||||
chr1:27489362
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C | A | 3 | a0002c0003t0013g0089a0002c0003t0022g0091a0002c0003t0035g0092 | 3 | HG02615.hp2 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-44+624G>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489362 | ||||||
chr1:27489364
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CACACACA others(82): Show |
C | 1 | a0001c0001t0044g0258 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-44+533_-44+621del others(89): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489364 | ||||||
chr1:27489449
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T | TAC | 49 | a0001c0001t0003g0011a0001c0001t0019g0025a0001c0001t0020g0256others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.-44+535_-44+536dup others(2): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489449 | ||||||
chr1:27489449
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T | TACAC | 8 | a0001c0001t0007g0059a0001c0002t0005g0053a0001c0002t0005g0054others(5): Show | 8 | HG00621.hp1 HG02886.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.-44+536_-44+537ins others(4): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489449 | ||||||
chr1:27489449
|
T | TACACAC | 18 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0073others(15): Show | 18 | HG00140.hp1 HG00597.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.-44+536_-44+537ins others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489449 | ||||||
chr1:27489449
|
T | TACACACA others(1): Show |
3 | a0001c0001t0003g0081a0001c0001t0032g0080a0001c0001t0033g0079 | 3 | HG01074.hp1 HG02738.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-44+536_-44+537ins others(8): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489449 | ||||||
chr1:27489449
|
T | TACACACA others(3): Show |
7 | a0001c0001t0003g0083a0001c0001t0003g0084a0001c0001t0003g0085others(4): Show | 7 | HG02572.hp1 HG02615.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.-44+536_-44+537ins others(10): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489449 | ||||||
chr1:27489449
|
T | TACACACA others(5): Show |
3 | a0001c0001t0003g0090a0001c0001t0055g0260a0002c0003t0022g0091 | 3 | HG02647.hp1 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-44+536_-44+537ins others(12): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489449 | ||||||
chr1:27489449
|
T | TACACACA others(13): Show |
1 | a0002c0003t0035g0092 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-44+536_-44+537ins others(20): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489449 | ||||||
chr1:27489452
|
G | A | 89 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(86): Show | 89 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.-44+534C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489452 | ||||||
chr1:27489453
|
T | C | 89 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(86): Show | 89 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.-44+533A>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489453 | ||||||
chr1:27489453
|
T | TAC | 13 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0209others(10): Show | 13 | HG01255.hp2 HG02074.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-44+531_-44+532dup others(2): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489453 | ||||||
chr1:27489453
|
T | TACAC | 3 | a0001c0001t0004g0217a0001c0001t0016g0254a0001c0001t0028g0003 | 3 | HG03579.hp1 NA18957.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-44+529_-44+532dup others(4): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489453 | ||||||
chr1:27489453
|
T | TACACAC | 4 | a0001c0001t0012g0218a0001c0001t0014g0219a0001c0001t0014g0220others(1): Show | 4 | HG02886.hp1 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+527_-44+532dup others(6): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489453 | ||||||
chr1:27489453
|
T | TACACACA others(1): Show |
3 | a0001c0001t0012g0222a0001c0001t0012g0225a0001c0001t0014g0221 | 3 | HG02451.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-44+525_-44+532dup others(8): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489453 | ||||||
chr1:27489453
|
T | TACACACA others(5): Show |
3 | a0001c0001t0013g0082a0001c0004t0012g0223a0001c0004t0030g0224 | 3 | HG01884.hp2 HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-44+521_-44+532dup others(12): Show |
WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489453 | ||||||
chr1:27489587
|
A | G | 91 | a0001c0001t0003g0011a0001c0001t0003g0069a0001c0001t0003g0070others(88): Show | 91 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.-44+399T>C | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489587 | ||||||
chr1:27489610
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A | C | 1 | a0001c0001t0026g0002 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-44+376T>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489610 | ||||||
chr1:27489815
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G | A | 1 | a0001c0001t0012g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-44+171C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489815 | ||||||
chr1:27489921
|
G | C | 34 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(31): Show | 34 | HG00408.hp1 HG00597.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.-44+65C>G | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489921 | ||||||
chr1:27489937
|
G | A | 1 | a0001c0001t0017g0259 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-44+49C>T | WASF2 | ENSG00000158195.11 | transcript | ENST00000618852.5 | protein_coding | 1/8 | chr1 | 27489937 |