geneid | 5470 |
---|---|
ensemblid | ENSG00000156194.19 |
hgncid | 9244 |
symbol | PPEF2 |
name | protein phosphatase with EF-hand domain 2 |
refseq_nuc | NM_006239.3 |
refseq_prot | NP_006230.2 |
ensembl_nuc | ENST00000286719.12 |
ensembl_prot | ENSP00000286719.6 |
mane_status | MANE Select |
chr | chr4 |
start | 75859867 |
end | 75902452 |
strand | - |
ver | v1.2 |
region | chr4:75859867-75902452 |
region5000 | chr4:75854867-75907452 |
regionname0 | PPEF2_chr4_75859867_75902452 |
regionname5000 | PPEF2_chr4_75854867_75907452 |
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 | 0/1 | 753 | 212 | 48 | 51 | 72 | 16 | 24 | 45 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0002 | 0/0 | 753 | 15 | 13 | 2 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0003 | 0/0 | 753 | 12 | 3 | 4 | 0 | 0 | 5 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0004 | 0/0 | 753 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0005 | 0/0 | 753 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0006 | 0/0 | 447 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0007 | 0/0 | 753 | 3 | 1 | 1 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0008 | 0/0 | 753 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0009 | 0/0 | 753 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0010 | 0/0 | 753 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0011 | 0/0 | 653 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0012 | 0/0 | 747 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0013 | 1/0 | 753 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0014 | 0/0 | 753 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0015 | 0/0 | 753 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0016 | 0/0 | 753 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
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 | 0/1 | 2262 | 196 | 36 | 48 | 71 | 16 | 24 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
c0002 | 0/0 | 2262 | 13 | 10 | 3 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
c0003 | 0/0 | 2262 | 12 | 3 | 4 | 0 | 0 | 5 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
c0004 | 0/0 | 2262 | 10 | 8 | 2 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
c0005 | 0/0 | 2262 | 7 | 7 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
c0006 | 0/0 | 2262 | 4 | 4 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
c0007 | 0/0 | 2263 | 4 | 4 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
c0008 | 0/0 | 2262 | 3 | 3 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
c0009 | 0/0 | 2262 | 3 | 1 | 1 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
c0010 | 0/0 | 2262 | 2 | 1 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
c0011 | 0/0 | 2262 | 2 | 2 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
c0012 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
c0013 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
c0014 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
c0015 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
c0016 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
c0017 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
c0018 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
c0019 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
c0020 | 0/0 | 2262 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
c0021 | 0/0 | 2278 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
c0022 | 0/0 | 2262 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
c0023 | 0/0 | 2262 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
c0024 | 1/0 | 2262 | 1 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
c0025 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
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 | 1/1 | 1082 | 184 | 49 | 39 | 69 | 7 | 18 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
t0002 | 0/0 | 1082 | 54 | 12 | 18 | 4 | 9 | 11 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
t0003 | 0/0 | 1082 | 23 | 22 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
t0004 | 0/0 | 1082 | 3 | 1 | 1 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
t0005 | 0/0 | 1082 | 2 | 2 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
t0006 | 0/0 | 1082 | 2 | 1 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
t0007 | 0/0 | 1082 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
t0008 | 0/0 | 1082 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
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 | 2 | 0 | 2 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0053 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0182 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
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 | 0/1 | 2262 | 196 | 36 | 48 | 71 | 16 | 24 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0001c0002 | 0/0 | 2262 | 13 | 10 | 3 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0001c0015 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0001c0016 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0001c0020 | 0/0 | 2262 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0002c0004 | 0/0 | 2262 | 10 | 8 | 2 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0002c0008 | 0/0 | 2262 | 3 | 3 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0002c0011 | 0/0 | 2262 | 2 | 2 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0003c0003 | 0/0 | 2262 | 12 | 3 | 4 | 0 | 0 | 5 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0004c0005 | 0/0 | 2262 | 7 | 7 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0005c0006 | 0/0 | 2262 | 4 | 4 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0005c0017 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0005c0018 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0006c0007 | 0/0 | 2263 | 4 | 4 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0007c0009 | 0/0 | 2262 | 3 | 1 | 1 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0008c0010 | 0/0 | 2262 | 2 | 1 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0008c0019 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0009c0012 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0010c0025 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0011c0023 | 0/0 | 2262 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0012c0021 | 0/0 | 2278 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0013c0024 | 1/0 | 2262 | 1 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0014c0022 | 0/0 | 2262 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0015c0014 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0016c0013 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3343 | 153 | 27 | 35 | 66 | 7 | 17 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0001c0001t0002 | 0/0 | 3343 | 37 | 5 | 12 | 4 | 9 | 7 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0001c0001t0003 | 0/0 | 3343 | 3 | 3 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0001c0001t0004 | 0/0 | 3343 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0001c0001t0005 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0001c0001t0007 | 0/0 | 3343 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0001c0002t0001 | 0/0 | 3343 | 6 | 4 | 2 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0001c0002t0002 | 0/0 | 3343 | 7 | 6 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0001c0015t0001 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0001c0016t0008 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0001c0020t0001 | 0/0 | 3343 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0002c0004t0001 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0002c0004t0003 | 0/0 | 3343 | 7 | 6 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0002c0004t0006 | 0/0 | 3343 | 2 | 1 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0002c0008t0001 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0002c0008t0003 | 0/0 | 3343 | 2 | 2 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0002c0011t0001 | 0/0 | 3343 | 2 | 2 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0003c0003t0001 | 0/0 | 3343 | 2 | 2 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0003c0003t0002 | 0/0 | 3343 | 8 | 0 | 4 | 0 | 0 | 4 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0003c0003t0004 | 0/0 | 3343 | 2 | 1 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0004c0005t0003 | 0/0 | 3343 | 7 | 7 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0005c0006t0001 | 0/0 | 3343 | 4 | 4 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0005c0017t0001 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0005c0018t0005 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0006c0007t0003 | 0/0 | 3344 | 4 | 4 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0007c0009t0001 | 0/0 | 3343 | 2 | 0 | 1 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0007c0009t0002 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0008c0010t0001 | 0/0 | 3343 | 2 | 1 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0008c0019t0001 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0009c0012t0001 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0010c0025t0001 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0011c0023t0002 | 0/0 | 3343 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0012c0021t0001 | 0/0 | 3359 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0013c0024t0001 | 1/0 | 3343 | 1 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0014c0022t0001 | 0/0 | 3343 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0015c0014t0001 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
a0016c0013t0001 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | copy fasta | chr4 | 75854867 | 75907452 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0182 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0004g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0001t0007g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0002t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0002t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0002t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0002t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0002t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0002t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0002t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0015t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0016t0008g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0001c0020t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0002c0004t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0002c0004t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0002c0004t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0002c0004t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0002c0004t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0002c0004t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0002c0004t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0002c0004t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0002c0004t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0002c0004t0006g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0002c0008t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0002c0008t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0002c0008t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0002c0011t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0002c0011t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0003c0003t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0003c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0003c0003t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0003c0003t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0003c0003t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0003c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0003c0003t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0003c0003t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0003c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0003c0003t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0003c0003t0004g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0004c0005t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0004c0005t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0004c0005t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0004c0005t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0004c0005t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0004c0005t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0004c0005t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0005c0006t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0005c0006t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0005c0006t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0005c0006t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0005c0017t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0005c0018t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0006c0007t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0006c0007t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0006c0007t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0006c0007t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0007c0009t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0007c0009t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0007c0009t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0008c0010t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0008c0010t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0008c0019t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0009c0012t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0010c0025t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0011c0023t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0012c0021t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0013c0024t0001g0053 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0014c0022t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0015c0014t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
a0016c0013t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | GBR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0006 | EUR | GBR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0042 | EUR | GBR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | GBR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | FIN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0008 | EUR | FIN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0184 | EUR | FIN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | FIN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01081 | hp2 | a0003 | c0003 | t0002 | g0252 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01167 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01167 | hp2 | a0003 | c0003 | t0002 | g0257 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01175 | hp2 | a0002 | c0004 | t0006 | g0264 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01192 | hp2 | a0007 | c0009 | t0001 | g0216 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01243 | hp1 | a0002 | c0004 | t0003 | g0262 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01243 | hp2 | a0008 | c0010 | t0001 | g0208 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0230 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01256 | hp1 | a0003 | c0003 | t0002 | g0004 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01258 | hp1 | a0003 | c0003 | t0002 | g0004 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0211 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01496 | hp2 | a0011 | c0023 | t0002 | g0232 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0014 | EUR | IBS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0026 | EUR | IBS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0025 | EUR | IBS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0033 | EUR | IBS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01891 | hp2 | a0005 | c0006 | t0001 | g0220 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0212 | AMR | PEL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0228 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02055 | hp2 | a0003 | c0003 | t0004 | g0250 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02083 | hp1 | a0001 | c0001 | t0007 | g0157 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02132 | hp1 | a0014 | c0022 | t0001 | g0185 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02145 | hp2 | a0006 | c0007 | t0003 | g0204 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CDX | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CDX | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CDX | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CDX | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02258 | hp1 | a0002 | c0004 | t0003 | g0261 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02258 | hp2 | a0002 | c0011 | t0001 | g0056 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0227 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02451 | hp2 | a0009 | c0012 | t0001 | g0086 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02572 | hp1 | a0008 | c0019 | t0001 | g0032 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02572 | hp2 | a0004 | c0005 | t0003 | g0248 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02615 | hp1 | a0005 | c0006 | t0001 | g0236 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02615 | hp2 | a0002 | c0008 | t0003 | g0241 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02630 | hp2 | a0004 | c0005 | t0003 | g0246 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02647 | hp2 | a0002 | c0004 | t0003 | g0041 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02723 | hp1 | a0002 | c0008 | t0003 | g0242 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02723 | hp2 | a0001 | c0002 | t0002 | g0231 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02809 | hp1 | a0004 | c0005 | t0003 | g0253 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02809 | hp2 | a0006 | c0007 | t0003 | g0205 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02818 | hp1 | a0004 | c0005 | t0003 | g0016 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02818 | hp2 | a0001 | c0002 | t0002 | g0233 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02896 | hp1 | a0001 | c0002 | t0002 | g0239 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02922 | hp2 | a0005 | c0018 | t0005 | g0229 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02965 | hp1 | a0002 | c0004 | t0003 | g0226 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02970 | hp1 | a0006 | c0007 | t0003 | g0207 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02976 | hp1 | a0015 | c0014 | t0001 | g0217 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02976 | hp2 | a0006 | c0007 | t0003 | g0209 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03017 | hp2 | a0003 | c0003 | t0004 | g0251 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03098 | hp1 | a0016 | c0013 | t0001 | g0244 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03098 | hp2 | a0004 | c0005 | t0003 | g0259 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0221 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03139 | hp2 | a0002 | c0004 | t0003 | g0210 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03195 | hp1 | a0003 | c0003 | t0001 | g0266 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03195 | hp2 | a0003 | c0003 | t0001 | g0254 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03209 | hp2 | a0008 | c0010 | t0001 | g0265 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03225 | hp2 | a0001 | c0016 | t0008 | g0260 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03239 | hp2 | a0003 | c0003 | t0002 | g0256 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0237 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03453 | hp2 | a0002 | c0008 | t0001 | g0213 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03486 | hp1 | a0002 | c0004 | t0001 | g0095 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03486 | hp2 | a0005 | c0006 | t0001 | g0238 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03516 | hp2 | a0005 | c0006 | t0001 | g0235 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03540 | hp2 | a0002 | c0004 | t0006 | g0263 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03579 | hp1 | a0001 | c0002 | t0002 | g0240 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03669 | hp1 | a0003 | c0003 | t0002 | g0255 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03688 | hp1 | a0003 | c0003 | t0002 | g0245 | SAS | STU | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | STU | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03710 | hp1 | a0007 | c0009 | t0001 | g0214 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0101 | SAS | BEB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0112 | SAS | BEB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0197 | SAS | BEB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | STU | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG04199 | hp2 | a0003 | c0003 | t0002 | g0258 | SAS | STU | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | YRI | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18522 | hp2 | a0002 | c0011 | t0001 | g0054 | AFR | YRI | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18960 | hp1 | a0012 | c0021 | t0001 | g0057 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18971 | hp2 | a0001 | c0020 | t0001 | g0115 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | LWK | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | LWK | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | YRI | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0218 | AFR | YRI | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA20129 | hp1 | a0002 | c0004 | t0003 | g0052 | AFR | ASW | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA20129 | hp2 | a0001 | c0002 | t0002 | g0243 | AFR | ASW | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0038 | EUR | TSI | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | TSI | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02109 | hp1 | a0007 | c0009 | t0002 | g0215 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02109 | hp2 | a0001 | c0002 | t0002 | g0234 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02486 | hp1 | a0004 | c0005 | t0003 | g0247 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02486 | hp2 | a0001 | c0001 | t0005 | g0046 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02559 | hp1 | a0005 | c0017 | t0001 | g0189 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03471 | hp1 | a0001 | c0015 | t0001 | g0055 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG06807 | hp1 | a0010 | c0025 | t0001 | g0206 | AFR | USA | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
HG06807 | hp2 | a0002 | c0004 | t0003 | g0049 | AFR | USA | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA21309 | hp1 | a0004 | c0005 | t0003 | g0249 | AFR | LWK | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0182 | REF | REF | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
homoSapiens_grch38 | hp1 | a0013 | c0024 | t0001 | g0053 | REF | REF | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:75860716
|
T | TGTGGGCA others(9): Show |
1 | a0012 | 1 | NA18960.hp1 | frameshift_variant | HIGH | c.2197_2212dupGCCTCA others(10): Show |
p.Gln738fs | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 17/17 | 2493/3343 | 2212/2262 | 738/753 | chr4 | 75860716 | ||
chr4:75864488
|
G | A | 1 | a0011 | 1 | HG01496.hp2 | stop_gained | HIGH | c.1960C>T | p.Arg654* | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/17 | 2241/3343 | 1960/2262 | 654/753 | chr4 | 75864488 | ||
chr4:75866193
|
C | T | 1 | a0016 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.1916G>A | p.Arg639His | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 15/17 | 2197/3343 | 1916/2262 | 639/753 | chr4 | 75866193 | ||
chr4:75867346
|
T | A | 5 | a0002a0004a0005others(2): Show | 33 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(30): Show |
missense_variant | MODERATE | c.1723A>T | p.Ser575Cys | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 14/17 | 2004/3343 | 1723/2262 | 575/753 | chr4 | 75867346 | ||
chr4:75867411
|
C | T | 5 | a0002a0004a0005others(2): Show | 33 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(30): Show |
missense_variant | MODERATE | c.1658G>A | p.Arg553Lys | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 14/17 | 1939/3343 | 1658/2262 | 553/753 | chr4 | 75867411 | ||
chr4:75873192
|
T | G | 15 | a0001a0002a0003others(12): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
missense_variant | MODERATE | c.1441A>C | p.Met481Leu | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 12/17 | 1722/3343 | 1441/2262 | 481/753 | chr4 | 75873192 | ||
chr4:75873297
|
A | AC | 1 | a0006 | 4 | HG02145.hp2 HG02809.hp2 HG02970.hp1 others(1): Show |
frameshift_variant | HIGH | c.1335dupG | p.Trp446fs | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 12/17 | 1616/3343 | 1335/2262 | 445/753 | chr4 | 75873297 | ||
chr4:75876373
|
C | T | 2 | a0008a0010 | 4 | HG01243.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
missense_variant | MODERATE | c.1234G>A | p.Glu412Lys | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/17 | 1515/3343 | 1234/2262 | 412/753 | chr4 | 75876373 | ||
chr4:75876427
|
C | G | 1 | a0005 | 6 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(3): Show |
missense_variant | MODERATE | c.1180G>C | p.Val394Leu | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/17 | 1461/3343 | 1180/2262 | 394/753 | chr4 | 75876427 | ||
chr4:75882984
|
T | C | 1 | a0014 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.875A>G | p.His292Arg | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/17 | 1156/3343 | 875/2262 | 292/753 | chr4 | 75882984 | ||
chr4:75888232
|
C | T | 1 | a0015 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.514G>A | p.Glu172Lys | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/17 | 795/3343 | 514/2262 | 172/753 | chr4 | 75888232 | ||
chr4:75888243
|
G | A | 1 | a0007 | 3 | HG01192.hp2 HG02109.hp1 HG03710.hp1 |
missense_variant | MODERATE | c.503C>T | p.Thr168Ile | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/17 | 784/3343 | 503/2262 | 168/753 | chr4 | 75888243 | ||
chr4:75890022
|
G | A | 2 | a0006a0010 | 5 | HG02145.hp2 HG02809.hp2 HG02970.hp1 others(2): Show |
missense_variant | MODERATE | c.352C>T | p.Arg118Cys | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/17 | 633/3343 | 352/2262 | 118/753 | chr4 | 75890022 | ||
chr4:75890022
|
G | T | 3 | a0003a0004a0016 | 20 | HG01081.hp2 HG01167.hp2 HG01256.hp1 others(17): Show |
missense_variant | MODERATE | c.352C>A | p.Arg118Ser | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/17 | 633/3343 | 352/2262 | 118/753 | chr4 | 75890022 | ||
chr4:75891927
|
C | T | 1 | a0009 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.107G>A | p.Arg36His | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 3/17 | 388/3343 | 107/2262 | 36/753 | chr4 | 75891927 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:75864441
|
T | G | 3 | a0001c0016a0005c0006a0005c0018 | 6 | HG01891.hp2 HG02615.hp1 HG02922.hp2 others(3): Show |
splice_region_variant&synonymous_variant | LOW | c.2007A>C | p.Ser669Ser | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/17 | 2288/3343 | 2007/2262 | 669/753 | chr4 | 75864441 | ||
chr4:75867398
|
C | T | 1 | a0001c0020 | 1 | NA18971.hp2 | synonymous_variant | LOW | c.1671G>A | p.Ser557Ser | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 14/17 | 1952/3343 | 1671/2262 | 557/753 | chr4 | 75867398 | ||
chr4:75872075
|
A | G | 21 | a0001c0001a0001c0002a0001c0015others(18): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
synonymous_variant | LOW | c.1599T>C | p.Ile533Ile | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/17 | 1880/3343 | 1599/2262 | 533/753 | chr4 | 75872075 | ||
chr4:75884749
|
C | T | 13 | a0001c0001a0001c0020a0002c0004others(10): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
synonymous_variant | LOW | c.591G>A | p.Pro197Pro | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/17 | 872/3343 | 591/2262 | 197/753 | chr4 | 75884749 | ||
chr4:75886872
|
A | G | 4 | a0001c0015a0001c0016a0002c0011others(1): Show | 6 | HG01243.hp2 HG02258.hp2 HG03209.hp2 others(3): Show |
synonymous_variant | LOW | c.559T>C | p.Leu187Leu | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/17 | 840/3343 | 559/2262 | 187/753 | chr4 | 75886872 | ||
chr4:75888233
|
A | G | 24 | a0001c0001a0001c0002a0001c0015others(21): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
synonymous_variant | LOW | c.513T>C | p.Ser171Ser | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/17 | 794/3343 | 513/2262 | 171/753 | chr4 | 75888233 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:75859918
|
T | C | 2 | a0001c0001t0005a0005c0018t0005 | 2 | HG02486.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*749A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 17/17 | 749 | chr4 | 75859918 | |||||
chr4:75859952
|
T | C | 1 | a0002c0004t0006 | 2 | HG01175.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*715A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 17/17 | 715 | chr4 | 75859952 | |||||
chr4:75860005
|
T | A | 1 | a0001c0016t0008 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*662A>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 17/17 | 662 | chr4 | 75860005 | |||||
chr4:75860018
|
C | G | 8 | a0001c0001t0002a0001c0001t0004a0001c0002t0002others(5): Show | 58 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*649G>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 17/17 | 649 | chr4 | 75860018 | |||||
chr4:75860033
|
A | G | 1 | a0001c0001t0007 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*634T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 17/17 | 634 | chr4 | 75860033 | |||||
chr4:75860202
|
G | T | 2 | a0001c0001t0004a0003c0003t0004 | 3 | HG01167.hp1 HG02055.hp2 HG03017.hp2 |
3_prime_UTR_variant | MODIFIER | c.*465C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 17/17 | 465 | chr4 | 75860202 | |||||
chr4:75860524
|
C | A | 6 | a0001c0001t0003a0002c0004t0003a0002c0004t0006others(3): Show | 25 | HG01175.hp2 HG01243.hp1 HG02055.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*143G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 17/17 | 143 | chr4 | 75860524 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:75861090
|
A | G | 1 | a0015c0014t0001g0217 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2009-170T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861090 | ||||||
chr4:75861171
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2009-251C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861171 | ||||||
chr4:75861179
|
T | C | 1 | a0003c0003t0001g0254 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2009-259A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861179 | ||||||
chr4:75861202
|
C | T | 34 | a0001c0016t0008g0260a0002c0004t0001g0095a0002c0004t0003g0041others(31): Show | 34 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.2009-282G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861202 | ||||||
chr4:75861441
|
T | TG | 132 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(129): Show | 134 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.2009-522dupC | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861441 | ||||||
chr4:75861479
|
G | A | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2009-559C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861479 | ||||||
chr4:75861491
|
C | T | 1 | a0001c0001t0002g0014 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2009-571G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861491 | ||||||
chr4:75861500
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2009-580T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861500 | ||||||
chr4:75861522
|
A | G | 8 | a0001c0016t0008g0260a0002c0004t0006g0263a0002c0004t0006g0264others(5): Show | 8 | HG01175.hp2 HG01891.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2009-602T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861522 | ||||||
chr4:75861614
|
G | GT | 33 | a0001c0016t0008g0260a0002c0004t0001g0095a0002c0004t0003g0041others(30): Show | 33 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.2009-695dupA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTT | 66 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(63): Show | 68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.2009-696_2009-695d others(4): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(298): Show |
4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02895.hp2 HG02896.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2009-695_2009-694i others(307): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(303): Show |
1 | a0001c0001t0001g0144 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2009-695_2009-694i others(312): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(306): Show |
2 | a0001c0001t0001g0105a0001c0001t0001g0141 | 2 | HG02056.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(315): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(309): Show |
1 | a0001c0001t0001g0160 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2009-695_2009-694i others(318): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(310): Show |
3 | a0001c0001t0001g0104a0001c0001t0001g0176a0001c0001t0001g0190 | 3 | NA18952.hp1 NA19068.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(319): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(310): Show |
20 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0061others(17): Show | 21 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.2009-695_2009-694i others(319): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(311): Show |
1 | a0001c0001t0001g0171 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2009-695_2009-694i others(320): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(311): Show |
21 | a0001c0001t0001g0021a0001c0001t0001g0062a0001c0001t0001g0065others(18): Show | 21 | HG00099.hp1 HG00741.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.2009-695_2009-694i others(320): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(312): Show |
2 | a0001c0001t0001g0116a0001c0001t0001g0172 | 2 | HG01123.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(321): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(311): Show |
1 | a0001c0001t0001g0124 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2009-695_2009-694i others(320): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(312): Show |
9 | a0001c0001t0001g0023a0001c0001t0001g0063a0001c0001t0001g0076others(6): Show | 9 | HG01168.hp1 HG02155.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2009-695_2009-694i others(321): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(313): Show |
3 | a0001c0001t0001g0064a0001c0001t0001g0128a0001c0001t0001g0145 | 3 | HG01496.hp1 HG01934.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(322): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(314): Show |
1 | a0001c0001t0001g0132 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2009-695_2009-694i others(323): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(316): Show |
1 | a0001c0001t0001g0202 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2009-695_2009-694i others(325): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(317): Show |
2 | a0001c0001t0001g0148a0001c0001t0001g0174 | 2 | HG01934.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(326): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(318): Show |
2 | a0001c0001t0001g0162a0001c0002t0001g0212 | 2 | HG01975.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(327): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(319): Show |
3 | a0001c0001t0001g0069a0001c0001t0001g0097a0014c0022t0001g0185 | 3 | HG02132.hp1 NA18973.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(328): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(320): Show |
2 | a0001c0001t0001g0129a0001c0001t0001g0198 | 2 | HG02155.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(329): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(321): Show |
2 | a0001c0001t0001g0098a0001c0001t0001g0192 | 2 | NA18951.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(330): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(322): Show |
4 | a0001c0001t0001g0096a0001c0001t0001g0099a0001c0001t0001g0121others(1): Show | 4 | HG00423.hp1 HG00423.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.2009-695_2009-694i others(331): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(323): Show |
1 | a0001c0001t0001g0138 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2009-695_2009-694i others(332): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(322): Show |
1 | a0001c0020t0001g0115 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2009-695_2009-694i others(331): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(323): Show |
2 | a0001c0001t0001g0022a0001c0001t0001g0131 | 2 | HG03669.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(332): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(324): Show |
2 | a0001c0001t0001g0060a0001c0001t0001g0139 | 2 | HG00621.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(333): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(325): Show |
2 | a0001c0001t0001g0024a0001c0001t0001g0070 | 2 | HG02622.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(334): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(326): Show |
1 | a0001c0001t0001g0030 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2009-695_2009-694i others(335): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(328): Show |
3 | a0001c0001t0001g0059a0001c0001t0001g0163a0001c0002t0001g0211 | 3 | HG01261.hp1 HG02129.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(337): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(328): Show |
2 | a0001c0001t0001g0031a0001c0001t0001g0153 | 2 | NA18998.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(337): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(329): Show |
16 | a0001c0001t0001g0058a0001c0001t0001g0089a0001c0001t0001g0094others(13): Show | 17 | HG00140.hp2 HG00280.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.2009-695_2009-694i others(338): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(330): Show |
1 | a0001c0001t0001g0133 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2009-695_2009-694i others(339): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(329): Show |
1 | a0001c0001t0001g0140 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2009-695_2009-694i others(338): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(329): Show |
1 | a0001c0001t0001g0029 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2009-695_2009-694i others(338): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(330): Show |
17 | a0001c0001t0001g0073a0001c0001t0001g0087a0001c0001t0001g0088others(14): Show | 17 | HG01192.hp2 HG01255.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.2009-695_2009-694i others(339): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(331): Show |
8 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0078others(5): Show | 8 | HG01358.hp1 HG03710.hp2 NA18992.hp1 others(5): Show |
intron_variant | MODIFIER | c.2009-695_2009-694i others(340): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(332): Show |
4 | a0001c0001t0001g0066a0001c0001t0001g0108a0001c0001t0001g0143others(1): Show | 4 | HG00438.hp2 HG01175.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2009-695_2009-694i others(341): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(333): Show |
4 | a0001c0001t0001g0074a0001c0001t0001g0084a0001c0001t0001g0114others(1): Show | 4 | HG02165.hp1 HG02165.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2009-695_2009-694i others(342): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(334): Show |
6 | a0001c0001t0001g0110a0001c0001t0001g0117a0001c0001t0001g0135others(3): Show | 6 | HG02083.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2009-695_2009-694i others(343): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(335): Show |
3 | a0001c0001t0001g0111a0001c0001t0001g0136a0001c0001t0001g0194 | 3 | HG00673.hp1 HG02071.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(344): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861614
|
G | GTTTTTTT others(339): Show |
1 | a0001c0001t0001g0113 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2009-695_2009-694i others(348): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | ||||||
chr4:75861640
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2009-720G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861640 | ||||||
chr4:75861687
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2009-767T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861687 | ||||||
chr4:75861692
|
C | T | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | HG00099.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.2009-772G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861692 | ||||||
chr4:75861702
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2009-782A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861702 | ||||||
chr4:75861755
|
A | G | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2009-835T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861755 | ||||||
chr4:75861767
|
T | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2009-847A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861767 | ||||||
chr4:75861898
|
C | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2009-978G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861898 | ||||||
chr4:75861904
|
T | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2009-984A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861904 | ||||||
chr4:75861905
|
A | G | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2009-985T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861905 | ||||||
chr4:75861951
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2009-1031C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861951 | ||||||
chr4:75861966
|
A | G | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2009-1046T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861966 | ||||||
chr4:75861982
|
C | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2009-1062G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861982 | ||||||
chr4:75862020
|
C | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2009-1100G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75862020 | ||||||
chr4:75862118
|
C | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2009-1198G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75862118 | ||||||
chr4:75862248
|
G | A | 1 | a0002c0008t0001g0213 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2009-1328C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75862248 | ||||||
chr4:75862292
|
CAAAAAAA others(4): Show |
C | 5 | a0001c0001t0001g0151a0001c0001t0001g0187a0002c0004t0006g0264others(2): Show | 5 | HG00741.hp2 HG01175.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.2009-1383_2009-137 others(15): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75862292 | ||||||
chr4:75862292
|
CAAAAAAA others(5): Show |
C | 251 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(248): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.2009-1384_2009-137 others(16): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75862292 | ||||||
chr4:75862292
|
CAAAAAAA others(6): Show |
C | 5 | a0001c0001t0001g0058a0001c0001t0001g0222a0001c0001t0001g0223others(2): Show | 5 | HG02895.hp2 HG02896.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.2009-1385_2009-137 others(17): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75862292 | ||||||
chr4:75862589
|
C | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2009-1669G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75862589 | ||||||
chr4:75862622
|
C | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0153 | 2 | NA18950.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.2009-1702G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75862622 | ||||||
chr4:75863076
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2008+1364A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863076 | ||||||
chr4:75863192
|
G | A | 1 | a0001c0001t0002g0010 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2008+1248C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863192 | ||||||
chr4:75863208
|
TA | T | 4 | a0002c0004t0001g0095a0002c0011t0001g0054a0002c0011t0001g0056others(1): Show | 4 | HG02258.hp2 HG02559.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2008+1231delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863208 | ||||||
chr4:75863210
|
G | A | 227 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(224): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.2008+1230C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863210 | ||||||
chr4:75863335
|
CA | C | 35 | a0001c0001t0001g0147a0001c0001t0001g0164a0001c0001t0001g0172others(32): Show | 35 | HG01069.hp1 HG01071.hp1 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.2008+1104delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863335 | ||||||
chr4:75863335
|
CAA | C | 220 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(217): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.2008+1103_2008+110 others(6): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863335 | ||||||
chr4:75863448
|
C | T | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0078others(1): Show | 4 | HG02165.hp1 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.2008+992G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863448 | ||||||
chr4:75863449
|
G | A | 34 | a0001c0016t0008g0260a0002c0004t0001g0095a0002c0004t0003g0041others(31): Show | 34 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.2008+991C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863449 | ||||||
chr4:75863499
|
CAA | C | 237 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(234): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.2008+939_2008+940d others(4): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863499 | ||||||
chr4:75863499
|
CAAA | C | 23 | a0001c0001t0001g0094a0001c0001t0001g0222a0001c0001t0001g0223others(20): Show | 23 | HG01070.hp1 HG01243.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.2008+938_2008+940d others(5): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863499 | ||||||
chr4:75863504
|
A | T | 1 | a0001c0001t0001g0161 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2008+936T>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863504 | ||||||
chr4:75863672
|
C | T | 1 | a0002c0004t0001g0095 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2008+768G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863672 | ||||||
chr4:75863851
|
A | T | 1 | a0001c0001t0001g0160 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2008+589T>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863851 | ||||||
chr4:75863915
|
G | A | 1 | a0001c0016t0008g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2008+525C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863915 | ||||||
chr4:75863941
|
C | T | 1 | a0008c0010t0001g0208 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2008+499G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863941 | ||||||
chr4:75863971
|
C | A | 1 | a0001c0001t0001g0196 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2008+469G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863971 | ||||||
chr4:75864031
|
C | G | 2 | a0001c0001t0002g0067a0001c0001t0002g0203 | 2 | HG01361.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.2008+409G>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75864031 | ||||||
chr4:75864034
|
G | A | 28 | a0002c0004t0001g0095a0002c0004t0003g0041a0002c0004t0003g0049others(25): Show | 28 | HG01175.hp2 HG01243.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.2008+406C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75864034 | ||||||
chr4:75864151
|
C | T | 5 | a0002c0004t0003g0210a0004c0005t0003g0246a0004c0005t0003g0247others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2008+289G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75864151 | ||||||
chr4:75864563
|
C | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1921-36G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 15/16 | chr4 | 75864563 | ||||||
chr4:75864570
|
A | G | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1921-43T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 15/16 | chr4 | 75864570 | ||||||
chr4:75864583
|
T | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1921-56A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 15/16 | chr4 | 75864583 | ||||||
chr4:75864617
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1921-90G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 15/16 | chr4 | 75864617 | ||||||
chr4:75864624
|
G | GA | 4 | a0002c0004t0003g0226a0002c0004t0003g0261a0002c0004t0006g0263others(1): Show | 4 | HG01175.hp2 HG02258.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1921-98dupT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 15/16 | chr4 | 75864624 | ||||||
chr4:75865053
|
C | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1921-526G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 15/16 | chr4 | 75865053 | ||||||
chr4:75865227
|
G | A | 1 | a0004c0005t0003g0016 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1921-700C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 15/16 | chr4 | 75865227 | ||||||
chr4:75865544
|
G | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1920+645C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 15/16 | chr4 | 75865544 | ||||||
chr4:75866520
|
T | C | 228 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(225): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1757-168A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 14/16 | chr4 | 75866520 | ||||||
chr4:75866692
|
C | T | 1 | a0001c0016t0008g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1757-340G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 14/16 | chr4 | 75866692 | ||||||
chr4:75866761
|
T | C | 33 | a0002c0004t0001g0095a0002c0004t0003g0041a0002c0004t0003g0049others(30): Show | 33 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.1757-409A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 14/16 | chr4 | 75866761 | ||||||
chr4:75866804
|
G | A | 5 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(2): Show | 5 | HG02165.hp1 NA18973.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.1757-452C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 14/16 | chr4 | 75866804 | ||||||
chr4:75866970
|
A | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1756+343T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 14/16 | chr4 | 75866970 | ||||||
chr4:75867086
|
G | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1756+227C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 14/16 | chr4 | 75867086 | ||||||
chr4:75867115
|
A | G | 161 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(158): Show | 163 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1756+198T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 14/16 | chr4 | 75867115 | ||||||
chr4:75867259
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1756+54T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 14/16 | chr4 | 75867259 | ||||||
chr4:75867299
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1756+14A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 14/16 | chr4 | 75867299 | ||||||
chr4:75867424
|
G | A | 1 | a0007c0009t0001g0214 | 1 | HG03710.hp1 | splice_region_variant&intron_variant | LOW | c.1650-5C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75867424 | ||||||
chr4:75867539
|
C | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1650-120G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75867539 | ||||||
chr4:75867623
|
G | A | 33 | a0002c0004t0001g0095a0002c0004t0003g0041a0002c0004t0003g0049others(30): Show | 33 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.1650-204C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75867623 | ||||||
chr4:75867704
|
G | A | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1650-285C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75867704 | ||||||
chr4:75867927
|
T | C | 161 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(158): Show | 163 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1650-508A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75867927 | ||||||
chr4:75867985
|
C | G | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1650-566G>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75867985 | ||||||
chr4:75868062
|
C | G | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1650-643G>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868062 | ||||||
chr4:75868156
|
C | CAA | 256 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(253): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.1650-739_1650-738d others(4): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868156 | ||||||
chr4:75868185
|
G | A | 1 | a0005c0018t0005g0229 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1650-766C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868185 | ||||||
chr4:75868240
|
C | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1650-821G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868240 | ||||||
chr4:75868258
|
G | C | 2 | a0004c0005t0003g0247a0004c0005t0003g0248 | 2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1650-839C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868258 | ||||||
chr4:75868309
|
C | T | 1 | a0001c0001t0002g0009 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1650-890G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868309 | ||||||
chr4:75868315
|
C | CAA | 19 | a0002c0004t0003g0041a0002c0004t0003g0049a0002c0004t0003g0052others(16): Show | 19 | HG01243.hp1 HG02145.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.1650-898_1650-897d others(4): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868315 | ||||||
chr4:75868315
|
C | CAAA | 8 | a0002c0004t0001g0095a0002c0004t0003g0226a0002c0004t0003g0261others(5): Show | 8 | HG02258.hp1 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1650-899_1650-897d others(5): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868315 | ||||||
chr4:75868315
|
C | CAAAAA | 13 | a0001c0001t0001g0124a0001c0001t0001g0142a0001c0001t0001g0165others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.1650-901_1650-897d others(7): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868315 | ||||||
chr4:75868315
|
C | CAAAAAA | 206 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(203): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1650-902_1650-897d others(8): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868315 | ||||||
chr4:75868315
|
C | CAAAAAAA | 13 | a0001c0001t0001g0030a0001c0001t0001g0070a0001c0001t0001g0135others(10): Show | 13 | HG02145.hp1 HG02486.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.1650-903_1650-897d others(9): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868315 | ||||||
chr4:75868342
|
A | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1650-923T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868342 | ||||||
chr4:75868363
|
C | T | 228 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(225): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1650-944G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868363 | ||||||
chr4:75868453
|
T | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1650-1034A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868453 | ||||||
chr4:75868528
|
T | G | 1 | a0001c0001t0002g0011 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1650-1109A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868528 | ||||||
chr4:75868563
|
G | A | 1 | a0008c0010t0001g0265 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1650-1144C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868563 | ||||||
chr4:75868566
|
C | T | 33 | a0002c0004t0001g0095a0002c0004t0003g0041a0002c0004t0003g0049others(30): Show | 33 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.1650-1147G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868566 | ||||||
chr4:75868652
|
T | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1650-1233A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868652 | ||||||
chr4:75868738
|
C | T | 1 | a0001c0001t0002g0025 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1650-1319G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868738 | ||||||
chr4:75868745
|
A | G | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1650-1326T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868745 | ||||||
chr4:75868851
|
T | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1650-1432A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868851 | ||||||
chr4:75868883
|
C | T | 5 | a0002c0004t0001g0095a0002c0008t0001g0213a0002c0011t0001g0054others(2): Show | 5 | HG02258.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1650-1464G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868883 | ||||||
chr4:75869121
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1650-1702T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75869121 | ||||||
chr4:75869418
|
G | A | 228 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(225): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1650-1999C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75869418 | ||||||
chr4:75869600
|
A | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1650-2181T>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75869600 | ||||||
chr4:75869611
|
C | T | 5 | a0005c0006t0001g0220a0005c0006t0001g0235a0005c0006t0001g0236others(2): Show | 5 | HG01891.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1650-2192G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75869611 | ||||||
chr4:75869627
|
A | G | 260 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(257): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1650-2208T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75869627 | ||||||
chr4:75869674
|
T | A | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1650-2255A>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75869674 | ||||||
chr4:75869712
|
A | G | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1650-2293T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75869712 | ||||||
chr4:75869838
|
C | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1649+2187G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75869838 | ||||||
chr4:75869854
|
GA | G | 260 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(257): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1649+2170delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75869854 | ||||||
chr4:75869868
|
A | C | 4 | a0002c0004t0001g0095a0002c0011t0001g0054a0002c0011t0001g0056others(1): Show | 4 | HG02258.hp2 HG02559.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1649+2157T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75869868 | ||||||
chr4:75869868
|
A | G | 257 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(254): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1649+2157T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75869868 | ||||||
chr4:75870104
|
A | G | 4 | a0002c0004t0003g0226a0002c0004t0003g0261a0002c0004t0006g0263others(1): Show | 4 | HG01175.hp2 HG02258.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1649+1921T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870104 | ||||||
chr4:75870153
|
C | T | 33 | a0002c0004t0001g0095a0002c0004t0003g0041a0002c0004t0003g0049others(30): Show | 33 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.1649+1872G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870153 | ||||||
chr4:75870325
|
A | G | 4 | a0001c0001t0001g0121a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 4 | HG00621.hp2 NA18951.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1649+1700T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870325 | ||||||
chr4:75870500
|
T | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1649+1525A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870500 | ||||||
chr4:75870588
|
A | G | 1 | a0008c0010t0001g0208 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1649+1437T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870588 | ||||||
chr4:75870643
|
T | A | 228 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(225): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1649+1382A>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870643 | ||||||
chr4:75870676
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1649+1349C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870676 | ||||||
chr4:75870875
|
T | C | 33 | a0002c0004t0001g0095a0002c0004t0003g0041a0002c0004t0003g0049others(30): Show | 33 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.1649+1150A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870875 | ||||||
chr4:75870878
|
C | CATTTATT others(1): Show |
12 | a0001c0001t0001g0045a0001c0001t0001g0083a0001c0001t0001g0154others(9): Show | 13 | HG00323.hp1 HG01081.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1649+1139_1649+114 others(12): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870878 | ||||||
chr4:75870878
|
C | CATTTATT others(5): Show |
208 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1649+1135_1649+114 others(16): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870878 | ||||||
chr4:75870878
|
C | CATTTATT others(9): Show |
37 | a0001c0001t0001g0024a0001c0001t0001g0044a0001c0001t0001g0048others(34): Show | 38 | HG00673.hp1 HG01099.hp1 HG01169.hp2 others(35): Show |
intron_variant | MODIFIER | c.1649+1131_1649+114 others(20): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870878 | ||||||
chr4:75870878
|
C | CATTTATT others(13): Show |
2 | a0001c0001t0001g0133a0001c0001t0002g0027 | 2 | HG01257.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1649+1127_1649+114 others(24): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870878 | ||||||
chr4:75870878
|
C | CATTTATT others(17): Show |
1 | a0001c0001t0001g0222 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1649+1123_1649+114 others(28): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870878 | ||||||
chr4:75871002
|
CA | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1649+1022delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871002 | ||||||
chr4:75871080
|
G | C | 2 | a0001c0001t0001g0120a0001c0001t0001g0124 | 2 | HG02015.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1649+945C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871080 | ||||||
chr4:75871093
|
T | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1649+932A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871093 | ||||||
chr4:75871111
|
G | C | 1 | a0001c0001t0002g0197 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1649+914C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871111 | ||||||
chr4:75871121
|
T | C | 1 | a0001c0001t0002g0013 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1649+904A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871121 | ||||||
chr4:75871158
|
C | G | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1649+867G>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871158 | ||||||
chr4:75871166
|
C | T | 2 | a0001c0001t0002g0039a0001c0001t0002g0040 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1649+859G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871166 | ||||||
chr4:75871172
|
A | G | 260 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(257): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1649+853T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871172 | ||||||
chr4:75871210
|
G | A | 1 | a0005c0018t0005g0229 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1649+815C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871210 | ||||||
chr4:75871236
|
G | A | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1649+789C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871236 | ||||||
chr4:75871245
|
T | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1649+780A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871245 | ||||||
chr4:75871463
|
T | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1649+562A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871463 | ||||||
chr4:75871517
|
C | A | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1649+508G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871517 | ||||||
chr4:75871644
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1649+381T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871644 | ||||||
chr4:75871723
|
A | C | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1649+302T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871723 | ||||||
chr4:75871746
|
C | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1649+279G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871746 | ||||||
chr4:75871755
|
G | C | 4 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0188others(1): Show | 4 | HG01255.hp1 HG01975.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1649+270C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871755 | ||||||
chr4:75871776
|
T | A | 4 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0188others(1): Show | 4 | HG01255.hp1 HG01975.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1649+249A>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871776 | ||||||
chr4:75872429
|
C | A | 1 | a0001c0001t0002g0025 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1507-262G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 12/16 | chr4 | 75872429 | ||||||
chr4:75872614
|
G | A | 1 | a0005c0006t0001g0235 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1507-447C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 12/16 | chr4 | 75872614 | ||||||
chr4:75872715
|
C | T | 1 | a0005c0018t0005g0229 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1506+412G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 12/16 | chr4 | 75872715 | ||||||
chr4:75872905
|
G | C | 4 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0188others(1): Show | 4 | HG01255.hp1 HG01975.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1506+222C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 12/16 | chr4 | 75872905 | ||||||
chr4:75873509
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1321-197A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75873509 | ||||||
chr4:75873742
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0020 | 2 | HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1321-430G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75873742 | ||||||
chr4:75873794
|
A | AT | 8 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0050others(5): Show | 9 | HG01243.hp2 HG01891.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1321-483dupA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75873794 | ||||||
chr4:75874056
|
A | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1321-744T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874056 | ||||||
chr4:75874062
|
C | G | 1 | a0001c0001t0001g0129 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1321-750G>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874062 | ||||||
chr4:75874115
|
CAAACAAA others(9): Show |
C | 1 | a0001c0001t0001g0021 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1321-819_1321-804d others(18): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874115 | ||||||
chr4:75874123
|
CAAACAAA others(1): Show |
C | 4 | a0001c0001t0001g0106a0001c0001t0001g0110a0001c0001t0001g0186others(1): Show | 4 | HG02083.hp1 HG02083.hp2 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.1321-819_1321-812d others(10): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874123 | ||||||
chr4:75874127
|
CAAAT | C | 224 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(221): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1321-819_1321-816d others(6): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874127 | ||||||
chr4:75874393
|
T | C | 1 | a0001c0002t0002g0233 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1321-1081A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874393 | ||||||
chr4:75874396
|
A | G | 1 | a0004c0005t0003g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1321-1084T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874396 | ||||||
chr4:75874505
|
C | T | 5 | a0001c0001t0001g0045a0001c0001t0001g0083a0001c0001t0001g0154others(2): Show | 5 | HG01109.hp2 HG02647.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1321-1193G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874505 | ||||||
chr4:75874548
|
C | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0164 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1321-1236G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874548 | ||||||
chr4:75874752
|
T | C | 12 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(9): Show | 12 | HG00423.hp1 HG00621.hp2 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.1321-1440A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874752 | ||||||
chr4:75874760
|
C | T | 3 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG00099.hp1 HG00741.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.1321-1448G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874760 | ||||||
chr4:75874796
|
C | T | 2 | a0001c0001t0002g0012a0001c0001t0002g0013 | 2 | HG01081.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1321-1484G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874796 | ||||||
chr4:75874902
|
C | CT | 28 | a0001c0001t0001g0060a0001c0001t0002g0067a0002c0004t0001g0095others(25): Show | 28 | HG00621.hp1 HG01243.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1320+1384dupA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874902 | ||||||
chr4:75874902
|
CT | C | 6 | a0001c0001t0001g0050a0001c0001t0001g0169a0001c0001t0001g0175others(3): Show | 6 | HG01175.hp2 HG02451.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1320+1384delA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874902 | ||||||
chr4:75874906
|
T | C | 1 | a0001c0002t0002g0231 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1320+1381A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874906 | ||||||
chr4:75874961
|
G | T | 1 | a0001c0001t0001g0121 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1320+1326C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874961 | ||||||
chr4:75875466
|
A | G | 5 | a0005c0006t0001g0220a0005c0006t0001g0235a0005c0006t0001g0236others(2): Show | 5 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1320+821T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75875466 | ||||||
chr4:75875718
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1320+569G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75875718 | ||||||
chr4:75875767
|
T | C | 6 | a0005c0006t0001g0220a0005c0006t0001g0235a0005c0006t0001g0236others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1320+520A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75875767 | ||||||
chr4:75876026
|
A | G | 265 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(262): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1320+261T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75876026 | ||||||
chr4:75876184
|
A | AAGAG | 260 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(257): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1320+99_1320+102du others(5): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75876184 | ||||||
chr4:75876237
|
T | G | 4 | a0002c0004t0001g0095a0002c0008t0001g0213a0002c0011t0001g0054others(1): Show | 4 | HG02258.hp2 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1320+50A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75876237 | ||||||
chr4:75876797
|
G | A | 68 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(65): Show | 70 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.934-124C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75876797 | ||||||
chr4:75876991
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.934-318C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75876991 | ||||||
chr4:75876995
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.934-322C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75876995 | ||||||
chr4:75877006
|
A | AAAAAGAA others(42): Show |
1 | a0001c0001t0001g0120 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.934-334_934-333ins others(49): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | ||||||
chr4:75877006
|
A | AAAAGAAA others(43): Show |
1 | a0001c0001t0001g0088 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.934-334_934-333ins others(50): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | ||||||
chr4:75877006
|
A | AAAAGAAA others(50): Show |
1 | a0001c0001t0002g0035 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.934-334_934-333ins others(57): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | ||||||
chr4:75877006
|
A | AAAAGAAA others(58): Show |
1 | a0001c0001t0002g0036 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.934-334_934-333ins others(65): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | ||||||
chr4:75877006
|
A | AAAAGAAA others(9): Show |
3 | a0001c0001t0001g0087a0001c0001t0001g0091a0001c0001t0001g0193 | 3 | HG01358.hp1 HG02040.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.934-349_934-334dup others(16): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | ||||||
chr4:75877006
|
A | AAAAGAAA others(21): Show |
1 | a0001c0001t0001g0060 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.934-361_934-334dup others(28): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | ||||||
chr4:75877006
|
A | AAAAGAAA others(25): Show |
3 | a0001c0001t0001g0094a0001c0001t0001g0098a0001c0001t0001g0132 | 3 | HG01070.hp1 HG03942.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.934-365_934-334dup others(32): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | ||||||
chr4:75877006
|
A | AAAAGAAA others(29): Show |
16 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0130others(13): Show | 16 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.934-334_934-333ins others(36): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | ||||||
chr4:75877006
|
A | AAAAGAAA others(33): Show |
28 | a0001c0001t0001g0021a0001c0001t0001g0051a0001c0001t0001g0070others(25): Show | 29 | HG00323.hp2 HG00738.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.934-334_934-333ins others(40): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | ||||||
chr4:75877006
|
A | AAAAGAAA others(37): Show |
35 | a0001c0001t0001g0048a0001c0001t0001g0063a0001c0001t0001g0089others(32): Show | 36 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.934-334_934-333ins others(44): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | ||||||
chr4:75877006
|
A | AAAAGAAA others(41): Show |
45 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0020others(42): Show | 46 | HG00738.hp2 HG00741.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.934-334_934-333ins others(48): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | ||||||
chr4:75877006
|
A | AAAAGAAA others(45): Show |
38 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0031others(35): Show | 39 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.934-334_934-333ins others(52): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | ||||||
chr4:75877006
|
A | AAAAGAAA others(49): Show |
16 | a0001c0001t0001g0050a0001c0001t0001g0065a0001c0001t0001g0096others(13): Show | 16 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(13): Show |
intron_variant | MODIFIER | c.934-334_934-333ins others(56): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | ||||||
chr4:75877006
|
A | AAAAGAAA others(53): Show |
11 | a0001c0001t0001g0030a0001c0001t0001g0076a0001c0001t0001g0133others(8): Show | 11 | HG00423.hp2 HG01081.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.934-334_934-333ins others(60): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | ||||||
chr4:75877006
|
A | AAAAGAAA others(57): Show |
8 | a0001c0001t0001g0062a0001c0001t0001g0074a0001c0001t0001g0148others(5): Show | 8 | HG01358.hp2 HG02155.hp2 NA18983.hp1 others(5): Show |
intron_variant | MODIFIER | c.934-334_934-333ins others(64): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | ||||||
chr4:75877006
|
A | AAAAGAAA others(61): Show |
2 | a0001c0001t0001g0029a0001c0001t0001g0113 | 2 | NA18950.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.934-334_934-333ins others(68): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | ||||||
chr4:75877006
|
A | AAAGAAAG others(28): Show |
1 | a0001c0001t0001g0145 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-334_934-333ins others(35): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | ||||||
chr4:75877006
|
A | AAAGAAAG others(40): Show |
1 | a0001c0001t0001g0097 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.934-334_934-333ins others(47): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | ||||||
chr4:75877006
|
A | AAGAAAGA others(43): Show |
3 | a0001c0001t0001g0174a0001c0001t0002g0100a0001c0001t0003g0227 | 3 | HG01934.hp1 HG02280.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.934-334_934-333ins others(50): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | ||||||
chr4:75877006
|
A | AGAAAGAA others(34): Show |
1 | a0001c0001t0001g0022 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.934-334_934-333ins others(41): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | ||||||
chr4:75877006
|
A | AGAAAGAA others(42): Show |
1 | a0001c0001t0001g0064 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.934-334_934-333ins others(49): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | ||||||
chr4:75877006
|
AAAAGAAA others(1): Show |
A | 35 | a0001c0001t0001g0169a0002c0004t0001g0095a0002c0004t0003g0041others(32): Show | 35 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.934-341_934-334del others(8): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | ||||||
chr4:75877013
|
A | AAGAAAGA others(59): Show |
1 | a0001c0001t0002g0037 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.934-341_934-340ins others(66): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877013 | ||||||
chr4:75877014
|
G | A | 1 | a0001c0001t0002g0037 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.934-341C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877014 | ||||||
chr4:75877028
|
A | AAGAAAGA others(45): Show |
1 | a0001c0001t0001g0134 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.934-356_934-355ins others(52): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877028 | ||||||
chr4:75877038
|
G | GAAAGAAA others(46): Show |
1 | a0001c0001t0001g0079 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.934-366_934-365ins others(53): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877038 | ||||||
chr4:75877039
|
A | AAAGAAAG others(36): Show |
2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG00673.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.934-367_934-366ins others(43): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877039 | ||||||
chr4:75877039
|
A | AAAGAAAG others(40): Show |
1 | a0001c0001t0004g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.934-367_934-366ins others(47): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877039 | ||||||
chr4:75877039
|
A | AAAGAAAG others(44): Show |
2 | a0001c0001t0001g0023a0001c0001t0001g0071 | 2 | NA18992.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.934-367_934-366ins others(51): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877039 | ||||||
chr4:75877039
|
A | AAAGAAAG others(48): Show |
1 | a0001c0002t0001g0212 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.934-367_934-366ins others(55): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877039 | ||||||
chr4:75877115
|
A | G | 8 | a0002c0004t0003g0210a0002c0008t0003g0241a0002c0008t0003g0242others(5): Show | 8 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.934-442T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877115 | ||||||
chr4:75877135
|
C | T | 1 | a0005c0018t0005g0229 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.934-462G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877135 | ||||||
chr4:75877173
|
C | A | 6 | a0005c0006t0001g0220a0005c0006t0001g0235a0005c0006t0001g0236others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.934-500G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877173 | ||||||
chr4:75877213
|
T | C | 3 | a0001c0001t0003g0221a0001c0001t0003g0227a0001c0001t0003g0228 | 3 | HG02055.hp1 HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.934-540A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877213 | ||||||
chr4:75877246
|
G | A | 30 | a0001c0001t0001g0169a0002c0004t0003g0041a0002c0004t0003g0049others(27): Show | 30 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.934-573C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877246 | ||||||
chr4:75877268
|
C | T | 1 | a0005c0018t0005g0229 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.934-595G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877268 | ||||||
chr4:75877376
|
AAG | A | 9 | a0002c0004t0001g0095a0002c0008t0001g0213a0002c0011t0001g0054others(6): Show | 9 | HG01891.hp2 HG02258.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.934-705_934-704del others(2): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877376 | ||||||
chr4:75877378
|
G | GAGAAAGA others(1): Show |
5 | a0005c0018t0005g0229a0008c0010t0001g0208a0008c0010t0001g0265others(2): Show | 5 | HG01243.hp2 HG02572.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.934-706_934-705ins others(8): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877378 | ||||||
chr4:75877380
|
G | GAA | 226 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(223): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.934-708_934-707ins others(2): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877380 | ||||||
chr4:75877382
|
G | A | 25 | a0001c0001t0001g0169a0002c0004t0003g0041a0002c0004t0003g0049others(22): Show | 25 | HG01175.hp2 HG01243.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.934-709C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877382 | ||||||
chr4:75877384
|
A | G | 25 | a0001c0001t0001g0169a0002c0004t0003g0041a0002c0004t0003g0049others(22): Show | 25 | HG01175.hp2 HG01243.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.934-711T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877384 | ||||||
chr4:75877386
|
G | A | 25 | a0001c0001t0001g0169a0002c0004t0003g0041a0002c0004t0003g0049others(22): Show | 25 | HG01175.hp2 HG01243.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.934-713C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877386 | ||||||
chr4:75877386
|
GA | G | 226 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(223): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.934-714delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877386 | ||||||
chr4:75877594
|
T | C | 5 | a0001c0001t0001g0169a0002c0004t0003g0226a0002c0004t0003g0261others(2): Show | 5 | HG01175.hp2 HG02258.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.934-921A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877594 | ||||||
chr4:75877670
|
C | T | 260 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(257): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.934-997G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877670 | ||||||
chr4:75877672
|
CT | C | 71 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(68): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.934-1000delA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877672 | ||||||
chr4:75877674
|
T | G | 1 | a0001c0016t0008g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.934-1001A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877674 | ||||||
chr4:75877741
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.934-1068A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877741 | ||||||
chr4:75877791
|
A | G | 4 | a0008c0010t0001g0208a0008c0010t0001g0265a0008c0019t0001g0032others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.934-1118T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877791 | ||||||
chr4:75877916
|
C | T | 25 | a0001c0001t0001g0169a0002c0004t0003g0041a0002c0004t0003g0049others(22): Show | 25 | HG01175.hp2 HG01243.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.934-1243G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877916 | ||||||
chr4:75877946
|
T | C | 34 | a0001c0001t0001g0169a0002c0004t0003g0041a0002c0004t0003g0049others(31): Show | 34 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.934-1273A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877946 | ||||||
chr4:75877957
|
C | A | 1 | a0001c0015t0001g0055 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.934-1284G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877957 | ||||||
chr4:75878022
|
T | C | 1 | a0005c0006t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.934-1349A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75878022 | ||||||
chr4:75878204
|
T | C | 10 | a0001c0001t0001g0058a0002c0004t0001g0095a0002c0008t0001g0213others(7): Show | 10 | HG01891.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.934-1531A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75878204 | ||||||
chr4:75878214
|
T | A | 29 | a0001c0001t0001g0169a0002c0004t0003g0041a0002c0004t0003g0049others(26): Show | 29 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.934-1541A>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75878214 | ||||||
chr4:75878450
|
C | T | 38 | a0001c0001t0001g0169a0002c0004t0001g0095a0002c0004t0003g0041others(35): Show | 38 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.934-1777G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75878450 | ||||||
chr4:75878784
|
T | C | 4 | a0008c0010t0001g0208a0008c0010t0001g0265a0008c0019t0001g0032others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.934-2111A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75878784 | ||||||
chr4:75878802
|
T | G | 1 | a0002c0004t0003g0052 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.934-2129A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75878802 | ||||||
chr4:75878811
|
G | T | 29 | a0001c0001t0001g0169a0002c0004t0003g0041a0002c0004t0003g0049others(26): Show | 29 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.934-2138C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75878811 | ||||||
chr4:75878830
|
G | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0075 | 2 | NA18965.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.934-2157C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75878830 | ||||||
chr4:75878903
|
G | A | 41 | a0001c0001t0001g0169a0001c0002t0002g0230a0001c0002t0002g0231others(38): Show | 41 | HG01175.hp2 HG01243.hp1 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.934-2230C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75878903 | ||||||
chr4:75879005
|
G | T | 1 | a0010c0025t0001g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.934-2332C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879005 | ||||||
chr4:75879181
|
C | T | 1 | a0002c0008t0003g0241 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.934-2508G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879181 | ||||||
chr4:75879195
|
A | G | 41 | a0001c0001t0001g0169a0001c0002t0002g0230a0001c0002t0002g0231others(38): Show | 41 | HG01175.hp2 HG01243.hp1 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.934-2522T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879195 | ||||||
chr4:75879229
|
T | G | 41 | a0001c0001t0001g0169a0001c0002t0002g0230a0001c0002t0002g0231others(38): Show | 41 | HG01175.hp2 HG01243.hp1 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.934-2556A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879229 | ||||||
chr4:75879272
|
A | G | 41 | a0001c0001t0001g0169a0001c0002t0002g0230a0001c0002t0002g0231others(38): Show | 41 | HG01175.hp2 HG01243.hp1 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.934-2599T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879272 | ||||||
chr4:75879323
|
A | G | 265 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(262): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.934-2650T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879323 | ||||||
chr4:75879327
|
T | C | 41 | a0001c0001t0001g0169a0001c0002t0002g0230a0001c0002t0002g0231others(38): Show | 41 | HG01175.hp2 HG01243.hp1 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.934-2654A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879327 | ||||||
chr4:75879332
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.934-2659C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879332 | ||||||
chr4:75879350
|
C | T | 16 | a0001c0002t0002g0230a0001c0002t0002g0231a0001c0002t0002g0233others(13): Show | 16 | HG01255.hp2 HG01496.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.934-2677G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879350 | ||||||
chr4:75879384
|
T | G | 25 | a0001c0001t0001g0169a0002c0004t0003g0041a0002c0004t0003g0049others(22): Show | 25 | HG01175.hp2 HG01243.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.934-2711A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879384 | ||||||
chr4:75879398
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.934-2725C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879398 | ||||||
chr4:75879558
|
T | C | 41 | a0001c0001t0001g0169a0001c0002t0002g0230a0001c0002t0002g0231others(38): Show | 41 | HG01175.hp2 HG01243.hp1 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.934-2885A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879558 | ||||||
chr4:75879576
|
A | G | 219 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(216): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.934-2903T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879576 | ||||||
chr4:75879613
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.934-2940A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879613 | ||||||
chr4:75879838
|
A | AT | 216 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(213): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.933+3087dupA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879838 | ||||||
chr4:75879954
|
G | A | 219 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(216): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.933+2972C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879954 | ||||||
chr4:75879964
|
G | C | 1 | a0001c0001t0001g0058 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.933+2962C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879964 | ||||||
chr4:75879986
|
A | G | 219 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(216): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.933+2940T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879986 | ||||||
chr4:75880064
|
G | A | 8 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(5): Show | 8 | HG01070.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.933+2862C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880064 | ||||||
chr4:75880144
|
A | G | 219 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(216): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.933+2782T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880144 | ||||||
chr4:75880229
|
C | T | 16 | a0001c0002t0002g0230a0001c0002t0002g0231a0001c0002t0002g0233others(13): Show | 16 | HG01255.hp2 HG01496.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.933+2697G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880229 | ||||||
chr4:75880230
|
G | A | 1 | a0001c0002t0001g0237 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.933+2696C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880230 | ||||||
chr4:75880275
|
C | G | 1 | a0001c0001t0002g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.933+2651G>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880275 | ||||||
chr4:75880595
|
C | T | 219 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(216): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.933+2331G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880595 | ||||||
chr4:75880625
|
A | T | 219 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(216): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.933+2301T>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880625 | ||||||
chr4:75880670
|
T | C | 12 | a0001c0002t0002g0230a0001c0002t0002g0231a0001c0002t0002g0233others(9): Show | 12 | HG01255.hp2 HG01496.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.933+2256A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880670 | ||||||
chr4:75880804
|
C | CT | 17 | a0001c0002t0002g0230a0001c0002t0002g0231a0001c0002t0002g0233others(14): Show | 17 | HG01255.hp2 HG01496.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.933+2121dupA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880804 | ||||||
chr4:75880804
|
C | CTT | 29 | a0001c0001t0001g0169a0002c0004t0003g0041a0002c0004t0003g0049others(26): Show | 29 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.933+2120_933+2121d others(4): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880804 | ||||||
chr4:75880818
|
T | TTTTG | 214 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(211): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.933+2107_933+2108i others(6): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880818 | ||||||
chr4:75880818
|
T | TTTTTG | 5 | a0001c0001t0001g0020a0001c0001t0001g0105a0001c0001t0001g0141others(2): Show | 5 | HG02056.hp1 HG02056.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.933+2107_933+2108i others(7): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880818 | ||||||
chr4:75880907
|
C | T | 4 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0033others(1): Show | 4 | HG01257.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.933+2019G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880907 | ||||||
chr4:75880945
|
G | A | 12 | a0001c0002t0002g0230a0001c0002t0002g0231a0001c0002t0002g0233others(9): Show | 12 | HG01255.hp2 HG01496.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.933+1981C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880945 | ||||||
chr4:75880948
|
C | T | 219 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(216): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.933+1978G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880948 | ||||||
chr4:75880960
|
C | T | 1 | a0004c0005t0003g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.933+1966G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880960 | ||||||
chr4:75880991
|
G | A | 158 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(155): Show | 160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.933+1935C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880991 | ||||||
chr4:75881047
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.933+1879T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881047 | ||||||
chr4:75881102
|
A | AT | 191 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(188): Show | 193 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.933+1823dupA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881102 | ||||||
chr4:75881102
|
A | ATT | 67 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(64): Show | 69 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.933+1822_933+1823d others(4): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881102 | ||||||
chr4:75881243
|
A | G | 248 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(245): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.933+1683T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881243 | ||||||
chr4:75881289
|
A | G | 219 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(216): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.933+1637T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881289 | ||||||
chr4:75881320
|
G | A | 219 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(216): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.933+1606C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881320 | ||||||
chr4:75881358
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.933+1568T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881358 | ||||||
chr4:75881487
|
C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(151): Show | 156 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.933+1439G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881487 | ||||||
chr4:75881628
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.933+1298C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881628 | ||||||
chr4:75881668
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.933+1258C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881668 | ||||||
chr4:75881807
|
G | A | 1 | a0001c0002t0002g0233 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.933+1119C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881807 | ||||||
chr4:75881917
|
T | C | 16 | a0001c0002t0002g0230a0001c0002t0002g0231a0001c0002t0002g0233others(13): Show | 16 | HG01255.hp2 HG01496.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.933+1009A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881917 | ||||||
chr4:75881974
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.933+952A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881974 | ||||||
chr4:75881988
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.933+938C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881988 | ||||||
chr4:75882016
|
A | G | 219 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(216): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.933+910T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882016 | ||||||
chr4:75882033
|
A | C | 219 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(216): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.933+893T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882033 | ||||||
chr4:75882172
|
G | A | 219 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(216): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.933+754C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882172 | ||||||
chr4:75882232
|
T | C | 219 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(216): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.933+694A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882232 | ||||||
chr4:75882304
|
G | A | 219 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(216): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.933+622C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882304 | ||||||
chr4:75882460
|
C | T | 3 | a0002c0004t0001g0095a0002c0011t0001g0054a0002c0011t0001g0056 | 3 | HG02258.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.933+466G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882460 | ||||||
chr4:75882476
|
A | G | 1 | a0003c0003t0004g0251 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.933+450T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882476 | ||||||
chr4:75882518
|
G | T | 61 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(58): Show | 63 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.933+408C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882518 | ||||||
chr4:75882530
|
G | A | 219 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(216): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.933+396C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882530 | ||||||
chr4:75882539
|
C | CT | 7 | a0001c0001t0001g0074a0001c0001t0001g0181a0001c0001t0002g0007others(4): Show | 7 | HG00323.hp2 HG01167.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.933+386dupA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882539 | ||||||
chr4:75882539
|
C | CTT | 212 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(209): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.933+385_933+386dup others(2): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882539 | ||||||
chr4:75882591
|
G | T | 2 | a0004c0005t0003g0247a0004c0005t0003g0248 | 2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.933+335C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882591 | ||||||
chr4:75882914
|
A | G | 219 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(216): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.933+12T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882914 | ||||||
chr4:75883348
|
A | C | 223 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(220): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.747-146T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883348 | ||||||
chr4:75883351
|
C | T | 223 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(220): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.747-149G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883351 | ||||||
chr4:75883355
|
G | A | 223 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(220): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.747-153C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883355 | ||||||
chr4:75883532
|
A | G | 235 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(232): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.747-330T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883532 | ||||||
chr4:75883593
|
C | T | 1 | a0001c0016t0008g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.747-391G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883593 | ||||||
chr4:75883594
|
G | A | 237 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(234): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.747-392C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883594 | ||||||
chr4:75883601
|
G | C | 237 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(234): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.747-399C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883601 | ||||||
chr4:75883767
|
G | A | 226 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(223): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.747-565C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883767 | ||||||
chr4:75883817
|
C | CA | 23 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(20): Show | 23 | HG01255.hp2 HG01496.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.747-616dupT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883817 | ||||||
chr4:75883817
|
C | CAA | 8 | a0001c0002t0002g0240a0001c0015t0001g0055a0002c0004t0003g0262others(5): Show | 8 | HG01175.hp2 HG01243.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.747-617_747-616dup others(2): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883817 | ||||||
chr4:75883817
|
CA | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(173): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.747-616delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883817 | ||||||
chr4:75883847
|
G | A | 225 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(222): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.747-645C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883847 | ||||||
chr4:75883852
|
G | A | 15 | a0001c0002t0001g0003a0001c0002t0001g0218a0001c0002t0001g0237others(12): Show | 16 | HG01255.hp2 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.747-650C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883852 | ||||||
chr4:75883870
|
G | A | 157 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0024others(154): Show | 158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.747-668C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883870 | ||||||
chr4:75883889
|
G | A | 156 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0024others(153): Show | 157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.747-687C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883889 | ||||||
chr4:75883895
|
T | C | 227 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(224): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.747-693A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883895 | ||||||
chr4:75883938
|
T | A | 1 | a0001c0001t0001g0144 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.746+656A>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883938 | ||||||
chr4:75883940
|
A | G | 226 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.746+654T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883940 | ||||||
chr4:75884114
|
G | C | 48 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(45): Show | 49 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.746+480C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75884114 | ||||||
chr4:75884312
|
T | C | 233 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(230): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.746+282A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75884312 | ||||||
chr4:75884424
|
C | CA | 151 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(148): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.746+169dupT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75884424 | ||||||
chr4:75884424
|
C | CAA | 78 | a0001c0001t0001g0021a0001c0001t0001g0058a0001c0001t0001g0060others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.746+168_746+169dup others(2): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75884424 | ||||||
chr4:75884438
|
AT | A | 5 | a0006c0007t0003g0204a0006c0007t0003g0205a0006c0007t0003g0207others(2): Show | 5 | HG02145.hp2 HG02809.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.746+155delA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75884438 | ||||||
chr4:75884439
|
T | A | 3 | a0001c0002t0001g0003a0001c0002t0001g0218a0015c0014t0001g0217 | 4 | HG01891.hp1 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.746+155A>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75884439 | ||||||
chr4:75884532
|
A | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG00673.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.746+62T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75884532 | ||||||
chr4:75884539
|
A | G | 233 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(230): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.746+55T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75884539 | ||||||
chr4:75884566
|
A | G | 3 | a0001c0015t0001g0055a0002c0011t0001g0054a0002c0011t0001g0056 | 3 | HG02258.hp2 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.746+28T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75884566 | ||||||
chr4:75884592
|
A | G | 5 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(2): Show | 5 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(2): Show |
splice_donor_variant&intron_variant | HIGH | c.746+2T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75884592 | ||||||
chr4:75884809
|
G | A | 233 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(230): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.580-49C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75884809 | ||||||
chr4:75884825
|
C | T | 233 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(230): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.580-65G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75884825 | ||||||
chr4:75885141
|
G | A | 1 | a0001c0002t0002g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.580-381C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75885141 | ||||||
chr4:75885478
|
T | G | 233 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(230): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.580-718A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75885478 | ||||||
chr4:75885693
|
G | A | 8 | a0001c0001t0001g0081a0001c0001t0001g0179a0001c0001t0001g0180others(5): Show | 8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.580-933C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75885693 | ||||||
chr4:75885701
|
AAAAAATA others(32): Show |
A | 1 | a0001c0001t0001g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.580-980_580-942del others(39): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75885701 | ||||||
chr4:75885737
|
G | A | 1 | a0005c0006t0001g0235 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.580-977C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75885737 | ||||||
chr4:75885739
|
G | A | 232 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(229): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.580-979C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75885739 | ||||||
chr4:75885802
|
A | G | 233 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(230): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.580-1042T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75885802 | ||||||
chr4:75885862
|
A | G | 3 | a0001c0002t0001g0211a0001c0002t0001g0212a0002c0008t0001g0213 | 3 | HG01261.hp1 HG01975.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.579+990T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75885862 | ||||||
chr4:75886009
|
T | TA | 203 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(200): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.579+842dupT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886009 | ||||||
chr4:75886009
|
T | TAA | 14 | a0001c0001t0001g0141a0001c0001t0001g0222a0001c0001t0001g0223others(11): Show | 14 | HG01175.hp2 HG01243.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.579+841_579+842dup others(2): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886009 | ||||||
chr4:75886011
|
A | AG | 20 | a0003c0003t0001g0254a0003c0003t0001g0266a0003c0003t0002g0004others(17): Show | 21 | HG01081.hp2 HG01167.hp2 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.579+840_579+841ins others(1): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886011 | ||||||
chr4:75886054
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.579+798G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886054 | ||||||
chr4:75886265
|
A | G | 5 | a0006c0007t0003g0204a0006c0007t0003g0205a0006c0007t0003g0207others(2): Show | 5 | HG02145.hp2 HG02809.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+587T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886265 | ||||||
chr4:75886308
|
A | C | 1 | a0001c0001t0001g0149 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.579+544T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886308 | ||||||
chr4:75886336
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.579+516G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886336 | ||||||
chr4:75886389
|
G | T | 1 | a0001c0001t0001g0051 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.579+463C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886389 | ||||||
chr4:75886446
|
T | G | 1 | a0001c0001t0001g0069 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.579+406A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886446 | ||||||
chr4:75886557
|
T | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0068a0001c0001t0001g0082others(2): Show | 6 | HG00323.hp1 HG00741.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.579+295A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886557 | ||||||
chr4:75886614
|
G | A | 3 | a0001c0002t0001g0211a0001c0002t0001g0212a0002c0008t0001g0213 | 3 | HG01261.hp1 HG01975.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.579+238C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886614 | ||||||
chr4:75886711
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.579+141G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886711 | ||||||
chr4:75886715
|
CA | C | 3 | a0001c0002t0001g0211a0001c0002t0001g0212a0002c0008t0001g0213 | 3 | HG01261.hp1 HG01975.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.579+136delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886715 | ||||||
chr4:75886742
|
A | T | 6 | a0001c0015t0001g0055a0001c0016t0008g0260a0002c0011t0001g0054others(3): Show | 6 | HG01243.hp2 HG02258.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.579+110T>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886742 | ||||||
chr4:75886925
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.533-27T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75886925 | ||||||
chr4:75886980
|
C | G | 13 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(10): Show | 13 | HG01175.hp2 HG01243.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.533-82G>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75886980 | ||||||
chr4:75887011
|
G | T | 1 | a0002c0008t0001g0213 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.533-113C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887011 | ||||||
chr4:75887063
|
T | C | 3 | a0001c0002t0001g0211a0001c0002t0001g0212a0002c0008t0001g0213 | 3 | HG01261.hp1 HG01975.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.533-165A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887063 | ||||||
chr4:75887100
|
G | T | 1 | a0004c0005t0003g0016 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.533-202C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887100 | ||||||
chr4:75887149
|
C | T | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.533-251G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887149 | ||||||
chr4:75887150
|
G | A | 1 | a0014c0022t0001g0185 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.533-252C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887150 | ||||||
chr4:75887157
|
T | C | 236 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(233): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.533-259A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887157 | ||||||
chr4:75887234
|
G | A | 233 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(230): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.533-336C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887234 | ||||||
chr4:75887351
|
G | T | 5 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02895.hp2 HG02896.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.533-453C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887351 | ||||||
chr4:75887437
|
C | T | 3 | a0001c0002t0001g0211a0001c0002t0001g0212a0002c0008t0001g0213 | 3 | HG01261.hp1 HG01975.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.533-539G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887437 | ||||||
chr4:75887477
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.533-579G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887477 | ||||||
chr4:75887516
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.533-618C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887516 | ||||||
chr4:75887620
|
CA | C | 66 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(63): Show | 68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.532+593delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887620 | ||||||
chr4:75887620
|
CAA | C | 148 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0024others(145): Show | 149 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.532+592_532+593del others(2): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887620 | ||||||
chr4:75887620
|
CAAA | C | 13 | a0001c0001t0001g0107a0001c0001t0001g0146a0001c0001t0001g0147others(10): Show | 13 | HG01069.hp1 HG01175.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.532+591_532+593del others(3): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887620 | ||||||
chr4:75887921
|
T | C | 50 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(47): Show | 51 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.532+293A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887921 | ||||||
chr4:75887926
|
T | G | 1 | a0001c0001t0001g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.532+288A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887926 | ||||||
chr4:75888067
|
G | A | 5 | a0006c0007t0003g0204a0006c0007t0003g0205a0006c0007t0003g0207others(2): Show | 5 | HG02145.hp2 HG02809.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.532+147C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75888067 | ||||||
chr4:75888089
|
T | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0196 | 2 | HG02015.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.532+125A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75888089 | ||||||
chr4:75888166
|
A | G | 236 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(233): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.532+48T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75888166 | ||||||
chr4:75888416
|
C | T | 72 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.418-88G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75888416 | ||||||
chr4:75888464
|
A | G | 6 | a0001c0001t0001g0106a0006c0007t0003g0204a0006c0007t0003g0205others(3): Show | 6 | HG02145.hp2 HG02809.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.418-136T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75888464 | ||||||
chr4:75888724
|
G | C | 1 | a0009c0012t0001g0086 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.418-396C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75888724 | ||||||
chr4:75888726
|
G | A | 1 | a0004c0005t0003g0016 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.418-398C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75888726 | ||||||
chr4:75888875
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.418-547G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75888875 | ||||||
chr4:75888961
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.418-633G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75888961 | ||||||
chr4:75888965
|
A | G | 5 | a0006c0007t0003g0204a0006c0007t0003g0205a0006c0007t0003g0207others(2): Show | 5 | HG02145.hp2 HG02809.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.418-637T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75888965 | ||||||
chr4:75888977
|
T | C | 236 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(233): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.418-649A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75888977 | ||||||
chr4:75889046
|
C | T | 152 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0059others(149): Show | 153 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.418-718G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889046 | ||||||
chr4:75889068
|
C | T | 2 | a0003c0003t0002g0004a0003c0003t0002g0252 | 3 | HG01081.hp2 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.418-740G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889068 | ||||||
chr4:75889111
|
G | C | 241 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(238): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.418-783C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889111 | ||||||
chr4:75889161
|
G | A | 52 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(49): Show | 53 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.417+796C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889161 | ||||||
chr4:75889198
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.417+759G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889198 | ||||||
chr4:75889428
|
C | T | 10 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(7): Show | 10 | HG00280.hp1 HG01070.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.417+529G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889428 | ||||||
chr4:75889519
|
A | C | 13 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(10): Show | 13 | HG01175.hp2 HG01243.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.417+438T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889519 | ||||||
chr4:75889553
|
G | T | 15 | a0001c0002t0001g0237a0001c0002t0002g0230a0001c0002t0002g0231others(12): Show | 15 | HG01255.hp2 HG01496.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.417+404C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889553 | ||||||
chr4:75889619
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.417+338A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889619 | ||||||
chr4:75889621
|
G | C | 15 | a0001c0002t0001g0237a0001c0002t0002g0230a0001c0002t0002g0231others(12): Show | 15 | HG01255.hp2 HG01496.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.417+336C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889621 | ||||||
chr4:75889628
|
A | G | 52 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(49): Show | 53 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.417+329T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889628 | ||||||
chr4:75889672
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.417+285T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889672 | ||||||
chr4:75889703
|
C | A | 68 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(65): Show | 70 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.417+254G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889703 | ||||||
chr4:75889732
|
G | T | 1 | a0001c0001t0002g0025 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.417+225C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889732 | ||||||
chr4:75889787
|
T | C | 241 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(238): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.417+170A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889787 | ||||||
chr4:75889874
|
G | C | 1 | a0001c0001t0001g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.417+83C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889874 | ||||||
chr4:75889913
|
T | G | 1 | a0001c0001t0001g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.417+44A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889913 | ||||||
chr4:75890218
|
C | T | 2 | a0001c0001t0002g0100a0001c0001t0002g0101 | 2 | HG02735.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.242-86G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75890218 | ||||||
chr4:75890470
|
T | C | 32 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(29): Show | 33 | HG01081.hp2 HG01167.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.242-338A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75890470 | ||||||
chr4:75890475
|
T | C | 32 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(29): Show | 33 | HG01081.hp2 HG01167.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.242-343A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75890475 | ||||||
chr4:75890481
|
C | T | 32 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(29): Show | 33 | HG01081.hp2 HG01167.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.242-349G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75890481 | ||||||
chr4:75890483
|
T | C | 32 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(29): Show | 33 | HG01081.hp2 HG01167.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.242-351A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75890483 | ||||||
chr4:75890488
|
C | CAAAAAA | 10 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(7): Show | 10 | HG02055.hp1 HG02280.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.242-362_242-357dup others(6): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75890488 | ||||||
chr4:75890488
|
C | CAAAAAAA | 18 | a0003c0003t0001g0254a0003c0003t0001g0266a0003c0003t0002g0004others(15): Show | 19 | HG01081.hp2 HG01167.hp2 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.242-363_242-357dup others(7): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75890488 | ||||||
chr4:75890488
|
CA | C | 197 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(194): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.242-357delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75890488 | ||||||
chr4:75890608
|
A | C | 1 | a0001c0001t0001g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.242-476T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75890608 | ||||||
chr4:75890657
|
A | C | 4 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(1): Show | 4 | HG00423.hp1 NA18971.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.242-525T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75890657 | ||||||
chr4:75890878
|
T | C | 19 | a0003c0003t0001g0254a0003c0003t0001g0266a0003c0003t0002g0004others(16): Show | 20 | HG01081.hp2 HG01167.hp2 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.242-746A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75890878 | ||||||
chr4:75890882
|
A | G | 1 | a0001c0001t0002g0017 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.242-750T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75890882 | ||||||
chr4:75891043
|
G | A | 151 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0059others(148): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.241+605C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891043 | ||||||
chr4:75891081
|
A | G | 49 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(46): Show | 50 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.241+567T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891081 | ||||||
chr4:75891134
|
T | G | 1 | a0001c0001t0001g0187 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.241+514A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891134 | ||||||
chr4:75891152
|
G | T | 6 | a0002c0004t0003g0210a0006c0007t0003g0204a0006c0007t0003g0205others(3): Show | 6 | HG02145.hp2 HG02809.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.241+496C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891152 | ||||||
chr4:75891168
|
G | A | 17 | a0001c0002t0001g0003a0001c0002t0001g0218a0001c0002t0001g0237others(14): Show | 18 | HG01255.hp2 HG01496.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.241+480C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891168 | ||||||
chr4:75891180
|
C | CA | 44 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(41): Show | 45 | HG01081.hp2 HG01167.hp2 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.241+467dupT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891180 | ||||||
chr4:75891188
|
AAAAAGAA others(3): Show |
A | 1 | a0001c0001t0002g0014 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.241+450_241+459del others(10): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891188 | ||||||
chr4:75891222
|
C | T | 1 | a0002c0004t0003g0261 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.241+426G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891222 | ||||||
chr4:75891250
|
G | T | 3 | a0001c0002t0001g0211a0001c0002t0001g0212a0002c0008t0001g0213 | 3 | HG01261.hp1 HG01975.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.241+398C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891250 | ||||||
chr4:75891279
|
A | G | 3 | a0001c0002t0001g0211a0001c0002t0001g0212a0002c0008t0001g0213 | 3 | HG01261.hp1 HG01975.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.241+369T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891279 | ||||||
chr4:75891331
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.241+317G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891331 | ||||||
chr4:75891347
|
C | T | 1 | a0004c0005t0003g0016 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.241+301G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891347 | ||||||
chr4:75891520
|
C | G | 218 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.241+128G>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891520 | ||||||
chr4:75891526
|
C | G | 1 | a0001c0001t0001g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.241+122G>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891526 | ||||||
chr4:75891611
|
C | T | 1 | a0002c0004t0001g0095 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.241+37G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891611 | ||||||
chr4:75891617
|
GA | G | 8 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(5): Show | 8 | HG01070.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.241+30delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891617 | ||||||
chr4:75891711
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG01975.hp2 | splice_region_variant&intron_variant | LOW | c.184-6C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 3/16 | chr4 | 75891711 | ||||||
chr4:75891797
|
G | A | 1 | a0005c0017t0001g0189 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.183+54C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 3/16 | chr4 | 75891797 | ||||||
chr4:75892087
|
C | G | 1 | a0001c0001t0001g0085 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.56-109G>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75892087 | ||||||
chr4:75892112
|
T | C | 6 | a0002c0004t0003g0210a0006c0007t0003g0204a0006c0007t0003g0205others(3): Show | 6 | HG02145.hp2 HG02809.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.56-134A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75892112 | ||||||
chr4:75892353
|
G | A | 1 | a0005c0018t0005g0229 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.56-375C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75892353 | ||||||
chr4:75892503
|
A | C | 1 | a0001c0001t0001g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.56-525T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75892503 | ||||||
chr4:75892519
|
G | A | 19 | a0003c0003t0001g0254a0003c0003t0001g0266a0003c0003t0002g0004others(16): Show | 20 | HG01081.hp2 HG01167.hp2 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.56-541C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75892519 | ||||||
chr4:75892532
|
GA | G | 6 | a0002c0004t0003g0210a0006c0007t0003g0204a0006c0007t0003g0205others(3): Show | 6 | HG02145.hp2 HG02809.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.56-555delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75892532 | ||||||
chr4:75892641
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.56-663G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75892641 | ||||||
chr4:75892703
|
T | C | 18 | a0001c0002t0001g0003a0001c0002t0001g0218a0001c0002t0001g0237others(15): Show | 19 | HG01255.hp2 HG01496.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.56-725A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75892703 | ||||||
chr4:75892742
|
G | C | 2 | a0002c0004t0006g0263a0002c0004t0006g0264 | 2 | HG01175.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.56-764C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75892742 | ||||||
chr4:75892894
|
AGCTGGAT others(14): Show |
A | 1 | a0001c0001t0001g0190 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.56-937_56-917delCT others(19): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75892894 | ||||||
chr4:75892973
|
T | G | 3 | a0001c0002t0001g0211a0001c0002t0001g0212a0002c0008t0001g0213 | 3 | HG01261.hp1 HG01975.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.56-995A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75892973 | ||||||
chr4:75892989
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.56-1011C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75892989 | ||||||
chr4:75893001
|
C | T | 15 | a0001c0002t0001g0237a0001c0002t0002g0230a0001c0002t0002g0231others(12): Show | 15 | HG01255.hp2 HG01496.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.56-1023G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893001 | ||||||
chr4:75893078
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.56-1100A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893078 | ||||||
chr4:75893223
|
C | T | 1 | a0008c0010t0001g0208 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.56-1245G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893223 | ||||||
chr4:75893251
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.56-1273T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893251 | ||||||
chr4:75893252
|
C | T | 3 | a0001c0002t0001g0003a0001c0002t0001g0218a0015c0014t0001g0217 | 4 | HG01891.hp1 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-1274G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893252 | ||||||
chr4:75893281
|
T | C | 33 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(30): Show | 34 | HG01081.hp2 HG01167.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.56-1303A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893281 | ||||||
chr4:75893296
|
A | G | 157 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0059others(154): Show | 158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.56-1318T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893296 | ||||||
chr4:75893314
|
A | G | 33 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(30): Show | 34 | HG01081.hp2 HG01167.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.56-1336T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893314 | ||||||
chr4:75893352
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024 | 3 | HG02622.hp1 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.56-1374C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893352 | ||||||
chr4:75893433
|
G | T | 1 | a0001c0001t0001g0083 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.56-1455C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893433 | ||||||
chr4:75893487
|
G | GAC | 171 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0059others(168): Show | 172 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.56-1511_56-1510dup others(2): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893487 | ||||||
chr4:75893487
|
G | GACACAC | 51 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(48): Show | 52 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.56-1515_56-1510dup others(6): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893487 | ||||||
chr4:75893487
|
GAC | G | 3 | a0001c0002t0001g0211a0001c0002t0001g0212a0002c0008t0001g0213 | 3 | HG01261.hp1 HG01975.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.56-1511_56-1510del others(2): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893487 | ||||||
chr4:75893505
|
C | CAT | 18 | a0001c0002t0001g0003a0001c0002t0001g0218a0001c0002t0001g0237others(15): Show | 19 | HG01255.hp2 HG01496.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.56-1528_56-1527ins others(2): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893505 | ||||||
chr4:75893510
|
T | A | 1 | a0001c0001t0001g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.56-1532A>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893510 | ||||||
chr4:75893512
|
A | T | 1 | a0001c0001t0001g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.56-1534T>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893512 | ||||||
chr4:75893540
|
G | A | 3 | a0001c0015t0001g0055a0002c0011t0001g0054a0002c0011t0001g0056 | 3 | HG02258.hp2 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.56-1562C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893540 | ||||||
chr4:75893684
|
C | T | 19 | a0003c0003t0001g0254a0003c0003t0001g0266a0003c0003t0002g0004others(16): Show | 20 | HG01081.hp2 HG01167.hp2 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.56-1706G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893684 | ||||||
chr4:75893831
|
G | GCAGCAGA others(12): Show |
5 | a0001c0015t0001g0055a0002c0011t0001g0054a0002c0011t0001g0056others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-1872_56-1854dup others(19): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893831 | ||||||
chr4:75893861
|
C | CTTTTTTT others(2): Show |
151 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0059others(148): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.56-1884_56-1883ins others(9): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893861 | ||||||
chr4:75893862
|
C | T | 151 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0059others(148): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.56-1884G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893862 | ||||||
chr4:75893880
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0068 | 3 | HG01109.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.56-1902G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893880 | ||||||
chr4:75893882
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.56-1904C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893882 | ||||||
chr4:75893966
|
C | G | 1 | a0001c0001t0001g0082 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.56-1988G>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893966 | ||||||
chr4:75894373
|
TAGAG | T | 4 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0007others(1): Show | 5 | HG00099.hp2 HG00323.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+1894_55+1897del others(4): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75894373 | ||||||
chr4:75894388
|
C | T | 3 | a0001c0002t0001g0211a0001c0002t0001g0212a0002c0008t0001g0213 | 3 | HG01261.hp1 HG01975.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.55+1883G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75894388 | ||||||
chr4:75894641
|
C | A | 1 | a0003c0003t0001g0266 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.55+1630G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75894641 | ||||||
chr4:75894648
|
G | A | 15 | a0001c0002t0001g0237a0001c0002t0002g0230a0001c0002t0002g0231others(12): Show | 15 | HG01255.hp2 HG01496.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.55+1623C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75894648 | ||||||
chr4:75894990
|
G | A | 30 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(27): Show | 31 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.55+1281C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75894990 | ||||||
chr4:75895127
|
A | AT | 9 | a0001c0001t0002g0067a0001c0001t0003g0221a0002c0004t0003g0210others(6): Show | 9 | HG02055.hp2 HG02257.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.55+1143dupA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895127 | ||||||
chr4:75895127
|
A | ATT | 5 | a0004c0005t0003g0246a0004c0005t0003g0247a0004c0005t0003g0248others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.55+1142_55+1143dup others(2): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895127 | ||||||
chr4:75895127
|
A | ATTT | 44 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(41): Show | 45 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.55+1141_55+1143dup others(3): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895127 | ||||||
chr4:75895127
|
AT | A | 144 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0059others(141): Show | 146 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.55+1143delA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895127 | ||||||
chr4:75895230
|
C | T | 5 | a0001c0016t0008g0260a0002c0004t0003g0261a0002c0004t0003g0262others(2): Show | 5 | HG01175.hp2 HG01243.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+1041G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895230 | ||||||
chr4:75895257
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.55+1014C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895257 | ||||||
chr4:75895301
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.55+970G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895301 | ||||||
chr4:75895336
|
G | A | 4 | a0001c0001t0001g0059a0001c0001t0001g0192a0001c0001t0001g0193others(1): Show | 4 | HG02040.hp1 HG02071.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+935C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895336 | ||||||
chr4:75895343
|
C | T | 17 | a0003c0003t0001g0254a0003c0003t0002g0004a0003c0003t0002g0245others(14): Show | 18 | HG01081.hp2 HG01167.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.55+928G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895343 | ||||||
chr4:75895444
|
T | A | 19 | a0003c0003t0001g0254a0003c0003t0001g0266a0003c0003t0002g0004others(16): Show | 20 | HG01081.hp2 HG01167.hp2 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.55+827A>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895444 | ||||||
chr4:75895470
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.55+801G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895470 | ||||||
chr4:75895485
|
C | A | 3 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037 | 3 | NA18951.hp1 NA18965.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.55+786G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895485 | ||||||
chr4:75895498
|
C | T | 49 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(46): Show | 50 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.55+773G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895498 | ||||||
chr4:75895601
|
G | A | 6 | a0001c0002t0001g0211a0001c0002t0001g0212a0001c0002t0002g0243others(3): Show | 6 | HG01261.hp1 HG01975.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.55+670C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895601 | ||||||
chr4:75895605
|
G | T | 4 | a0002c0004t0003g0261a0002c0004t0003g0262a0002c0004t0006g0263others(1): Show | 4 | HG01175.hp2 HG01243.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+666C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895605 | ||||||
chr4:75895728
|
C | T | 106 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(103): Show | 109 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.55+543G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895728 | ||||||
chr4:75895731
|
C | CA | 39 | a0001c0001t0001g0195a0001c0001t0001g0222a0001c0001t0001g0223others(36): Show | 40 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.55+539dupT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895731 | ||||||
chr4:75895743
|
A | AT | 19 | a0003c0003t0001g0254a0003c0003t0001g0266a0003c0003t0002g0004others(16): Show | 20 | HG01081.hp2 HG01167.hp2 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.55+527dupA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895743 | ||||||
chr4:75895743
|
A | T | 1 | a0001c0001t0001g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.55+528T>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895743 | ||||||
chr4:75895839
|
G | T | 15 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(12): Show | 15 | HG01175.hp2 HG01243.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.55+432C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895839 | ||||||
chr4:75895884
|
T | TA | 23 | a0003c0003t0001g0254a0003c0003t0001g0266a0003c0003t0002g0004others(20): Show | 24 | HG01081.hp2 HG01167.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.55+386dupT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895884 | ||||||
chr4:75895912
|
A | T | 1 | a0001c0001t0001g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.55+359T>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895912 | ||||||
chr4:75895918
|
A | T | 1 | a0001c0001t0002g0017 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.55+353T>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895918 | ||||||
chr4:75896068
|
T | C | 57 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(54): Show | 59 | HG01081.hp2 HG01167.hp2 HG01175.hp2 others(56): Show |
intron_variant | MODIFIER | c.55+203A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75896068 | ||||||
chr4:75896259
|
G | A | 49 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(46): Show | 50 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.55+12C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75896259 | ||||||
chr4:75896267
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02071.hp2 | splice_region_variant&intron_variant | LOW | c.55+4C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75896267 | ||||||
chr4:75896710
|
A | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0059others(151): Show | 155 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-58-327T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75896710 | ||||||
chr4:75896868
|
CA | C | 207 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(204): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.-58-486delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75896868 | ||||||
chr4:75896869
|
A | T | 1 | a0001c0015t0001g0055 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-58-486T>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75896869 | ||||||
chr4:75896870
|
C | A | 1 | a0001c0015t0001g0055 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-58-487G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75896870 | ||||||
chr4:75896870
|
C | T | 207 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(204): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.-58-487G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75896870 | ||||||
chr4:75896871
|
A | C | 1 | a0001c0015t0001g0055 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-58-488T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75896871 | ||||||
chr4:75896875
|
T | A | 1 | a0001c0001t0002g0042 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-58-492A>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75896875 | ||||||
chr4:75896876
|
T | C | 1 | a0001c0001t0002g0042 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-58-493A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75896876 | ||||||
chr4:75896897
|
T | C | 21 | a0001c0002t0001g0211a0001c0002t0001g0212a0002c0008t0001g0213others(18): Show | 22 | HG01081.hp2 HG01167.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.-58-514A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75896897 | ||||||
chr4:75897010
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-58-627G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75897010 | ||||||
chr4:75897172
|
A | G | 1 | a0005c0006t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-58-789T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75897172 | ||||||
chr4:75897214
|
A | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.-58-831T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75897214 | ||||||
chr4:75897293
|
A | G | 1 | a0002c0011t0001g0054 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-58-910T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75897293 | ||||||
chr4:75897500
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-58-1117A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75897500 | ||||||
chr4:75897729
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-58-1346C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75897729 | ||||||
chr4:75897797
|
A | G | 1 | a0016c0013t0001g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-58-1414T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75897797 | ||||||
chr4:75897822
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-58-1439G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75897822 | ||||||
chr4:75897880
|
A | G | 49 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(46): Show | 50 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.-58-1497T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75897880 | ||||||
chr4:75897887
|
G | C | 1 | a0001c0001t0002g0219 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-58-1504C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75897887 | ||||||
chr4:75897946
|
C | A | 1 | a0001c0001t0002g0015 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-58-1563G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75897946 | ||||||
chr4:75897976
|
C | A | 209 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.-58-1593G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75897976 | ||||||
chr4:75898015
|
G | A | 49 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(46): Show | 50 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.-58-1632C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898015 | ||||||
chr4:75898073
|
G | A | 18 | a0003c0003t0001g0254a0003c0003t0001g0266a0003c0003t0002g0004others(15): Show | 19 | HG01081.hp2 HG01167.hp2 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.-58-1690C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898073 | ||||||
chr4:75898257
|
G | A | 1 | a0001c0001t0002g0197 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-58-1874C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898257 | ||||||
chr4:75898297
|
T | G | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | NA19000.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.-58-1914A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898297 | ||||||
chr4:75898301
|
C | T | 209 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.-58-1918G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898301 | ||||||
chr4:75898332
|
T | C | 212 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(209): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.-58-1949A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898332 | ||||||
chr4:75898346
|
C | T | 49 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(46): Show | 50 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.-58-1963G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898346 | ||||||
chr4:75898534
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-58-2151C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898534 | ||||||
chr4:75898664
|
T | C | 5 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0040others(2): Show | 5 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58-2281A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898664 | ||||||
chr4:75898721
|
T | A | 1 | a0003c0003t0001g0266 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-58-2338A>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898721 | ||||||
chr4:75898761
|
G | C | 1 | a0001c0001t0001g0202 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-58-2378C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898761 | ||||||
chr4:75898857
|
T | G | 1 | a0001c0016t0008g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-58-2474A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898857 | ||||||
chr4:75898921
|
G | T | 1 | a0001c0001t0001g0062 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-58-2538C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898921 | ||||||
chr4:75899145
|
A | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG00438.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.-58-2762T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75899145 | ||||||
chr4:75899309
|
A | G | 4 | a0001c0001t0002g0219a0001c0002t0001g0003a0001c0002t0001g0218others(1): Show | 5 | HG01891.hp1 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-59+2921T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75899309 | ||||||
chr4:75899392
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG02129.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-59+2838G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75899392 | ||||||
chr4:75899499
|
C | T | 1 | a0012c0021t0001g0057 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-59+2731G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75899499 | ||||||
chr4:75899512
|
TC | T | 3 | a0001c0002t0001g0211a0001c0002t0001g0212a0002c0008t0001g0213 | 3 | HG01261.hp1 HG01975.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-59+2717delG | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75899512 | ||||||
chr4:75899589
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-59+2641A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75899589 | ||||||
chr4:75899780
|
C | T | 157 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0059others(154): Show | 158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-59+2450G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75899780 | ||||||
chr4:75899781
|
A | G | 157 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0059others(154): Show | 158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-59+2449T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75899781 | ||||||
chr4:75899782
|
A | ATGGC | 157 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0059others(154): Show | 158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-59+2447_-59+2448i others(6): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75899782 | ||||||
chr4:75899783
|
C | T | 157 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0059others(154): Show | 158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-59+2447G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75899783 | ||||||
chr4:75900941
|
G | A | 264 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(261): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.-59+1289C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75900941 | ||||||
chr4:75901222
|
A | G | 3 | a0001c0015t0001g0055a0002c0011t0001g0054a0002c0011t0001g0056 | 3 | HG02258.hp2 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-59+1008T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75901222 | ||||||
chr4:75901445
|
T | C | 5 | a0002c0004t0003g0261a0002c0004t0003g0262a0002c0004t0006g0263others(2): Show | 5 | HG01175.hp2 HG01243.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-59+785A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75901445 | ||||||
chr4:75901520
|
C | CA | 9 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(6): Show | 9 | HG02280.hp1 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-59+709dupT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75901520 | ||||||
chr4:75901520
|
CA | C | 157 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0059others(154): Show | 158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-59+709delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75901520 | ||||||
chr4:75901595
|
T | G | 49 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(46): Show | 50 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.-59+635A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75901595 | ||||||
chr4:75901618
|
C | T | 12 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0007others(9): Show | 13 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.-59+612G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75901618 | ||||||
chr4:75901738
|
G | A | 1 | a0003c0003t0001g0266 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-59+492C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75901738 | ||||||
chr4:75901970
|
T | G | 2 | a0001c0001t0001g0051a0002c0004t0003g0052 | 2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-59+260A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75901970 | ||||||
chr4:75901981
|
T | C | 265 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(262): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.-59+249A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75901981 | ||||||
chr4:75902072
|
A | G | 49 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(46): Show | 50 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.-59+158T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75902072 |