geneid | 51588 |
---|---|
ensemblid | ENSG00000105229.7 |
hgncid | 17002 |
symbol | PIAS4 |
name | protein inhibitor of activated STAT 4 |
refseq_nuc | NM_015897.4 |
refseq_prot | NP_056981.2 |
ensembl_nuc | ENST00000262971.3 |
ensembl_prot | ENSP00000262971.1 |
mane_status | MANE Select |
chr | chr19 |
start | 4007736 |
end | 4039386 |
strand | + |
ver | v1.2 |
region | chr19:4007736-4039386 |
region5000 | chr19:4002736-4044386 |
regionname0 | PIAS4_chr19_4007736_4039386 |
regionname5000 | PIAS4_chr19_4002736_4044386 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 510 | 328 | 90 | 74 | 100 | 18 | 44 | 56 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0002 | 0/0 | 510 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0003 | 0/0 | 510 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0004 | 0/0 | 510 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
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 | 1533 | 173 | 11 | 49 | 75 | 11 | 26 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
c0002 | 0/0 | 1533 | 39 | 23 | 6 | 7 | 1 | 2 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
c0003 | 0/0 | 1533 | 28 | 6 | 8 | 5 | 5 | 4 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
c0004 | 0/0 | 1533 | 27 | 27 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
c0005 | 0/0 | 1533 | 23 | 8 | 4 | 2 | 0 | 9 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
c0006 | 0/0 | 1533 | 12 | 12 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
c0007 | 0/0 | 1533 | 9 | 0 | 6 | 0 | 1 | 2 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
c0008 | 1/0 | 1533 | 6 | 1 | 0 | 3 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
c0009 | 0/0 | 1533 | 5 | 0 | 0 | 5 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
c0010 | 0/0 | 1533 | 2 | 0 | 0 | 0 | 0 | 2 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
c0011 | 0/0 | 1533 | 2 | 2 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
c0012 | 0/0 | 1533 | 2 | 1 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
c0013 | 0/0 | 1533 | 2 | 0 | 2 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
c0014 | 0/0 | 1533 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
c0015 | 0/0 | 1533 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
c0016 | 0/0 | 1533 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
c0017 | 0/0 | 1533 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1537 | 209 | 27 | 58 | 83 | 13 | 27 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
t0002 | 0/0 | 1535 | 27 | 2 | 10 | 3 | 4 | 8 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
t0003 | 0/0 | 1535 | 26 | 24 | 2 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
t0004 | 0/0 | 1535 | 24 | 24 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
t0005 | 1/0 | 1537 | 18 | 0 | 1 | 7 | 0 | 9 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
t0006 | 0/0 | 1535 | 5 | 3 | 0 | 2 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
t0007 | 0/0 | 1537 | 3 | 0 | 2 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
t0008 | 0/0 | 1535 | 3 | 3 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
t0009 | 0/0 | 1537 | 2 | 0 | 2 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
t0010 | 0/0 | 1537 | 2 | 0 | 0 | 2 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
t0011 | 0/0 | 1535 | 2 | 2 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
t0012 | 0/0 | 1535 | 2 | 2 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
t0013 | 0/0 | 1537 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
t0014 | 0/0 | 1537 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
t0015 | 0/0 | 1537 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
t0016 | 0/0 | 1537 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
t0017 | 0/0 | 1537 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
t0018 | 0/0 | 1537 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
t0019 | 0/0 | 1537 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
t0020 | 0/0 | 1535 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
t0021 | 0/0 | 1537 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
t0022 | 0/0 | 1537 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
t0023 | 0/0 | 1537 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0067 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0149 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
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 | 1533 | 173 | 11 | 49 | 75 | 11 | 26 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0002 | 0/0 | 1533 | 39 | 23 | 6 | 7 | 1 | 2 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0003 | 0/0 | 1533 | 28 | 6 | 8 | 5 | 5 | 4 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0004 | 0/0 | 1533 | 27 | 27 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0005 | 0/0 | 1533 | 23 | 8 | 4 | 2 | 0 | 9 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0006 | 0/0 | 1533 | 12 | 12 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0007 | 0/0 | 1533 | 9 | 0 | 6 | 0 | 1 | 2 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0008 | 1/0 | 1533 | 6 | 1 | 0 | 3 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0009 | 0/0 | 1533 | 5 | 0 | 0 | 5 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0012 | 0/0 | 1533 | 2 | 1 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0014 | 0/0 | 1533 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0015 | 0/0 | 1533 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0016 | 0/0 | 1533 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0017 | 0/0 | 1533 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0002c0010 | 0/0 | 1533 | 2 | 0 | 0 | 0 | 0 | 2 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0003c0011 | 0/0 | 1533 | 2 | 2 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0004c0013 | 0/0 | 1533 | 2 | 0 | 2 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3069 | 164 | 10 | 47 | 71 | 10 | 25 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0001t0009 | 0/0 | 3069 | 2 | 0 | 2 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0001t0010 | 0/0 | 3069 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0001t0013 | 0/0 | 3069 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0001t0014 | 0/0 | 3069 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0001t0016 | 0/0 | 3069 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0001t0019 | 0/0 | 3069 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0001t0021 | 0/0 | 3069 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0001t0022 | 0/0 | 3069 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0002t0001 | 0/0 | 3069 | 16 | 5 | 5 | 5 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0002t0002 | 0/0 | 3067 | 3 | 0 | 0 | 1 | 0 | 2 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0002t0003 | 0/0 | 3067 | 4 | 3 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0002t0004 | 0/0 | 3067 | 11 | 11 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0002t0006 | 0/0 | 3067 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0002t0008 | 0/0 | 3067 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0002t0010 | 0/0 | 3069 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0002t0018 | 0/0 | 3069 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0002t0020 | 0/0 | 3067 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0003t0001 | 0/0 | 3069 | 4 | 0 | 2 | 1 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0003t0002 | 0/0 | 3067 | 17 | 2 | 5 | 2 | 4 | 4 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0003t0003 | 0/0 | 3067 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0003t0004 | 0/0 | 3067 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0003t0006 | 0/0 | 3067 | 4 | 2 | 0 | 2 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0003t0015 | 0/0 | 3069 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0004t0003 | 0/0 | 3067 | 20 | 20 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0004t0004 | 0/0 | 3067 | 2 | 2 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0004t0008 | 0/0 | 3067 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0004t0011 | 0/0 | 3067 | 2 | 2 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0004t0012 | 0/0 | 3067 | 2 | 2 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0005t0001 | 0/0 | 3069 | 7 | 7 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0005t0005 | 0/0 | 3069 | 11 | 0 | 1 | 2 | 0 | 8 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0005t0007 | 0/0 | 3069 | 3 | 0 | 2 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0005t0017 | 0/0 | 3069 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0005t0023 | 0/0 | 3069 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0006t0003 | 0/0 | 3067 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0006t0004 | 0/0 | 3067 | 10 | 10 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0006t0008 | 0/0 | 3067 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0007t0001 | 0/0 | 3069 | 4 | 0 | 1 | 0 | 1 | 2 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0007t0002 | 0/0 | 3067 | 5 | 0 | 5 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0008t0001 | 0/0 | 3069 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0008t0005 | 1/0 | 3069 | 5 | 0 | 0 | 3 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0009t0001 | 0/0 | 3069 | 5 | 0 | 0 | 5 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0012t0001 | 0/0 | 3069 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0012t0005 | 0/0 | 3069 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0014t0001 | 0/0 | 3069 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0015t0005 | 0/0 | 3069 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0016t0001 | 0/0 | 3069 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0001c0017t0001 | 0/0 | 3069 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0002c0010t0002 | 0/0 | 3067 | 2 | 0 | 0 | 0 | 0 | 2 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0003c0011t0001 | 0/0 | 3069 | 2 | 2 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
a0004c0013t0001 | 0/0 | 3069 | 2 | 0 | 2 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | copy fasta | chr19 | 4002736 | 4044386 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0149 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0009g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0009g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0010g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0013g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0014g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0016g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0019g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0021g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0001t0022g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0008g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0010g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0018g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0002t0020g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0002g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0002g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0006g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0006g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0006g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0006g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0003t0015g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0004t0003g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0004t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0004t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0004t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0004t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0004t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0004t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0004t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0004t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0004t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0004t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0004t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0004t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0004t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0004t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0004t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0004t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0004t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0004t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0004t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0004t0008g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0004t0011g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0004t0012g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0004t0012g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0005t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0005t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0005t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0005t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0005t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0005t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0005t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0005t0005g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0005t0005g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0005t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0005t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0005t0005g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0005t0005g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0005t0005g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0005t0005g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0005t0005g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0005t0005g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0005t0005g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0005t0007g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0005t0007g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0005t0007g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0005t0017g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0005t0023g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0006t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0006t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0006t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0006t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0006t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0006t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0006t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0006t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0006t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0006t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0006t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0006t0008g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0007t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0007t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0007t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0007t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0007t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0007t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0007t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0007t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0008t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0008t0005g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0008t0005g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0008t0005g0067 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0008t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0009t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0009t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0009t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0009t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0012t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0012t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0014t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0015t0005g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0016t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0001c0017t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0002c0010t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0002c0010t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0003c0011t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0003c0011t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
a0004c0013t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | GBR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | GBR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00280 | hp1 | a0001 | c0003 | t0001 | g0277 | EUR | FIN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | FIN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | FIN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00423 | hp1 | a0001 | c0003 | t0001 | g0294 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00423 | hp2 | a0001 | c0001 | t0016 | g0023 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00438 | hp1 | a0001 | c0001 | t0021 | g0117 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00558 | hp1 | a0001 | c0009 | t0001 | g0010 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00609 | hp1 | a0001 | c0012 | t0005 | g0233 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00609 | hp2 | a0001 | c0015 | t0005 | g0124 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00639 | hp1 | a0001 | c0005 | t0017 | g0019 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00642 | hp2 | a0004 | c0013 | t0001 | g0015 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0044 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00735 | hp2 | a0001 | c0014 | t0001 | g0204 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG00741 | hp2 | a0001 | c0003 | t0002 | g0276 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0206 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01070 | hp2 | a0004 | c0013 | t0001 | g0015 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0207 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0202 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01109 | hp2 | a0001 | c0002 | t0003 | g0199 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01168 | hp1 | a0001 | c0007 | t0002 | g0286 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01168 | hp2 | a0001 | c0005 | t0005 | g0274 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01169 | hp2 | a0001 | c0007 | t0002 | g0285 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01192 | hp2 | a0001 | c0003 | t0001 | g0217 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01243 | hp1 | a0001 | c0003 | t0003 | g0229 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01243 | hp2 | a0001 | c0003 | t0002 | g0266 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01255 | hp1 | a0001 | c0003 | t0002 | g0267 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01256 | hp1 | a0001 | c0001 | t0009 | g0093 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01256 | hp2 | a0001 | c0007 | t0001 | g0235 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01258 | hp2 | a0001 | c0001 | t0009 | g0095 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01261 | hp2 | a0001 | c0003 | t0002 | g0287 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01346 | hp2 | a0001 | c0003 | t0002 | g0275 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01361 | hp2 | a0001 | c0005 | t0007 | g0238 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01433 | hp1 | a0001 | c0003 | t0001 | g0218 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01496 | hp1 | a0001 | c0005 | t0007 | g0241 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01515 | hp1 | a0001 | c0007 | t0001 | g0279 | EUR | IBS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01515 | hp2 | a0001 | c0003 | t0002 | g0020 | EUR | IBS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01516 | hp2 | a0001 | c0003 | t0002 | g0270 | EUR | IBS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01517 | hp1 | a0001 | c0003 | t0002 | g0020 | EUR | IBS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01517 | hp2 | a0001 | c0003 | t0002 | g0269 | EUR | IBS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01884 | hp1 | a0001 | c0006 | t0004 | g0030 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01884 | hp2 | a0001 | c0005 | t0001 | g0260 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0201 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01891 | hp2 | a0001 | c0002 | t0004 | g0175 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02027 | hp1 | a0001 | c0008 | t0005 | g0009 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02055 | hp2 | a0001 | c0006 | t0004 | g0035 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02056 | hp1 | a0001 | c0008 | t0005 | g0070 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02071 | hp1 | a0001 | c0001 | t0014 | g0135 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02145 | hp1 | a0001 | c0004 | t0003 | g0251 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02145 | hp2 | a0001 | c0004 | t0003 | g0259 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02148 | hp2 | a0001 | c0007 | t0002 | g0022 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02155 | hp1 | a0001 | c0009 | t0001 | g0010 | EAS | CDX | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02155 | hp2 | a0001 | c0008 | t0005 | g0009 | EAS | CDX | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CDX | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CDX | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02257 | hp1 | a0001 | c0006 | t0004 | g0028 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02257 | hp2 | a0001 | c0006 | t0004 | g0032 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02258 | hp1 | a0001 | c0003 | t0015 | g0216 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0195 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02280 | hp2 | a0001 | c0004 | t0003 | g0257 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02300 | hp2 | a0001 | c0007 | t0002 | g0022 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02451 | hp1 | a0001 | c0004 | t0003 | g0252 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02451 | hp2 | a0001 | c0006 | t0004 | g0026 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02572 | hp1 | a0001 | c0002 | t0004 | g0297 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02572 | hp2 | a0001 | c0002 | t0004 | g0166 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02602 | hp2 | a0001 | c0007 | t0001 | g0230 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02615 | hp1 | a0001 | c0017 | t0001 | g0033 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02615 | hp2 | a0001 | c0004 | t0003 | g0250 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02622 | hp1 | a0001 | c0002 | t0006 | g0209 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02622 | hp2 | a0001 | c0002 | t0008 | g0212 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02630 | hp1 | a0001 | c0002 | t0018 | g0138 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02630 | hp2 | a0001 | c0004 | t0003 | g0246 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02647 | hp1 | a0001 | c0006 | t0004 | g0029 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02647 | hp2 | a0001 | c0002 | t0004 | g0178 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02717 | hp1 | a0001 | c0003 | t0006 | g0290 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02717 | hp2 | a0001 | c0002 | t0003 | g0227 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02738 | hp2 | a0001 | c0005 | t0005 | g0231 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02818 | hp1 | a0001 | c0006 | t0004 | g0036 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02818 | hp2 | a0001 | c0002 | t0004 | g0169 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02886 | hp1 | a0001 | c0005 | t0023 | g0243 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02886 | hp2 | a0001 | c0004 | t0003 | g0247 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02895 | hp1 | a0001 | c0005 | t0001 | g0039 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02895 | hp2 | a0003 | c0011 | t0001 | g0288 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02896 | hp1 | a0001 | c0004 | t0003 | g0303 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02896 | hp2 | a0001 | c0004 | t0004 | g0249 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02897 | hp1 | a0001 | c0004 | t0004 | g0248 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02897 | hp2 | a0003 | c0011 | t0001 | g0289 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02922 | hp1 | a0001 | c0004 | t0003 | g0255 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02922 | hp2 | a0001 | c0004 | t0012 | g0004 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02965 | hp1 | a0001 | c0005 | t0001 | g0263 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02965 | hp2 | a0001 | c0006 | t0004 | g0037 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02970 | hp1 | a0001 | c0003 | t0004 | g0228 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02970 | hp2 | a0001 | c0006 | t0004 | g0031 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02976 | hp2 | a0001 | c0002 | t0004 | g0200 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03041 | hp1 | a0001 | c0004 | t0003 | g0254 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03041 | hp2 | a0001 | c0004 | t0003 | g0005 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03098 | hp1 | a0001 | c0004 | t0003 | g0305 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03098 | hp2 | a0001 | c0002 | t0020 | g0299 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03139 | hp1 | a0001 | c0004 | t0003 | g0256 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03139 | hp2 | a0001 | c0004 | t0003 | g0005 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03195 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03209 | hp2 | a0001 | c0004 | t0011 | g0004 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03225 | hp1 | a0001 | c0006 | t0003 | g0038 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03225 | hp2 | a0001 | c0004 | t0003 | g0304 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0197 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03453 | hp2 | a0001 | c0002 | t0003 | g0198 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03486 | hp1 | a0001 | c0004 | t0003 | g0253 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03486 | hp2 | a0001 | c0004 | t0003 | g0301 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03490 | hp2 | a0002 | c0010 | t0002 | g0280 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03491 | hp1 | a0001 | c0003 | t0002 | g0272 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03491 | hp2 | a0001 | c0007 | t0001 | g0024 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03492 | hp1 | a0001 | c0003 | t0002 | g0271 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03492 | hp2 | a0002 | c0010 | t0002 | g0281 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03516 | hp1 | a0001 | c0002 | t0004 | g0157 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03516 | hp2 | a0001 | c0005 | t0001 | g0295 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03540 | hp1 | a0001 | c0004 | t0003 | g0302 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03540 | hp2 | a0001 | c0002 | t0004 | g0298 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03579 | hp1 | a0001 | c0004 | t0008 | g0300 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03579 | hp2 | a0001 | c0004 | t0003 | g0005 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0111 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03654 | hp2 | a0001 | c0003 | t0002 | g0021 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | STU | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03688 | hp2 | a0001 | c0003 | t0002 | g0021 | SAS | STU | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03704 | hp1 | a0001 | c0001 | t0022 | g0057 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03704 | hp2 | a0001 | c0005 | t0005 | g0237 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03710 | hp1 | a0001 | c0008 | t0005 | g0058 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03834 | hp2 | a0001 | c0005 | t0005 | g0019 | SAS | BEB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | BEB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03942 | hp1 | a0001 | c0005 | t0005 | g0242 | SAS | BEB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | STU | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | STU | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG04184 | hp1 | a0001 | c0005 | t0005 | g0239 | SAS | BEB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0112 | SAS | BEB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | STU | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG04199 | hp2 | a0001 | c0005 | t0005 | g0244 | SAS | STU | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG04204 | hp1 | a0001 | c0005 | t0005 | g0236 | SAS | STU | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18522 | hp1 | a0001 | c0004 | t0003 | g0258 | AFR | YRI | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18522 | hp2 | a0001 | c0002 | t0003 | g0196 | AFR | YRI | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18612 | hp2 | a0001 | c0005 | t0005 | g0234 | EAS | CHB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18747 | hp1 | a0001 | c0005 | t0005 | g0232 | EAS | CHB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | YRI | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18906 | hp2 | a0001 | c0006 | t0008 | g0027 | AFR | YRI | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18942 | hp1 | a0001 | c0009 | t0001 | g0073 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18968 | hp1 | a0001 | c0009 | t0001 | g0072 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18983 | hp1 | a0001 | c0003 | t0002 | g0283 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18983 | hp2 | a0001 | c0002 | t0010 | g0105 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18990 | hp2 | a0001 | c0016 | t0001 | g0125 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19007 | hp2 | a0001 | c0001 | t0010 | g0140 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19030 | hp1 | a0001 | c0006 | t0004 | g0034 | AFR | LWK | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19030 | hp2 | a0001 | c0001 | t0019 | g0176 | AFR | LWK | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | LWK | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19043 | hp2 | a0001 | c0005 | t0001 | g0262 | AFR | LWK | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19060 | hp2 | a0001 | c0009 | t0001 | g0074 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19079 | hp2 | a0001 | c0003 | t0006 | g0292 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19084 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19085 | hp1 | a0001 | c0003 | t0006 | g0291 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19089 | hp2 | a0001 | c0003 | t0002 | g0282 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19240 | hp1 | a0001 | c0005 | t0001 | g0261 | AFR | YRI | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA19240 | hp2 | a0001 | c0002 | t0004 | g0171 | AFR | YRI | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA20129 | hp1 | a0001 | c0003 | t0002 | g0268 | AFR | ASW | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA20129 | hp2 | a0001 | c0002 | t0004 | g0167 | AFR | ASW | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA20752 | hp1 | a0001 | c0001 | t0013 | g0052 | EUR | TSI | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0208 | EUR | TSI | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0064 | EUR | TSI | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | TSI | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA20905 | hp1 | a0001 | c0005 | t0007 | g0278 | SAS | GIH | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA20905 | hp2 | a0001 | c0005 | t0005 | g0240 | SAS | GIH | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG01123 | hp2 | a0001 | c0007 | t0002 | g0284 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02486 | hp1 | a0001 | c0003 | t0006 | g0293 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02486 | hp2 | a0001 | c0004 | t0011 | g0004 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02559 | hp1 | a0001 | c0008 | t0001 | g0168 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03471 | hp1 | a0001 | c0002 | t0004 | g0213 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG03471 | hp2 | a0001 | c0012 | t0001 | g0296 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG06807 | hp1 | a0001 | c0004 | t0012 | g0245 | AFR | USA | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | USA | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA20300 | hp1 | a0001 | c0005 | t0001 | g0264 | AFR | USA | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | USA | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0188 | AFR | LWK | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
NA21309 | hp2 | a0001 | c0003 | t0002 | g0273 | AFR | LWK | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0149 | REF | REF | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
homoSapiens_grch38 | hp1 | a0001 | c0008 | t0005 | g0067 | REF | REF | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4033489
|
G | A | 1 | a0002 | 2 | HG03490.hp2 HG03492.hp2 |
missense_variant | MODERATE | c.1051G>A | p.Val351Ile | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/11 | 1076/3069 | 1051/1533 | 351/510 | chr19 | 4033489 | ||
chr19:4033528
|
A | G | 1 | a0004 | 2 | HG00642.hp2 HG01070.hp2 |
missense_variant | MODERATE | c.1090A>G | p.Met364Val | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/11 | 1115/3069 | 1090/1533 | 364/510 | chr19 | 4033528 | ||
chr19:4037729
|
G | A | 1 | a0003 | 2 | HG02895.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.1387G>A | p.Ala463Thr | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 1412/3069 | 1387/1533 | 463/510 | chr19 | 4037729 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4012973
|
C | T | 3 | a0001c0004a0001c0006a0001c0017 | 40 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(37): Show |
synonymous_variant | LOW | c.78C>T | p.Phe26Phe | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/11 | 103/3069 | 78/1533 | 26/510 | chr19 | 4012973 | ||
chr19:4013231
|
C | T | 1 | a0001c0009 | 5 | HG00558.hp1 HG02155.hp1 NA18942.hp1 others(2): Show |
synonymous_variant | LOW | c.336C>T | p.Tyr112Tyr | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/11 | 361/3069 | 336/1533 | 112/510 | chr19 | 4013231 | ||
chr19:4013324
|
T | C | 7 | a0001c0003a0001c0004a0001c0005others(4): Show | 93 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(90): Show |
synonymous_variant | LOW | c.429T>C | p.Asp143Asp | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/11 | 454/3069 | 429/1533 | 143/510 | chr19 | 4013324 | ||
chr19:4028785
|
C | T | 8 | a0001c0001a0001c0007a0001c0009others(5): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
synonymous_variant | LOW | c.738C>T | p.Thr246Thr | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 6/11 | 763/3069 | 738/1533 | 246/510 | chr19 | 4028785 | ||
chr19:4033440
|
C | T | 1 | a0001c0016 | 1 | NA18990.hp2 | synonymous_variant | LOW | c.1002C>T | p.Ser334Ser | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/11 | 1027/3069 | 1002/1533 | 334/510 | chr19 | 4033440 | ||
chr19:4033464
|
T | C | 11 | a0001c0001a0001c0002a0001c0003others(8): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
synonymous_variant | LOW | c.1026T>C | p.Cys342Cys | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/11 | 1051/3069 | 1026/1533 | 342/510 | chr19 | 4033464 | ||
chr19:4037383
|
G | A | 1 | a0001c0014 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.1152G>A | p.Ser384Ser | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 10/11 | 1177/3069 | 1152/1533 | 384/510 | chr19 | 4037383 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4037968
|
T | C | 4 | a0001c0002t0002a0001c0003t0002a0001c0007t0002others(1): Show | 27 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*93T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 93 | chr19 | 4037968 | |||||
chr19:4037973
|
A | C | 3 | a0001c0002t0008a0001c0004t0008a0001c0006t0008 | 3 | HG02622.hp2 HG03579.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*98A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 98 | chr19 | 4037973 | |||||
chr19:4038047
|
G | C | 1 | a0001c0001t0009 | 2 | HG01256.hp1 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*172G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 172 | chr19 | 4038047 | |||||
chr19:4038129
|
C | T | 2 | a0001c0004t0011a0001c0004t0012 | 4 | HG02486.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*254C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 254 | chr19 | 4038129 | |||||
chr19:4038187
|
G | A | 1 | a0001c0005t0007 | 3 | HG01361.hp2 HG01496.hp1 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*312G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 312 | chr19 | 4038187 | |||||
chr19:4038275
|
C | T | 1 | a0001c0005t0023 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*400C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 400 | chr19 | 4038275 | |||||
chr19:4038323
|
A | G | 1 | a0001c0001t0022 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*448A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 448 | chr19 | 4038323 | |||||
chr19:4038330
|
C | T | 1 | a0001c0001t0021 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*455C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 455 | chr19 | 4038330 | |||||
chr19:4038373
|
C | T | 10 | a0001c0002t0004a0001c0002t0006a0001c0002t0008others(7): Show | 33 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*498C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 498 | chr19 | 4038373 | |||||
chr19:4038388
|
G | A | 1 | a0001c0001t0013 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*513G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 513 | chr19 | 4038388 | |||||
chr19:4038390
|
G | A | 1 | a0001c0001t0014 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*515G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 515 | chr19 | 4038390 | |||||
chr19:4038643
|
G | C | 1 | a0001c0003t0015 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*768G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 768 | chr19 | 4038643 | |||||
chr19:4038772
|
G | T | 1 | a0001c0001t0019 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*897G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 897 | chr19 | 4038772 | |||||
chr19:4038877
|
A | C | 3 | a0001c0002t0006a0001c0002t0020a0001c0003t0006 | 6 | HG02486.hp1 HG02622.hp1 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1002A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 1002 | chr19 | 4038877 | |||||
chr19:4038945
|
G | T | 1 | a0001c0002t0018 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1070G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 1070 | chr19 | 4038945 | |||||
chr19:4039058
|
G | C | 45 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(42): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
3_prime_UTR_variant | MODIFIER | c.*1183G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 1183 | chr19 | 4039058 | |||||
chr19:4039067
|
C | T | 1 | a0001c0001t0016 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1192C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 1192 | chr19 | 4039067 | |||||
chr19:4039104
|
C | T | 1 | a0001c0004t0012 | 2 | HG02922.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1229C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 1229 | chr19 | 4039104 | |||||
chr19:4039247
|
TCA | T | 20 | a0001c0002t0002a0001c0002t0003a0001c0002t0004others(17): Show | 90 | HG00741.hp2 HG01109.hp2 HG01123.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1374_*1375delAC | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 1374 | INFO_REALIGN_3_PRIME | chr19 | 4039247 | ||||
chr19:4039261
|
G | A | 1 | a0001c0002t0020 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1386G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 1386 | chr19 | 4039261 | |||||
chr19:4039273
|
G | A | 1 | a0001c0005t0017 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1398G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 1398 | chr19 | 4039273 | |||||
chr19:4039330
|
G | T | 2 | a0001c0001t0010a0001c0002t0010 | 2 | NA18983.hp2 NA19007.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1455G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 1455 | chr19 | 4039330 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4007862
|
C | T | 6 | a0001c0004t0003g0301a0001c0004t0003g0302a0001c0004t0003g0303others(3): Show | 6 | HG02896.hp1 HG03098.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+75C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4007862 | ||||||
chr19:4007878
|
C | T | 1 | a0001c0002t0020g0299 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.27+91C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4007878 | ||||||
chr19:4007944
|
T | TGAGGGCG others(15): Show |
1 | a0001c0007t0001g0024 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.27+159_27+180dupAG others(20): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4007944 | |||||
chr19:4007947
|
G | A | 1 | a0001c0001t0016g0023 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.27+160G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4007947 | ||||||
chr19:4007993
|
A | G | 86 | a0001c0001t0001g0265a0001c0002t0004g0297a0001c0002t0004g0298others(83): Show | 92 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.27+206A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4007993 | ||||||
chr19:4008070
|
C | T | 1 | a0001c0002t0003g0227 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.27+283C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4008070 | ||||||
chr19:4008192
|
G | A | 1 | a0001c0001t0001g0025 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.27+405G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4008192 | ||||||
chr19:4008208
|
C | T | 3 | a0001c0001t0001g0226a0001c0002t0004g0297a0001c0002t0004g0298 | 3 | HG02572.hp1 HG03540.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.27+421C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4008208 | ||||||
chr19:4008214
|
C | T | 2 | a0001c0005t0001g0295a0001c0012t0001g0296 | 2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.27+427C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4008214 | ||||||
chr19:4008387
|
G | C | 13 | a0001c0006t0003g0038a0001c0006t0004g0026a0001c0006t0004g0028others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.27+600G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4008387 | ||||||
chr19:4008389
|
C | T | 13 | a0001c0006t0003g0038a0001c0006t0004g0026a0001c0006t0004g0028others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.27+602C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4008389 | ||||||
chr19:4008519
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.27+732C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4008519 | ||||||
chr19:4008572
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.27+785C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4008572 | ||||||
chr19:4008590
|
T | C | 2 | a0001c0002t0004g0297a0001c0002t0004g0298 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.27+803T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4008590 | ||||||
chr19:4008711
|
C | T | 1 | a0001c0001t0001g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.27+924C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4008711 | ||||||
chr19:4009092
|
A | G | 1 | a0001c0002t0020g0299 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.27+1305A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4009092 | ||||||
chr19:4009097
|
C | T | 1 | a0001c0001t0001g0222 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.27+1310C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4009097 | ||||||
chr19:4009211
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.27+1424C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4009211 | ||||||
chr19:4009260
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.27+1473A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4009260 | ||||||
chr19:4009411
|
G | C | 52 | a0001c0003t0003g0229a0001c0003t0004g0228a0001c0004t0003g0005others(49): Show | 55 | HG00609.hp1 HG00639.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.27+1624G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4009411 | ||||||
chr19:4009437
|
C | T | 2 | a0001c0002t0004g0297a0001c0002t0004g0298 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.27+1650C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4009437 | ||||||
chr19:4009567
|
C | A | 1 | a0001c0003t0004g0228 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.27+1780C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4009567 | ||||||
chr19:4009580
|
A | G | 1 | a0001c0002t0004g0298 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.27+1793A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4009580 | ||||||
chr19:4009915
|
G | A | 17 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(14): Show | 17 | HG00099.hp2 HG00735.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.27+2128G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4009915 | ||||||
chr19:4010038
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.27+2251A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4010038 | ||||||
chr19:4010334
|
A | G | 64 | a0001c0002t0004g0297a0001c0002t0004g0298a0001c0003t0001g0217others(61): Show | 67 | HG00423.hp1 HG00609.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.27+2547A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4010334 | ||||||
chr19:4010691
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.28-2232G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4010691 | ||||||
chr19:4010767
|
C | T | 1 | a0001c0003t0001g0218 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.28-2156C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4010767 | ||||||
chr19:4010869
|
C | T | 8 | a0001c0005t0001g0039a0001c0005t0001g0260a0001c0005t0001g0261others(5): Show | 8 | HG01884.hp2 HG02895.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.28-2054C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4010869 | ||||||
chr19:4010939
|
C | T | 1 | a0001c0003t0002g0287 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.28-1984C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4010939 | ||||||
chr19:4011014
|
C | T | 5 | a0001c0003t0001g0294a0001c0003t0006g0290a0001c0003t0006g0291others(2): Show | 5 | HG00423.hp1 HG02486.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-1909C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011014 | ||||||
chr19:4011267
|
A | G | 182 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0055others(179): Show | 194 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(191): Show |
intron_variant | MODIFIER | c.28-1656A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011267 | ||||||
chr19:4011435
|
A | T | 24 | a0001c0004t0003g0005a0001c0004t0003g0246a0001c0004t0003g0247others(21): Show | 27 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(24): Show |
intron_variant | MODIFIER | c.28-1488A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011435 | ||||||
chr19:4011437
|
T | G | 64 | a0001c0002t0004g0297a0001c0002t0004g0298a0001c0003t0001g0217others(61): Show | 67 | HG00423.hp1 HG00609.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.28-1486T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011437 | ||||||
chr19:4011459
|
G | C | 13 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(10): Show | 13 | HG01106.hp2 HG01167.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.28-1464G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011459 | ||||||
chr19:4011556
|
C | T | 18 | a0001c0005t0005g0019a0001c0005t0005g0231a0001c0005t0005g0232others(15): Show | 18 | HG00609.hp1 HG00639.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.28-1367C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011556 | ||||||
chr19:4011574
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.28-1349C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011574 | ||||||
chr19:4011641
|
T | TGGTGTGG others(95): Show |
3 | a0001c0003t0001g0217a0001c0003t0001g0218a0001c0003t0015g0216 | 3 | HG01192.hp2 HG01433.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.28-1267_28-1266ins others(102): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011641 | |||||
chr19:4011641
|
TGGTGTGG others(44): Show |
T | 1 | a0001c0002t0004g0157 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.28-1266_28-1216del others(51): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011641 | |||||
chr19:4011656
|
T | G | 1 | a0001c0001t0001g0056 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.28-1267T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011656 | ||||||
chr19:4011657
|
T | G | 10 | a0001c0001t0001g0056a0001c0001t0001g0158a0001c0001t0001g0159others(7): Show | 10 | HG01192.hp2 HG01433.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.28-1266T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011657 | ||||||
chr19:4011658
|
T | G | 10 | a0001c0001t0001g0056a0001c0001t0001g0158a0001c0001t0001g0159others(7): Show | 10 | HG01192.hp2 HG01433.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.28-1265T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011658 | ||||||
chr19:4011658
|
T | TGGTGTGG others(229): Show |
1 | a0001c0004t0003g0247 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.28-1251_28-1250ins others(236): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | |||||
chr19:4011658
|
T | TGGTGTGG others(331): Show |
2 | a0001c0004t0003g0246a0001c0004t0003g0256 | 2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.28-1251_28-1250ins others(338): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | |||||
chr19:4011658
|
T | TGGTGTGG others(348): Show |
11 | a0001c0004t0003g0005a0001c0004t0003g0250a0001c0004t0003g0251others(8): Show | 14 | HG02145.hp1 HG02451.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.28-1251_28-1250ins others(355): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | |||||
chr19:4011658
|
T | TGGTGTGG others(365): Show |
2 | a0001c0004t0003g0301a0001c0004t0008g0300 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.28-1251_28-1250ins others(372): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | |||||
chr19:4011658
|
T | TGGTGTGG others(227): Show |
2 | a0001c0004t0003g0304a0001c0004t0003g0305 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.28-1251_28-1250ins others(234): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | |||||
chr19:4011658
|
T | TGGTGTGG others(363): Show |
1 | a0001c0004t0003g0303 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.28-1251_28-1250ins others(370): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | |||||
chr19:4011658
|
T | TGGTGTGG others(586): Show |
1 | a0001c0004t0003g0257 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.28-1251_28-1250ins others(593): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | |||||
chr19:4011658
|
T | TGGTGTGG others(501): Show |
1 | a0001c0004t0003g0258 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.28-1251_28-1250ins others(508): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | |||||
chr19:4011658
|
T | TGGTGTGG others(499): Show |
1 | a0001c0004t0003g0259 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.28-1251_28-1250ins others(506): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | |||||
chr19:4011658
|
T | TGGTGTGG others(142): Show |
1 | a0001c0005t0001g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.28-1251_28-1250ins others(149): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | |||||
chr19:4011658
|
TGGTGTGG others(10): Show |
T | 1 | a0001c0002t0008g0212 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.28-1250_28-1234del others(17): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | |||||
chr19:4011658
|
TGGTGTGG others(27): Show |
T | 1 | a0001c0002t0004g0213 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.28-1250_28-1217del others(34): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | |||||
chr19:4011658
|
TGGTGTGG others(44): Show |
T | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.28-1250_28-1200del others(51): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | |||||
chr19:4011658
|
TGGTGTGG others(180): Show |
T | 1 | a0001c0001t0001g0144 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.28-1250_28-1064del | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | |||||
chr19:4011667
|
G | A | 1 | a0001c0007t0001g0230 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.28-1256G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011667 | ||||||
chr19:4011668
|
G | C | 17 | a0001c0005t0005g0019a0001c0005t0005g0231a0001c0005t0005g0232others(14): Show | 17 | HG00609.hp1 HG00639.hp1 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.28-1255G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011668 | ||||||
chr19:4011671
|
TGG | T | 17 | a0001c0005t0005g0019a0001c0005t0005g0231a0001c0005t0005g0232others(14): Show | 17 | HG00609.hp1 HG00639.hp1 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.28-1247_28-1246del others(2): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011671 | |||||
chr19:4011673
|
G | A | 6 | a0001c0003t0001g0217a0001c0003t0001g0218a0001c0003t0015g0216others(3): Show | 6 | HG01192.hp2 HG01433.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-1250G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011673 | ||||||
chr19:4011673
|
G | GGGGGTGT others(10): Show |
1 | a0001c0001t0001g0066 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.28-1079_28-1063dup others(17): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011673 | |||||
chr19:4011673
|
G | GGGGGTGT others(212): Show |
1 | a0001c0002t0004g0171 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.28-1080_28-1079ins others(219): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011673 | |||||
chr19:4011673
|
G | T | 53 | a0001c0001t0001g0056a0001c0001t0001g0141a0001c0001t0001g0142others(50): Show | 56 | HG00423.hp1 HG01243.hp1 HG01884.hp2 others(53): Show |
intron_variant | MODIFIER | c.28-1250G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011673 | ||||||
chr19:4011673
|
GGGGGTGT others(10): Show |
G | 33 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(30): Show | 37 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(34): Show |
intron_variant | MODIFIER | c.28-1079_28-1063del others(17): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011673 | |||||
chr19:4011673
|
GGGGGTGT others(27): Show |
G | 60 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(57): Show | 66 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.28-1096_28-1063del others(34): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011673 | |||||
chr19:4011673
|
GGGGGTGT others(44): Show |
G | 5 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0205others(2): Show | 5 | HG00438.hp2 HG01081.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-1113_28-1063del others(51): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011673 | |||||
chr19:4011673
|
GGGGGTGT others(61): Show |
G | 1 | a0001c0001t0001g0139 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.28-1130_28-1063del others(68): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011673 | |||||
chr19:4011674
|
G | T | 5 | a0001c0001t0001g0214a0001c0002t0004g0297a0001c0002t0004g0298others(2): Show | 5 | HG01243.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-1249G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011674 | ||||||
chr19:4011675
|
G | GGGTGTGG others(27): Show |
1 | a0003c0011t0001g0288 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.28-1234_28-1233ins others(34): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011675 | |||||
chr19:4011675
|
G | T | 5 | a0001c0001t0001g0214a0001c0002t0004g0297a0001c0002t0004g0298others(2): Show | 5 | HG01243.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-1248G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011675 | ||||||
chr19:4011686
|
T | TGTGTTTG others(298): Show |
1 | a0001c0003t0001g0294 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.28-1233_28-1232ins others(305): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011686 | |||||
chr19:4011687
|
G | GTGTGGGG others(193): Show |
3 | a0001c0003t0002g0020a0001c0003t0002g0266a0001c0003t0002g0267 | 4 | HG01243.hp2 HG01255.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-1205_28-1204ins others(200): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011687 | |||||
chr19:4011687
|
G | GTGTGGGG others(244): Show |
21 | a0001c0003t0001g0277a0001c0003t0002g0021a0001c0003t0002g0268others(18): Show | 23 | HG00280.hp1 HG00741.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.28-1205_28-1204ins others(251): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011687 | |||||
chr19:4011690
|
T | A | 1 | a0003c0011t0001g0289 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.28-1233T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011690 | ||||||
chr19:4011690
|
T | TTTGGTGT others(212): Show |
1 | a0001c0004t0012g0245 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.28-1233_28-1232ins others(219): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011690 | ||||||
chr19:4011690
|
T | TTTGGTGT others(841): Show |
1 | a0001c0004t0003g0302 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.28-1233_28-1232ins others(848): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011690 | ||||||
chr19:4011691
|
G | T | 11 | a0001c0003t0006g0290a0001c0003t0006g0291a0001c0003t0006g0292others(8): Show | 11 | HG01884.hp2 HG02486.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-1232G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011691 | ||||||
chr19:4011692
|
G | T | 11 | a0001c0003t0006g0290a0001c0003t0006g0291a0001c0003t0006g0292others(8): Show | 11 | HG01884.hp2 HG02486.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-1231G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011692 | ||||||
chr19:4011704
|
G | GTGTTTGG others(72): Show |
4 | a0001c0003t0006g0290a0001c0003t0006g0291a0001c0003t0006g0292others(1): Show | 4 | HG02486.hp1 HG02717.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-1216_28-1215ins others(79): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011704 | |||||
chr19:4011704
|
G | GTGTTTGG others(91): Show |
4 | a0001c0005t0001g0039a0001c0005t0001g0260a0001c0005t0001g0261others(1): Show | 4 | HG01884.hp2 HG02895.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-1216_28-1215ins others(98): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011704 | |||||
chr19:4011704
|
G | GTGTTTGG others(274): Show |
1 | a0001c0005t0001g0264 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.28-1216_28-1215ins others(281): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011704 | |||||
chr19:4011707
|
T | A | 3 | a0001c0003t0001g0217a0001c0003t0001g0218a0001c0003t0015g0216 | 3 | HG01192.hp2 HG01433.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.28-1216T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011707 | ||||||
chr19:4011707
|
T | G | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(7): Show | 13 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(10): Show |
intron_variant | MODIFIER | c.28-1216T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011707 | ||||||
chr19:4011707
|
T | TGGGGTGT others(161): Show |
1 | a0001c0001t0001g0075 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.28-1080_28-1079ins others(168): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011707 | |||||
chr19:4011707
|
T | TGGGGTGT others(214): Show |
1 | a0001c0001t0001g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.28-1080_28-1079ins others(221): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011707 | |||||
chr19:4011708
|
G | T | 4 | a0001c0005t0001g0295a0001c0007t0001g0230a0001c0012t0001g0296others(1): Show | 4 | HG02602.hp2 HG02897.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-1215G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011708 | ||||||
chr19:4011709
|
G | GGGTGTGG others(76): Show |
1 | a0001c0003t0002g0287 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.28-1205_28-1204ins others(83): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011709 | |||||
chr19:4011709
|
G | T | 4 | a0001c0005t0001g0295a0001c0007t0001g0230a0001c0012t0001g0296others(1): Show | 4 | HG02602.hp2 HG02897.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-1214G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011709 | ||||||
chr19:4011718
|
G | A | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164 | 3 | NA18955.hp1 NA19070.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.28-1205G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011718 | ||||||
chr19:4011718
|
G | GCTGTGGG others(325): Show |
1 | a0001c0007t0001g0230 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.28-1205_28-1204ins others(332): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011718 | ||||||
chr19:4011718
|
G | GGTGTGTG others(293): Show |
3 | a0001c0005t0005g0232a0001c0005t0005g0234a0001c0012t0005g0233 | 3 | HG00609.hp1 NA18612.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.28-1165_28-1164ins others(300): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011718 | |||||
chr19:4011721
|
G | C | 2 | a0001c0005t0001g0295a0001c0012t0001g0296 | 2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.28-1202G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011721 | ||||||
chr19:4011721
|
G | GTGTGGGG others(178): Show |
1 | a0003c0011t0001g0289 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.28-1149_28-1148ins others(185): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011721 | |||||
chr19:4011721
|
G | GTGTGGGG others(91): Show |
12 | a0001c0005t0005g0019a0001c0005t0005g0231a0001c0005t0005g0236others(9): Show | 12 | HG00639.hp1 HG01256.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.28-1165_28-1164ins others(98): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011721 | |||||
chr19:4011721
|
G | GTGTTTGG others(8): Show |
1 | a0001c0005t0001g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.28-1199_28-1198ins others(15): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011721 | |||||
chr19:4011724
|
T | A | 1 | a0001c0004t0003g0302 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.28-1199T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011724 | ||||||
chr19:4011724
|
T | G | 3 | a0001c0001t0001g0064a0001c0002t0001g0210a0001c0002t0001g0211 | 3 | NA18964.hp2 NA19064.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.28-1199T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011724 | ||||||
chr19:4011735
|
G | GGTGTGTG others(276): Show |
1 | a0001c0005t0023g0243 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.28-1165_28-1164ins others(283): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011735 | |||||
chr19:4011735
|
GGT | G | 9 | a0001c0003t0006g0290a0001c0003t0006g0291a0001c0003t0006g0292others(6): Show | 10 | HG02486.hp1 HG02486.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.28-1182_28-1181del others(2): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011735 | |||||
chr19:4011737
|
T | TGTGTGGG others(610): Show |
1 | a0001c0003t0001g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.28-1165_28-1164ins others(617): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011737 | |||||
chr19:4011738
|
G | GTGTGGGG others(74): Show |
1 | a0001c0005t0005g0244 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.28-1165_28-1164ins others(81): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011738 | |||||
chr19:4011741
|
T | A | 2 | a0001c0002t0004g0157a0003c0011t0001g0288 | 2 | HG02895.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.28-1182T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011741 | ||||||
chr19:4011742
|
G | T | 1 | a0001c0003t0002g0287 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.28-1181G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011742 | ||||||
chr19:4011743
|
G | T | 1 | a0001c0003t0002g0287 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.28-1180G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011743 | ||||||
chr19:4011752
|
GGT | G | 13 | a0001c0004t0003g0005a0001c0004t0003g0246a0001c0004t0003g0250others(10): Show | 15 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.28-1165_28-1164del others(2): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011752 | |||||
chr19:4011754
|
T | TGTGGGGT others(38): Show |
1 | a0001c0003t0001g0294 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.28-1166_28-1165ins others(45): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011754 | |||||
chr19:4011754
|
T | TGTGTTTG others(8): Show |
24 | a0001c0003t0001g0277a0001c0003t0002g0020a0001c0003t0002g0021others(21): Show | 27 | HG00280.hp1 HG00741.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.28-1165_28-1164ins others(15): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011754 | |||||
chr19:4011758
|
T | A | 1 | a0001c0004t0003g0302 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.28-1165T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011758 | ||||||
chr19:4011758
|
TGGGGTGT others(127): Show |
T | 1 | a0001c0002t0004g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.28-1062_28-929del | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011758 | |||||
chr19:4011759
|
G | T | 2 | a0001c0003t0001g0218a0001c0003t0015g0216 | 2 | HG01433.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.28-1164G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011759 | ||||||
chr19:4011760
|
G | T | 2 | a0001c0003t0001g0218a0001c0003t0015g0216 | 2 | HG01433.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.28-1163G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011760 | ||||||
chr19:4011772
|
G | GTGTTTGG others(25): Show |
2 | a0001c0002t0004g0297a0001c0002t0004g0298 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.28-1148_28-1147ins others(32): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011772 | |||||
chr19:4011775
|
T | A | 1 | a0003c0011t0001g0288 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.28-1148T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011775 | ||||||
chr19:4011775
|
T | G | 1 | a0001c0001t0001g0165 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.28-1148T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011775 | ||||||
chr19:4011776
|
G | T | 2 | a0001c0001t0001g0018a0001c0003t0002g0287 | 3 | HG01261.hp2 NA18944.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.28-1147G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011776 | ||||||
chr19:4011777
|
G | T | 2 | a0001c0001t0001g0018a0001c0003t0002g0287 | 3 | HG01261.hp2 NA18944.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.28-1146G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011777 | ||||||
chr19:4011787
|
G | C | 1 | a0001c0001t0001g0018 | 2 | NA18944.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.28-1136G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011787 | ||||||
chr19:4011789
|
G | GTGTGGGG others(8): Show |
24 | a0001c0003t0001g0277a0001c0003t0002g0020a0001c0003t0002g0021others(21): Show | 27 | HG00280.hp1 HG00741.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.28-1120_28-1119ins others(15): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011789 | |||||
chr19:4011789
|
G | GTGTTTGG others(8): Show |
3 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208 | 3 | HG01069.hp2 HG01071.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.28-1131_28-1130ins others(15): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011789 | |||||
chr19:4011790
|
TGTGGGGT others(95): Show |
T | 1 | a0001c0001t0001g0018 | 2 | NA18944.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.28-1131_28-1030del | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011790 | |||||
chr19:4011792
|
T | A | 1 | a0001c0003t0004g0228 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.28-1131T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011792 | ||||||
chr19:4011792
|
T | TGGGGTGT others(59): Show |
1 | a0001c0016t0001g0125 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.28-1097_28-1096ins others(66): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011792 | |||||
chr19:4011792
|
T | TGGGGTGT others(42): Show |
2 | a0001c0002t0001g0017a0001c0002t0001g0201 | 3 | HG01891.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.28-1114_28-1113ins others(49): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011792 | |||||
chr19:4011793
|
G | T | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0002t0006g0209 | 3 | HG02622.hp1 NA18973.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.28-1130G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011793 | ||||||
chr19:4011794
|
G | GGGTGTGG others(261): Show |
2 | a0001c0003t0001g0218a0001c0003t0015g0216 | 2 | HG01433.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.28-1114_28-1113ins others(268): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011794 | |||||
chr19:4011794
|
G | T | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0002t0006g0209 | 3 | HG02622.hp1 NA18973.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.28-1129G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011794 | ||||||
chr19:4011806
|
G | C | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | NA18973.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.28-1117G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011806 | ||||||
chr19:4011806
|
G | GTGTTTGG others(8): Show |
6 | a0001c0001t0001g0134a0001c0001t0001g0155a0001c0001t0001g0156others(3): Show | 6 | HG00735.hp2 HG01074.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-1114_28-1113ins others(15): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011806 | |||||
chr19:4011809
|
T | A | 1 | a0001c0003t0003g0229 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.28-1114T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011809 | ||||||
chr19:4011809
|
T | G | 3 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208 | 3 | HG01069.hp2 HG01071.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.28-1114T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011809 | ||||||
chr19:4011809
|
T | TGGGGTGT others(42): Show |
1 | a0001c0001t0019g0176 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.28-1097_28-1096ins others(49): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011809 | |||||
chr19:4011809
|
T | TTTGGTGT others(10): Show |
1 | a0001c0002t0006g0209 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.28-1114_28-1113ins others(17): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011809 | ||||||
chr19:4011810
|
G | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0003c0011t0001g0288 | 3 | HG02895.hp2 NA18964.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.28-1113G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011810 | ||||||
chr19:4011811
|
G | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0003c0011t0001g0288 | 3 | HG02895.hp2 NA18964.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.28-1112G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011811 | ||||||
chr19:4011819
|
A | G | 1 | a0001c0001t0013g0052 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.28-1104A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011819 | ||||||
chr19:4011823
|
G | C | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | NA18964.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.28-1100G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011823 | ||||||
chr19:4011823
|
G | GTGTTTGG others(8): Show |
8 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(5): Show | 8 | HG01106.hp2 HG01167.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.28-1097_28-1096ins others(15): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011823 | |||||
chr19:4011826
|
T | G | 8 | a0001c0001t0001g0134a0001c0001t0001g0155a0001c0001t0001g0156others(5): Show | 8 | HG00735.hp2 HG01074.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.28-1097T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011826 | ||||||
chr19:4011826
|
T | TTTGGTGT others(25): Show |
3 | a0001c0001t0001g0146a0001c0001t0001g0177a0001c0002t0004g0178 | 3 | HG01975.hp2 HG02647.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.28-1097_28-1096ins others(32): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011826 | ||||||
chr19:4011827
|
G | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(66): Show | 75 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.28-1096G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011827 | ||||||
chr19:4011828
|
G | GTGTGGAG others(59): Show |
1 | a0001c0003t0002g0287 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.28-1095_28-1094ins others(66): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011828 | ||||||
chr19:4011828
|
G | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(66): Show | 75 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.28-1095G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011828 | ||||||
chr19:4011837
|
GGT | G | 64 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(61): Show | 70 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.28-1080_28-1079del others(2): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011837 | |||||
chr19:4011838
|
G | C | 4 | a0001c0001t0001g0065a0001c0001t0001g0129a0001c0001t0001g0145others(1): Show | 4 | HG02523.hp2 HG03239.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-1085G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011838 | ||||||
chr19:4011840
|
G | C | 63 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(60): Show | 69 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.28-1083G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011840 | ||||||
chr19:4011841
|
TGTGGGGT others(44): Show |
T | 1 | a0001c0001t0001g0129 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.28-1080_28-1030del others(51): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011841 | |||||
chr19:4011842
|
G | GGGGTGTG others(5): Show |
1 | a0001c0001t0001g0145 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.28-1081_28-1080ins others(12): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011842 | ||||||
chr19:4011843
|
T | A | 1 | a0001c0004t0003g0302 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.28-1080T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011843 | ||||||
chr19:4011843
|
T | G | 11 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0148others(8): Show | 11 | HG01106.hp2 HG01167.hp1 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.28-1080T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011843 | ||||||
chr19:4011843
|
TGGGGTGT others(42): Show |
T | 1 | a0001c0002t0006g0209 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.28-1062_28-1014del others(49): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011843 | |||||
chr19:4011844
|
G | T | 3 | a0001c0001t0001g0065a0001c0002t0004g0157a0001c0006t0004g0037 | 3 | HG02965.hp2 HG03516.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.28-1079G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011844 | ||||||
chr19:4011845
|
G | T | 3 | a0001c0001t0001g0065a0001c0002t0004g0157a0001c0006t0004g0037 | 3 | HG02965.hp2 HG03516.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.28-1078G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011845 | ||||||
chr19:4011855
|
G | C | 1 | a0001c0006t0004g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.28-1068G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011855 | ||||||
chr19:4011857
|
GTGTTTGG others(8): Show |
G | 21 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0076others(18): Show | 21 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.28-1062_28-1048del others(15): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011857 | |||||
chr19:4011858
|
TGTTTGGT others(27): Show |
T | 1 | a0001c0006t0004g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.28-1063_28-1030del others(34): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011858 | |||||
chr19:4011860
|
T | A | 1 | a0001c0003t0003g0229 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.28-1063T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011860 | ||||||
chr19:4011860
|
T | G | 55 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0040others(52): Show | 61 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.28-1063T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011860 | ||||||
chr19:4011860
|
TTTGGTGT others(25): Show |
T | 2 | a0001c0001t0001g0134a0001c0001t0001g0161 | 2 | HG02280.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.28-1062_28-1031del others(32): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011860 | ||||||
chr19:4011861
|
T | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0040others(76): Show | 86 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.28-1062T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011861 | ||||||
chr19:4011862
|
T | G | 80 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0040others(77): Show | 87 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.28-1061T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011862 | ||||||
chr19:4011862
|
TGGTGTGG others(8): Show |
T | 1 | a0001c0002t0004g0157 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.28-1051_28-1037del others(15): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011862 | |||||
chr19:4011871
|
G | GGT | 73 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0040others(70): Show | 80 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.28-1052_28-1051ins others(2): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011871 | ||||||
chr19:4011871
|
G | GGTGTGTG others(476): Show |
1 | a0001c0003t0004g0228 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.28-1052_28-1051ins others(483): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011871 | ||||||
chr19:4011872
|
C | CTGTGGGG others(10): Show |
1 | a0001c0001t0001g0063 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.28-1048_28-1032dup others(17): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011872 | |||||
chr19:4011872
|
C | CTGTGGGG others(189): Show |
1 | a0001c0003t0006g0290 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.28-1032_28-1031ins others(196): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011872 | |||||
chr19:4011872
|
C | CTGTGGGG others(142): Show |
4 | a0001c0003t0001g0294a0001c0003t0006g0291a0001c0003t0006g0292others(1): Show | 4 | HG00423.hp1 HG02486.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-1032_28-1031ins others(149): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011872 | |||||
chr19:4011872
|
C | CTGTGGGG others(161): Show |
1 | a0001c0004t0003g0303 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.28-1032_28-1031ins others(168): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011872 | |||||
chr19:4011872
|
C | CTGTGGGG others(463): Show |
1 | a0001c0005t0001g0262 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.28-1032_28-1031ins others(470): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011872 | |||||
chr19:4011872
|
C | CTGTGGGG others(414): Show |
17 | a0001c0004t0003g0005a0001c0004t0003g0246a0001c0004t0003g0250others(14): Show | 20 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.28-1032_28-1031ins others(421): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011872 | |||||
chr19:4011872
|
C | CTGTGGGG others(312): Show |
1 | a0001c0005t0001g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.28-1032_28-1031ins others(319): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011872 | |||||
chr19:4011872
|
C | CTGTGGGG others(414): Show |
1 | a0001c0004t0003g0301 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.28-1032_28-1031ins others(421): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011872 | |||||
chr19:4011872
|
C | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 122 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.28-1051C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011872 | ||||||
chr19:4011875
|
T | G | 8 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0076others(5): Show | 8 | HG01975.hp1 HG02004.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.28-1048T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011875 | ||||||
chr19:4011875
|
T | TGGGGTGT others(493): Show |
1 | a0001c0007t0001g0230 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.28-1032_28-1031ins others(500): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011875 | |||||
chr19:4011875
|
T | TGGGGTGT others(495): Show |
1 | a0001c0005t0005g0232 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.28-1032_28-1031ins others(502): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011875 | |||||
chr19:4011877
|
G | T | 1 | a0001c0001t0001g0144 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.28-1046G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011877 | ||||||
chr19:4011879
|
G | A | 1 | a0003c0011t0001g0289 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.28-1044G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011879 | ||||||
chr19:4011892
|
G | A | 20 | a0001c0004t0003g0005a0001c0004t0003g0246a0001c0004t0003g0250others(17): Show | 23 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.28-1031G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011892 | ||||||
chr19:4011892
|
G | GGGGGTGT others(27): Show |
1 | a0001c0002t0008g0212 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.28-1015_28-1014ins others(34): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011892 | |||||
chr19:4011892
|
G | GGGGGTGT others(10): Show |
59 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(56): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.28-860_28-844dupGG others(15): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011892 | |||||
chr19:4011892
|
G | GGGGGTGT others(27): Show |
10 | a0001c0001t0001g0170a0001c0001t0001g0174a0001c0001t0001g0219others(7): Show | 10 | HG00140.hp1 HG01261.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.28-877_28-844dupGG others(32): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011892 | |||||
chr19:4011892
|
G | GGGGGTGT others(44): Show |
5 | a0001c0006t0004g0028a0001c0006t0004g0029a0001c0006t0004g0030others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-894_28-844dupGG others(49): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011892 | |||||
chr19:4011892
|
G | GGGGGTGT others(61): Show |
1 | a0001c0006t0008g0027 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.28-911_28-844dupGG others(66): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011892 | |||||
chr19:4011892
|
G | GGGGGTGT others(78): Show |
1 | a0001c0006t0004g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.28-928_28-844dupGG others(83): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011892 | |||||
chr19:4011892
|
G | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(157): Show | 170 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.28-1031G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011892 | ||||||
chr19:4011892
|
GGGGGTGT others(10): Show |
G | 5 | a0001c0001t0001g0051a0001c0001t0001g0123a0001c0001t0001g0144others(2): Show | 6 | HG00558.hp1 HG00609.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-860_28-844delGG others(15): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011892 | |||||
chr19:4011895
|
G | TGTGTGGA others(10): Show |
4 | a0001c0001t0001g0025a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG02083.hp1 NA18966.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-1029_28-1028ins others(17): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011895 | ||||||
chr19:4011909
|
T | G | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.28-1014T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011909 | ||||||
chr19:4011909
|
T | TGGGGTGT others(459): Show |
1 | a0001c0005t0023g0243 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.28-998_28-997insGG others(464): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011909 | |||||
chr19:4011909
|
T | TGGGGTGT others(546): Show |
2 | a0001c0005t0005g0234a0001c0012t0005g0233 | 2 | HG00609.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.28-998_28-997insGG others(551): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011909 | |||||
chr19:4011910
|
G | T | 13 | a0001c0005t0005g0019a0001c0005t0005g0231a0001c0005t0005g0236others(10): Show | 13 | HG00639.hp1 HG01256.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.28-1013G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011910 | ||||||
chr19:4011911
|
G | T | 13 | a0001c0005t0005g0019a0001c0005t0005g0231a0001c0005t0005g0236others(10): Show | 13 | HG00639.hp1 HG01256.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.28-1012G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011911 | ||||||
chr19:4011920
|
G | A | 13 | a0001c0005t0005g0019a0001c0005t0005g0231a0001c0005t0005g0236others(10): Show | 13 | HG00639.hp1 HG01256.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.28-1003G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011920 | ||||||
chr19:4011922
|
T | TGTGTGGG others(178): Show |
14 | a0001c0003t0001g0277a0001c0003t0002g0021a0001c0003t0002g0266others(11): Show | 15 | HG00280.hp1 HG00741.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.28-844_28-843insGG others(183): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011922 | |||||
chr19:4011922
|
T | TGTGTGGG others(127): Show |
1 | a0001c0003t0001g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.28-878_28-877insTT others(132): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011922 | |||||
chr19:4011922
|
T | TGTGTGGG others(763): Show |
1 | a0003c0011t0001g0288 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.28-946_28-945insTT others(768): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011922 | |||||
chr19:4011922
|
T | TGTGTGGG others(25): Show |
2 | a0001c0003t0001g0218a0001c0003t0015g0216 | 2 | HG01433.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.28-980_28-979insTT others(30): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011922 | |||||
chr19:4011922
|
T | TGTGTTTG others(612): Show |
1 | a0003c0011t0001g0289 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.28-997_28-996insTT others(617): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011922 | |||||
chr19:4011939
|
T | TGTGTGGG others(344): Show |
1 | a0001c0003t0001g0218 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.28-952_28-951insCT others(349): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011939 | |||||
chr19:4011939
|
T | TGTGTGGG others(178): Show |
1 | a0001c0003t0002g0020 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.28-844_28-843insGG others(183): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011939 | |||||
chr19:4011939
|
T | TGTGTGGG others(161): Show |
11 | a0001c0003t0002g0282a0001c0003t0002g0283a0001c0006t0004g0034others(8): Show | 12 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.28-844_28-843insGG others(166): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011939 | |||||
chr19:4011943
|
T | A | 2 | a0001c0005t0001g0262a0001c0005t0001g0263 | 2 | HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.28-980T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011943 | ||||||
chr19:4011943
|
T | TGGGGTGT others(463): Show |
1 | a0001c0012t0001g0296 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.28-912_28-911insTT others(468): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011943 | |||||
chr19:4011943
|
T | TGGGGTGT others(463): Show |
2 | a0001c0005t0001g0260a0001c0005t0001g0264 | 2 | HG01884.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.28-912_28-911insTT others(468): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011943 | |||||
chr19:4011943
|
T | TGGGGTGT others(495): Show |
1 | a0001c0005t0001g0039 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.28-912_28-911insTT others(500): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011943 | |||||
chr19:4011943
|
T | TGGGGTGT others(497): Show |
1 | a0001c0004t0012g0245 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.28-929_28-928insTT others(502): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011943 | |||||
chr19:4011943
|
T | TGGGGTGT others(480): Show |
1 | a0001c0004t0003g0247 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.28-946_28-945insTT others(485): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011943 | |||||
chr19:4011944
|
G | T | 1 | a0001c0003t0002g0287 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.28-979G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011944 | ||||||
chr19:4011945
|
G | T | 1 | a0001c0003t0002g0287 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.28-978G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011945 | ||||||
chr19:4011956
|
T | TGTGTGGG others(310): Show |
1 | a0001c0003t0015g0216 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.28-952_28-951insCT others(315): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011956 | |||||
chr19:4011956
|
T | TGTGTGGG others(614): Show |
1 | a0001c0004t0003g0304 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.28-929_28-928insTT others(619): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011956 | |||||
chr19:4011956
|
T | TGTGTGGG others(597): Show |
1 | a0001c0004t0003g0305 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.28-929_28-928insTT others(602): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011956 | |||||
chr19:4011957
|
G | GTGGGGTG others(393): Show |
1 | a0001c0003t0002g0287 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.28-964_28-963insGG others(398): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011957 | |||||
chr19:4011960
|
T | A | 1 | a0001c0005t0005g0232 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.28-963T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011960 | ||||||
chr19:4011960
|
T | G | 2 | a0001c0002t0001g0210a0001c0002t0001g0211 | 2 | NA18964.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.28-963T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011960 | ||||||
chr19:4011965
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.28-958T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011965 | ||||||
chr19:4011977
|
T | A | 1 | a0001c0004t0003g0303 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.28-946T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011977 | ||||||
chr19:4011983
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.28-940G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011983 | ||||||
chr19:4011990
|
T | TGTGTGGG others(8): Show |
1 | a0001c0001t0001g0075 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.28-927_28-913dupGG others(13): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011990 | |||||
chr19:4011990
|
T | TGTGTGGG others(25): Show |
3 | a0001c0005t0005g0234a0001c0005t0023g0243a0001c0012t0005g0233 | 3 | HG00609.hp1 HG02886.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.28-927_28-896dupGG others(30): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011990 | |||||
chr19:4012007
|
T | TGTGGGGT others(40): Show |
18 | a0001c0004t0003g0005a0001c0004t0003g0246a0001c0004t0003g0250others(15): Show | 21 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.28-913_28-912insGG others(45): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012007 | |||||
chr19:4012007
|
T | TGTGTGGG others(8): Show |
4 | a0001c0003t0001g0294a0001c0003t0006g0291a0001c0003t0006g0292others(1): Show | 4 | HG00423.hp1 HG02486.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-910_28-896dupGG others(13): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012007 | |||||
chr19:4012007
|
T | TGTGTGGG others(59): Show |
1 | a0001c0001t0019g0176 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.28-910_28-845dupGG others(64): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012007 | |||||
chr19:4012007
|
T | TGTGTTTG others(561): Show |
1 | a0001c0005t0001g0295 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.28-912_28-911insTT others(566): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012007 | |||||
chr19:4012007
|
T | TGTGTTTG others(971): Show |
1 | a0001c0005t0001g0261 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.28-912_28-911insTT others(976): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012007 | |||||
chr19:4012030
|
G | GGGTGTGG others(776): Show |
1 | a0001c0003t0003g0229 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.28-878_28-877insTT others(781): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012030 | |||||
chr19:4012045
|
T | G | 2 | a0001c0004t0003g0247a0001c0004t0012g0245 | 2 | HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.28-878T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012045 | ||||||
chr19:4012046
|
G | T | 28 | a0001c0003t0004g0228a0001c0004t0003g0005a0001c0004t0003g0246others(25): Show | 31 | HG00609.hp1 HG02145.hp1 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.28-877G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012046 | ||||||
chr19:4012047
|
G | GGGTGTGG others(59): Show |
1 | a0001c0005t0005g0232 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.28-862_28-861insGG others(64): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012047 | |||||
chr19:4012047
|
G | GGGTGTGG others(59): Show |
1 | a0001c0012t0001g0296 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.28-845_28-844insGG others(64): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012047 | |||||
chr19:4012047
|
G | GGGTGTGG others(27): Show |
6 | a0001c0004t0003g0303a0001c0005t0001g0039a0001c0005t0001g0260others(3): Show | 6 | HG01884.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-872_28-839dupGT others(32): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012047 | |||||
chr19:4012047
|
G | GGGTGTGG others(693): Show |
5 | a0001c0005t0005g0019a0001c0005t0005g0231a0001c0005t0005g0244others(2): Show | 5 | HG00639.hp1 HG02738.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-861_28-860insTT others(698): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012047 | |||||
chr19:4012047
|
G | GGGTGTGG others(710): Show |
1 | a0001c0007t0001g0235 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.28-861_28-860insTT others(715): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012047 | |||||
chr19:4012047
|
G | GGGTGTGG others(793): Show |
1 | a0001c0005t0005g0236 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.28-861_28-860insTT others(798): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012047 | |||||
chr19:4012047
|
G | GGGTGTGG others(810): Show |
1 | a0001c0005t0005g0237 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.28-861_28-860insTT others(815): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012047 | |||||
chr19:4012047
|
G | GGGTGTGG others(695): Show |
5 | a0001c0005t0005g0239a0001c0005t0005g0240a0001c0005t0005g0242others(2): Show | 5 | HG01361.hp2 HG01496.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-861_28-860insTT others(700): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012047 | |||||
chr19:4012047
|
G | GTGTGGAG others(74): Show |
2 | a0001c0004t0003g0247a0001c0004t0012g0245 | 2 | HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.28-876_28-875insTG others(79): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012047 | ||||||
chr19:4012047
|
G | T | 28 | a0001c0003t0004g0228a0001c0004t0003g0005a0001c0004t0003g0246others(25): Show | 31 | HG00609.hp1 HG02145.hp1 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.28-876G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012047 | ||||||
chr19:4012099
|
G | A | 52 | a0001c0003t0003g0229a0001c0003t0004g0228a0001c0004t0003g0005others(49): Show | 55 | HG00609.hp1 HG00639.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.28-824G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012099 | ||||||
chr19:4012149
|
A | G | 91 | a0001c0002t0004g0297a0001c0002t0004g0298a0001c0003t0001g0217others(88): Show | 97 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.28-774A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012149 | ||||||
chr19:4012250
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.28-673C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012250 | ||||||
chr19:4012339
|
A | G | 4 | a0001c0002t0003g0198a0001c0002t0003g0199a0001c0002t0006g0209others(1): Show | 4 | HG01109.hp2 HG02622.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-584A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012339 | ||||||
chr19:4012493
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.28-430C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012493 | ||||||
chr19:4012528
|
C | T | 1 | a0001c0003t0006g0293 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.28-395C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012528 | ||||||
chr19:4012567
|
G | A | 3 | a0001c0003t0002g0268a0001c0003t0002g0269a0001c0003t0002g0270 | 3 | HG01516.hp2 HG01517.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.28-356G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012567 | ||||||
chr19:4012740
|
G | T | 1 | a0001c0002t0004g0213 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.28-183G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012740 | ||||||
chr19:4012857
|
G | C | 1 | a0001c0001t0001g0114 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.28-66G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012857 | ||||||
chr19:4012880
|
G | A | 1 | a0001c0007t0001g0279 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.28-43G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012880 | ||||||
chr19:4012917
|
C | T | 1 | a0001c0002t0004g0213 | 1 | HG03471.hp1 | splice_region_variant&intron_variant | LOW | c.28-6C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012917 | ||||||
chr19:4013391
|
C | T | 52 | a0001c0003t0003g0229a0001c0003t0004g0228a0001c0004t0003g0005others(49): Show | 55 | HG00609.hp1 HG00639.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.454+42C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4013391 | ||||||
chr19:4013449
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.454+100G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4013449 | ||||||
chr19:4013456
|
A | G | 2 | a0001c0002t0004g0297a0001c0002t0004g0298 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.454+107A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4013456 | ||||||
chr19:4013652
|
C | CA | 35 | a0001c0003t0001g0217a0001c0003t0001g0218a0001c0003t0001g0277others(32): Show | 38 | HG00280.hp1 HG00423.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.454+304dupA | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4013652 | |||||
chr19:4013685
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.454+336G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4013685 | ||||||
chr19:4013689
|
A | G | 1 | a0001c0001t0001g0018 | 2 | NA18944.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.454+340A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4013689 | ||||||
chr19:4013707
|
T | A | 5 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 5 | HG00323.hp2 HG01069.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.454+358T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4013707 | ||||||
chr19:4013740
|
C | T | 2 | a0001c0002t0002g0111a0001c0002t0002g0112 | 2 | HG03654.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.454+391C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4013740 | ||||||
chr19:4013859
|
G | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG00323.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.454+510G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4013859 | ||||||
chr19:4013901
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.454+552C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4013901 | ||||||
chr19:4014053
|
GGC | G | 3 | a0001c0005t0005g0019a0001c0005t0005g0244a0001c0005t0017g0019 | 3 | HG00639.hp1 HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.454+705_454+706del others(2): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014053 | ||||||
chr19:4014067
|
G | A | 53 | a0001c0002t0004g0166a0001c0003t0003g0229a0001c0003t0004g0228others(50): Show | 56 | HG00609.hp1 HG00639.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.454+718G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014067 | ||||||
chr19:4014112
|
G | T | 24 | a0001c0004t0003g0005a0001c0004t0003g0246a0001c0004t0003g0247others(21): Show | 27 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(24): Show |
intron_variant | MODIFIER | c.454+763G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014112 | ||||||
chr19:4014177
|
G | A | 1 | a0001c0002t0004g0157 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.454+828G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014177 | ||||||
chr19:4014276
|
A | G | 1 | a0001c0002t0004g0213 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.454+927A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014276 | ||||||
chr19:4014279
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.454+930G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014279 | ||||||
chr19:4014284
|
C | T | 1 | a0001c0002t0004g0298 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.454+935C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014284 | ||||||
chr19:4014334
|
G | T | 4 | a0001c0003t0001g0294a0001c0003t0006g0291a0001c0003t0006g0292others(1): Show | 4 | HG00423.hp1 HG02486.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.454+985G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014334 | ||||||
chr19:4014402
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.454+1053G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014402 | ||||||
chr19:4014472
|
C | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0134others(1): Show | 4 | HG00323.hp1 HG01255.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.454+1123C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014472 | ||||||
chr19:4014664
|
C | T | 3 | a0001c0007t0002g0284a0001c0007t0002g0285a0001c0007t0002g0286 | 3 | HG01123.hp2 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.454+1315C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014664 | ||||||
chr19:4014665
|
G | A | 2 | a0001c0003t0002g0271a0001c0003t0002g0272 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.454+1316G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014665 | ||||||
chr19:4014787
|
C | T | 10 | a0001c0004t0003g0247a0001c0004t0003g0253a0001c0004t0003g0254others(7): Show | 10 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.454+1438C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014787 | ||||||
chr19:4014834
|
G | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0055a0001c0001t0001g0172others(8): Show | 14 | HG00639.hp2 HG01074.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.454+1485G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014834 | ||||||
chr19:4014834
|
G | T | 1 | a0001c0001t0001g0018 | 2 | NA18944.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.454+1485G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014834 | ||||||
chr19:4014904
|
TC | T | 8 | a0001c0002t0004g0213a0001c0003t0001g0294a0001c0003t0006g0290others(5): Show | 8 | HG00423.hp1 HG02486.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.454+1557delC | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4014904 | |||||
chr19:4015066
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.454+1717A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4015066 | ||||||
chr19:4015082
|
G | A | 1 | a0001c0002t0004g0213 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.454+1733G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4015082 | ||||||
chr19:4015123
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.454+1774A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4015123 | ||||||
chr19:4015411
|
T | C | 20 | a0001c0002t0004g0298a0001c0004t0003g0005a0001c0004t0003g0246others(17): Show | 23 | HG02145.hp1 HG02280.hp2 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.454+2062T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4015411 | ||||||
chr19:4015417
|
CACCAGTG others(10): Show |
C | 2 | a0003c0011t0001g0288a0003c0011t0001g0289 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.454+2069_454+2085d others(19): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4015417 | ||||||
chr19:4015557
|
G | A | 6 | a0001c0002t0001g0017a0001c0002t0001g0201a0001c0002t0001g0202others(3): Show | 7 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.454+2208G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4015557 | ||||||
chr19:4015590
|
T | C | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | HG01106.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.454+2241T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4015590 | ||||||
chr19:4015751
|
A | G | 7 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0152others(4): Show | 7 | HG03239.hp1 HG03669.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.454+2402A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4015751 | ||||||
chr19:4015953
|
A | T | 1 | a0001c0001t0001g0062 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.454+2604A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4015953 | ||||||
chr19:4015969
|
G | C | 1 | a0001c0001t0001g0018 | 2 | NA18944.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.454+2620G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4015969 | ||||||
chr19:4015986
|
C | T | 1 | a0001c0003t0006g0293 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.454+2637C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4015986 | ||||||
chr19:4016007
|
T | G | 53 | a0001c0001t0001g0170a0001c0002t0003g0227a0001c0002t0004g0166others(50): Show | 56 | HG00280.hp1 HG00423.hp1 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.454+2658T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4016007 | ||||||
chr19:4016031
|
C | T | 26 | a0001c0003t0001g0218a0001c0003t0001g0277a0001c0003t0002g0020others(23): Show | 29 | HG00280.hp1 HG00741.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.454+2682C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4016031 | ||||||
chr19:4016107
|
G | T | 2 | a0001c0003t0002g0271a0001c0003t0002g0272 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.454+2758G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4016107 | ||||||
chr19:4016141
|
C | T | 1 | a0001c0007t0001g0279 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.454+2792C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4016141 | ||||||
chr19:4016313
|
C | A | 1 | a0001c0001t0001g0115 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.454+2964C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4016313 | ||||||
chr19:4016424
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.454+3075T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4016424 | ||||||
chr19:4016577
|
T | C | 1 | a0001c0005t0001g0039 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.454+3228T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4016577 | ||||||
chr19:4016793
|
A | G | 1 | a0001c0002t0004g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.454+3444A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4016793 | ||||||
chr19:4016912
|
TGCTTGCC others(7): Show |
T | 1 | a0001c0005t0001g0039 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.454+3564_454+3577d others(16): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4016912 | ||||||
chr19:4017483
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.454+4134C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4017483 | ||||||
chr19:4017561
|
T | A | 1 | a0001c0001t0001g0126 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.454+4212T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4017561 | ||||||
chr19:4017583
|
C | T | 7 | a0001c0006t0004g0028a0001c0006t0004g0029a0001c0006t0004g0030others(4): Show | 7 | HG01884.hp1 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.454+4234C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4017583 | ||||||
chr19:4017680
|
C | CT | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(213): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.454+4350dupT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4017680 | |||||
chr19:4017680
|
C | CTT | 36 | a0001c0001t0001g0046a0001c0001t0001g0061a0001c0001t0001g0108others(33): Show | 39 | HG00423.hp1 HG00741.hp1 HG02145.hp1 others(36): Show |
intron_variant | MODIFIER | c.454+4349_454+4350d others(4): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4017680 | |||||
chr19:4017680
|
C | CTTT | 29 | a0001c0003t0001g0217a0001c0003t0001g0218a0001c0003t0001g0277others(26): Show | 32 | HG00280.hp1 HG00741.hp2 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.454+4348_454+4350d others(5): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4017680 | |||||
chr19:4017740
|
C | T | 1 | a0001c0007t0001g0235 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.454+4391C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4017740 | ||||||
chr19:4017921
|
T | C | 87 | a0001c0002t0004g0298a0001c0003t0001g0217a0001c0003t0001g0218others(84): Show | 93 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.454+4572T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4017921 | ||||||
chr19:4017955
|
G | A | 34 | a0001c0002t0003g0227a0001c0002t0004g0167a0001c0002t0004g0169others(31): Show | 37 | HG00280.hp1 HG00741.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.454+4606G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4017955 | ||||||
chr19:4018083
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.454+4734A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018083 | ||||||
chr19:4018096
|
G | A | 1 | a0001c0001t0022g0057 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.454+4747G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018096 | ||||||
chr19:4018102
|
A | G | 87 | a0001c0002t0004g0298a0001c0003t0001g0217a0001c0003t0001g0218others(84): Show | 93 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.454+4753A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018102 | ||||||
chr19:4018107
|
C | T | 1 | a0001c0003t0015g0216 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.454+4758C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018107 | ||||||
chr19:4018266
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.454+4917C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018266 | ||||||
chr19:4018425
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.454+5076C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018425 | ||||||
chr19:4018442
|
T | C | 34 | a0001c0003t0001g0217a0001c0003t0001g0218a0001c0003t0001g0277others(31): Show | 37 | HG00280.hp1 HG00423.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.454+5093T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018442 | ||||||
chr19:4018483
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.454+5134G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018483 | ||||||
chr19:4018486
|
C | A | 29 | a0001c0003t0003g0229a0001c0003t0004g0228a0001c0004t0003g0253others(26): Show | 29 | HG00609.hp1 HG00639.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.454+5137C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018486 | ||||||
chr19:4018520
|
C | T | 1 | a0001c0014t0001g0204 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.454+5171C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018520 | ||||||
chr19:4018528
|
C | T | 18 | a0001c0005t0005g0019a0001c0005t0005g0231a0001c0005t0005g0232others(15): Show | 18 | HG00609.hp1 HG00639.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.454+5179C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018528 | ||||||
chr19:4018543
|
G | A | 1 | a0001c0001t0001g0006 | 2 | HG01496.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.454+5194G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018543 | ||||||
chr19:4018579
|
A | G | 18 | a0001c0005t0005g0019a0001c0005t0005g0231a0001c0005t0005g0232others(15): Show | 18 | HG00609.hp1 HG00639.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.454+5230A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018579 | ||||||
chr19:4018749
|
G | C | 28 | a0001c0003t0001g0294a0001c0003t0006g0290a0001c0003t0006g0291others(25): Show | 31 | HG00423.hp1 HG02145.hp1 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.455-5287G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018749 | ||||||
chr19:4018758
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.455-5278C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018758 | ||||||
chr19:4018880
|
C | T | 9 | a0001c0004t0003g0253a0001c0005t0001g0039a0001c0005t0001g0260others(6): Show | 9 | HG01884.hp2 HG02895.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.455-5156C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018880 | ||||||
chr19:4019258
|
G | C | 2 | a0002c0010t0002g0280a0002c0010t0002g0281 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.455-4778G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019258 | ||||||
chr19:4019269
|
C | G | 31 | a0001c0002t0003g0196a0001c0003t0003g0229a0001c0003t0004g0228others(28): Show | 31 | HG00609.hp1 HG00639.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.455-4767C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019269 | ||||||
chr19:4019272
|
C | T | 2 | a0001c0006t0004g0034a0001c0006t0004g0035 | 2 | HG02055.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.455-4764C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019272 | ||||||
chr19:4019436
|
G | A | 30 | a0001c0003t0003g0229a0001c0003t0004g0228a0001c0004t0003g0253others(27): Show | 30 | HG00609.hp1 HG00639.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.455-4600G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019436 | ||||||
chr19:4019642
|
C | T | 1 | a0001c0003t0003g0229 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.455-4394C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019642 | ||||||
chr19:4019675
|
C | A | 1 | a0001c0004t0008g0300 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.455-4361C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019675 | ||||||
chr19:4019700
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.455-4336A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019700 | ||||||
chr19:4019769
|
G | A | 1 | a0001c0005t0001g0039 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.455-4267G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019769 | ||||||
chr19:4019771
|
A | C | 1 | a0001c0005t0001g0039 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.455-4265A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019771 | ||||||
chr19:4019774
|
G | A | 1 | a0001c0005t0005g0232 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.455-4262G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019774 | ||||||
chr19:4019784
|
G | T | 1 | a0001c0001t0001g0142 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.455-4252G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019784 | ||||||
chr19:4019815
|
C | T | 29 | a0001c0003t0003g0229a0001c0003t0004g0228a0001c0004t0003g0253others(26): Show | 29 | HG00609.hp1 HG00639.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.455-4221C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019815 | ||||||
chr19:4019816
|
G | T | 1 | a0001c0005t0001g0039 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.455-4220G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019816 | ||||||
chr19:4019821
|
C | T | 1 | a0001c0002t0004g0298 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.455-4215C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019821 | ||||||
chr19:4019846
|
T | G | 1 | a0001c0001t0001g0160 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.455-4190T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019846 | ||||||
chr19:4019856
|
G | T | 6 | a0001c0001t0001g0170a0001c0002t0003g0227a0001c0002t0004g0167others(3): Show | 6 | HG02559.hp1 HG02717.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.455-4180G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019856 | ||||||
chr19:4019865
|
G | C | 30 | a0001c0003t0003g0229a0001c0003t0004g0228a0001c0004t0003g0253others(27): Show | 30 | HG00609.hp1 HG00639.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.455-4171G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019865 | ||||||
chr19:4019922
|
CT | C | 26 | a0001c0001t0001g0081a0001c0001t0001g0180a0001c0004t0003g0005others(23): Show | 29 | HG00639.hp2 HG02145.hp1 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.455-4100delT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4019922 | |||||
chr19:4019927
|
T | C | 24 | a0001c0003t0001g0277a0001c0003t0002g0020a0001c0003t0002g0021others(21): Show | 27 | HG00280.hp1 HG00741.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.455-4109T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019927 | ||||||
chr19:4019940
|
A | G | 13 | a0001c0006t0003g0038a0001c0006t0004g0026a0001c0006t0004g0028others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.455-4096A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019940 | ||||||
chr19:4019956
|
G | A | 2 | a0003c0011t0001g0288a0003c0011t0001g0289 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.455-4080G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019956 | ||||||
chr19:4019960
|
G | A | 88 | a0001c0002t0004g0298a0001c0003t0001g0217a0001c0003t0001g0218others(85): Show | 94 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.455-4076G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019960 | ||||||
chr19:4019963
|
C | T | 88 | a0001c0002t0004g0298a0001c0003t0001g0217a0001c0003t0001g0218others(85): Show | 94 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.455-4073C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019963 | ||||||
chr19:4019969
|
T | C | 88 | a0001c0002t0004g0298a0001c0003t0001g0217a0001c0003t0001g0218others(85): Show | 94 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.455-4067T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019969 | ||||||
chr19:4020013
|
T | C | 1 | a0001c0004t0003g0301 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.455-4023T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020013 | ||||||
chr19:4020165
|
C | G | 1 | a0001c0001t0001g0192 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.455-3871C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020165 | ||||||
chr19:4020304
|
G | A | 2 | a0003c0011t0001g0288a0003c0011t0001g0289 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.455-3732G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020304 | ||||||
chr19:4020370
|
T | C | 2 | a0003c0011t0001g0288a0003c0011t0001g0289 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.455-3666T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020370 | ||||||
chr19:4020372
|
C | T | 27 | a0001c0003t0001g0217a0001c0003t0001g0218a0001c0003t0001g0277others(24): Show | 30 | HG00280.hp1 HG00741.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.455-3664C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020372 | ||||||
chr19:4020447
|
T | C | 27 | a0001c0003t0001g0217a0001c0003t0001g0218a0001c0003t0001g0277others(24): Show | 30 | HG00280.hp1 HG00741.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.455-3589T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020447 | ||||||
chr19:4020460
|
G | C | 1 | a0001c0002t0004g0200 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.455-3576G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020460 | ||||||
chr19:4020495
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.455-3541G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020495 | ||||||
chr19:4020529
|
A | G | 4 | a0001c0007t0002g0022a0001c0007t0002g0284a0001c0007t0002g0285others(1): Show | 5 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.455-3507A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020529 | ||||||
chr19:4020599
|
C | T | 3 | a0001c0002t0004g0213a0001c0003t0003g0229a0001c0003t0004g0228 | 3 | HG01243.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.455-3437C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020599 | ||||||
chr19:4020611
|
T | A | 1 | a0001c0002t0003g0196 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.455-3425T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020611 | ||||||
chr19:4020631
|
A | T | 5 | a0001c0002t0003g0227a0001c0002t0004g0167a0001c0002t0004g0169others(2): Show | 5 | HG02559.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.455-3405A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020631 | ||||||
chr19:4020637
|
T | G | 27 | a0001c0003t0001g0217a0001c0003t0001g0218a0001c0003t0001g0277others(24): Show | 30 | HG00280.hp1 HG00741.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.455-3399T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020637 | ||||||
chr19:4020712
|
A | T | 23 | a0001c0004t0003g0005a0001c0004t0003g0246a0001c0004t0003g0247others(20): Show | 26 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.455-3324A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020712 | ||||||
chr19:4020739
|
T | C | 1 | a0001c0003t0015g0216 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.455-3297T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020739 | ||||||
chr19:4020793
|
G | T | 14 | a0001c0001t0001g0002a0001c0001t0001g0055a0001c0001t0001g0139others(11): Show | 17 | HG00639.hp2 HG00673.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.455-3243G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020793 | ||||||
chr19:4020814
|
TG | T | 23 | a0001c0001t0001g0170a0001c0002t0003g0227a0001c0002t0004g0166others(20): Show | 23 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.455-3219delG | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4020814 | |||||
chr19:4020816
|
G | C | 22 | a0001c0001t0001g0170a0001c0002t0003g0227a0001c0002t0004g0166others(19): Show | 22 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.455-3220G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020816 | ||||||
chr19:4020872
|
G | T | 2 | a0003c0011t0001g0288a0003c0011t0001g0289 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.455-3164G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020872 | ||||||
chr19:4020939
|
G | A | 1 | a0001c0005t0001g0039 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.455-3097G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020939 | ||||||
chr19:4021037
|
T | A | 5 | a0001c0003t0001g0294a0001c0003t0006g0290a0001c0003t0006g0291others(2): Show | 5 | HG00423.hp1 HG02486.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.455-2999T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021037 | ||||||
chr19:4021165
|
A | G | 1 | a0001c0006t0003g0038 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.455-2871A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021165 | ||||||
chr19:4021170
|
T | C | 5 | a0001c0003t0001g0294a0001c0003t0006g0290a0001c0003t0006g0291others(2): Show | 5 | HG00423.hp1 HG02486.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.455-2866T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021170 | ||||||
chr19:4021241
|
C | T | 30 | a0001c0003t0003g0229a0001c0003t0004g0228a0001c0004t0003g0253others(27): Show | 30 | HG00609.hp1 HG00639.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.455-2795C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021241 | ||||||
chr19:4021257
|
A | G | 1 | a0001c0001t0001g0003 | 3 | HG02080.hp1 HG02132.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.455-2779A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021257 | ||||||
chr19:4021273
|
C | T | 1 | a0001c0002t0020g0299 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.455-2763C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021273 | ||||||
chr19:4021374
|
T | C | 4 | a0001c0003t0001g0294a0001c0003t0006g0291a0001c0003t0006g0292others(1): Show | 4 | HG00423.hp1 HG02486.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-2662T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021374 | ||||||
chr19:4021469
|
C | T | 23 | a0001c0004t0003g0005a0001c0004t0003g0246a0001c0004t0003g0247others(20): Show | 26 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.455-2567C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021469 | ||||||
chr19:4021471
|
GT | G | 19 | a0001c0005t0005g0019a0001c0005t0005g0231a0001c0005t0005g0232others(16): Show | 19 | HG00609.hp1 HG00639.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.455-2564delT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021471 | ||||||
chr19:4021473
|
C | G | 19 | a0001c0005t0005g0019a0001c0005t0005g0231a0001c0005t0005g0232others(16): Show | 19 | HG00609.hp1 HG00639.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.455-2563C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021473 | ||||||
chr19:4021580
|
G | A | 19 | a0001c0005t0005g0019a0001c0005t0005g0231a0001c0005t0005g0232others(16): Show | 19 | HG00609.hp1 HG00639.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.455-2456G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021580 | ||||||
chr19:4021585
|
T | C | 1 | a0001c0002t0004g0213 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.455-2451T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021585 | ||||||
chr19:4021639
|
T | C | 1 | a0001c0001t0014g0135 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.455-2397T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021639 | ||||||
chr19:4021727
|
C | T | 2 | a0001c0002t0004g0178a0001c0002t0004g0297 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.455-2309C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021727 | ||||||
chr19:4021740
|
T | G | 7 | a0001c0004t0003g0253a0001c0005t0001g0039a0001c0005t0001g0260others(4): Show | 7 | HG01884.hp2 HG02895.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.455-2296T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021740 | ||||||
chr19:4021742
|
C | CT | 28 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(25): Show | 28 | HG00609.hp1 HG00639.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.455-2273dupT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4021742 | |||||
chr19:4021742
|
CT | C | 57 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0064others(54): Show | 60 | HG00423.hp1 HG00639.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.455-2273delT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4021742 | |||||
chr19:4021880
|
G | C | 1 | a0001c0002t0004g0213 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.455-2156G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021880 | ||||||
chr19:4021955
|
C | T | 1 | a0001c0004t0003g0252 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.455-2081C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021955 | ||||||
chr19:4022097
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.455-1939A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022097 | ||||||
chr19:4022167
|
G | A | 61 | a0001c0002t0004g0298a0001c0003t0001g0294a0001c0003t0003g0229others(58): Show | 64 | HG00423.hp1 HG00609.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.455-1869G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022167 | ||||||
chr19:4022337
|
G | T | 1 | a0001c0002t0004g0175 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.455-1699G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022337 | ||||||
chr19:4022364
|
T | C | 1 | a0001c0004t0003g0256 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.455-1672T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022364 | ||||||
chr19:4022413
|
G | A | 1 | a0001c0008t0001g0168 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.455-1623G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022413 | ||||||
chr19:4022453
|
G | A | 1 | a0001c0003t0004g0228 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.455-1583G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022453 | ||||||
chr19:4022465
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.455-1571C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022465 | ||||||
chr19:4022546
|
T | G | 6 | a0001c0002t0001g0017a0001c0002t0001g0201a0001c0002t0001g0202others(3): Show | 7 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.455-1490T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022546 | ||||||
chr19:4022550
|
T | G | 1 | a0001c0001t0001g0183 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.455-1486T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022550 | ||||||
chr19:4022568
|
G | A | 9 | a0001c0004t0003g0253a0001c0005t0001g0039a0001c0005t0001g0260others(6): Show | 9 | HG01884.hp2 HG02895.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.455-1468G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022568 | ||||||
chr19:4022617
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0146 | 2 | HG02735.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.455-1419C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022617 | ||||||
chr19:4022629
|
A | G | 88 | a0001c0002t0004g0298a0001c0003t0001g0217a0001c0003t0001g0218others(85): Show | 94 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.455-1407A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022629 | ||||||
chr19:4022658
|
G | A | 1 | a0001c0002t0004g0298 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.455-1378G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022658 | ||||||
chr19:4022665
|
C | T | 30 | a0001c0003t0003g0229a0001c0003t0004g0228a0001c0004t0003g0253others(27): Show | 30 | HG00609.hp1 HG00639.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.455-1371C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022665 | ||||||
chr19:4022837
|
AT | A | 29 | a0001c0003t0003g0229a0001c0003t0004g0228a0001c0004t0003g0253others(26): Show | 29 | HG00609.hp1 HG00639.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.455-1185delT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4022837 | |||||
chr19:4022886
|
C | T | 1 | a0001c0015t0005g0124 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.455-1150C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022886 | ||||||
chr19:4022901
|
G | A | 2 | a0001c0003t0002g0282a0001c0003t0002g0283 | 2 | NA18983.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.455-1135G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022901 | ||||||
chr19:4023032
|
G | A | 1 | a0001c0002t0004g0157 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.455-1004G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023032 | ||||||
chr19:4023100
|
A | G | 1 | a0001c0002t0001g0078 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.455-936A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023100 | ||||||
chr19:4023140
|
C | T | 1 | a0001c0002t0004g0213 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.455-896C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023140 | ||||||
chr19:4023172
|
C | CA | 97 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0055others(94): Show | 106 | HG00609.hp1 HG00639.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.455-847dupA | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4023172 | |||||
chr19:4023172
|
C | CAA | 34 | a0001c0001t0001g0226a0001c0002t0001g0044a0001c0002t0002g0111others(31): Show | 37 | HG00280.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.455-848_455-847dup others(2): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4023172 | |||||
chr19:4023172
|
CA | C | 6 | a0001c0001t0001g0060a0001c0001t0001g0110a0001c0001t0001g0203others(3): Show | 6 | HG01255.hp2 HG01256.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.455-847delA | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4023172 | |||||
chr19:4023190
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.455-846T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023190 | ||||||
chr19:4023254
|
G | A | 1 | a0001c0002t0004g0298 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.455-782G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023254 | ||||||
chr19:4023265
|
G | A | 1 | a0001c0002t0004g0200 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.455-771G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023265 | ||||||
chr19:4023312
|
C | G | 9 | a0001c0001t0001g0106a0001c0002t0010g0105a0001c0003t0001g0294others(6): Show | 9 | HG00423.hp1 HG02165.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.455-724C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023312 | ||||||
chr19:4023350
|
T | C | 1 | a0001c0014t0001g0204 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.455-686T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023350 | ||||||
chr19:4023459
|
C | CCAAAA | 6 | a0001c0003t0001g0294a0001c0003t0002g0273a0001c0003t0006g0290others(3): Show | 6 | HG00423.hp1 HG02717.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.455-552_455-548dup others(5): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4023459 | |||||
chr19:4023459
|
C | CCAAAACA others(3): Show |
2 | a0001c0005t0001g0295a0001c0012t0001g0296 | 2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.455-557_455-548dup others(10): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4023459 | |||||
chr19:4023521
|
C | T | 3 | a0001c0002t0004g0157a0003c0011t0001g0288a0003c0011t0001g0289 | 3 | HG02895.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.455-515C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023521 | ||||||
chr19:4023748
|
C | T | 1 | a0001c0003t0006g0290 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.455-288C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023748 | ||||||
chr19:4023764
|
C | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0192 | 2 | NA18969.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.455-272C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023764 | ||||||
chr19:4023830
|
A | G | 65 | a0001c0001t0001g0018a0001c0001t0001g0080a0001c0001t0001g0108others(62): Show | 69 | HG00609.hp1 HG00639.hp1 HG01168.hp2 others(66): Show |
intron_variant | MODIFIER | c.455-206A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023830 | ||||||
chr19:4023840
|
G | T | 17 | a0001c0001t0001g0097a0001c0001t0001g0137a0001c0001t0001g0159others(14): Show | 18 | HG00438.hp2 HG02273.hp1 NA18944.hp1 others(15): Show |
intron_variant | MODIFIER | c.455-196G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023840 | ||||||
chr19:4024022
|
G | A | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.455-14G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4024022 | ||||||
chr19:4024339
|
T | C | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(248): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.539+219T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024339 | ||||||
chr19:4024351
|
G | T | 1 | a0001c0001t0001g0104 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.539+231G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024351 | ||||||
chr19:4024353
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.539+233G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024353 | ||||||
chr19:4024367
|
C | A | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(247): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.539+247C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024367 | ||||||
chr19:4024371
|
T | G | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(247): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.539+251T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024371 | ||||||
chr19:4024377
|
G | A | 4 | a0001c0009t0001g0010a0001c0009t0001g0072a0001c0009t0001g0073others(1): Show | 5 | HG00558.hp1 HG02155.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.539+257G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024377 | ||||||
chr19:4024461
|
A | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.539+341A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024461 | ||||||
chr19:4024519
|
G | A | 11 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(8): Show | 13 | HG01109.hp2 HG02145.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.539+399G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024519 | ||||||
chr19:4024527
|
G | A | 27 | a0001c0002t0001g0044a0001c0002t0002g0111a0001c0002t0002g0112others(24): Show | 30 | HG00280.hp1 HG00735.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.539+407G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024527 | ||||||
chr19:4024550
|
G | A | 26 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(23): Show | 29 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.539+430G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024550 | ||||||
chr19:4024655
|
G | C | 1 | a0001c0009t0001g0072 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.539+535G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024655 | ||||||
chr19:4024657
|
A | G | 1 | a0001c0009t0001g0072 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.539+537A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024657 | ||||||
chr19:4024691
|
T | G | 1 | a0001c0009t0001g0072 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.539+571T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024691 | ||||||
chr19:4024757
|
T | A | 1 | a0001c0001t0001g0048 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.539+637T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024757 | ||||||
chr19:4024762
|
GT | G | 26 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(23): Show | 29 | HG01109.hp2 HG01243.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.539+654delT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4024762 | |||||
chr19:4024762
|
GTT | G | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.539+653_539+654del others(2): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4024762 | |||||
chr19:4024808
|
C | T | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(247): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.539+688C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024808 | ||||||
chr19:4024853
|
C | T | 2 | a0001c0005t0005g0239a0001c0005t0005g0242 | 2 | HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.539+733C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024853 | ||||||
chr19:4024892
|
A | G | 7 | a0001c0001t0001g0056a0001c0001t0001g0091a0001c0001t0001g0092others(4): Show | 7 | HG02074.hp1 HG02080.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.539+772A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024892 | ||||||
chr19:4024893
|
G | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.539+773G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024893 | ||||||
chr19:4024984
|
C | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.539+864C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024984 | ||||||
chr19:4025043
|
C | T | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(247): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.539+923C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025043 | ||||||
chr19:4025056
|
G | T | 7 | a0001c0002t0006g0209a0001c0002t0020g0299a0001c0003t0001g0294others(4): Show | 7 | HG00423.hp1 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.539+936G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025056 | ||||||
chr19:4025062
|
C | T | 7 | a0001c0002t0006g0209a0001c0002t0020g0299a0001c0003t0001g0294others(4): Show | 7 | HG00423.hp1 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.539+942C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025062 | ||||||
chr19:4025115
|
T | G | 1 | a0001c0005t0005g0240 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.539+995T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025115 | ||||||
chr19:4025147
|
G | A | 26 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(23): Show | 29 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.539+1027G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025147 | ||||||
chr19:4025156
|
G | A | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.539+1036G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025156 | ||||||
chr19:4025159
|
C | T | 1 | a0001c0003t0006g0290 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.539+1039C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025159 | ||||||
chr19:4025281
|
G | A | 5 | a0001c0003t0002g0268a0001c0003t0002g0269a0001c0003t0002g0270others(2): Show | 5 | HG01346.hp2 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.539+1161G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025281 | ||||||
chr19:4025299
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.539+1179T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025299 | ||||||
chr19:4025379
|
C | G | 1 | a0001c0006t0004g0029 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.539+1259C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025379 | ||||||
chr19:4025486
|
C | T | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.539+1366C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025486 | ||||||
chr19:4025539
|
C | T | 2 | a0001c0003t0003g0229a0001c0003t0004g0228 | 2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.539+1419C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025539 | ||||||
chr19:4025540
|
G | A | 1 | a0001c0001t0010g0140 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.539+1420G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025540 | ||||||
chr19:4025618
|
G | A | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.539+1498G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025618 | ||||||
chr19:4025669
|
A | ACCTCATC others(8): Show |
2 | a0001c0002t0001g0206a0001c0002t0001g0207 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.539+1553_539+1554i others(17): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4025669 | |||||
chr19:4025673
|
C | CGTCTTTC others(8): Show |
1 | a0001c0001t0001g0048 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.539+1567_539+1568i others(17): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4025673 | |||||
chr19:4025673
|
C | T | 26 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(23): Show | 29 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.539+1553C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025673 | ||||||
chr19:4025688
|
C | CGTCTTTC others(8): Show |
247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(244): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.539+1573_539+1574i others(17): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4025688 | |||||
chr19:4025688
|
C | T | 3 | a0001c0001t0001g0048a0001c0002t0001g0206a0001c0002t0001g0207 | 3 | HG01069.hp2 HG01071.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.539+1568C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025688 | ||||||
chr19:4025752
|
G | GT | 26 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(23): Show | 29 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.539+1633dupT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4025752 | |||||
chr19:4025911
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.539+1791A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025911 | ||||||
chr19:4025947
|
G | A | 1 | a0001c0001t0001g0006 | 2 | HG01496.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.539+1827G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025947 | ||||||
chr19:4025966
|
C | T | 12 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0053others(9): Show | 15 | HG00642.hp2 HG01070.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.539+1846C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025966 | ||||||
chr19:4025980
|
A | C | 26 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(23): Show | 29 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.539+1860A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025980 | ||||||
chr19:4025991
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.539+1871G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025991 | ||||||
chr19:4025998
|
C | T | 1 | a0001c0002t0002g0151 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.539+1878C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025998 | ||||||
chr19:4026006
|
G | A | 26 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(23): Show | 29 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.539+1886G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026006 | ||||||
chr19:4026073
|
C | CA | 34 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(31): Show | 37 | HG01109.hp2 HG01884.hp2 HG02145.hp1 others(34): Show |
intron_variant | MODIFIER | c.539+1973dupA | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026073 | |||||
chr19:4026073
|
C | CAAAA | 14 | a0001c0002t0004g0166a0001c0002t0004g0200a0001c0002t0004g0213others(11): Show | 14 | HG02055.hp2 HG02451.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.539+1970_539+1973d others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026073 | |||||
chr19:4026073
|
C | CAAAAA | 8 | a0001c0002t0004g0157a0001c0002t0004g0175a0001c0002t0004g0178others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.539+1969_539+1973d others(7): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026073 | |||||
chr19:4026073
|
CA | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(184): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.539+1973delA | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026073 | |||||
chr19:4026073
|
CAA | C | 27 | a0001c0002t0002g0111a0001c0002t0002g0112a0001c0002t0002g0151others(24): Show | 30 | HG00280.hp1 HG00741.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.539+1972_539+1973d others(4): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026073 | |||||
chr19:4026158
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.540-1988T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026158 | ||||||
chr19:4026201
|
C | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0134a0001c0002t0018g0138 | 4 | HG02280.hp1 HG02630.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-1945C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026201 | ||||||
chr19:4026259
|
A | C | 1 | a0001c0001t0001g0046 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.540-1887A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026259 | ||||||
chr19:4026279
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.540-1867C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026279 | ||||||
chr19:4026295
|
G | GCTAATTT others(300): Show |
1 | a0001c0002t0004g0171 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.540-1842_540-1841i others(309): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026295 | |||||
chr19:4026295
|
G | GCTAATTT others(311): Show |
5 | a0001c0002t0004g0157a0001c0002t0004g0167a0001c0002t0004g0175others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.540-1842_540-1841i others(320): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026295 | |||||
chr19:4026295
|
G | GCTAATTT others(312): Show |
7 | a0001c0002t0004g0169a0001c0002t0004g0178a0001c0002t0004g0200others(4): Show | 7 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.540-1842_540-1841i others(321): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026295 | |||||
chr19:4026295
|
G | GCTAATTT others(313): Show |
9 | a0001c0002t0003g0227a0001c0002t0004g0166a0001c0002t0004g0297others(6): Show | 9 | HG02257.hp2 HG02572.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.540-1842_540-1841i others(322): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026295 | |||||
chr19:4026295
|
G | GCTAATTT others(314): Show |
1 | a0001c0002t0004g0298 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.540-1842_540-1841i others(323): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026295 | |||||
chr19:4026295
|
G | GCTAATTT others(315): Show |
2 | a0001c0002t0004g0213a0001c0006t0004g0035 | 2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.540-1842_540-1841i others(324): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026295 | |||||
chr19:4026295
|
G | GCTAATTT others(316): Show |
2 | a0001c0002t0008g0212a0001c0004t0008g0300 | 2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.540-1842_540-1841i others(325): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026295 | |||||
chr19:4026381
|
A | C | 303 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(300): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.540-1765A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026381 | ||||||
chr19:4026397
|
G | C | 1 | a0001c0001t0001g0221 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.540-1749G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026397 | ||||||
chr19:4026411
|
C | T | 2 | a0001c0005t0001g0295a0001c0012t0001g0296 | 2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.540-1735C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026411 | ||||||
chr19:4026478
|
T | G | 1 | a0001c0001t0001g0114 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.540-1668T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026478 | ||||||
chr19:4026550
|
A | C | 27 | a0001c0002t0003g0227a0001c0002t0004g0157a0001c0002t0004g0166others(24): Show | 27 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.540-1596A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026550 | ||||||
chr19:4026571
|
A | G | 1 | a0001c0001t0001g0185 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.540-1575A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026571 | ||||||
chr19:4026573
|
C | CCCCA | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(247): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.540-1572_540-1569d others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026573 | |||||
chr19:4026769
|
G | T | 27 | a0001c0002t0003g0227a0001c0002t0004g0157a0001c0002t0004g0166others(24): Show | 27 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.540-1377G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026769 | ||||||
chr19:4026810
|
C | G | 303 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(300): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.540-1336C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026810 | ||||||
chr19:4026822
|
A | T | 1 | a0001c0006t0003g0038 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.540-1324A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026822 | ||||||
chr19:4026922
|
A | T | 1 | a0001c0001t0001g0150 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.540-1224A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026922 | ||||||
chr19:4026934
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.540-1212G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026934 | ||||||
chr19:4027014
|
A | AT | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.540-1121dupT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4027014 | |||||
chr19:4027110
|
C | T | 7 | a0001c0002t0001g0202a0001c0002t0001g0206a0001c0002t0001g0207others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.540-1036C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027110 | ||||||
chr19:4027240
|
C | T | 1 | a0004c0013t0001g0015 | 2 | HG00642.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.540-906C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027240 | ||||||
chr19:4027270
|
G | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0161 | 2 | NA18973.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.540-876G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027270 | ||||||
chr19:4027291
|
C | G | 27 | a0001c0002t0003g0227a0001c0002t0004g0157a0001c0002t0004g0166others(24): Show | 27 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.540-855C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027291 | ||||||
chr19:4027394
|
G | A | 1 | a0001c0012t0005g0233 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.540-752G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027394 | ||||||
chr19:4027501
|
T | C | 2 | a0001c0003t0003g0229a0001c0003t0004g0228 | 2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.540-645T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027501 | ||||||
chr19:4027562
|
G | GT | 39 | a0001c0001t0001g0059a0001c0001t0001g0062a0001c0001t0001g0063others(36): Show | 42 | HG00280.hp1 HG00280.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.540-579dupT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4027562 | |||||
chr19:4027568
|
G | T | 274 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(271): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.540-578G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027568 | ||||||
chr19:4027579
|
T | G | 1 | a0001c0003t0002g0270 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.540-567T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027579 | ||||||
chr19:4027592
|
T | C | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | HG02132.hp1 NA18612.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.540-554T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027592 | ||||||
chr19:4027627
|
A | G | 2 | a0001c0005t0001g0295a0001c0012t0001g0296 | 2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.540-519A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027627 | ||||||
chr19:4027677
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.540-469C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027677 | ||||||
chr19:4027726
|
A | T | 26 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(23): Show | 29 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.540-420A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027726 | ||||||
chr19:4027764
|
C | G | 2 | a0001c0006t0004g0034a0001c0006t0004g0035 | 2 | HG02055.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.540-382C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027764 | ||||||
chr19:4027854
|
C | A | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(272): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.540-292C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027854 | ||||||
chr19:4028016
|
G | T | 3 | a0001c0006t0004g0030a0001c0006t0004g0031a0001c0006t0004g0032 | 3 | HG01884.hp1 HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.540-130G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4028016 | ||||||
chr19:4028069
|
C | T | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(248): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.540-77C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4028069 | ||||||
chr19:4028075
|
G | C | 1 | a0001c0001t0001g0265 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.540-71G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4028075 | ||||||
chr19:4028077
|
G | A | 7 | a0001c0002t0006g0209a0001c0002t0020g0299a0001c0003t0001g0294others(4): Show | 7 | HG00423.hp1 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.540-69G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4028077 | ||||||
chr19:4028292
|
G | A | 27 | a0001c0001t0001g0081a0001c0002t0001g0044a0001c0002t0002g0111others(24): Show | 30 | HG00280.hp1 HG00735.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.581+105G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 4/10 | chr19 | 4028292 | ||||||
chr19:4028636
|
T | C | 16 | a0001c0001t0001g0183a0001c0002t0001g0201a0001c0002t0004g0175others(13): Show | 17 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.672+36T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 5/10 | chr19 | 4028636 | ||||||
chr19:4028692
|
C | G | 67 | a0001c0002t0001g0201a0001c0002t0003g0196a0001c0002t0003g0198others(64): Show | 70 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(67): Show |
intron_variant | MODIFIER | c.673-28C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 5/10 | chr19 | 4028692 | ||||||
chr19:4028862
|
C | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0055a0001c0001t0001g0132others(8): Show | 14 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.801+14C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 6/10 | chr19 | 4028862 | ||||||
chr19:4028915
|
T | G | 27 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(24): Show | 30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.802-16T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 6/10 | chr19 | 4028915 | ||||||
chr19:4028916
|
T | C | 27 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(24): Show | 30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.802-15T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 6/10 | chr19 | 4028916 | ||||||
chr19:4029058
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.907+22G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029058 | ||||||
chr19:4029077
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.907+41C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029077 | ||||||
chr19:4029109
|
C | T | 3 | a0001c0005t0007g0238a0001c0005t0007g0241a0001c0005t0007g0278 | 3 | HG01361.hp2 HG01496.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.907+73C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029109 | ||||||
chr19:4029121
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.907+85C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029121 | ||||||
chr19:4029127
|
G | A | 25 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(22): Show | 28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.907+91G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029127 | ||||||
chr19:4029136
|
G | A | 1 | a0001c0005t0005g0231 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.907+100G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029136 | ||||||
chr19:4029146
|
C | T | 2 | a0001c0005t0007g0238a0001c0005t0007g0241 | 2 | HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.907+110C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029146 | ||||||
chr19:4029266
|
A | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.907+230A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029266 | ||||||
chr19:4029271
|
G | T | 1 | a0001c0001t0010g0140 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.907+235G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029271 | ||||||
chr19:4029291
|
T | C | 277 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(274): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.907+255T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029291 | ||||||
chr19:4029345
|
C | G | 4 | a0001c0003t0001g0294a0001c0003t0006g0291a0001c0003t0006g0292others(1): Show | 4 | HG00423.hp1 HG02486.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.907+309C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029345 | ||||||
chr19:4029354
|
C | T | 1 | a0001c0005t0005g0234 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.907+318C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029354 | ||||||
chr19:4029445
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0133 | 2 | HG01981.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.907+409G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029445 | ||||||
chr19:4029455
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.907+419C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029455 | ||||||
chr19:4029494
|
G | A | 1 | a0001c0006t0004g0035 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.907+458G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029494 | ||||||
chr19:4029497
|
C | T | 1 | a0001c0002t0004g0157 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.907+461C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029497 | ||||||
chr19:4029571
|
G | T | 2 | a0001c0001t0001g0080a0001c0001t0001g0220 | 2 | HG03490.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.907+535G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029571 | ||||||
chr19:4029659
|
C | G | 2 | a0001c0001t0009g0093a0001c0001t0009g0095 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.907+623C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029659 | ||||||
chr19:4029696
|
A | G | 2 | a0001c0003t0003g0229a0001c0003t0004g0228 | 2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.907+660A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029696 | ||||||
chr19:4029786
|
A | G | 26 | a0001c0002t0001g0044a0001c0002t0002g0111a0001c0002t0002g0112others(23): Show | 29 | HG00280.hp1 HG00735.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.907+750A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029786 | ||||||
chr19:4029811
|
AT | A | 20 | a0001c0002t0003g0199a0001c0003t0002g0269a0001c0003t0002g0275others(17): Show | 21 | HG00609.hp1 HG01109.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.907+804delT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr19 | 4029811 | |||||
chr19:4029811
|
ATT | A | 73 | a0001c0001t0001g0051a0001c0001t0001g0062a0001c0001t0001g0069others(70): Show | 80 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.907+803_907+804del others(2): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr19 | 4029811 | |||||
chr19:4029811
|
ATTT | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(154): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.907+802_907+804del others(3): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr19 | 4029811 | |||||
chr19:4029811
|
ATTTT | A | 7 | a0001c0001t0001g0053a0001c0001t0001g0083a0001c0001t0001g0127others(4): Show | 7 | HG01070.hp1 HG01081.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.907+801_907+804del others(4): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr19 | 4029811 | |||||
chr19:4029811
|
ATTTTTTT others(3): Show |
A | 4 | a0001c0002t0003g0227a0001c0002t0004g0167a0001c0002t0004g0171others(1): Show | 4 | HG01891.hp2 HG02717.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.907+795_907+804del others(10): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr19 | 4029811 | |||||
chr19:4029811
|
ATTTTTTT others(4): Show |
A | 22 | a0001c0002t0004g0157a0001c0002t0004g0166a0001c0002t0004g0169others(19): Show | 22 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.907+794_907+804del others(11): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr19 | 4029811 | |||||
chr19:4029811
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0004t0004g0248 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.907+793_907+804del others(12): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr19 | 4029811 | |||||
chr19:4029811
|
ATTTTTTT others(7): Show |
A | 5 | a0001c0005t0001g0295a0001c0008t0001g0168a0001c0012t0001g0296others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.907+791_907+804del others(14): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr19 | 4029811 | |||||
chr19:4029892
|
G | A | 28 | a0001c0001t0001g0142a0001c0002t0003g0227a0001c0002t0004g0157others(25): Show | 28 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.907+856G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029892 | ||||||
chr19:4029980
|
G | T | 1 | a0001c0003t0002g0267 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.907+944G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029980 | ||||||
chr19:4029983
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.907+947C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029983 | ||||||
chr19:4030118
|
G | C | 26 | a0001c0002t0001g0044a0001c0002t0002g0111a0001c0002t0002g0112others(23): Show | 29 | HG00280.hp1 HG00735.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.907+1082G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4030118 | ||||||
chr19:4030167
|
TGCCCAGG others(208): Show |
T | 5 | a0001c0001t0001g0047a0001c0001t0001g0050a0001c0001t0001g0149others(2): Show | 5 | HG01106.hp1 HG02735.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.907+1135_907+1349d others(2): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr19 | 4030167 | |||||
chr19:4030181
|
G | T | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(265): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.907+1145G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4030181 | ||||||
chr19:4030192
|
A | G | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(265): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.907+1156A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4030192 | ||||||
chr19:4030345
|
C | T | 11 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(8): Show | 13 | HG01109.hp2 HG02145.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.907+1309C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4030345 | ||||||
chr19:4030348
|
A | G | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.907+1312A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4030348 | ||||||
chr19:4030354
|
TCA | T | 9 | a0001c0002t0001g0017a0001c0002t0001g0201a0001c0002t0001g0202others(6): Show | 10 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.907+1322_907+1323d others(4): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr19 | 4030354 | |||||
chr19:4030575
|
T | C | 1 | a0001c0003t0006g0290 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.907+1539T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4030575 | ||||||
chr19:4030618
|
C | CA | 11 | a0001c0001t0001g0041a0001c0001t0001g0142a0001c0002t0003g0227others(8): Show | 11 | HG02055.hp1 HG02572.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.907+1596dupA | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr19 | 4030618 | |||||
chr19:4030628
|
A | G | 5 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0040others(2): Show | 7 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(4): Show |
intron_variant | MODIFIER | c.907+1592A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4030628 | ||||||
chr19:4030777
|
A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(218): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.907+1741A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4030777 | ||||||
chr19:4030875
|
A | T | 1 | a0001c0007t0001g0230 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.907+1839A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4030875 | ||||||
chr19:4030959
|
C | G | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(270): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.907+1923C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4030959 | ||||||
chr19:4031046
|
A | T | 1 | a0001c0002t0004g0175 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.907+2010A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031046 | ||||||
chr19:4031101
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.908-1999C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031101 | ||||||
chr19:4031192
|
C | G | 1 | a0001c0001t0001g0014 | 2 | HG01934.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.908-1908C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031192 | ||||||
chr19:4031332
|
T | C | 26 | a0001c0002t0001g0044a0001c0002t0002g0111a0001c0002t0002g0112others(23): Show | 29 | HG00280.hp1 HG00735.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.908-1768T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031332 | ||||||
chr19:4031344
|
C | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.908-1756C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031344 | ||||||
chr19:4031369
|
G | A | 1 | a0001c0002t0004g0175 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.908-1731G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031369 | ||||||
chr19:4031428
|
A | C | 303 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(300): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.908-1672A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031428 | ||||||
chr19:4031484
|
T | A | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(270): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.908-1616T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031484 | ||||||
chr19:4031539
|
G | A | 1 | a0001c0001t0021g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.908-1561G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031539 | ||||||
chr19:4031545
|
G | T | 1 | a0001c0012t0001g0296 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.908-1555G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031545 | ||||||
chr19:4031583
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.908-1517A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031583 | ||||||
chr19:4031632
|
G | A | 1 | a0001c0003t0006g0290 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.908-1468G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031632 | ||||||
chr19:4031771
|
C | T | 26 | a0001c0002t0001g0044a0001c0002t0002g0111a0001c0002t0002g0112others(23): Show | 29 | HG00280.hp1 HG00735.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.908-1329C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031771 | ||||||
chr19:4031812
|
C | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.908-1288C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031812 | ||||||
chr19:4031921
|
C | T | 48 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(45): Show | 55 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.908-1179C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031921 | ||||||
chr19:4031924
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.908-1176C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031924 | ||||||
chr19:4032078
|
G | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(190): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.908-1022G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032078 | ||||||
chr19:4032109
|
G | T | 1 | a0001c0004t0008g0300 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.908-991G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032109 | ||||||
chr19:4032358
|
C | G | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(270): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.908-742C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032358 | ||||||
chr19:4032531
|
T | C | 27 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(24): Show | 30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.908-569T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032531 | ||||||
chr19:4032551
|
A | G | 27 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(24): Show | 30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.908-549A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032551 | ||||||
chr19:4032626
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.908-474T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032626 | ||||||
chr19:4032678
|
A | G | 27 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(24): Show | 30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.908-422A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032678 | ||||||
chr19:4032683
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.908-417C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032683 | ||||||
chr19:4032684
|
A | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(184): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.908-416A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032684 | ||||||
chr19:4032746
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.908-354G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032746 | ||||||
chr19:4032818
|
T | C | 1 | a0001c0001t0001g0115 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.908-282T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032818 | ||||||
chr19:4032943
|
A | G | 27 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(24): Show | 30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.908-157A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032943 | ||||||
chr19:4032951
|
A | G | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(270): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.908-149A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032951 | ||||||
chr19:4032987
|
C | T | 27 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(24): Show | 30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.908-113C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032987 | ||||||
chr19:4033029
|
G | A | 27 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(24): Show | 30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.908-71G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4033029 | ||||||
chr19:4033064
|
A | T | 1 | a0001c0002t0004g0157 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.908-36A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4033064 | ||||||
chr19:4033181
|
G | A | 7 | a0001c0002t0006g0209a0001c0002t0020g0299a0001c0003t0001g0294others(4): Show | 7 | HG00423.hp1 HG02486.hp1 HG02622.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.981+8G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 8/10 | chr19 | 4033181 | ||||||
chr19:4033246
|
G | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.981+73G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 8/10 | chr19 | 4033246 | ||||||
chr19:4033281
|
G | A | 27 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(24): Show | 30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.981+108G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 8/10 | chr19 | 4033281 | ||||||
chr19:4033303
|
G | A | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(270): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.982-117G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 8/10 | chr19 | 4033303 | ||||||
chr19:4033616
|
G | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1142+36G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4033616 | ||||||
chr19:4033720
|
C | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.1142+140C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4033720 | ||||||
chr19:4033751
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1142+171C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4033751 | ||||||
chr19:4033791
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0180 | 2 | HG00639.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1142+211G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4033791 | ||||||
chr19:4033856
|
A | T | 1 | a0001c0001t0001g0108 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1142+276A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4033856 | ||||||
chr19:4033992
|
G | T | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(243): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1142+412G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4033992 | ||||||
chr19:4033996
|
T | TCTGG | 27 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(24): Show | 30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.1142+419_1142+422d others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4033996 | |||||
chr19:4034136
|
C | T | 5 | a0001c0005t0005g0019a0001c0005t0005g0231a0001c0005t0005g0244others(2): Show | 5 | HG00639.hp1 HG02738.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1142+556C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034136 | ||||||
chr19:4034156
|
G | A | 24 | a0001c0002t0002g0111a0001c0002t0002g0112a0001c0002t0002g0151others(21): Show | 27 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1142+576G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034156 | ||||||
chr19:4034157
|
C | T | 7 | a0001c0002t0006g0209a0001c0002t0020g0299a0001c0003t0001g0294others(4): Show | 7 | HG00423.hp1 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1142+577C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034157 | ||||||
chr19:4034175
|
G | A | 2 | a0001c0004t0004g0248a0001c0004t0004g0249 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1142+595G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034175 | ||||||
chr19:4034208
|
A | G | 27 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(24): Show | 30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.1142+628A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034208 | ||||||
chr19:4034215
|
G | A | 1 | a0001c0002t0006g0209 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1142+635G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034215 | ||||||
chr19:4034225
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG00323.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.1142+645C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034225 | ||||||
chr19:4034238
|
C | T | 27 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(24): Show | 30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.1142+658C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034238 | ||||||
chr19:4034258
|
GGCCCTGC others(24): Show |
G | 5 | a0001c0003t0002g0268a0001c0003t0002g0269a0001c0003t0002g0270others(2): Show | 5 | HG01346.hp2 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1142+684_1142+714d others(33): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4034258 | |||||
chr19:4034281
|
G | A | 1 | a0001c0002t0020g0299 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1142+701G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034281 | ||||||
chr19:4034343
|
C | T | 1 | a0001c0006t0003g0038 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1142+763C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034343 | ||||||
chr19:4034379
|
C | T | 2 | a0001c0004t0004g0248a0001c0004t0004g0249 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1142+799C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034379 | ||||||
chr19:4034385
|
A | G | 1 | a0001c0001t0001g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1142+805A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034385 | ||||||
chr19:4034456
|
A | G | 1 | a0001c0005t0005g0232 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1142+876A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034456 | ||||||
chr19:4034471
|
G | A | 2 | a0001c0003t0003g0229a0001c0003t0004g0228 | 2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1142+891G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034471 | ||||||
chr19:4034710
|
C | T | 25 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(22): Show | 28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1142+1130C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034710 | ||||||
chr19:4034795
|
C | T | 1 | a0001c0003t0015g0216 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1142+1215C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034795 | ||||||
chr19:4034844
|
T | C | 25 | a0001c0002t0003g0227a0001c0002t0004g0166a0001c0002t0004g0167others(22): Show | 25 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1142+1264T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034844 | ||||||
chr19:4034909
|
A | G | 27 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(24): Show | 30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.1142+1329A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034909 | ||||||
chr19:4034963
|
G | A | 10 | a0001c0005t0001g0039a0001c0005t0001g0260a0001c0005t0001g0261others(7): Show | 10 | HG01884.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1142+1383G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034963 | ||||||
chr19:4035103
|
C | T | 3 | a0001c0002t0006g0209a0001c0002t0020g0299a0001c0003t0006g0290 | 3 | HG02622.hp1 HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1142+1523C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035103 | ||||||
chr19:4035210
|
T | C | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(270): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1142+1630T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035210 | ||||||
chr19:4035278
|
G | A | 27 | a0001c0002t0003g0227a0001c0002t0004g0157a0001c0002t0004g0166others(24): Show | 27 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.1142+1698G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035278 | ||||||
chr19:4035300
|
C | T | 27 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(24): Show | 30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.1142+1720C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035300 | ||||||
chr19:4035359
|
T | C | 27 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(24): Show | 30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.1142+1779T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035359 | ||||||
chr19:4035373
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0061others(1): Show | 6 | HG00099.hp1 HG00280.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.1142+1793G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035373 | ||||||
chr19:4035410
|
G | C | 1 | a0001c0002t0004g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1142+1830G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035410 | ||||||
chr19:4035496
|
A | T | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(270): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1143-1878A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035496 | ||||||
chr19:4035517
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1143-1857C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035517 | ||||||
chr19:4035544
|
G | T | 27 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(24): Show | 30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.1143-1830G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035544 | ||||||
chr19:4035568
|
C | G | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(270): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1143-1806C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035568 | ||||||
chr19:4035574
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1143-1800C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035574 | ||||||
chr19:4035638
|
C | G | 1 | a0001c0001t0001g0065 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1143-1736C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035638 | ||||||
chr19:4035704
|
C | T | 27 | a0001c0001t0001g0088a0001c0002t0001g0188a0001c0002t0001g0197others(24): Show | 30 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.1143-1670C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035704 | ||||||
chr19:4035752
|
TCACA | T | 25 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(22): Show | 28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-1612_1143-160 others(8): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035752 | |||||
chr19:4035830
|
TCACA | T | 4 | a0001c0002t0004g0213a0001c0006t0004g0030a0001c0006t0004g0031others(1): Show | 4 | HG01884.hp1 HG02257.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143-1536_1143-153 others(8): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035830 | |||||
chr19:4035831
|
C | A | 27 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(24): Show | 30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.1143-1543C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035831 | ||||||
chr19:4035839
|
C | T | 6 | a0001c0002t0006g0209a0001c0002t0020g0299a0001c0003t0006g0290others(3): Show | 6 | HG02486.hp1 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1143-1535C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035839 | ||||||
chr19:4035864
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1143-1510C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035864 | ||||||
chr19:4035870
|
C | A | 1 | a0001c0001t0001g0219 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1143-1504C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035870 | ||||||
chr19:4035872
|
C | A | 1 | a0001c0001t0001g0219 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1143-1502C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035872 | ||||||
chr19:4035885
|
G | A | 27 | a0001c0002t0003g0227a0001c0002t0004g0157a0001c0002t0004g0166others(24): Show | 27 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.1143-1489G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035885 | ||||||
chr19:4035892
|
T | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(184): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.1143-1482T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035892 | ||||||
chr19:4035911
|
C | A | 1 | a0001c0001t0001g0219 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1143-1463C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035911 | ||||||
chr19:4035913
|
C | A | 1 | a0001c0001t0001g0219 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1143-1461C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035913 | ||||||
chr19:4035925
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1143-1449T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035925 | ||||||
chr19:4035959
|
A | ACACCCGC others(238): Show |
10 | a0001c0005t0001g0039a0001c0005t0001g0260a0001c0005t0001g0261others(7): Show | 10 | HG01884.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(249): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1246): Show |
20 | a0001c0002t0003g0196a0001c0004t0003g0005a0001c0004t0003g0247others(17): Show | 23 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1257): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1246): Show |
2 | a0001c0002t0003g0198a0001c0002t0003g0199 | 2 | HG01109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1257): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1360): Show |
1 | a0001c0004t0003g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1371): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1246): Show |
1 | a0001c0004t0003g0254 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1257): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1246): Show |
1 | a0001c0004t0003g0301 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1257): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(521): Show |
1 | a0001c0001t0001g0091 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(532): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(238): Show |
21 | a0001c0005t0001g0295a0001c0005t0005g0019a0001c0005t0005g0231others(18): Show | 22 | HG00609.hp2 HG00639.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(249): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(236): Show |
1 | a0001c0005t0005g0236 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(247): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1326): Show |
1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1337): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1390): Show |
2 | a0001c0003t0002g0271a0001c0003t0002g0272 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1401): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1326): Show |
16 | a0001c0002t0002g0111a0001c0002t0002g0112a0001c0003t0002g0020others(13): Show | 18 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1337): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1326): Show |
1 | a0001c0003t0002g0021 | 2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1337): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1287): Show |
2 | a0002c0010t0002g0280a0002c0010t0002g0281 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1298): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(732): Show |
1 | a0001c0001t0001g0088 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(743): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1244): Show |
2 | a0001c0003t0003g0229a0001c0003t0004g0228 | 2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1255): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(238): Show |
1 | a0001c0012t0005g0233 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(249): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1367): Show |
4 | a0001c0003t0006g0290a0001c0003t0006g0291a0001c0003t0006g0292others(1): Show | 4 | HG02486.hp1 HG02717.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1378): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1393): Show |
2 | a0001c0002t0006g0209a0001c0002t0020g0299 | 2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1404): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(204): Show |
7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(215): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(599): Show |
1 | a0001c0001t0001g0040 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(610): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(520): Show |
1 | a0001c0001t0001g0062 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(531): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(521): Show |
71 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(68): Show | 78 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(532): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1365): Show |
1 | a0001c0001t0001g0060 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1376): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1365): Show |
1 | a0001c0001t0001g0224 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1376): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1365): Show |
46 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(43): Show | 51 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1376): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1363): Show |
7 | a0001c0002t0001g0017a0001c0002t0001g0201a0001c0002t0001g0202others(4): Show | 8 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1374): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1282): Show |
1 | a0001c0001t0001g0121 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1293): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1361): Show |
1 | a0001c0001t0019g0176 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1372): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1365): Show |
5 | a0001c0001t0001g0011a0001c0001t0001g0097a0001c0001t0001g0104others(2): Show | 6 | NA18994.hp2 NA19007.hp1 NA19064.hp2 others(3): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1376): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1363): Show |
28 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0055others(25): Show | 32 | HG00438.hp2 HG00673.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1374): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1363): Show |
2 | a0001c0001t0001g0203a0001c0014t0001g0204 | 2 | HG00735.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1374): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1361): Show |
1 | a0001c0001t0001g0132 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1372): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1363): Show |
1 | a0001c0001t0001g0193 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1374): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(480): Show |
1 | a0001c0001t0001g0087 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(491): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1365): Show |
2 | a0001c0001t0001g0012a0001c0001t0001g0101 | 3 | NA18973.hp1 NA19070.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1376): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1361): Show |
4 | a0001c0002t0001g0016a0001c0002t0001g0195a0001c0002t0001g0210others(1): Show | 5 | HG02273.hp1 NA18955.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1372): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1359): Show |
1 | a0001c0003t0015g0216 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1370): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(517): Show |
1 | a0001c0001t0001g0107 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(528): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1595): Show |
2 | a0001c0006t0004g0034a0001c0006t0004g0035 | 2 | HG02055.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1606): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1595): Show |
1 | a0001c0006t0004g0036 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1606): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1677): Show |
1 | a0001c0002t0004g0175 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1688): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1636): Show |
3 | a0001c0002t0008g0212a0001c0004t0008g0300a0001c0006t0008g0027 | 3 | HG02622.hp2 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1647): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1636): Show |
6 | a0001c0002t0003g0227a0001c0002t0004g0166a0001c0002t0004g0167others(3): Show | 6 | HG02572.hp2 HG02717.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1647): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1636): Show |
8 | a0001c0002t0004g0178a0001c0002t0004g0297a0001c0002t0004g0298others(5): Show | 8 | HG02257.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1647): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1633): Show |
3 | a0001c0006t0004g0030a0001c0006t0004g0031a0001c0006t0004g0032 | 3 | HG01884.hp1 HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1644): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1634): Show |
1 | a0001c0006t0004g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1645): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1790): Show |
1 | a0001c0002t0004g0213 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1801): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1635): Show |
1 | a0001c0002t0004g0157 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1646): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACACCCGC others(1324): Show |
3 | a0001c0002t0002g0151a0001c0003t0002g0282a0001c0003t0002g0283 | 3 | NA18983.hp1 NA19087.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1335): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035959
|
A | ACCCGCAC others(1361): Show |
1 | a0001c0001t0001g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1143-1414_1143-141 others(1372): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | |||||
chr19:4035960
|
C | CACCCGCA others(602): Show |
2 | a0001c0001t0001g0158a0001c0001t0021g0117 | 2 | HG00438.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(613): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035960 | |||||
chr19:4035962
|
T | G | 2 | a0001c0001t0001g0158a0001c0001t0021g0117 | 2 | HG00438.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1143-1412T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035962 | ||||||
chr19:4035971
|
C | T | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1403C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035971 | ||||||
chr19:4035975
|
G | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(81): Show | 91 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1143-1399G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035975 | ||||||
chr19:4035975
|
G | GTC | 4 | a0001c0004t0003g0247a0001c0004t0003g0253a0001c0004t0003g0255others(1): Show | 4 | HG02145.hp2 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1143-1398_1143-139 others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035975 | |||||
chr19:4035979
|
T | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(132): Show | 148 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.1143-1395T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035979 | ||||||
chr19:4035980
|
A | T | 1 | a0001c0001t0001g0158 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1143-1394A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035980 | ||||||
chr19:4035984
|
A | ACACATCT others(45): Show |
24 | a0001c0002t0002g0111a0001c0002t0002g0112a0001c0002t0002g0151others(21): Show | 27 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1143-1386_1143-138 others(56): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035984 | |||||
chr19:4035986
|
A | ATCCATAT others(4): Show |
77 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(74): Show | 84 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1143-1388_1143-138 others(15): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035986 | ||||||
chr19:4035986
|
A | C | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1388A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035986 | ||||||
chr19:4035995
|
T | C | 27 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(24): Show | 30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.1143-1379T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035995 | ||||||
chr19:4035997
|
T | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(81): Show | 91 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1143-1377T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035997 | ||||||
chr19:4035998
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(107): Show | 120 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1143-1376G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035998 | ||||||
chr19:4036012
|
T | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(105): Show | 118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1143-1362T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036012 | ||||||
chr19:4036012
|
T | G | 2 | a0001c0001t0001g0158a0001c0001t0021g0117 | 2 | HG00438.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1143-1362T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036012 | ||||||
chr19:4036013
|
T | TAACACAC others(7): Show |
7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1361_1143-136 others(18): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036013 | ||||||
chr19:4036013
|
T | TCACACAC others(1): Show |
79 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(76): Show | 86 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1143-1355_1143-135 others(12): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036013 | |||||
chr19:4036022
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(74): Show | 84 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1143-1352C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036022 | ||||||
chr19:4036024
|
T | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(74): Show | 84 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1143-1350T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036024 | ||||||
chr19:4036036
|
C | T | 1 | a0001c0003t0015g0216 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1143-1338C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036036 | ||||||
chr19:4036037
|
G | A | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1337G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036037 | ||||||
chr19:4036039
|
C | A | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1335C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036039 | ||||||
chr19:4036040
|
A | ACACACAC others(197): Show |
2 | a0001c0001t0001g0158a0001c0001t0021g0117 | 2 | HG00438.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1143-1334_1143-133 others(208): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036040 | ||||||
chr19:4036041
|
T | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(83): Show | 93 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1143-1333T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036041 | ||||||
chr19:4036041
|
T | TACACAC | 24 | a0001c0002t0002g0111a0001c0002t0002g0112a0001c0002t0002g0151others(21): Show | 27 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1143-1327_1143-132 others(10): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036041 | |||||
chr19:4036046
|
A | ACACCCG | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1325_1143-132 others(10): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036046 | |||||
chr19:4036055
|
T | C | 9 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0001t0001g0158others(6): Show | 9 | HG00438.hp1 HG01192.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.1143-1319T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036055 | ||||||
chr19:4036056
|
A | G | 24 | a0001c0002t0002g0111a0001c0002t0002g0112a0001c0002t0002g0151others(21): Show | 27 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1143-1318A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036056 | ||||||
chr19:4036067
|
A | G | 2 | a0001c0001t0001g0158a0001c0001t0021g0117 | 2 | HG00438.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1143-1307A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036067 | ||||||
chr19:4036069
|
T | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(107): Show | 120 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1143-1305T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036069 | ||||||
chr19:4036070
|
G | A | 9 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0001t0001g0158others(6): Show | 9 | HG00438.hp1 HG01192.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.1143-1304G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036070 | ||||||
chr19:4036070
|
G | T | 24 | a0001c0002t0002g0111a0001c0002t0002g0112a0001c0002t0002g0151others(21): Show | 27 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1143-1304G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036070 | ||||||
chr19:4036071
|
T | TAACACAC others(7): Show |
7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1303_1143-130 others(18): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036071 | ||||||
chr19:4036071
|
T | TCACACAC others(1): Show |
77 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(74): Show | 84 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1143-1297_1143-129 others(12): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036071 | |||||
chr19:4036081
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(107): Show | 120 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1143-1293G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036081 | ||||||
chr19:4036094
|
C | A | 2 | a0001c0001t0001g0158a0001c0001t0021g0117 | 2 | HG00438.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1143-1280C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036094 | ||||||
chr19:4036098
|
A | T | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1276A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036098 | ||||||
chr19:4036099
|
T | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(81): Show | 91 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1143-1275T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036099 | ||||||
chr19:4036099
|
TACAA | T | 24 | a0001c0002t0002g0111a0001c0002t0002g0112a0001c0002t0002g0151others(21): Show | 27 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1143-1271_1143-126 others(8): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036099 | |||||
chr19:4036101
|
CAA | C | 4 | a0001c0002t0003g0227a0001c0002t0004g0167a0001c0002t0004g0169others(1): Show | 4 | HG02717.hp2 HG02818.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143-1271_1143-127 others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036101 | |||||
chr19:4036102
|
A | ACACAATC others(193): Show |
77 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(74): Show | 84 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1143-1272_1143-127 others(204): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036102 | ||||||
chr19:4036103
|
A | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(106): Show | 116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1143-1271A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036103 | ||||||
chr19:4036108
|
A | ACCCG | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1265_1143-126 others(8): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036108 | |||||
chr19:4036117
|
T | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(81): Show | 91 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1143-1257T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036117 | ||||||
chr19:4036122
|
A | G | 3 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0225 | 3 | HG01192.hp1 HG02055.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1143-1252A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036122 | ||||||
chr19:4036129
|
A | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(74): Show | 84 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1143-1245A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036129 | ||||||
chr19:4036131
|
C | T | 24 | a0001c0002t0002g0111a0001c0002t0002g0112a0001c0002t0002g0151others(21): Show | 27 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1143-1243C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036131 | ||||||
chr19:4036132
|
G | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(81): Show | 91 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1143-1242G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036132 | ||||||
chr19:4036133
|
T | TAACACAC others(7): Show |
7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1241_1143-124 others(18): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036133 | ||||||
chr19:4036143
|
G | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(81): Show | 91 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1143-1231G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036143 | ||||||
chr19:4036155
|
C | T | 2 | a0001c0001t0001g0158a0001c0001t0021g0117 | 2 | HG00438.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1143-1219C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036155 | ||||||
chr19:4036156
|
C | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(74): Show | 84 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1143-1218C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036156 | ||||||
chr19:4036157
|
G | A | 9 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0001t0001g0158others(6): Show | 9 | HG00438.hp1 HG01192.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.1143-1217G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036157 | ||||||
chr19:4036161
|
T | C | 9 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0001t0001g0158others(6): Show | 9 | HG00438.hp1 HG01192.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.1143-1213T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036161 | ||||||
chr19:4036161
|
TACAAACA others(1): Show |
T | 26 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(23): Show | 29 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.1143-1209_1143-120 others(12): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036161 | |||||
chr19:4036163
|
C | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(133): Show | 149 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1143-1211C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036163 | ||||||
chr19:4036164
|
A | ACATCCAT others(12): Show |
1 | a0001c0001t0021g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1143-1210_1143-120 others(23): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036164 | ||||||
chr19:4036164
|
A | ACATCCAT others(101): Show |
1 | a0001c0001t0001g0158 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1143-1210_1143-120 others(112): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036164 | ||||||
chr19:4036165
|
A | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(81): Show | 91 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1143-1209A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036165 | ||||||
chr19:4036166
|
A | T | 2 | a0001c0001t0001g0158a0001c0001t0021g0117 | 2 | HG00438.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1143-1208A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036166 | ||||||
chr19:4036168
|
A | ATCCATAC others(12): Show |
7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1206_1143-120 others(23): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036168 | ||||||
chr19:4036169
|
C | CACACACA others(47): Show |
1 | a0001c0004t0003g0254 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1143-1170_1143-116 others(58): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036169 | |||||
chr19:4036179
|
T | C | 8 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0001t0021g0117others(5): Show | 8 | HG00438.hp1 HG01192.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143-1195T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036179 | ||||||
chr19:4036180
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1143-1194A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036180 | ||||||
chr19:4036185
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1143-1189G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036185 | ||||||
chr19:4036194
|
G | A | 111 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(108): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1143-1180G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036194 | ||||||
chr19:4036194
|
G | T | 1 | a0001c0001t0001g0158 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1143-1180G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036194 | ||||||
chr19:4036195
|
T | TCA | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1174_1143-117 others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036195 | |||||
chr19:4036195
|
T | TCACACAT others(167): Show |
73 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(70): Show | 80 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1143-1170_1143-116 others(178): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036195 | |||||
chr19:4036195
|
T | TCACACAT others(252): Show |
3 | a0001c0001t0001g0040a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | HG00099.hp2 HG00597.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.1143-1170_1143-116 others(263): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036195 | |||||
chr19:4036195
|
T | TCACACAT others(167): Show |
1 | a0001c0001t0001g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1143-1170_1143-116 others(178): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036195 | |||||
chr19:4036205
|
A | G | 24 | a0001c0002t0002g0111a0001c0002t0002g0112a0001c0002t0002g0151others(21): Show | 27 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1143-1169A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036205 | ||||||
chr19:4036218
|
T | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(110): Show | 123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1143-1156T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036218 | ||||||
chr19:4036219
|
G | A | 82 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(79): Show | 89 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.1143-1155G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036219 | ||||||
chr19:4036221
|
CAT | C | 4 | a0001c0001t0001g0040a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 4 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143-1151_1143-115 others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036221 | |||||
chr19:4036222
|
A | ACACACAC others(76): Show |
1 | a0001c0002t0001g0078 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1143-1152_1143-115 others(87): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036222 | ||||||
chr19:4036223
|
T | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(79): Show | 89 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.1143-1151T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036223 | ||||||
chr19:4036224
|
A | ACACACAT others(45): Show |
74 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(71): Show | 81 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.1143-1144_1143-114 others(56): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036224 | |||||
chr19:4036226
|
A | ACACATCC others(8): Show |
7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1144_1143-114 others(19): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036226 | |||||
chr19:4036237
|
T | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(78): Show | 88 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1143-1137T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036237 | ||||||
chr19:4036238
|
A | G | 2 | a0001c0002t0004g0178a0001c0002t0004g0297 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1143-1136A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036238 | ||||||
chr19:4036252
|
A | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(71): Show | 81 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.1143-1122A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036252 | ||||||
chr19:4036255
|
ACATG | A | 5 | a0001c0001t0001g0040a0001c0001t0001g0086a0001c0001t0001g0087others(2): Show | 5 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(2): Show |
intron_variant | MODIFIER | c.1143-1116_1143-111 others(8): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036255 | |||||
chr19:4036257
|
ATG | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(71): Show | 81 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.1143-1116_1143-111 others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036257 | ||||||
chr19:4036258
|
T | C | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1116T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036258 | ||||||
chr19:4036259
|
G | A | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1115G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036259 | ||||||
chr19:4036270
|
T | C | 4 | a0001c0001t0001g0040a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 4 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143-1104T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036270 | ||||||
chr19:4036271
|
A | G | 1 | a0001c0001t0021g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1143-1103A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036271 | ||||||
chr19:4036272
|
T | G | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1102T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036272 | ||||||
chr19:4036274
|
T | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(83): Show | 93 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1143-1100T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036274 | ||||||
chr19:4036275
|
G | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(83): Show | 93 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1143-1099G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036275 | ||||||
chr19:4036276
|
G | A | 1 | a0001c0001t0021g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1143-1098G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036276 | ||||||
chr19:4036279
|
T | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(83): Show | 93 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1143-1095T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036279 | ||||||
chr19:4036280
|
A | G | 2 | a0001c0002t0004g0167a0001c0002t0004g0169 | 2 | HG02818.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1143-1094A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036280 | ||||||
chr19:4036284
|
C | T | 2 | a0001c0005t0001g0295a0001c0012t0001g0296 | 2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1143-1090C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036284 | ||||||
chr19:4036285
|
G | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(75): Show | 85 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1143-1089G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036285 | ||||||
chr19:4036285
|
G | T | 1 | a0001c0001t0021g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1143-1089G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036285 | ||||||
chr19:4036286
|
T | TCA | 124 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(121): Show | 140 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1143-1075_1143-107 others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036286 | |||||
chr19:4036286
|
T | TCACACAC others(483): Show |
1 | a0001c0001t0001g0141 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1143-1074_1143-107 others(494): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036286 | |||||
chr19:4036294
|
A | ACATCCAT others(188): Show |
1 | a0001c0001t0021g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1143-1078_1143-107 others(199): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036294 | |||||
chr19:4036294
|
A | ACATCCAT others(43): Show |
74 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(71): Show | 81 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.1143-1078_1143-107 others(54): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036294 | |||||
chr19:4036294
|
A | ACATCTAT others(14): Show |
4 | a0001c0001t0001g0040a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 4 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143-1078_1143-107 others(25): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036294 | |||||
chr19:4036303
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(76): Show | 86 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1143-1071T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036303 | ||||||
chr19:4036317
|
C | CG | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1057_1143-105 others(5): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036317 | ||||||
chr19:4036317
|
CT | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(76): Show | 86 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1143-1056delT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036317 | ||||||
chr19:4036319
|
G | C | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1055G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036319 | ||||||
chr19:4036320
|
T | A | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1054T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036320 | ||||||
chr19:4036320
|
T | TCATACAC others(1): Show |
79 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(76): Show | 86 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1143-1054_1143-105 others(12): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036320 | ||||||
chr19:4036321
|
T | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(83): Show | 93 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1143-1053T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036321 | ||||||
chr19:4036325
|
T | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(83): Show | 93 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1143-1049T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036325 | ||||||
chr19:4036326
|
G | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(83): Show | 93 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1143-1048G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036326 | ||||||
chr19:4036335
|
T | C | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1039T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036335 | ||||||
chr19:4036336
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(76): Show | 86 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1143-1038A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036336 | ||||||
chr19:4036350
|
G | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(76): Show | 86 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1143-1024G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036350 | ||||||
chr19:4036356
|
C | CACACA | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1017_1143-101 others(9): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036356 | |||||
chr19:4036360
|
T | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(84): Show | 94 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1143-1014T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036360 | ||||||
chr19:4036373
|
C | A | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1001C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036373 | ||||||
chr19:4036374
|
C | T | 2 | a0002c0010t0002g0280a0002c0010t0002g0281 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1143-1000C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036374 | ||||||
chr19:4036375
|
G | A | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-999G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036375 | ||||||
chr19:4036379
|
T | C | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-995T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036379 | ||||||
chr19:4036381
|
C | G | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-993C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036381 | ||||||
chr19:4036388
|
A | ATCCATAT others(10): Show |
7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-986_1143-985i others(19): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036388 | ||||||
chr19:4036390
|
G | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(83): Show | 93 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1143-984G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036390 | ||||||
chr19:4036393
|
T | C | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-981T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036393 | ||||||
chr19:4036407
|
T | C | 34 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0002t0003g0196others(31): Show | 37 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.1143-967T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036407 | ||||||
chr19:4036408
|
G | A | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-966G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036408 | ||||||
chr19:4036409
|
T | TCACACG | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-960_1143-959i others(8): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036409 | |||||
chr19:4036419
|
G | A | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-955G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036419 | ||||||
chr19:4036432
|
T | C | 8 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0001t0001g0131others(5): Show | 8 | HG01081.hp2 HG01192.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143-942T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036432 | ||||||
chr19:4036433
|
G | A | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-941G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036433 | ||||||
chr19:4036434
|
TCATA | T | 4 | a0001c0003t0002g0282a0001c0003t0002g0283a0002c0010t0002g0280others(1): Show | 4 | HG03490.hp2 HG03492.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1143-937_1143-934d others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036434 | |||||
chr19:4036435
|
CATACAA | C | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-937_1143-932d others(8): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036435 | |||||
chr19:4036437
|
TACAA | T | 27 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(24): Show | 30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.1143-933_1143-930d others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036437 | |||||
chr19:4036449
|
C | T | 2 | a0001c0005t0001g0295a0001c0012t0001g0296 | 2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1143-925C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036449 | ||||||
chr19:4036450
|
A | T | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-924A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036450 | ||||||
chr19:4036460
|
G | A | 34 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0002t0003g0196others(31): Show | 37 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.1143-914G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036460 | ||||||
chr19:4036470
|
G | A | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-904G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036470 | ||||||
chr19:4036471
|
T | TCACACA | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-902_1143-897d others(8): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036471 | |||||
chr19:4036480
|
C | G | 1 | a0001c0001t0001g0063 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1143-894C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036480 | ||||||
chr19:4036481
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1143-893A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036481 | ||||||
chr19:4036495
|
G | A | 34 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0002t0003g0196others(31): Show | 37 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.1143-879G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036495 | ||||||
chr19:4036496
|
TCATA | T | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-875_1143-872d others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036496 | |||||
chr19:4036503
|
A | C | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-871A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036503 | ||||||
chr19:4036508
|
ACACACAT others(25): Show |
A | 3 | a0001c0001t0001g0087a0001c0003t0003g0229a0001c0003t0004g0228 | 3 | HG00621.hp2 HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1143-842_1143-811d others(34): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036508 | |||||
chr19:4036512
|
A | T | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-862A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036512 | ||||||
chr19:4036531
|
C | CGTCACAC others(19): Show |
25 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(22): Show | 28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-843_1143-842i others(28): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036531 | ||||||
chr19:4036531
|
CT | C | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-842delT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036531 | ||||||
chr19:4036533
|
G | A | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-841G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036533 | ||||||
chr19:4036533
|
G | C | 25 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(22): Show | 28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-841G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036533 | ||||||
chr19:4036534
|
T | A | 25 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(22): Show | 28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-840T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036534 | ||||||
chr19:4036535
|
T | C | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-839T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036535 | ||||||
chr19:4036539
|
T | C | 32 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0002t0003g0196others(29): Show | 35 | HG01109.hp2 HG01192.hp2 HG01256.hp2 others(32): Show |
intron_variant | MODIFIER | c.1143-835T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036539 | ||||||
chr19:4036540
|
G | A | 32 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0002t0003g0196others(29): Show | 35 | HG01109.hp2 HG01192.hp2 HG01256.hp2 others(32): Show |
intron_variant | MODIFIER | c.1143-834G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036540 | ||||||
chr19:4036549
|
T | C | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-825T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036549 | ||||||
chr19:4036550
|
A | C | 25 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(22): Show | 28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-824A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036550 | ||||||
chr19:4036561
|
A | G | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-813A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036561 | ||||||
chr19:4036564
|
G | A | 32 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0002t0003g0196others(29): Show | 35 | HG01109.hp2 HG01192.hp2 HG01256.hp2 others(32): Show |
intron_variant | MODIFIER | c.1143-810G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036564 | ||||||
chr19:4036565
|
T | TCACATGC others(1): Show |
25 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(22): Show | 28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-805_1143-804i others(10): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036565 | |||||
chr19:4036574
|
C | T | 25 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(22): Show | 28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-800C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036574 | ||||||
chr19:4036578
|
C | T | 25 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(22): Show | 28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-796C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036578 | ||||||
chr19:4036579
|
A | G | 25 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(22): Show | 28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-795A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036579 | ||||||
chr19:4036583
|
C | T | 25 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(22): Show | 28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-791C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036583 | ||||||
chr19:4036588
|
C | A | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-786C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036588 | ||||||
chr19:4036588
|
C | T | 2 | a0001c0004t0004g0248a0001c0004t0004g0249 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1143-786C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036588 | ||||||
chr19:4036593
|
T | C | 25 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(22): Show | 28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-781T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036593 | ||||||
chr19:4036593
|
T | TACAC | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-773_1143-770d others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036593 | |||||
chr19:4036608
|
A | C | 2 | a0001c0003t0003g0229a0001c0003t0004g0228 | 2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1143-766A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036608 | ||||||
chr19:4036622
|
G | A | 2 | a0001c0003t0003g0229a0001c0003t0004g0228 | 2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1143-752G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036622 | ||||||
chr19:4036625
|
T | A | 35 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0002t0003g0196others(32): Show | 38 | HG00741.hp2 HG01109.hp2 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.1143-749T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036625 | ||||||
chr19:4036632
|
T | C | 32 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0002t0003g0196others(29): Show | 35 | HG01109.hp2 HG01192.hp2 HG01256.hp2 others(32): Show |
intron_variant | MODIFIER | c.1143-742T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036632 | ||||||
chr19:4036633
|
A | G | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-741A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036633 | ||||||
chr19:4036636
|
C | T | 2 | a0001c0003t0003g0229a0001c0003t0004g0228 | 2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1143-738C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036636 | ||||||
chr19:4036637
|
A | G | 2 | a0001c0003t0003g0229a0001c0003t0004g0228 | 2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1143-737A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036637 | ||||||
chr19:4036638
|
G | A | 2 | a0003c0011t0001g0288a0003c0011t0001g0289 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1143-736G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036638 | ||||||
chr19:4036641
|
C | T | 2 | a0001c0003t0003g0229a0001c0003t0004g0228 | 2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1143-733C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036641 | ||||||
chr19:4036644
|
ACTG | A | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-729_1143-727d others(5): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036644 | ||||||
chr19:4036646
|
T | C | 27 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(24): Show | 30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.1143-728T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036646 | ||||||
chr19:4036651
|
T | C | 2 | a0001c0003t0003g0229a0001c0003t0004g0228 | 2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1143-723T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036651 | ||||||
chr19:4036651
|
T | TCACACAC others(50): Show |
7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-723_1143-722i others(59): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036651 | ||||||
chr19:4036663
|
T | C | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0003t0001g0217others(4): Show | 7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-711T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036663 | ||||||
chr19:4036664
|
A | C | 25 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(22): Show | 28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-710A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036664 | ||||||
chr19:4036678
|
G | A | 25 | a0001c0002t0003g0196a0001c0002t0003g0198a0001c0002t0003g0199others(22): Show | 28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-696G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036678 | ||||||
chr19:4036679
|
T | TCACATGC others(3): Show |
26 | a0001c0001t0001g0170a0001c0002t0003g0196a0001c0002t0003g0198others(23): Show | 29 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.1143-691_1143-690i others(12): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036679 | |||||
chr19:4036688
|
C | T | 26 | a0001c0001t0001g0170a0001c0002t0003g0196a0001c0002t0003g0198others(23): Show | 29 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.1143-686C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036688 | ||||||
chr19:4036692
|
T | C | 2 | a0001c0003t0003g0229a0001c0003t0004g0228 | 2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1143-682T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036692 | ||||||
chr19:4036693
|
A | G | 26 | a0001c0001t0001g0170a0001c0002t0003g0196a0001c0002t0003g0198others(23): Show | 29 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.1143-681A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036693 | ||||||
chr19:4036697
|
C | T | 26 | a0001c0001t0001g0170a0001c0002t0003g0196a0001c0002t0003g0198others(23): Show | 29 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.1143-677C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036697 | ||||||
chr19:4036703
|
A | G | 28 | a0001c0001t0001g0170a0001c0002t0003g0196a0001c0002t0003g0198others(25): Show | 31 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.1143-671A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036703 | ||||||
chr19:4036704
|
T | TCA | 26 | a0001c0001t0001g0170a0001c0002t0003g0196a0001c0002t0003g0198others(23): Show | 29 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.1143-669_1143-668d others(4): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036704 | |||||
chr19:4036707
|
T | C | 26 | a0001c0001t0001g0170a0001c0002t0003g0196a0001c0002t0003g0198others(23): Show | 29 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.1143-667T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036707 | ||||||
chr19:4036717
|
C | CA | 17 | a0001c0002t0002g0111a0001c0002t0002g0112a0001c0002t0002g0151others(14): Show | 20 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.1143-656dupA | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036717 | |||||
chr19:4036765
|
TACACCGT others(53): Show |
T | 1 | a0001c0001t0001g0040 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1143-590_1143-531d others(62): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036765 | |||||
chr19:4036772
|
TCACA | T | 22 | a0001c0001t0001g0170a0001c0002t0003g0196a0001c0002t0003g0198others(19): Show | 24 | HG01109.hp2 HG02145.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.1143-589_1143-586d others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036772 | |||||
chr19:4036772
|
TCACACAC others(1): Show |
T | 3 | a0001c0004t0011g0004a0001c0004t0012g0004a0001c0004t0012g0245 | 4 | HG02486.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143-593_1143-586d others(10): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036772 | |||||
chr19:4036820
|
CAGTCCAC others(279): Show |
C | 1 | a0001c0001t0001g0086 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1143-550_1143-265d others(2): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036820 | |||||
chr19:4036853
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1143-521C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036853 | ||||||
chr19:4036917
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1143-457T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036917 | ||||||
chr19:4036924
|
G | C | 2 | a0001c0001t0001g0194a0001c0003t0006g0290 | 2 | HG02717.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1143-450G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036924 | ||||||
chr19:4036926
|
TCA | T | 6 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0003t0001g0218others(3): Show | 6 | HG01433.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1143-437_1143-436d others(4): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036926 | |||||
chr19:4036926
|
TCACA | T | 3 | a0001c0004t0004g0248a0001c0004t0004g0249a0001c0006t0004g0037 | 3 | HG02896.hp2 HG02897.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1143-439_1143-436d others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036926 | |||||
chr19:4036974
|
C | T | 2 | a0003c0011t0001g0288a0003c0011t0001g0289 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1143-400C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036974 | ||||||
chr19:4036995
|
A | G | 2 | a0001c0002t0003g0198a0001c0002t0003g0199 | 2 | HG01109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1143-379A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036995 | ||||||
chr19:4037014
|
C | T | 1 | a0001c0006t0004g0032 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1143-360C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4037014 | ||||||
chr19:4037082
|
T | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(215): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1143-292T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4037082 | ||||||
chr19:4037088
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1143-286A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4037088 | ||||||
chr19:4037178
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1143-196G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4037178 | ||||||
chr19:4037295
|
T | A | 1 | a0001c0002t0010g0105 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1143-79T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4037295 | ||||||
chr19:4037324
|
G | A | 34 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(31): Show | 36 | HG00609.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1143-50G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4037324 | ||||||
chr19:4037527
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.1273+23C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 10/10 | chr19 | 4037527 |