geneid | 57661 |
---|---|
ensemblid | ENSG00000070047.13 |
hgncid | 24351 |
symbol | PHRF1 |
name | PHD and ring finger domains 1 |
refseq_nuc | NM_001286581.2 |
refseq_prot | NP_001273510.1 |
ensembl_nuc | ENST00000264555.10 |
ensembl_prot | ENSP00000264555.5 |
mane_status | MANE Select |
chr | chr11 |
start | 576470 |
end | 612222 |
strand | + |
ver | v1.2 |
region | chr11:576470-612222 |
region5000 | chr11:571470-617222 |
regionname0 | PHRF1_chr11_576470_612222 |
regionname5000 | PHRF1_chr11_571470_617222 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1649 | 149 | 33 | 32 | 54 | 9 | 20 | 34 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0002 | 0/0 | 1649 | 63 | 15 | 10 | 32 | 1 | 5 | 18 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0003 | 0/0 | 1645 | 12 | 7 | 5 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0004 | 0/0 | 1649 | 10 | 0 | 9 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0005 | 0/0 | 1649 | 8 | 0 | 2 | 1 | 1 | 4 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0006 | 0/0 | 1645 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0007 | 0/0 | 1649 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0008 | 0/0 | 1649 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0009 | 0/0 | 1645 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0010 | 0/0 | 1649 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0011 | 0/0 | 1649 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0012 | 0/0 | 1649 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0013 | 0/0 | 1645 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0014 | 0/0 | 1649 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0015 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0016 | 0/0 | 1645 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0017 | 0/0 | 1649 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0018 | 0/0 | 1649 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0019 | 0/0 | 1649 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0020 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0021 | 0/0 | 1649 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0022 | 0/0 | 1649 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0023 | 0/0 | 1649 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0024 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0025 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 4950 | 95 | 7 | 19 | 48 | 4 | 17 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0002 | 0/0 | 4950 | 59 | 11 | 10 | 32 | 1 | 5 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0003 | 0/1 | 4950 | 29 | 11 | 10 | 3 | 2 | 2 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0004 | 0/0 | 4938 | 12 | 7 | 5 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0005 | 0/0 | 4950 | 10 | 0 | 9 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0006 | 0/0 | 4950 | 9 | 7 | 1 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0007 | 0/0 | 4950 | 8 | 0 | 2 | 1 | 1 | 4 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0008 | 0/0 | 4938 | 6 | 6 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0009 | 0/0 | 4950 | 5 | 4 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0010 | 0/0 | 4950 | 4 | 4 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0011 | 0/0 | 4950 | 4 | 4 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0012 | 0/0 | 4938 | 3 | 3 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0013 | 0/0 | 4950 | 3 | 3 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0014 | 0/0 | 4950 | 3 | 2 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0015 | 0/0 | 4950 | 2 | 0 | 2 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0016 | 0/0 | 4950 | 2 | 2 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0017 | 0/0 | 4950 | 2 | 2 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0018 | 0/0 | 4950 | 2 | 0 | 0 | 2 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0019 | 0/0 | 4950 | 2 | 0 | 0 | 2 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0020 | 0/0 | 4938 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0021 | 0/0 | 4938 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0022 | 0/0 | 4938 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0023 | 0/0 | 4950 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0024 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0025 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0026 | 0/0 | 4950 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0027 | 0/0 | 4950 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0028 | 0/0 | 4950 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0029 | 0/0 | 4950 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0030 | 0/0 | 4950 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0031 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0032 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0033 | 0/0 | 4950 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0034 | 0/0 | 4950 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0035 | 0/0 | 4950 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0036 | 0/0 | 4950 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0037 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
c0038 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 590 | 186 | 32 | 36 | 82 | 8 | 28 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
t0002 | 0/0 | 590 | 54 | 31 | 16 | 2 | 4 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
t0003 | 0/0 | 590 | 15 | 10 | 5 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
t0004 | 0/0 | 590 | 5 | 5 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
t0005 | 0/1 | 590 | 5 | 0 | 3 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
t0006 | 0/0 | 590 | 4 | 0 | 0 | 4 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
t0007 | 0/0 | 590 | 2 | 0 | 0 | 2 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
t0008 | 0/0 | 590 | 2 | 2 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
t0009 | 0/0 | 590 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
t0010 | 0/0 | 512 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
t0011 | 0/0 | 590 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
t0012 | 0/0 | 590 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
t0013 | 0/0 | 590 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
t0014 | 0/0 | 590 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0002 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4950 | 95 | 7 | 19 | 48 | 4 | 17 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0003 | 0/1 | 4950 | 29 | 11 | 10 | 3 | 2 | 2 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0006 | 0/0 | 4950 | 9 | 7 | 1 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0009 | 0/0 | 4950 | 5 | 4 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0014 | 0/0 | 4950 | 3 | 2 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0018 | 0/0 | 4950 | 2 | 0 | 0 | 2 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0023 | 0/0 | 4950 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0025 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0027 | 0/0 | 4950 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0031 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0033 | 0/0 | 4950 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0034 | 0/0 | 4950 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0002c0002 | 0/0 | 4950 | 59 | 11 | 10 | 32 | 1 | 5 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0002c0011 | 0/0 | 4950 | 4 | 4 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0003c0004 | 0/0 | 4938 | 12 | 7 | 5 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0004c0005 | 0/0 | 4950 | 10 | 0 | 9 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0005c0007 | 0/0 | 4950 | 8 | 0 | 2 | 1 | 1 | 4 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0006c0008 | 0/0 | 4938 | 6 | 6 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0007c0010 | 0/0 | 4950 | 4 | 4 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0008c0013 | 0/0 | 4950 | 3 | 3 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0009c0012 | 0/0 | 4938 | 3 | 3 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0010c0015 | 0/0 | 4950 | 2 | 0 | 2 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0011c0016 | 0/0 | 4950 | 2 | 2 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0012c0017 | 0/0 | 4950 | 2 | 2 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0013c0021 | 0/0 | 4938 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0013c0022 | 0/0 | 4938 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0014c0019 | 0/0 | 4950 | 2 | 0 | 0 | 2 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0015c0024 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0016c0020 | 0/0 | 4938 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0017c0028 | 0/0 | 4950 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0018c0029 | 0/0 | 4950 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0019c0030 | 0/0 | 4950 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0020c0032 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0021c0026 | 0/0 | 4950 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0022c0035 | 0/0 | 4950 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0023c0036 | 0/0 | 4950 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0024c0037 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0025c0038 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5539 | 89 | 7 | 19 | 42 | 4 | 17 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0001t0006 | 0/0 | 5539 | 4 | 0 | 0 | 4 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0001t0007 | 0/0 | 5539 | 2 | 0 | 0 | 2 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0003t0002 | 0/0 | 5539 | 22 | 11 | 6 | 2 | 2 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0003t0005 | 0/1 | 5539 | 5 | 0 | 3 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0003t0012 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0003t0013 | 0/0 | 5539 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0006t0002 | 0/0 | 5539 | 9 | 7 | 1 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0009t0002 | 0/0 | 5539 | 4 | 4 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0009t0011 | 0/0 | 5539 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0014t0001 | 0/0 | 5539 | 3 | 2 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0018t0001 | 0/0 | 5539 | 2 | 0 | 0 | 2 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0023t0001 | 0/0 | 5539 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0025t0002 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0027t0001 | 0/0 | 5539 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0031t0001 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0033t0014 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0001c0034t0001 | 0/0 | 5539 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0002c0002t0001 | 0/0 | 5539 | 59 | 11 | 10 | 32 | 1 | 5 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0002c0011t0001 | 0/0 | 5539 | 4 | 4 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0003c0004t0003 | 0/0 | 5527 | 12 | 7 | 5 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0004c0005t0002 | 0/0 | 5539 | 10 | 0 | 9 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0005c0007t0001 | 0/0 | 5539 | 8 | 0 | 2 | 1 | 1 | 4 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0006c0008t0004 | 0/0 | 5527 | 5 | 5 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0006c0008t0010 | 0/0 | 5449 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0007c0010t0002 | 0/0 | 5539 | 4 | 4 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0008c0013t0002 | 0/0 | 5539 | 3 | 3 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0009c0012t0003 | 0/0 | 5527 | 3 | 3 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0010c0015t0001 | 0/0 | 5539 | 2 | 0 | 2 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0011c0016t0001 | 0/0 | 5539 | 2 | 2 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0012c0017t0001 | 0/0 | 5539 | 2 | 2 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0013c0021t0008 | 0/0 | 5527 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0013c0022t0008 | 0/0 | 5527 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0014c0019t0001 | 0/0 | 5539 | 2 | 0 | 0 | 2 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0015c0024t0002 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0016c0020t0009 | 0/0 | 5527 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0017c0028t0001 | 0/0 | 5539 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0018c0029t0001 | 0/0 | 5539 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0019c0030t0001 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0020c0032t0001 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0021c0026t0001 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0022c0035t0001 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0023c0036t0001 | 0/0 | 5539 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0024c0037t0001 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
a0025c0038t0001 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | copy fasta | chr11 | 571470 | 617222 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0006g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0006g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0006g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0007g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0001t0007g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0005g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0005g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0005g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0005g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0005g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0012g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0003t0013g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0006t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0006t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0006t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0006t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0006t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0006t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0006t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0006t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0006t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0009t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0009t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0009t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0009t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0009t0011g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0014t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0014t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0014t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0018t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0018t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0023t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0025t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0027t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0031t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0033t0014g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0001c0034t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0002 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0011t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0011t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0011t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0002c0011t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0003c0004t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0003c0004t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0003c0004t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0003c0004t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0003c0004t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0003c0004t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0003c0004t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0003c0004t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0003c0004t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0003c0004t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0003c0004t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0003c0004t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0004c0005t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0004c0005t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0004c0005t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0004c0005t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0004c0005t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0004c0005t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0004c0005t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0004c0005t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0004c0005t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0005c0007t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0005c0007t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0005c0007t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0005c0007t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0005c0007t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0005c0007t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0005c0007t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0005c0007t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0006c0008t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0006c0008t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0006c0008t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0006c0008t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0006c0008t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0006c0008t0010g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0007c0010t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0007c0010t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0007c0010t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0007c0010t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0008c0013t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0008c0013t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0009c0012t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0009c0012t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0009c0012t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0010c0015t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0011c0016t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0011c0016t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0012c0017t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0012c0017t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0013c0021t0008g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0013c0022t0008g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0014c0019t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0014c0019t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0015c0024t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0016c0020t0009g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0017c0028t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0018c0029t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0019c0030t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0020c0032t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0021c0026t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0022c0035t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0023c0036t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0024c0037t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
a0025c0038t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0004 | c0005 | t0002 | g0042 | EUR | GBR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG00099 | hp2 | a0001 | c0027 | t0001 | g0254 | EUR | GBR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG00140 | hp1 | a0001 | c0006 | t0002 | g0124 | EUR | GBR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0266 | EUR | GBR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0218 | EUR | FIN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | FIN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG00408 | hp2 | a0001 | c0001 | t0006 | g0212 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG00544 | hp2 | a0019 | c0030 | t0001 | g0182 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0234 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG00597 | hp2 | a0001 | c0001 | t0007 | g0201 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG00639 | hp1 | a0001 | c0003 | t0005 | g0035 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG00639 | hp2 | a0003 | c0004 | t0003 | g0083 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | CHS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG00735 | hp1 | a0001 | c0003 | t0013 | g0051 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG00741 | hp2 | a0001 | c0003 | t0005 | g0026 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0255 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01074 | hp1 | a0001 | c0009 | t0011 | g0097 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01074 | hp2 | a0001 | c0003 | t0002 | g0052 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01099 | hp1 | a0001 | c0003 | t0002 | g0043 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01106 | hp2 | a0023 | c0036 | t0001 | g0110 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01168 | hp1 | a0003 | c0004 | t0003 | g0174 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01168 | hp2 | a0005 | c0007 | t0001 | g0179 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01169 | hp1 | a0003 | c0004 | t0003 | g0175 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0169 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01175 | hp1 | a0004 | c0005 | t0002 | g0033 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01192 | hp1 | a0001 | c0006 | t0002 | g0016 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01192 | hp2 | a0001 | c0003 | t0005 | g0014 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01243 | hp2 | a0018 | c0029 | t0001 | g0217 | AMR | PUR | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0185 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01255 | hp2 | a0001 | c0003 | t0002 | g0028 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0224 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01256 | hp2 | a0010 | c0015 | t0001 | g0004 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01257 | hp1 | a0001 | c0003 | t0002 | g0027 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01257 | hp2 | a0004 | c0005 | t0002 | g0023 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01258 | hp1 | a0004 | c0005 | t0002 | g0032 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01258 | hp2 | a0010 | c0015 | t0001 | g0004 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01346 | hp1 | a0003 | c0004 | t0003 | g0222 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01346 | hp2 | a0004 | c0005 | t0002 | g0034 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01361 | hp2 | a0001 | c0003 | t0002 | g0029 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01433 | hp2 | a0003 | c0004 | t0003 | g0084 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01516 | hp1 | a0001 | c0003 | t0002 | g0054 | EUR | IBS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0240 | EUR | IBS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01517 | hp1 | a0001 | c0003 | t0002 | g0055 | EUR | IBS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0245 | EUR | IBS | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01884 | hp2 | a0003 | c0004 | t0003 | g0216 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01891 | hp1 | a0007 | c0010 | t0002 | g0011 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01928 | hp2 | a0004 | c0005 | t0002 | g0041 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0223 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01943 | hp2 | a0001 | c0014 | t0001 | g0262 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0267 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01975 | hp2 | a0004 | c0005 | t0002 | g0031 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01981 | hp2 | a0004 | c0005 | t0002 | g0018 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02004 | hp2 | a0005 | c0007 | t0001 | g0253 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02015 | hp1 | a0001 | c0003 | t0002 | g0022 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0221 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02040 | hp1 | a0014 | c0019 | t0001 | g0126 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02056 | hp1 | a0005 | c0007 | t0001 | g0180 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0248 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0135 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02083 | hp1 | a0014 | c0019 | t0001 | g0090 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | KHV | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02145 | hp1 | a0025 | c0038 | t0001 | g0181 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02145 | hp2 | a0006 | c0008 | t0004 | g0121 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | CDX | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CDX | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CDX | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CDX | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02257 | hp1 | a0024 | c0037 | t0001 | g0125 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0137 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0133 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02258 | hp2 | a0001 | c0031 | t0001 | g0261 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0227 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02280 | hp1 | a0001 | c0003 | t0002 | g0038 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02280 | hp2 | a0001 | c0003 | t0002 | g0053 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02293 | hp1 | a0004 | c0005 | t0002 | g0003 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02300 | hp2 | a0004 | c0005 | t0002 | g0003 | AMR | PEL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02451 | hp1 | a0001 | c0025 | t0002 | g0092 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02451 | hp2 | a0006 | c0008 | t0004 | g0080 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02572 | hp1 | a0001 | c0009 | t0002 | g0094 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02572 | hp2 | a0002 | c0011 | t0001 | g0166 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02602 | hp1 | a0005 | c0007 | t0001 | g0268 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02602 | hp2 | a0001 | c0003 | t0005 | g0044 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02615 | hp1 | a0002 | c0011 | t0001 | g0165 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02615 | hp2 | a0001 | c0003 | t0002 | g0040 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02622 | hp1 | a0011 | c0016 | t0001 | g0069 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02622 | hp2 | a0003 | c0004 | t0003 | g0177 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02630 | hp1 | a0009 | c0012 | t0003 | g0176 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02630 | hp2 | a0006 | c0008 | t0004 | g0247 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02683 | hp1 | a0005 | c0007 | t0001 | g0089 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02717 | hp1 | a0002 | c0011 | t0001 | g0065 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02717 | hp2 | a0003 | c0004 | t0003 | g0269 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0188 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02723 | hp2 | a0001 | c0006 | t0002 | g0036 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0095 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02818 | hp2 | a0009 | c0012 | t0003 | g0067 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0220 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02886 | hp2 | a0001 | c0014 | t0001 | g0263 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02896 | hp1 | a0013 | c0022 | t0008 | g0123 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02896 | hp2 | a0008 | c0013 | t0002 | g0005 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02897 | hp1 | a0008 | c0013 | t0002 | g0005 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02897 | hp2 | a0002 | c0011 | t0001 | g0058 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02922 | hp1 | a0001 | c0009 | t0002 | g0131 | AFR | ESN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02922 | hp2 | a0007 | c0010 | t0002 | g0012 | AFR | ESN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0132 | AFR | ESN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03041 | hp1 | a0003 | c0004 | t0003 | g0164 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03041 | hp2 | a0003 | c0004 | t0003 | g0190 | AFR | GWD | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03098 | hp1 | a0007 | c0010 | t0002 | g0010 | AFR | MSL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03098 | hp2 | a0001 | c0009 | t0002 | g0093 | AFR | MSL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03130 | hp1 | a0001 | c0006 | t0002 | g0008 | AFR | ESN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03130 | hp2 | a0007 | c0010 | t0002 | g0272 | AFR | ESN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03139 | hp1 | a0001 | c0006 | t0002 | g0019 | AFR | ESN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03195 | hp1 | a0001 | c0003 | t0002 | g0039 | AFR | ESN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03209 | hp1 | a0009 | c0012 | t0003 | g0082 | AFR | MSL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03209 | hp2 | a0001 | c0006 | t0002 | g0013 | AFR | MSL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03225 | hp1 | a0001 | c0003 | t0002 | g0037 | AFR | MSL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03225 | hp2 | a0003 | c0004 | t0003 | g0250 | AFR | MSL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03453 | hp2 | a0001 | c0003 | t0002 | g0015 | AFR | MSL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03486 | hp1 | a0006 | c0008 | t0004 | g0178 | AFR | MSL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03486 | hp2 | a0008 | c0013 | t0002 | g0184 | AFR | MSL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0072 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03516 | hp1 | a0001 | c0003 | t0002 | g0048 | AFR | ESN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03516 | hp2 | a0003 | c0004 | t0003 | g0025 | AFR | ESN | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03579 | hp1 | a0011 | c0016 | t0001 | g0087 | AFR | MSL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0136 | AFR | MSL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03710 | hp2 | a0017 | c0028 | t0001 | g0129 | SAS | PJL | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0194 | SAS | BEB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0172 | SAS | STU | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG04115 | hp2 | a0001 | c0034 | t0001 | g0120 | SAS | STU | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG04184 | hp1 | a0005 | c0007 | t0001 | g0128 | SAS | BEB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | STU | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | STU | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG04204 | hp1 | a0001 | c0003 | t0002 | g0030 | SAS | STU | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | STU | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18522 | hp1 | a0001 | c0006 | t0002 | g0009 | AFR | YRI | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0085 | AFR | YRI | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18612 | hp2 | a0001 | c0001 | t0007 | g0196 | EAS | CHB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | CHB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | CHB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18906 | hp1 | a0006 | c0008 | t0004 | g0081 | AFR | YRI | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18906 | hp2 | a0020 | c0032 | t0001 | g0167 | AFR | YRI | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18946 | hp2 | a0001 | c0018 | t0001 | g0113 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18947 | hp2 | a0001 | c0001 | t0006 | g0242 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18967 | hp2 | a0001 | c0003 | t0012 | g0049 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18974 | hp1 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18983 | hp2 | a0001 | c0033 | t0014 | g0105 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18984 | hp1 | a0001 | c0018 | t0001 | g0112 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18984 | hp2 | a0001 | c0001 | t0006 | g0163 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA18985 | hp2 | a0001 | c0001 | t0006 | g0241 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19000 | hp1 | a0001 | c0003 | t0002 | g0017 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19011 | hp2 | a0022 | c0035 | t0001 | g0243 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19030 | hp2 | a0001 | c0006 | t0002 | g0057 | AFR | LWK | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19043 | hp1 | a0001 | c0003 | t0002 | g0046 | AFR | LWK | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19043 | hp2 | a0012 | c0017 | t0001 | g0103 | AFR | LWK | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19066 | hp2 | a0021 | c0026 | t0001 | g0096 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19240 | hp1 | a0016 | c0020 | t0009 | g0249 | AFR | YRI | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA19240 | hp2 | a0006 | c0008 | t0010 | g0068 | AFR | YRI | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA20129 | hp1 | a0001 | c0014 | t0001 | g0144 | AFR | ASW | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA20129 | hp2 | a0001 | c0003 | t0002 | g0045 | AFR | ASW | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA20752 | hp1 | a0005 | c0007 | t0001 | g0252 | EUR | TSI | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA20752 | hp2 | a0001 | c0023 | t0001 | g0231 | EUR | TSI | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | GIH | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA20905 | hp2 | a0005 | c0007 | t0001 | g0127 | SAS | GIH | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0139 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG01123 | hp2 | a0001 | c0003 | t0002 | g0056 | AMR | CLM | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02486 | hp1 | a0012 | c0017 | t0001 | g0148 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02486 | hp2 | a0001 | c0006 | t0002 | g0021 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02559 | hp1 | a0001 | c0003 | t0002 | g0020 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0086 | AFR | ACB | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0104 | AFR | USA | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
HG06807 | hp2 | a0001 | c0009 | t0002 | g0183 | AFR | USA | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA20300 | hp1 | a0001 | c0003 | t0002 | g0047 | AFR | USA | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA20300 | hp2 | a0013 | c0021 | t0008 | g0251 | AFR | USA | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0070 | AFR | LWK | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
NA21309 | hp2 | a0015 | c0024 | t0002 | g0024 | AFR | LWK | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0005 | g0050 | REF | REF | PHRF1_chr11_571470_617222 | PHRF1 | chr11 | 571470 | 617222 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:581591
|
C | T | 1 | a0025 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.79C>T | p.Pro27Ser | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 2/18 | 223/5539 | 79/4950 | 27/1649 | chr11 | 581591 | ||
chr11:581973
|
G | C | 1 | a0010 | 2 | HG01256.hp2 HG01258.hp2 |
missense_variant | MODERATE | c.106G>C | p.Val36Leu | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/18 | 250/5539 | 106/4950 | 36/1649 | chr11 | 581973 | ||
chr11:587372
|
A | G | 1 | a0014 | 2 | HG02040.hp1 HG02083.hp1 |
missense_variant | MODERATE | c.328A>G | p.Ile110Val | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/18 | 472/5539 | 328/4950 | 110/1649 | chr11 | 587372 | ||
chr11:597398
|
C | T | 1 | a0024 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.722C>T | p.Ala241Val | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 8/18 | 866/5539 | 722/4950 | 241/1649 | chr11 | 597398 | ||
chr11:598481
|
G | T | 1 | a0023 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.1003G>T | p.Ala335Ser | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/18 | 1147/5539 | 1003/4950 | 335/1649 | chr11 | 598481 | ||
chr11:607068
|
C | T | 1 | a0022 | 1 | NA19011.hp2 | missense_variant&splice_region_variant | MODERATE | c.1612C>T | p.Pro538Ser | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 1756/5539 | 1612/4950 | 538/1649 | chr11 | 607068 | ||
chr11:607356
|
G | A | 1 | a0009 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
missense_variant | MODERATE | c.1900G>A | p.Gly634Ser | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 2044/5539 | 1900/4950 | 634/1649 | chr11 | 607356 | ||
chr11:607680
|
G | A | 1 | a0021 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.2224G>A | p.Gly742Arg | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 2368/5539 | 2224/4950 | 742/1649 | chr11 | 607680 | ||
chr11:607819
|
C | A | 1 | a0008 | 3 | HG02896.hp2 HG02897.hp1 HG03486.hp2 |
missense_variant | MODERATE | c.2363C>A | p.Ser788Tyr | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 2507/5539 | 2363/4950 | 788/1649 | chr11 | 607819 | ||
chr11:607933
|
G | A | 1 | a0015 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2477G>A | p.Arg826Gln | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 2621/5539 | 2477/4950 | 826/1649 | chr11 | 607933 | ||
chr11:608184
|
G | T | 1 | a0013 | 2 | HG02896.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.2728G>T | p.Ala910Ser | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 2872/5539 | 2728/4950 | 910/1649 | chr11 | 608184 | ||
chr11:608502
|
CGGACGCG others(5): Show |
C | 5 | a0003a0006a0009others(2): Show | 24 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(21): Show |
disruptive_inframe_deletion | MODERATE | c.3059_3070delGGACGC others(6): Show |
p.Gly1020_Ser1023del | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 3203/5539 | 3059/4950 | 1020/1649 | INFO_REALIGN_3_PRIME | chr11 | 608502 | |
chr11:608593
|
G | A | 5 | a0005a0014a0017others(2): Show | 13 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(10): Show |
missense_variant | MODERATE | c.3137G>A | p.Arg1046Gln | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 3281/5539 | 3137/4950 | 1046/1649 | chr11 | 608593 | ||
chr11:608871
|
C | T | 1 | a0012 | 2 | HG02486.hp1 NA19043.hp2 |
missense_variant | MODERATE | c.3415C>T | p.Arg1139Trp | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 3559/5539 | 3415/4950 | 1139/1649 | chr11 | 608871 | ||
chr11:608959
|
C | T | 1 | a0007 | 4 | HG01891.hp1 HG02922.hp2 HG03098.hp1 others(1): Show |
missense_variant | MODERATE | c.3503C>T | p.Ser1168Leu | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 3647/5539 | 3503/4950 | 1168/1649 | chr11 | 608959 | ||
chr11:609019
|
G | C | 1 | a0019 | 1 | HG00544.hp2 | missense_variant | MODERATE | c.3563G>C | p.Arg1188Pro | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 3707/5539 | 3563/4950 | 1188/1649 | chr11 | 609019 | ||
chr11:609081
|
G | C | 2 | a0011a0024 | 3 | HG02257.hp1 HG02622.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.3625G>C | p.Gly1209Arg | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 3769/5539 | 3625/4950 | 1209/1649 | chr11 | 609081 | ||
chr11:609145
|
C | T | 1 | a0013 | 2 | HG02896.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.3689C>T | p.Pro1230Leu | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 3833/5539 | 3689/4950 | 1230/1649 | chr11 | 609145 | ||
chr11:609148
|
A | C | 1 | a0006 | 6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
missense_variant | MODERATE | c.3692A>C | p.Glu1231Ala | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 3836/5539 | 3692/4950 | 1231/1649 | chr11 | 609148 | ||
chr11:609577
|
C | T | 5 | a0003a0006a0009others(2): Show | 24 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(21): Show |
missense_variant | MODERATE | c.4121C>T | p.Ala1374Val | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 4265/5539 | 4121/4950 | 1374/1649 | chr11 | 609577 | ||
chr11:610277
|
T | C | 17 | a0001a0003a0004others(14): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
missense_variant | MODERATE | c.4346T>C | p.Val1449Ala | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 15/18 | 4490/5539 | 4346/4950 | 1449/1649 | chr11 | 610277 | ||
chr11:610724
|
C | T | 1 | a0004 | 10 | HG00099.hp1 HG01175.hp1 HG01257.hp2 others(7): Show |
missense_variant | MODERATE | c.4640C>T | p.Ala1547Val | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 16/18 | 4784/5539 | 4640/4950 | 1547/1649 | chr11 | 610724 | ||
chr11:611740
|
C | T | 1 | a0016 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.4913C>T | p.Ala1638Val | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 5057/5539 | 4913/4950 | 1638/1649 | chr11 | 611740 | ||
chr11:611752
|
C | T | 2 | a0017a0020 | 2 | HG03710.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.4925C>T | p.Pro1642Leu | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 5069/5539 | 4925/4950 | 1642/1649 | chr11 | 611752 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:581587
|
G | A | 5 | a0006c0008a0009c0012a0013c0021others(2): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
synonymous_variant | LOW | c.75G>A | p.Ala25Ala | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 2/18 | 219/5539 | 75/4950 | 25/1649 | chr11 | 581587 | ||
chr11:582056
|
G | A | 1 | a0001c0023 | 1 | NA20752.hp2 | synonymous_variant | LOW | c.189G>A | p.Glu63Glu | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/18 | 333/5539 | 189/4950 | 63/1649 | chr11 | 582056 | ||
chr11:587425
|
C | A | 5 | a0001c0003a0001c0006a0004c0005others(2): Show | 53 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(50): Show |
synonymous_variant | LOW | c.381C>A | p.Ala127Ala | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/18 | 525/5539 | 381/4950 | 127/1649 | chr11 | 587425 | ||
chr11:587452
|
C | T | 1 | a0002c0011 | 4 | HG02572.hp2 HG02615.hp1 HG02717.hp1 others(1): Show |
synonymous_variant | LOW | c.408C>T | p.Val136Val | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/18 | 552/5539 | 408/4950 | 136/1649 | chr11 | 587452 | ||
chr11:592666
|
C | T | 2 | a0013c0021a0013c0022 | 2 | HG02896.hp1 NA20300.hp2 |
synonymous_variant | LOW | c.612C>T | p.Cys204Cys | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/18 | 756/5539 | 612/4950 | 204/1649 | chr11 | 592666 | ||
chr11:605277
|
T | C | 5 | a0006c0008a0009c0012a0013c0021others(2): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
synonymous_variant | LOW | c.1311T>C | p.Pro437Pro | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 11/18 | 1455/5539 | 1311/4950 | 437/1649 | chr11 | 605277 | ||
chr11:607175
|
G | A | 4 | a0001c0003a0001c0025a0004c0005others(1): Show | 41 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(38): Show |
synonymous_variant | LOW | c.1719G>A | p.Pro573Pro | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 1863/5539 | 1719/4950 | 573/1649 | chr11 | 607175 | ||
chr11:607649
|
C | T | 1 | a0001c0018 | 2 | NA18946.hp2 NA18984.hp1 |
synonymous_variant | LOW | c.2193C>T | p.Ser731Ser | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 2337/5539 | 2193/4950 | 731/1649 | chr11 | 607649 | ||
chr11:608180
|
A | G | 1 | a0006c0008 | 6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
synonymous_variant | LOW | c.2724A>G | p.Ala908Ala | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 2868/5539 | 2724/4950 | 908/1649 | chr11 | 608180 | ||
chr11:608333
|
G | A | 1 | a0001c0027 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.2877G>A | p.Thr959Thr | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 3021/5539 | 2877/4950 | 959/1649 | chr11 | 608333 | ||
chr11:608378
|
G | A | 1 | a0013c0021 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.2922G>A | p.Pro974Pro | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 3066/5539 | 2922/4950 | 974/1649 | chr11 | 608378 | ||
chr11:609068
|
G | A | 8 | a0001c0003a0001c0006a0001c0009others(5): Show | 62 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(59): Show |
synonymous_variant | LOW | c.3612G>A | p.Ala1204Ala | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 3756/5539 | 3612/4950 | 1204/1649 | chr11 | 609068 | ||
chr11:609242
|
C | T | 1 | a0001c0034 | 1 | HG04115.hp2 | synonymous_variant | LOW | c.3786C>T | p.Gly1262Gly | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 3930/5539 | 3786/4950 | 1262/1649 | chr11 | 609242 | ||
chr11:609347
|
T | G | 2 | a0013c0021a0013c0022 | 2 | HG02896.hp1 NA20300.hp2 |
synonymous_variant | LOW | c.3891T>G | p.Ser1297Ser | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 4035/5539 | 3891/4950 | 1297/1649 | chr11 | 609347 | ||
chr11:609353
|
G | A | 8 | a0001c0003a0001c0006a0001c0009others(5): Show | 62 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(59): Show |
synonymous_variant | LOW | c.3897G>A | p.Pro1299Pro | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 4041/5539 | 3897/4950 | 1299/1649 | chr11 | 609353 | ||
chr11:609521
|
T | C | 2 | a0001c0014a0001c0031 | 4 | HG01943.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
synonymous_variant | LOW | c.4065T>C | p.Ala1355Ala | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 4209/5539 | 4065/4950 | 1355/1649 | chr11 | 609521 | ||
chr11:609701
|
C | T | 1 | a0001c0031 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.4245C>T | p.Pro1415Pro | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/18 | 4389/5539 | 4245/4950 | 1415/1649 | chr11 | 609701 | ||
chr11:610680
|
C | T | 1 | a0001c0033 | 1 | NA18983.hp2 | synonymous_variant | LOW | c.4596C>T | p.Ala1532Ala | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 16/18 | 4740/5539 | 4596/4950 | 1532/1649 | chr11 | 610680 | ||
chr11:611052
|
C | T | 2 | a0018c0029a0025c0038 | 2 | HG01243.hp2 HG02145.hp1 |
synonymous_variant | LOW | c.4776C>T | p.Tyr1592Tyr | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 17/18 | 4920/5539 | 4776/4950 | 1592/1649 | chr11 | 611052 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:576517
|
C | T | 1 | a0001c0033t0014 | 1 | NA18983.hp2 | 5_prime_UTR_variant | MODIFIER | c.-97C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/18 | 4996 | chr11 | 576517 | |||||
chr11:611796
|
TATGCCCG others(71): Show |
T | 1 | a0006c0008t0010 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*51_*128delTCGGGGC others(71): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 51 | INFO_REALIGN_3_PRIME | chr11 | 611796 | ||||
chr11:611802
|
C | G | 1 | a0001c0003t0005 | 5 | HG00639.hp1 HG00741.hp2 HG01192.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*25C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 25 | chr11 | 611802 | |||||
chr11:611814
|
G | C | 1 | a0016c0020t0009 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*37G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 37 | chr11 | 611814 | |||||
chr11:611830
|
G | A | 1 | a0001c0001t0006 | 4 | HG00408.hp2 NA18947.hp2 NA18984.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*53G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 53 | chr11 | 611830 | |||||
chr11:611841
|
C | T | 1 | a0001c0003t0013 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*64C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 64 | chr11 | 611841 | |||||
chr11:611868
|
C | T | 14 | a0001c0003t0002a0001c0003t0005a0001c0003t0012others(11): Show | 68 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*91C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 91 | chr11 | 611868 | |||||
chr11:611869
|
G | A | 1 | a0001c0001t0007 | 2 | HG00597.hp2 NA18612.hp2 |
3_prime_UTR_variant | MODIFIER | c.*92G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 92 | chr11 | 611869 | |||||
chr11:611919
|
C | G | 19 | a0001c0003t0002a0001c0003t0005a0001c0003t0012others(16): Show | 86 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*142C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 142 | chr11 | 611919 | |||||
chr11:611923
|
G | A | 1 | a0016c0020t0009 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*146G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 146 | chr11 | 611923 | |||||
chr11:611982
|
A | G | 1 | a0001c0003t0012 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*205A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 205 | chr11 | 611982 | |||||
chr11:612145
|
C | G | 1 | a0001c0009t0011 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*368C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 368 | chr11 | 612145 | |||||
chr11:612148
|
T | C | 17 | a0001c0003t0002a0001c0003t0005a0001c0003t0012others(14): Show | 71 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*371T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 371 | chr11 | 612148 | |||||
chr11:612176
|
G | A | 2 | a0006c0008t0004a0006c0008t0010 | 6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*399G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 399 | chr11 | 612176 | |||||
chr11:612182
|
T | C | 19 | a0001c0003t0002a0001c0003t0005a0001c0003t0012others(16): Show | 86 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*405T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 18/18 | 405 | chr11 | 612182 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:576634
|
C | T | 1 | a0007c0010t0002g0272 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-22+42C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 576634 | ||||||
chr11:576665
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-22+73G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 576665 | ||||||
chr11:576683
|
ACCGCGGG others(12): Show |
A | 1 | a0001c0001t0001g0007 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-22+97_-22+115delG others(18): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 576683 | |||||
chr11:576745
|
G | GCTGGGAG others(12): Show |
17 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0074others(14): Show | 18 | HG01256.hp2 HG01258.hp2 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.-22+317_-22+335dup others(19): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 576745 | |||||
chr11:576745
|
G | GCTGGGAG others(31): Show |
7 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(4): Show | 7 | HG00438.hp2 HG01981.hp1 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.-22+298_-22+335dup others(38): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 576745 | |||||
chr11:576745
|
G | GCTGGGAG others(69): Show |
1 | a0002c0011t0001g0058 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-22+260_-22+335dup others(76): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 576745 | |||||
chr11:576745
|
GCTGGGAG others(12): Show |
G | 51 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0130others(48): Show | 54 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.-22+317_-22+335del others(19): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 576745 | |||||
chr11:576745
|
GCTGGGAG others(31): Show |
G | 49 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(46): Show | 51 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.-22+298_-22+335del others(38): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 576745 | |||||
chr11:576745
|
GCTGGGAG others(50): Show |
G | 39 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(36): Show | 39 | HG00280.hp1 HG00558.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.-22+279_-22+335del others(57): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 576745 | |||||
chr11:576745
|
GCTGGGAG others(69): Show |
G | 22 | a0001c0001t0001g0257a0001c0001t0001g0259a0001c0001t0001g0260others(19): Show | 22 | HG00099.hp2 HG00140.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.-22+260_-22+335del others(76): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 576745 | |||||
chr11:576745
|
GCTGGGAG others(88): Show |
G | 9 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0003t0002g0017others(6): Show | 9 | HG01952.hp2 HG01981.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-22+241_-22+335del others(95): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 576745 | |||||
chr11:576745
|
GCTGGGAG others(107): Show |
G | 37 | a0001c0003t0002g0022a0001c0003t0002g0027a0001c0003t0002g0028others(34): Show | 38 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-22+222_-22+335del | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 576745 | |||||
chr11:576768
|
G | A | 2 | a0001c0006t0002g0008a0001c0006t0002g0009 | 2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-22+176G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 576768 | ||||||
chr11:576806
|
G | A | 6 | a0001c0003t0005g0014a0001c0006t0002g0013a0007c0010t0002g0010others(3): Show | 6 | HG01192.hp2 HG01891.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22+214G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 576806 | ||||||
chr11:576825
|
G | A | 2 | a0001c0003t0002g0015a0001c0006t0002g0016 | 2 | HG01192.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-22+233G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 576825 | ||||||
chr11:576844
|
G | A | 5 | a0001c0003t0002g0017a0001c0003t0002g0020a0001c0006t0002g0019others(2): Show | 5 | HG01981.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+252G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 576844 | ||||||
chr11:576863
|
G | A | 37 | a0001c0003t0002g0022a0001c0003t0002g0027a0001c0003t0002g0028others(34): Show | 38 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-22+271G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 576863 | ||||||
chr11:576871
|
C | G | 1 | a0001c0006t0002g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-22+279C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 576871 | ||||||
chr11:577167
|
T | G | 1 | a0020c0032t0001g0167 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-22+575T>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577167 | ||||||
chr11:577180
|
C | G | 4 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(1): Show | 4 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22+588C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577180 | ||||||
chr11:577238
|
C | T | 4 | a0002c0011t0001g0058a0002c0011t0001g0065a0002c0011t0001g0165others(1): Show | 4 | HG02572.hp2 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22+646C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577238 | ||||||
chr11:577269
|
A | G | 1 | a0001c0003t0002g0056 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-22+677A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577269 | ||||||
chr11:577296
|
G | C | 11 | a0002c0002t0001g0002a0002c0002t0001g0066a0002c0002t0001g0122others(8): Show | 13 | HG00597.hp1 HG00609.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.-22+704G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577296 | ||||||
chr11:577309
|
G | A | 19 | a0003c0004t0003g0083a0003c0004t0003g0084a0003c0004t0003g0174others(16): Show | 19 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-22+717G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577309 | ||||||
chr11:577330
|
C | T | 1 | a0003c0004t0003g0164 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-22+738C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577330 | ||||||
chr11:577354
|
T | C | 17 | a0003c0004t0003g0083a0003c0004t0003g0084a0003c0004t0003g0174others(14): Show | 17 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22+762T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577354 | ||||||
chr11:577442
|
C | T | 19 | a0003c0004t0003g0083a0003c0004t0003g0084a0003c0004t0003g0174others(16): Show | 19 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-22+850C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577442 | ||||||
chr11:577454
|
C | T | 17 | a0003c0004t0003g0083a0003c0004t0003g0084a0003c0004t0003g0174others(14): Show | 17 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22+862C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577454 | ||||||
chr11:577534
|
G | A | 72 | a0001c0003t0002g0015a0001c0003t0002g0017a0001c0003t0002g0020others(69): Show | 73 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.-22+942G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577534 | ||||||
chr11:577670
|
C | G | 17 | a0003c0004t0003g0083a0003c0004t0003g0084a0003c0004t0003g0174others(14): Show | 17 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22+1078C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577670 | ||||||
chr11:577684
|
G | A | 19 | a0003c0004t0003g0083a0003c0004t0003g0084a0003c0004t0003g0174others(16): Show | 19 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-22+1092G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577684 | ||||||
chr11:577696
|
A | T | 1 | a0002c0002t0001g0267 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-22+1104A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577696 | ||||||
chr11:577727
|
C | T | 1 | a0001c0001t0006g0163 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-22+1135C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577727 | ||||||
chr11:577735
|
C | T | 1 | a0002c0002t0001g0246 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-22+1143C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577735 | ||||||
chr11:577809
|
C | T | 71 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0060others(68): Show | 71 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.-22+1217C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577809 | ||||||
chr11:577903
|
T | G | 19 | a0003c0004t0003g0083a0003c0004t0003g0084a0003c0004t0003g0174others(16): Show | 19 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-22+1311T>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577903 | ||||||
chr11:577908
|
G | C | 19 | a0003c0004t0003g0083a0003c0004t0003g0084a0003c0004t0003g0174others(16): Show | 19 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-22+1316G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577908 | ||||||
chr11:577915
|
T | C | 19 | a0003c0004t0003g0083a0003c0004t0003g0084a0003c0004t0003g0174others(16): Show | 19 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-22+1323T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 577915 | ||||||
chr11:578078
|
G | T | 6 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(3): Show | 6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22+1486G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 578078 | ||||||
chr11:578222
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-22+1630G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 578222 | ||||||
chr11:578230
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-22+1638G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 578230 | ||||||
chr11:578294
|
C | T | 1 | a0002c0002t0001g0234 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-22+1702C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 578294 | ||||||
chr11:578634
|
T | C | 272 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0060others(269): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.-22+2042T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 578634 | ||||||
chr11:578759
|
A | G | 109 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0060others(106): Show | 110 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.-22+2167A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 578759 | ||||||
chr11:578844
|
C | G | 53 | a0001c0003t0002g0015a0001c0003t0002g0017a0001c0003t0002g0020others(50): Show | 54 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.-22+2252C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 578844 | ||||||
chr11:578954
|
A | G | 1 | a0002c0002t0001g0140 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-22+2362A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 578954 | ||||||
chr11:578976
|
A | G | 20 | a0002c0002t0001g0001a0002c0002t0001g0059a0002c0002t0001g0098others(17): Show | 22 | HG00558.hp1 HG00673.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.-22+2384A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 578976 | ||||||
chr11:578996
|
T | C | 199 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0060others(196): Show | 201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.-22+2404T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 578996 | ||||||
chr11:579048
|
T | C | 2 | a0003c0004t0003g0174a0003c0004t0003g0175 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-21-2444T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579048 | ||||||
chr11:579049
|
A | T | 2 | a0003c0004t0003g0174a0003c0004t0003g0175 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-21-2443A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579049 | ||||||
chr11:579078
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-21-2414C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579078 | ||||||
chr11:579188
|
G | C | 1 | a0013c0022t0008g0123 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-21-2304G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579188 | ||||||
chr11:579220
|
T | TCCCCCAG others(11): Show |
3 | a0009c0012t0003g0067a0009c0012t0003g0082a0009c0012t0003g0176 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-21-2238_-21-2221d others(20): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 579220 | |||||
chr11:579220
|
TCCCCCAG others(11): Show |
T | 2 | a0018c0029t0001g0217a0025c0038t0001g0181 | 2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-21-2238_-21-2221d others(20): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 579220 | |||||
chr11:579253
|
C | T | 1 | a0001c0006t0002g0124 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-21-2239C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579253 | ||||||
chr11:579254
|
C | CTCCCCCC others(11): Show |
68 | a0001c0003t0002g0015a0001c0003t0002g0017a0001c0003t0002g0020others(65): Show | 69 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-21-2222_-21-2221i others(20): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 579254 | |||||
chr11:579254
|
C | T | 1 | a0001c0006t0002g0124 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-21-2238C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579254 | ||||||
chr11:579256
|
C | A | 34 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0060others(31): Show | 34 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.-21-2236C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579256 | ||||||
chr11:579354
|
C | T | 13 | a0005c0007t0001g0089a0005c0007t0001g0127a0005c0007t0001g0128others(10): Show | 13 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.-21-2138C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579354 | ||||||
chr11:579412
|
T | C | 1 | a0001c0003t0002g0015 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-21-2080T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579412 | ||||||
chr11:579417
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-21-2075C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579417 | ||||||
chr11:579421
|
C | T | 1 | a0002c0002t0001g0227 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-21-2071C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579421 | ||||||
chr11:579467
|
G | C | 1 | a0001c0001t0007g0196 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-21-2025G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579467 | ||||||
chr11:579546
|
C | T | 7 | a0003c0004t0003g0083a0003c0004t0003g0084a0003c0004t0003g0174others(4): Show | 7 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-1946C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579546 | ||||||
chr11:579568
|
C | T | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-21-1924C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579568 | ||||||
chr11:579596
|
G | A | 4 | a0007c0010t0002g0010a0007c0010t0002g0011a0007c0010t0002g0012others(1): Show | 4 | HG01891.hp1 HG02922.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-1896G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579596 | ||||||
chr11:579608
|
G | C | 1 | a0001c0001t0001g0205 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-21-1884G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579608 | ||||||
chr11:579676
|
C | T | 7 | a0003c0004t0003g0083a0003c0004t0003g0084a0003c0004t0003g0174others(4): Show | 7 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-1816C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579676 | ||||||
chr11:579718
|
G | GAAGAAAG others(370): Show |
1 | a0001c0001t0007g0201 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-21-1757_-21-1756i others(379): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 579718 | |||||
chr11:579736
|
A | G | 4 | a0001c0001t0001g0232a0001c0001t0001g0264a0001c0001t0001g0270others(1): Show | 4 | HG01928.hp1 HG01952.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-1756A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579736 | ||||||
chr11:579757
|
C | T | 1 | a0002c0002t0001g0099 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-21-1735C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579757 | ||||||
chr11:579768
|
T | G | 1 | a0001c0006t0002g0124 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-21-1724T>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579768 | ||||||
chr11:579823
|
C | T | 2 | a0009c0012t0003g0082a0009c0012t0003g0176 | 2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-21-1669C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579823 | ||||||
chr11:579855
|
G | T | 1 | a0001c0009t0011g0097 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-21-1637G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579855 | ||||||
chr11:579948
|
C | T | 2 | a0001c0001t0001g0071a0007c0010t0002g0012 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-21-1544C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 579948 | ||||||
chr11:580020
|
T | C | 1 | a0019c0030t0001g0182 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-21-1472T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580020 | ||||||
chr11:580166
|
C | T | 2 | a0001c0003t0002g0054a0001c0003t0002g0055 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-21-1326C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580166 | ||||||
chr11:580199
|
G | A | 2 | a0018c0029t0001g0217a0025c0038t0001g0181 | 2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-21-1293G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580199 | ||||||
chr11:580290
|
C | A | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-21-1202C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580290 | ||||||
chr11:580309
|
G | A | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-21-1183G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580309 | ||||||
chr11:580349
|
T | C | 1 | a0002c0002t0001g0248 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-21-1143T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580349 | ||||||
chr11:580402
|
C | T | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-21-1090C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580402 | ||||||
chr11:580480
|
G | C | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-21-1012G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580480 | ||||||
chr11:580501
|
A | C | 3 | a0009c0012t0003g0067a0009c0012t0003g0082a0009c0012t0003g0176 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-21-991A>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580501 | ||||||
chr11:580668
|
T | C | 2 | a0001c0001t0001g0239a0001c0001t0001g0266 | 2 | HG00140.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-21-824T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580668 | ||||||
chr11:580732
|
A | G | 6 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(3): Show | 6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21-760A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580732 | ||||||
chr11:580770
|
C | T | 6 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(3): Show | 6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21-722C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580770 | ||||||
chr11:580911
|
A | G | 1 | a0002c0002t0001g0223 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-21-581A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580911 | ||||||
chr11:580969
|
G | A | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-21-523G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 580969 | ||||||
chr11:581051
|
C | T | 1 | a0001c0003t0002g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-21-441C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 581051 | ||||||
chr11:581092
|
G | A | 10 | a0001c0001t0001g0091a0001c0001t0001g0130a0001c0009t0002g0093others(7): Show | 11 | HG01074.hp1 HG02451.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-21-400G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 581092 | ||||||
chr11:581111
|
AT | A | 19 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0228others(16): Show | 19 | HG01257.hp2 HG02015.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.-21-365delT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 581111 | |||||
chr11:581189
|
G | A | 4 | a0007c0010t0002g0010a0007c0010t0002g0011a0007c0010t0002g0012others(1): Show | 4 | HG01891.hp1 HG02922.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-303G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 581189 | ||||||
chr11:581235
|
G | C | 1 | a0001c0001t0001g0114 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-21-257G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 581235 | ||||||
chr11:581256
|
T | TAGGGCTC others(94): Show |
6 | a0009c0012t0003g0067a0009c0012t0003g0082a0009c0012t0003g0176others(3): Show | 6 | HG02630.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21-226_-21-126dup others(101): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 581256 | |||||
chr11:581256
|
T | TAGGGCTC others(94): Show |
6 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(3): Show | 6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21-203_-21-202ins others(101): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 581256 | |||||
chr11:581455
|
G | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02080.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.-21-37G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 1/17 | chr11 | 581455 | ||||||
chr11:581769
|
A | G | 2 | a0001c0006t0002g0008a0001c0006t0002g0009 | 2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.94+163A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 2/17 | chr11 | 581769 | ||||||
chr11:581773
|
C | A | 1 | a0001c0001t0001g0202 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.94+167C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 2/17 | chr11 | 581773 | ||||||
chr11:581803
|
T | C | 8 | a0003c0004t0003g0025a0003c0004t0003g0083a0003c0004t0003g0084others(5): Show | 8 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-159T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 2/17 | chr11 | 581803 | ||||||
chr11:582107
|
C | G | 2 | a0002c0002t0001g0225a0002c0002t0001g0226 | 2 | NA18941.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.214+26C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 582107 | ||||||
chr11:582126
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02080.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.214+45C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 582126 | ||||||
chr11:582264
|
C | CT | 11 | a0001c0001t0001g0071a0002c0002t0001g0172a0006c0008t0004g0080others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.214+201dupT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 582264 | |||||
chr11:582264
|
CT | C | 177 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0060others(174): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.214+201delT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 582264 | |||||
chr11:582504
|
C | T | 2 | a0002c0002t0001g0085a0002c0002t0001g0086 | 2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.214+423C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 582504 | ||||||
chr11:582587
|
C | T | 1 | a0001c0006t0002g0124 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.214+506C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 582587 | ||||||
chr11:582727
|
C | T | 52 | a0001c0003t0002g0015a0001c0003t0002g0017a0001c0003t0002g0020others(49): Show | 53 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.214+646C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 582727 | ||||||
chr11:582803
|
C | T | 1 | a0013c0021t0008g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.214+722C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 582803 | ||||||
chr11:582815
|
C | T | 1 | a0016c0020t0009g0249 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.214+734C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 582815 | ||||||
chr11:582819
|
C | T | 1 | a0016c0020t0009g0249 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.214+738C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 582819 | ||||||
chr11:582927
|
G | A | 8 | a0005c0007t0001g0089a0005c0007t0001g0127a0005c0007t0001g0128others(5): Show | 8 | HG01168.hp2 HG02040.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.214+846G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 582927 | ||||||
chr11:583050
|
A | T | 1 | a0001c0001t0001g0213 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.214+969A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583050 | ||||||
chr11:583053
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.214+972C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583053 | ||||||
chr11:583078
|
C | A | 1 | a0001c0003t0005g0026 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.214+997C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583078 | ||||||
chr11:583083
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.214+1002G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583083 | ||||||
chr11:583107
|
G | A | 30 | a0001c0003t0002g0017a0001c0003t0002g0022a0001c0003t0002g0027others(27): Show | 31 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.214+1026G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583107 | ||||||
chr11:583111
|
C | T | 1 | a0013c0022t0008g0123 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.214+1030C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583111 | ||||||
chr11:583122
|
G | C | 18 | a0001c0003t0002g0027a0001c0003t0002g0028a0001c0003t0002g0029others(15): Show | 18 | HG00639.hp2 HG01123.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.214+1041G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583122 | ||||||
chr11:583145
|
T | C | 8 | a0002c0002t0001g0085a0002c0002t0001g0086a0002c0011t0001g0058others(5): Show | 8 | HG01975.hp2 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+1064T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583145 | ||||||
chr11:583146
|
G | C | 8 | a0002c0002t0001g0085a0002c0002t0001g0086a0002c0011t0001g0058others(5): Show | 8 | HG01975.hp2 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+1065G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583146 | ||||||
chr11:583147
|
T | C | 7 | a0002c0002t0001g0085a0002c0002t0001g0086a0002c0011t0001g0058others(4): Show | 7 | HG02559.hp2 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.214+1066T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583147 | ||||||
chr11:583156
|
T | C | 21 | a0001c0003t0002g0020a0001c0003t0002g0027a0001c0003t0002g0028others(18): Show | 21 | HG00140.hp1 HG01123.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.214+1075T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583156 | ||||||
chr11:583158
|
G | A | 21 | a0001c0003t0002g0020a0001c0003t0002g0027a0001c0003t0002g0028others(18): Show | 21 | HG00140.hp1 HG01123.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.214+1077G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583158 | ||||||
chr11:583168
|
G | A | 3 | a0002c0002t0001g0186a0002c0002t0001g0187a0019c0030t0001g0182 | 3 | HG00544.hp2 NA19010.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.214+1087G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583168 | ||||||
chr11:583223
|
C | T | 2 | a0003c0004t0003g0174a0003c0004t0003g0175 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.214+1142C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583223 | ||||||
chr11:583270
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG00544.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.214+1189C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583270 | ||||||
chr11:583327
|
ACT | A | 4 | a0001c0001t0001g0062a0001c0001t0001g0076a0001c0018t0001g0112others(1): Show | 4 | HG00438.hp2 NA18946.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+1249_214+1250d others(4): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 583327 | |||||
chr11:583350
|
A | G | 3 | a0009c0012t0003g0067a0009c0012t0003g0082a0009c0012t0003g0176 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.214+1269A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583350 | ||||||
chr11:583404
|
C | T | 3 | a0003c0004t0003g0190a0003c0004t0003g0222a0003c0004t0003g0269 | 3 | HG01346.hp1 HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.214+1323C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583404 | ||||||
chr11:583590
|
A | G | 2 | a0001c0003t0005g0035a0015c0024t0002g0024 | 2 | HG00639.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.214+1509A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583590 | ||||||
chr11:583612
|
G | A | 3 | a0002c0002t0001g0085a0002c0002t0001g0086a0003c0004t0003g0164 | 3 | HG02559.hp2 HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.214+1531G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583612 | ||||||
chr11:583731
|
TCAAA | T | 52 | a0001c0003t0002g0015a0001c0003t0002g0017a0001c0003t0002g0020others(49): Show | 53 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.214+1655_214+1658d others(6): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 583731 | |||||
chr11:583747
|
G | A | 2 | a0002c0002t0001g0085a0002c0002t0001g0086 | 2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.214+1666G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583747 | ||||||
chr11:583767
|
C | T | 52 | a0001c0003t0002g0015a0001c0003t0002g0017a0001c0003t0002g0020others(49): Show | 53 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.214+1686C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583767 | ||||||
chr11:583787
|
T | C | 64 | a0001c0003t0002g0015a0001c0003t0002g0017a0001c0003t0002g0020others(61): Show | 65 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.214+1706T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 583787 | ||||||
chr11:584010
|
C | T | 1 | a0002c0002t0001g0221 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.214+1929C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584010 | ||||||
chr11:584099
|
A | G | 1 | a0002c0002t0001g0172 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.214+2018A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584099 | ||||||
chr11:584112
|
G | A | 104 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0060others(101): Show | 104 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.214+2031G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584112 | ||||||
chr11:584243
|
C | T | 48 | a0001c0003t0002g0015a0001c0003t0002g0017a0001c0003t0002g0020others(45): Show | 49 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.214+2162C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584243 | ||||||
chr11:584371
|
C | T | 1 | a0006c0008t0004g0121 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.214+2290C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584371 | ||||||
chr11:584395
|
C | A | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.214+2314C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584395 | ||||||
chr11:584479
|
G | A | 1 | a0004c0005t0002g0041 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.214+2398G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584479 | ||||||
chr11:584514
|
G | T | 4 | a0001c0001t0001g0062a0001c0001t0001g0076a0001c0018t0001g0112others(1): Show | 4 | HG00438.hp2 NA18946.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+2433G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584514 | ||||||
chr11:584516
|
G | A | 3 | a0011c0016t0001g0069a0011c0016t0001g0087a0024c0037t0001g0125 | 3 | HG02257.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.214+2435G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584516 | ||||||
chr11:584572
|
G | A | 3 | a0009c0012t0003g0067a0009c0012t0003g0082a0009c0012t0003g0176 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.214+2491G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584572 | ||||||
chr11:584591
|
A | G | 72 | a0001c0003t0002g0015a0001c0003t0002g0017a0001c0003t0002g0020others(69): Show | 73 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.214+2510A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584591 | ||||||
chr11:584594
|
G | T | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.214+2513G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584594 | ||||||
chr11:584724
|
A | G | 1 | a0001c0001t0001g0238 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.215-2535A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584724 | ||||||
chr11:584729
|
C | CT | 34 | a0001c0001t0001g0061a0001c0001t0001g0102a0001c0001t0001g0114others(31): Show | 34 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.215-2505dupT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 584729 | |||||
chr11:584729
|
C | CTT | 11 | a0001c0001t0001g0149a0002c0002t0001g0085a0002c0002t0001g0086others(8): Show | 11 | HG00673.hp2 HG01433.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.215-2506_215-2505d others(4): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 584729 | |||||
chr11:584729
|
C | G | 1 | a0020c0032t0001g0167 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.215-2530C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584729 | ||||||
chr11:584729
|
CT | C | 16 | a0001c0001t0001g0141a0001c0001t0001g0159a0001c0001t0001g0197others(13): Show | 16 | HG00438.hp1 HG00597.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.215-2505delT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 584729 | |||||
chr11:584736
|
T | G | 1 | a0001c0001t0001g0115 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.215-2523T>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584736 | ||||||
chr11:584767
|
C | A | 4 | a0001c0001t0001g0232a0001c0001t0001g0264a0001c0001t0001g0270others(1): Show | 4 | HG01928.hp1 HG01952.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-2492C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584767 | ||||||
chr11:584769
|
C | T | 8 | a0003c0004t0003g0025a0003c0004t0003g0083a0003c0004t0003g0084others(5): Show | 8 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.215-2490C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584769 | ||||||
chr11:584790
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0229 | 2 | HG01106.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.215-2469T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584790 | ||||||
chr11:584791
|
G | T | 1 | a0001c0001t0001g0115 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.215-2468G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584791 | ||||||
chr11:584792
|
T | A | 1 | a0001c0001t0001g0115 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.215-2467T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584792 | ||||||
chr11:584846
|
T | C | 1 | a0001c0001t0001g0115 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.215-2413T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584846 | ||||||
chr11:584931
|
T | C | 1 | a0013c0022t0008g0123 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.215-2328T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 584931 | ||||||
chr11:585014
|
A | T | 1 | a0024c0037t0001g0125 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.215-2245A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585014 | ||||||
chr11:585026
|
C | A | 1 | a0001c0033t0014g0105 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.215-2233C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585026 | ||||||
chr11:585043
|
T | A | 1 | a0001c0001t0001g0115 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.215-2216T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585043 | ||||||
chr11:585175
|
C | T | 2 | a0005c0007t0001g0252a0005c0007t0001g0253 | 2 | HG02004.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.215-2084C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585175 | ||||||
chr11:585208
|
T | TGCCCTTT others(775): Show |
1 | a0001c0001t0001g0257 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.215-1865_215-1864i others(784): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585208 | |||||
chr11:585208
|
T | TGCCCTTT others(821): Show |
5 | a0002c0002t0001g0072a0002c0002t0001g0104a0002c0002t0001g0255others(2): Show | 6 | HG01069.hp2 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-1865_215-1864i others(830): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585208 | |||||
chr11:585208
|
T | TGCCCTTT others(338): Show |
1 | a0016c0020t0009g0249 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.215-2003_215-2002i others(347): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585208 | |||||
chr11:585208
|
T | TGCCCTTT others(223): Show |
3 | a0009c0012t0003g0067a0009c0012t0003g0082a0009c0012t0003g0176 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.215-2003_215-2002i others(232): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585208 | |||||
chr11:585208
|
TGCCCTTT others(108): Show |
T | 1 | a0001c0001t0001g0071 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.215-1864_215-1750d others(2): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585208 | |||||
chr11:585211
|
C | CCTTTCCA others(1396): Show |
1 | a0001c0006t0002g0124 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1405): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585211 | |||||
chr11:585211
|
C | CCTTTCCA others(1718): Show |
1 | a0001c0003t0002g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1727): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585211 | |||||
chr11:585221
|
T | TTGAGGTA others(775): Show |
1 | a0013c0021t0008g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.215-1957_215-1956i others(784): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585221 | |||||
chr11:585221
|
T | TTGAGGTA others(292): Show |
1 | a0006c0008t0004g0178 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.215-2003_215-2002i others(301): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585221 | |||||
chr11:585234
|
C | CCTTTCCA others(39): Show |
2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG02132.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.215-2016_215-2015i others(48): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | |||||
chr11:585234
|
C | CCTTTCCA others(1718): Show |
1 | a0001c0006t0002g0021 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.215-1842_215-1841i others(1727): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | |||||
chr11:585234
|
C | CCTTTCCA others(1718): Show |
3 | a0001c0003t0002g0015a0001c0006t0002g0008a0001c0006t0002g0009 | 3 | HG03130.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.215-1842_215-1841i others(1727): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | |||||
chr11:585234
|
C | CCTTTCCA others(1695): Show |
1 | a0001c0006t0002g0019 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.215-1865_215-1864i others(1704): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | |||||
chr11:585234
|
C | CCTTTCCA others(1741): Show |
1 | a0001c0003t0002g0022 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.215-1934_215-1933i others(1750): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | |||||
chr11:585234
|
C | CCTTTCCA others(1741): Show |
1 | a0001c0003t0002g0017 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.215-1934_215-1933i others(1750): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | |||||
chr11:585234
|
C | CCTTTCCA others(1741): Show |
1 | a0007c0010t0002g0272 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1750): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | |||||
chr11:585234
|
C | CCTTTCCA others(1741): Show |
1 | a0007c0010t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1750): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | |||||
chr11:585234
|
C | CCTTTCCA others(1718): Show |
2 | a0001c0003t0002g0037a0001c0003t0002g0038 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.215-1957_215-1956i others(1727): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | |||||
chr11:585234
|
C | CCTTTCCA others(1695): Show |
3 | a0001c0003t0002g0039a0001c0003t0002g0053a0001c0006t0002g0057 | 3 | HG02280.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.215-1957_215-1956i others(1704): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | |||||
chr11:585234
|
C | CCTTTCCA others(1718): Show |
1 | a0001c0003t0002g0029 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1727): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | |||||
chr11:585234
|
C | CCTTTCCA others(1718): Show |
1 | a0001c0003t0002g0040 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1727): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | |||||
chr11:585234
|
C | CCTTTCCA others(1718): Show |
12 | a0001c0003t0002g0027a0001c0003t0002g0028a0001c0003t0002g0030others(9): Show | 12 | HG01123.hp2 HG01255.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.215-1957_215-1956i others(1727): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | |||||
chr11:585234
|
C | CCTTTCCA others(1695): Show |
1 | a0001c0003t0002g0020 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1704): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | |||||
chr11:585234
|
C | CCTTTCCA others(1741): Show |
1 | a0001c0006t0002g0016 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1750): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | |||||
chr11:585234
|
C | CCTTTCCA others(1695): Show |
1 | a0001c0003t0002g0052 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1704): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | |||||
chr11:585234
|
C | CCTTTCCA others(292): Show |
4 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(1): Show | 4 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-2003_215-2002i others(301): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | |||||
chr11:585234
|
C | CCTTTCCA others(315): Show |
1 | a0006c0008t0010g0068 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.215-2003_215-2002i others(324): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585234 | |||||
chr11:585244
|
T | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0106 | 2 | NA18963.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.215-2015T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585244 | ||||||
chr11:585257
|
C | CCTTTCCA others(2017): Show |
1 | a0001c0006t0002g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.215-1842_215-1841i others(2026): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585257 | |||||
chr11:585257
|
C | CCTTTCCA others(1672): Show |
1 | a0004c0005t0002g0042 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.215-1842_215-1841i others(1681): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585257 | |||||
chr11:585257
|
C | CCTTTCCA others(1672): Show |
2 | a0001c0003t0005g0026a0001c0003t0005g0035 | 2 | HG00639.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.215-1957_215-1956i others(1681): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585257 | |||||
chr11:585257
|
C | CCTTTCCA others(1672): Show |
1 | a0001c0003t0002g0043 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1681): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585257 | |||||
chr11:585257
|
C | CCTTTCCA others(1603): Show |
1 | a0004c0005t0002g0031 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1612): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585257 | |||||
chr11:585257
|
C | CCTTTCCA others(1649): Show |
1 | a0001c0003t0005g0044 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1658): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585257 | |||||
chr11:585257
|
C | CCTTTCCA others(752): Show |
1 | a0015c0024t0002g0024 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.215-1957_215-1956i others(761): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585257 | |||||
chr11:585257
|
C | CCTTTCCA others(1672): Show |
1 | a0001c0003t0005g0014 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1681): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585257 | |||||
chr11:585257
|
C | CCTTTCCA others(1672): Show |
9 | a0001c0003t0005g0050a0001c0003t0013g0051a0004c0005t0002g0003others(6): Show | 10 | HG00735.hp1 HG01175.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.215-1957_215-1956i others(1681): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585257 | |||||
chr11:585257
|
C | T | 2 | a0018c0029t0001g0217a0025c0038t0001g0181 | 2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.215-2002C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585257 | ||||||
chr11:585280
|
C | CCTTTCCA others(16): Show |
1 | a0001c0006t0002g0013 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.215-1957_215-1956i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585280 | |||||
chr11:585280
|
C | CCTTTCCA others(1626): Show |
1 | a0013c0022t0008g0123 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.215-1957_215-1956i others(1635): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585280 | |||||
chr11:585280
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0106 | 2 | NA18963.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.215-1979C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585280 | ||||||
chr11:585290
|
T | TTGAGGTA others(16): Show |
3 | a0001c0001t0001g0232a0001c0001t0001g0264a0001c0023t0001g0231 | 3 | HG01928.hp1 HG02300.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.215-1947_215-1946i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585290 | |||||
chr11:585290
|
T | TTGAGGTA others(200): Show |
2 | a0018c0029t0001g0217a0025c0038t0001g0181 | 2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.215-1947_215-1946i others(209): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585290 | |||||
chr11:585303
|
C | T | 12 | a0003c0004t0003g0025a0003c0004t0003g0083a0003c0004t0003g0084others(9): Show | 12 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.215-1956C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585303 | ||||||
chr11:585313
|
T | A | 4 | a0001c0001t0001g0270a0009c0012t0003g0067a0009c0012t0003g0082others(1): Show | 4 | HG01952.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-1946T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585313 | ||||||
chr11:585326
|
C | T | 3 | a0009c0012t0003g0067a0009c0012t0003g0082a0009c0012t0003g0176 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.215-1933C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585326 | ||||||
chr11:585336
|
T | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG02132.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.215-1923T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585336 | ||||||
chr11:585336
|
T | TTGAGGTA others(39): Show |
2 | a0018c0029t0001g0217a0025c0038t0001g0181 | 2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.215-1888_215-1887i others(48): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585336 | |||||
chr11:585349
|
C | T | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0002c0002t0001g0246 | 3 | HG02132.hp1 NA18943.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.215-1910C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585349 | ||||||
chr11:585372
|
C | CCTTTCCA others(2385): Show |
2 | a0001c0001t0001g0073a0001c0001t0001g0106 | 2 | NA18963.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.215-1878_215-1877i others(2394): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585372 | |||||
chr11:585372
|
C | T | 18 | a0001c0009t0002g0093a0002c0002t0001g0059a0002c0002t0001g0132others(15): Show | 18 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.215-1887C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585372 | ||||||
chr11:585382
|
T | TTGAGGTA others(821): Show |
1 | a0002c0002t0001g0195 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.215-1865_215-1864i others(830): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585382 | |||||
chr11:585395
|
C | CCTTTCCA others(16): Show |
2 | a0001c0001t0001g0162a0001c0001t0001g0213 | 2 | NA18946.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.215-1842_215-1841i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585395 | |||||
chr11:585395
|
C | T | 66 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0130others(63): Show | 69 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.215-1864C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585395 | ||||||
chr11:585405
|
T | A | 6 | a0001c0001t0001g0257a0002c0002t0001g0072a0002c0002t0001g0104others(3): Show | 7 | HG01069.hp2 HG01256.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.215-1854T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585405 | ||||||
chr11:585405
|
T | TTGAGGTA others(844): Show |
2 | a0001c0027t0001g0254a0002c0002t0001g0185 | 2 | HG00099.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.215-1842_215-1841i others(853): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585405 | |||||
chr11:585405
|
T | TTGAGGTA others(844): Show |
3 | a0002c0002t0001g0186a0002c0002t0001g0187a0019c0030t0001g0182 | 3 | HG00544.hp2 NA19010.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.215-1842_215-1841i others(853): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585405 | |||||
chr11:585405
|
T | TTGAGGTA others(844): Show |
12 | a0002c0002t0001g0001a0002c0002t0001g0098a0002c0002t0001g0099others(9): Show | 14 | HG01123.hp1 HG01256.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.215-1842_215-1841i others(853): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585405 | |||||
chr11:585405
|
T | TTGAGGTA others(821): Show |
8 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0189others(5): Show | 8 | HG01943.hp1 HG02040.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-1842_215-1841i others(830): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585405 | |||||
chr11:585405
|
T | TTGAGGTA others(798): Show |
1 | a0002c0002t0001g0234 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.215-1842_215-1841i others(807): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585405 | |||||
chr11:585418
|
C | CCTTTCCA others(39): Show |
35 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0077others(32): Show | 35 | HG00280.hp2 HG00673.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.215-1796_215-1795i others(48): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585418 | |||||
chr11:585418
|
C | CCTTTCCA others(4156): Show |
1 | a0002c0002t0001g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.215-1796_215-1795i others(4165): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585418 | |||||
chr11:585418
|
C | CCTTTCCA others(4110): Show |
1 | a0002c0002t0001g0086 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.215-1796_215-1795i others(4119): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585418 | |||||
chr11:585418
|
C | CCTTTCCA others(4110): Show |
1 | a0003c0004t0003g0164 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.215-1796_215-1795i others(4119): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585418 | |||||
chr11:585418
|
C | CCTTTCCA others(16): Show |
32 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0060others(29): Show | 32 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.215-1819_215-1818i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585418 | |||||
chr11:585418
|
C | T | 32 | a0001c0001t0001g0073a0001c0001t0001g0088a0001c0001t0001g0106others(29): Show | 35 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.215-1841C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585418 | ||||||
chr11:585428
|
T | A | 1 | a0013c0022t0008g0123 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.215-1831T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585428 | ||||||
chr11:585441
|
C | CCTTTCCA others(39): Show |
4 | a0001c0001t0001g0159a0001c0001t0001g0200a0005c0007t0001g0252others(1): Show | 4 | HG00438.hp1 HG02004.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-1773_215-1772i others(48): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585441 | |||||
chr11:585441
|
C | T | 12 | a0001c0001t0001g0150a0001c0001t0001g0151a0002c0002t0001g0059others(9): Show | 12 | HG02080.hp2 HG02132.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.215-1818C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585441 | ||||||
chr11:585451
|
T | A | 2 | a0018c0029t0001g0217a0025c0038t0001g0181 | 2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.215-1808T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585451 | ||||||
chr11:585464
|
C | CCTTTCCA others(16): Show |
4 | a0003c0004t0003g0084a0003c0004t0003g0175a0003c0004t0003g0216others(1): Show | 4 | HG01169.hp1 HG01433.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-1786_215-1785i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585464 | |||||
chr11:585464
|
C | CCTTTCCA others(16): Show |
2 | a0001c0018t0001g0112a0001c0018t0001g0113 | 2 | NA18946.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.215-1773_215-1772i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585464 | |||||
chr11:585464
|
C | T | 28 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0101others(25): Show | 29 | HG00140.hp2 HG00408.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.215-1795C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585464 | ||||||
chr11:585474
|
T | A | 57 | a0001c0001t0001g0073a0001c0001t0001g0106a0001c0003t0002g0015others(54): Show | 58 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.215-1785T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585474 | ||||||
chr11:585474
|
T | ATGAGGTA others(16): Show |
4 | a0003c0004t0003g0025a0003c0004t0003g0083a0003c0004t0003g0174others(1): Show | 4 | HG00639.hp2 HG01168.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-1786_215-1785i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585474 | ||||||
chr11:585474
|
T | TTGAGGTA others(4685): Show |
1 | a0005c0007t0001g0179 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.215-1773_215-1772i others(4694): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585474 | |||||
chr11:585474
|
T | TTGAGGTA others(4685): Show |
1 | a0005c0007t0001g0089 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.215-1773_215-1772i others(4694): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585474 | |||||
chr11:585474
|
T | TTGAGGTA others(4708): Show |
1 | a0014c0019t0001g0126 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.215-1773_215-1772i others(4717): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585474 | |||||
chr11:585474
|
T | TTGAGGTA others(4708): Show |
1 | a0014c0019t0001g0090 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.215-1773_215-1772i others(4717): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585474 | |||||
chr11:585487
|
C | CCTTTCCA others(2339): Show |
1 | a0001c0001t0001g0150 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.215-1763_215-1762i others(2348): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | |||||
chr11:585487
|
C | CCTTTCCA others(2339): Show |
1 | a0001c0001t0001g0151 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.215-1763_215-1762i others(2348): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | |||||
chr11:585487
|
C | CCTTTCCA others(4793): Show |
1 | a0001c0001t0001g0115 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.215-1750_215-1749i others(4802): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | |||||
chr11:585487
|
C | CCTTTCCA others(3098): Show |
1 | a0001c0001t0001g0213 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.215-1750_215-1749i others(3107): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | |||||
chr11:585487
|
C | CCTTTCCA others(4639): Show |
1 | a0005c0007t0001g0128 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.215-1750_215-1749i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | |||||
chr11:585487
|
C | CCTTTCCA others(2868): Show |
1 | a0001c0001t0001g0266 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.215-1750_215-1749i others(2877): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | |||||
chr11:585487
|
C | CCTTTCCA others(4823): Show |
1 | a0001c0001t0001g0210 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.215-1750_215-1749i others(4832): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | |||||
chr11:585487
|
C | CCTTTCCA others(2362): Show |
1 | a0001c0001t0001g0160 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.215-1750_215-1749i others(2371): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | |||||
chr11:585487
|
C | CCTTTCCA others(936): Show |
1 | a0001c0001t0001g0118 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.215-1750_215-1749i others(945): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | |||||
chr11:585487
|
C | CCTTTCCA others(4823): Show |
1 | a0001c0001t0001g0211 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.215-1750_215-1749i others(4832): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | |||||
chr11:585487
|
C | CCTTTCCA others(3144): Show |
1 | a0001c0001t0001g0101 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.215-1750_215-1749i others(3153): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | |||||
chr11:585487
|
C | CCTTTCCA others(4225): Show |
1 | a0011c0016t0001g0087 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.215-1750_215-1749i others(4234): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | |||||
chr11:585487
|
C | CCTTTCCA others(2523): Show |
1 | a0011c0016t0001g0069 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.215-1750_215-1749i others(2532): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | |||||
chr11:585487
|
C | CCTTTCCA others(4892): Show |
1 | a0001c0001t0001g0232 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.215-1750_215-1749i others(4901): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | |||||
chr11:585487
|
C | CCTTTCCA others(39): Show |
2 | a0005c0007t0001g0127a0005c0007t0001g0180 | 2 | HG02056.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.215-1750_215-1749i others(48): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | |||||
chr11:585487
|
C | CCTTTCCA others(3742): Show |
1 | a0025c0038t0001g0181 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.215-1694_215-1693i others(3751): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | |||||
chr11:585487
|
C | CCTTTCCA others(3742): Show |
1 | a0018c0029t0001g0217 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.215-1694_215-1693i others(3751): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | |||||
chr11:585487
|
C | CCTTTCCA others(1718): Show |
1 | a0001c0006t0002g0013 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.215-1681_215-1680i others(1727): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585487 | |||||
chr11:585487
|
C | T | 68 | a0001c0001t0001g0073a0001c0001t0001g0106a0001c0003t0002g0015others(65): Show | 69 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.215-1772C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585487 | ||||||
chr11:585497
|
T | A | 10 | a0001c0006t0002g0036a0001c0009t0002g0093a0002c0002t0001g0059others(7): Show | 10 | HG02080.hp2 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.215-1762T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585497 | ||||||
chr11:585497
|
T | TTGAGGTA others(16): Show |
3 | a0001c0001t0001g0162a0003c0004t0003g0222a0003c0004t0003g0269 | 3 | HG01346.hp1 HG02717.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.215-1750_215-1749i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585497 | |||||
chr11:585510
|
T | C | 135 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0060others(132): Show | 138 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.215-1749T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585510 | ||||||
chr11:585511
|
C | G | 4 | a0001c0001t0001g0073a0001c0001t0001g0106a0001c0001t0001g0150others(1): Show | 4 | HG02132.hp1 NA18963.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-1748C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585511 | ||||||
chr11:585520
|
T | A | 64 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0130others(61): Show | 70 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.215-1739T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585520 | ||||||
chr11:585520
|
T | TTGAGGTA others(16): Show |
33 | a0001c0001t0001g0007a0001c0001t0001g0060a0001c0001t0001g0061others(30): Show | 33 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.215-1717_215-1716i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585520 | |||||
chr11:585533
|
C | T | 28 | a0001c0001t0001g0071a0001c0001t0001g0088a0001c0001t0001g0091others(25): Show | 31 | HG00280.hp1 HG00597.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.215-1726C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585533 | ||||||
chr11:585534
|
C | CTTTCCAG others(2224): Show |
1 | a0001c0001t0001g0202 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.215-1717_215-1716i others(2233): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585534 | |||||
chr11:585543
|
T | A | 38 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(35): Show | 38 | HG00280.hp2 HG00438.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.215-1716T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585543 | ||||||
chr11:585543
|
T | TTGAGGTA others(16): Show |
1 | a0001c0001t0001g0107 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.215-1694_215-1693i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585543 | |||||
chr11:585547
|
G | A | 8 | a0003c0004t0003g0025a0003c0004t0003g0083a0003c0004t0003g0084others(5): Show | 8 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.215-1712G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585547 | ||||||
chr11:585556
|
C | T | 1 | a0016c0020t0009g0249 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.215-1703C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585556 | ||||||
chr11:585566
|
T | A | 38 | a0001c0001t0001g0006a0001c0001t0001g0159a0001c0001t0001g0200others(35): Show | 41 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.215-1693T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585566 | ||||||
chr11:585566
|
T | TTGAGGTA others(16): Show |
8 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0208others(5): Show | 8 | HG00408.hp2 HG00609.hp2 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-1671_215-1670i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585566 | |||||
chr11:585579
|
C | CCTTTCCA others(4731): Show |
2 | a0001c0018t0001g0112a0001c0018t0001g0113 | 2 | NA18946.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.215-1671_215-1670i others(4740): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585579 | |||||
chr11:585579
|
C | CCTTTCCA others(2707): Show |
1 | a0001c0001t0001g0161 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.215-1671_215-1670i others(2716): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585579 | |||||
chr11:585579
|
C | CCTTTCCA others(637): Show |
1 | a0016c0020t0009g0249 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.215-1658_215-1657i others(646): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585579 | |||||
chr11:585579
|
C | T | 118 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0101others(115): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.215-1680C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585579 | ||||||
chr11:585589
|
T | TTGAGGTA others(16): Show |
2 | a0005c0007t0001g0268a0024c0037t0001g0125 | 2 | HG02257.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.215-1648_215-1647i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585589 | |||||
chr11:585602
|
C | CCTTTCCA others(729): Show |
1 | a0006c0008t0004g0247 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.215-1585_215-1584i others(738): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585602 | |||||
chr11:585602
|
C | CCTTTCCA others(752): Show |
3 | a0009c0012t0003g0067a0009c0012t0003g0082a0009c0012t0003g0176 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.215-1612_215-1611i others(761): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585602 | |||||
chr11:585602
|
C | CCTTTCCA others(729): Show |
2 | a0006c0008t0004g0178a0006c0008t0010g0068 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.215-1635_215-1634i others(738): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585602 | |||||
chr11:585602
|
C | CCTTTCCA others(729): Show |
3 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121 | 3 | HG02145.hp2 HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.215-1635_215-1634i others(738): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585602 | |||||
chr11:585602
|
C | T | 10 | a0001c0001t0001g0202a0003c0004t0003g0025a0003c0004t0003g0083others(7): Show | 10 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.215-1657C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585602 | ||||||
chr11:585603
|
C | T | 4 | a0001c0003t0002g0017a0001c0003t0002g0022a0001c0003t0002g0052others(1): Show | 4 | HG01074.hp2 HG02015.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-1656C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585603 | ||||||
chr11:585612
|
T | A | 2 | a0005c0007t0001g0127a0005c0007t0001g0180 | 2 | HG02056.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.215-1647T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585612 | ||||||
chr11:585612
|
T | TTGAGGTA others(16): Show |
1 | a0017c0028t0001g0129 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.215-1625_215-1624i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585612 | |||||
chr11:585635
|
T | A | 1 | a0013c0022t0008g0123 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.215-1624T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585635 | ||||||
chr11:585635
|
T | TTGAGGTA others(890): Show |
1 | a0013c0021t0008g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.215-1612_215-1611i others(899): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585635 | |||||
chr11:585640
|
G | A | 34 | a0001c0001t0001g0071a0001c0001t0001g0257a0001c0027t0001g0254others(31): Show | 37 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.215-1619G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585640 | ||||||
chr11:585658
|
T | A | 122 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0101others(119): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.215-1601T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585658 | ||||||
chr11:585658
|
T | TTGAGGTA others(16): Show |
1 | a0001c0001t0001g0202 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(25): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4892): Show |
1 | a0001c0023t0001g0231 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4901): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4616): Show |
1 | a0001c0001t0001g0155 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4625): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4616): Show |
1 | a0001c0001t0001g0156 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4625): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4593): Show |
1 | a0001c0001t0001g0271 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4602): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4593): Show |
1 | a0001c0001t0001g0236 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4602): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4708): Show |
1 | a0001c0001t0001g0162 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4717): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4731): Show |
1 | a0001c0001t0001g0214 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4740): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4639): Show |
1 | a0001c0001t0001g0152 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(6272): Show |
1 | a0001c0001t0001g0265 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(6281): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(6295): Show |
1 | a0001c0001t0001g0235 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(6304): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4754): Show |
1 | a0001c0001t0001g0237 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4763): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4616): Show |
1 | a0001c0001t0001g0060 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4625): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4731): Show |
1 | a0001c0001t0001g0114 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4740): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4754): Show |
1 | a0001c0001t0001g0063 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4763): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4731): Show |
1 | a0001c0001t0001g0078 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4740): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4616): Show |
1 | a0001c0001t0001g0108 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4625): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(3880): Show |
1 | a0001c0001t0001g0238 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(3889): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4754): Show |
1 | a0001c0001t0001g0240 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4763): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4639): Show |
2 | a0001c0001t0001g0109a0001c0001t0001g0153 | 2 | HG00558.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4639): Show |
1 | a0001c0001t0001g0203 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4639): Show |
1 | a0001c0001t0001g0141 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4639): Show |
1 | a0001c0001t0001g0102 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4639): Show |
1 | a0001c0001t0001g0074 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4616): Show |
1 | a0001c0001t0001g0233 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4625): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4616): Show |
1 | a0001c0001t0007g0201 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4625): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4823): Show |
1 | a0023c0036t0001g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4832): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(6111): Show |
1 | a0001c0033t0014g0105 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(6120): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4639): Show |
1 | a0001c0001t0001g0061 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4616): Show |
1 | a0001c0001t0001g0154 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4625): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4639): Show |
1 | a0001c0001t0001g0111 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4662): Show |
1 | a0001c0001t0001g0075 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4671): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(5904): Show |
1 | a0001c0001t0001g0204 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(5913): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4640): Show |
1 | a0001c0001t0001g0147 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4649): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(3167): Show |
1 | a0001c0014t0001g0144 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(3176): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(3167): Show |
3 | a0001c0014t0001g0262a0001c0014t0001g0263a0001c0031t0001g0261 | 3 | HG01943.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.215-1589_215-1588i others(3176): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4616): Show |
1 | a0001c0001t0001g0145 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4625): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4685): Show |
1 | a0001c0001t0001g0157 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4694): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4708): Show |
1 | a0001c0001t0001g0158 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4717): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4593): Show |
1 | a0001c0001t0001g0146 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4602): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4754): Show |
1 | a0001c0001t0001g0077 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4763): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4777): Show |
1 | a0001c0001t0006g0163 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4786): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4869): Show |
1 | a0001c0001t0001g0064 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4878): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4685): Show |
2 | a0001c0001t0001g0062a0001c0001t0001g0076 | 2 | HG00438.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.215-1589_215-1588i others(4694): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4547): Show |
1 | a0001c0001t0001g0206 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4556): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(6180): Show |
1 | a0001c0001t0001g0116 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(6189): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4547): Show |
1 | a0001c0001t0001g0107 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4556): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4639): Show |
4 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(1): Show | 4 | NA18948.hp2 NA18963.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4639): Show |
1 | a0001c0001t0007g0196 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4616): Show |
1 | a0001c0001t0001g0007 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4625): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4639): Show |
1 | a0001c0001t0001g0229 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4778): Show |
1 | a0001c0001t0006g0241 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4787): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4777): Show |
1 | a0001c0001t0006g0242 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4786): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4984): Show |
1 | a0001c0001t0001g0207 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4993): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4961): Show |
1 | a0001c0001t0001g0079 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4970): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4179): Show |
1 | a0001c0001t0001g0205 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4188): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4754): Show |
1 | a0001c0001t0001g0117 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4763): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4662): Show |
1 | a0012c0017t0001g0148 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4671): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4294): Show |
1 | a0001c0001t0001g0100 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4303): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4685): Show |
1 | a0012c0017t0001g0103 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4694): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(2960): Show |
1 | a0001c0001t0001g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(2969): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4756): Show |
1 | a0022c0035t0001g0243 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4765): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4639): Show |
1 | a0020c0032t0001g0167 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4708): Show |
1 | a0001c0034t0001g0120 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4717): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4777): Show |
2 | a0005c0007t0001g0252a0005c0007t0001g0253 | 2 | HG02004.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.215-1589_215-1588i others(4786): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4616): Show |
1 | a0001c0001t0001g0259 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4625): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4616): Show |
1 | a0001c0001t0001g0260 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4625): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4317): Show |
1 | a0001c0001t0001g0143 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4326): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4777): Show |
1 | a0001c0001t0001g0208 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4786): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(2638): Show |
1 | a0001c0001t0001g0006 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(2647): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4685): Show |
1 | a0001c0001t0001g0142 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4694): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4800): Show |
1 | a0001c0001t0006g0212 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4809): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(5007): Show |
1 | a0001c0001t0001g0159 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(5016): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4823): Show |
1 | a0001c0001t0001g0119 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4832): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4685): Show |
1 | a0001c0001t0001g0200 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4694): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4777): Show |
1 | a0001c0001t0001g0209 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4786): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4777): Show |
1 | a0005c0007t0001g0268 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4786): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(5053): Show |
1 | a0001c0001t0001g0239 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(5062): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4202): Show |
1 | a0024c0037t0001g0125 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4211): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4708): Show |
1 | a0005c0007t0001g0180 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4717): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4754): Show |
1 | a0005c0007t0001g0127 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4763): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4754): Show |
1 | a0017c0028t0001g0129 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4763): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(3305): Show |
1 | a0001c0001t0001g0244 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(3314): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4639): Show |
1 | a0001c0001t0001g0149 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(4648): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(890): Show |
1 | a0002c0002t0001g0066 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(899): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(844): Show |
2 | a0001c0001t0001g0088a0002c0002t0001g0133 | 2 | HG01243.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.215-1589_215-1588i others(853): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(913): Show |
1 | a0002c0002t0001g0095 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(922): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(821): Show |
1 | a0003c0004t0003g0190 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(830): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(913): Show |
5 | a0001c0009t0002g0094a0001c0009t0002g0131a0001c0009t0002g0183others(2): Show | 6 | HG02451.hp1 HG02572.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-1589_215-1588i others(922): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(936): Show |
1 | a0008c0013t0002g0184 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(945): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(798): Show |
1 | a0002c0002t0001g0132 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(807): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(798): Show |
2 | a0003c0004t0003g0222a0003c0004t0003g0269 | 2 | HG01346.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.215-1589_215-1588i others(807): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(844): Show |
1 | a0002c0002t0001g0221 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(853): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(867): Show |
1 | a0002c0002t0001g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(876): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(959): Show |
1 | a0002c0002t0001g0137 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(968): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(936): Show |
3 | a0001c0001t0001g0091a0002c0002t0001g0136a0002c0002t0001g0188 | 3 | HG02723.hp1 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.215-1589_215-1588i others(945): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(913): Show |
2 | a0001c0001t0001g0130a0001c0009t0011g0097 | 2 | HG01074.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.215-1589_215-1588i others(922): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(890): Show |
4 | a0002c0002t0001g0122a0002c0002t0001g0168a0002c0002t0001g0170others(1): Show | 4 | HG00597.hp1 HG00609.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-1589_215-1588i others(899): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(867): Show |
5 | a0002c0002t0001g0002a0002c0002t0001g0070a0002c0002t0001g0169others(2): Show | 7 | HG01167.hp1 HG01169.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.215-1589_215-1588i others(876): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(844): Show |
2 | a0002c0002t0001g0215a0002c0002t0001g0218 | 2 | HG00280.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.215-1589_215-1588i others(853): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(821): Show |
3 | a0002c0002t0001g0059a0002c0002t0001g0194a0002c0002t0001g0258 | 3 | HG02080.hp2 HG03831.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.215-1589_215-1588i others(830): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(821): Show |
1 | a0001c0009t0002g0093 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.215-1589_215-1588i others(830): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(729): Show |
1 | a0002c0002t0001g0172 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.215-1589_215-1588i others(738): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(844): Show |
4 | a0002c0011t0001g0058a0002c0011t0001g0065a0002c0011t0001g0165others(1): Show | 4 | HG02572.hp2 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-1589_215-1588i others(853): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(5030): Show |
1 | a0001c0001t0001g0245 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.215-1585_215-1584i others(5039): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(4938): Show |
2 | a0001c0001t0001g0264a0001c0001t0001g0270 | 2 | HG01928.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.215-1585_215-1584i others(4947): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585658
|
T | TTGAGGTA others(798): Show |
1 | a0002c0002t0001g0246 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.215-1585_215-1584i others(807): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585658 | |||||
chr11:585680
|
C | CT | 9 | a0001c0001t0001g0232a0001c0001t0001g0238a0001c0001t0001g0264others(6): Show | 9 | HG00099.hp2 HG01257.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.215-1561dupT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585680 | |||||
chr11:585680
|
C | CTTTTTTT others(1): Show |
6 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(3): Show | 6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-1568_215-1561d others(10): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585680 | |||||
chr11:585680
|
C | CTTTTTTT others(3): Show |
7 | a0003c0004t0003g0025a0003c0004t0003g0083a0003c0004t0003g0084others(4): Show | 7 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.215-1570_215-1561d others(12): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585680 | |||||
chr11:585680
|
C | CTTTTTTT others(4): Show |
2 | a0001c0006t0002g0016a0003c0004t0003g0177 | 2 | HG01192.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.215-1571_215-1561d others(13): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585680 | |||||
chr11:585680
|
C | CTTTTTTT others(5): Show |
11 | a0001c0003t0002g0022a0001c0003t0002g0027a0001c0003t0002g0055others(8): Show | 11 | HG00140.hp1 HG01257.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.215-1572_215-1561d others(14): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585680 | |||||
chr11:585680
|
C | CTTTTTTT others(6): Show |
24 | a0001c0003t0002g0015a0001c0003t0002g0028a0001c0003t0002g0029others(21): Show | 25 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.215-1573_215-1561d others(15): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585680 | |||||
chr11:585680
|
C | CTTTTTTT others(7): Show |
10 | a0001c0003t0002g0020a0001c0003t0002g0038a0001c0003t0002g0047others(7): Show | 10 | HG01074.hp2 HG01346.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.215-1574_215-1561d others(16): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585680 | |||||
chr11:585680
|
C | CTTTTTTT others(8): Show |
2 | a0001c0003t0002g0017a0001c0003t0012g0049 | 2 | NA18967.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.215-1575_215-1561d others(17): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585680 | |||||
chr11:585680
|
C | CTTTTTTT others(9): Show |
1 | a0001c0003t0002g0040 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.215-1576_215-1561d others(18): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585680 | |||||
chr11:585680
|
CT | C | 7 | a0001c0001t0001g0115a0001c0001t0001g0160a0001c0001t0001g0198others(4): Show | 7 | HG01943.hp1 HG03710.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.215-1561delT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 585680 | |||||
chr11:585744
|
G | C | 1 | a0016c0020t0009g0249 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.215-1515G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585744 | ||||||
chr11:585824
|
G | A | 6 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(3): Show | 6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-1435G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585824 | ||||||
chr11:585857
|
T | C | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.215-1402T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 585857 | ||||||
chr11:586050
|
G | A | 2 | a0013c0021t0008g0251a0013c0022t0008g0123 | 2 | HG02896.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.215-1209G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 586050 | ||||||
chr11:586129
|
A | G | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.215-1130A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 586129 | ||||||
chr11:586185
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.215-1074G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 586185 | ||||||
chr11:586334
|
A | T | 3 | a0009c0012t0003g0067a0009c0012t0003g0082a0009c0012t0003g0176 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.215-925A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 586334 | ||||||
chr11:586417
|
C | T | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.215-842C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 586417 | ||||||
chr11:586564
|
A | G | 3 | a0011c0016t0001g0069a0011c0016t0001g0087a0024c0037t0001g0125 | 3 | HG02257.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.215-695A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 586564 | ||||||
chr11:586635
|
G | C | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.215-624G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 586635 | ||||||
chr11:586661
|
C | CT | 3 | a0009c0012t0003g0067a0009c0012t0003g0082a0009c0012t0003g0176 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.215-597dupT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 586661 | |||||
chr11:586696
|
A | G | 52 | a0001c0003t0002g0015a0001c0003t0002g0017a0001c0003t0002g0020others(49): Show | 53 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.215-563A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 586696 | ||||||
chr11:586698
|
C | G | 3 | a0011c0016t0001g0069a0011c0016t0001g0087a0024c0037t0001g0125 | 3 | HG02257.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.215-561C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 586698 | ||||||
chr11:586833
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.215-426T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 586833 | ||||||
chr11:587014
|
C | T | 37 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0077others(34): Show | 37 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.215-245C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 587014 | ||||||
chr11:587238
|
G | T | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.215-21G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | chr11 | 587238 | ||||||
chr11:587528
|
C | T | 1 | a0022c0035t0001g0243 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.420+64C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 587528 | ||||||
chr11:587655
|
CAT | C | 3 | a0001c0001t0001g0088a0002c0002t0001g0132a0002c0002t0001g0133 | 3 | HG01243.hp1 HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.420+192_420+193del others(2): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 587655 | ||||||
chr11:587700
|
T | C | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.420+236T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 587700 | ||||||
chr11:587885
|
A | G | 1 | a0001c0001t0001g0203 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.420+421A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 587885 | ||||||
chr11:588067
|
G | A | 2 | a0013c0021t0008g0251a0013c0022t0008g0123 | 2 | HG02896.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.420+603G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 588067 | ||||||
chr11:588192
|
CCTGTT | C | 3 | a0011c0016t0001g0069a0011c0016t0001g0087a0024c0037t0001g0125 | 3 | HG02257.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.420+734_420+738del others(5): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 588192 | |||||
chr11:588289
|
T | C | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.420+825T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 588289 | ||||||
chr11:588292
|
C | T | 1 | a0007c0010t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.420+828C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 588292 | ||||||
chr11:588306
|
C | T | 1 | a0013c0022t0008g0123 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.420+842C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 588306 | ||||||
chr11:588377
|
C | CT | 12 | a0002c0002t0001g0002a0002c0002t0001g0066a0002c0002t0001g0122others(9): Show | 14 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.420+924dupT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 588377 | |||||
chr11:588489
|
C | G | 2 | a0003c0004t0003g0222a0003c0004t0003g0269 | 2 | HG01346.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.420+1025C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 588489 | ||||||
chr11:588504
|
C | T | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.420+1040C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 588504 | ||||||
chr11:588505
|
G | A | 1 | a0002c0002t0001g0099 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.420+1041G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 588505 | ||||||
chr11:588617
|
G | A | 1 | a0021c0026t0001g0096 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.420+1153G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 588617 | ||||||
chr11:588654
|
C | T | 117 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0060others(114): Show | 117 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.420+1190C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 588654 | ||||||
chr11:588659
|
G | A | 6 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0141others(3): Show | 6 | HG00741.hp1 HG01099.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.420+1195G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 588659 | ||||||
chr11:589029
|
G | C | 2 | a0018c0029t0001g0217a0025c0038t0001g0181 | 2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.420+1565G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589029 | ||||||
chr11:589072
|
G | A | 1 | a0002c0002t0001g0139 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.420+1608G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589072 | ||||||
chr11:589076
|
C | T | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.420+1612C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589076 | ||||||
chr11:589113
|
C | T | 1 | a0013c0021t0008g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.420+1649C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589113 | ||||||
chr11:589162
|
G | A | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.420+1698G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589162 | ||||||
chr11:589246
|
G | A | 11 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.420+1782G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589246 | ||||||
chr11:589392
|
T | G | 3 | a0001c0003t0005g0014a0001c0003t0005g0044a0001c0003t0005g0050 | 3 | HG01192.hp2 HG02602.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.420+1928T>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589392 | ||||||
chr11:589538
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.421-1846G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589538 | ||||||
chr11:589564
|
T | C | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0060others(186): Show | 192 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.421-1820T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589564 | ||||||
chr11:589570
|
C | A | 1 | a0013c0021t0008g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.421-1814C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589570 | ||||||
chr11:589579
|
G | GGA | 181 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0060others(178): Show | 184 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.421-1804_421-1803i others(4): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589579 | |||||
chr11:589581
|
G | A | 181 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0060others(178): Show | 184 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.421-1803G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589581 | ||||||
chr11:589589
|
C | T | 10 | a0001c0001t0001g0071a0006c0008t0004g0080a0006c0008t0004g0081others(7): Show | 10 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.421-1795C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589589 | ||||||
chr11:589595
|
T | A | 12 | a0001c0001t0001g0071a0001c0009t0002g0183a0002c0002t0001g0086others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.421-1789T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589595 | ||||||
chr11:589597
|
G | A | 13 | a0001c0001t0001g0071a0001c0009t0002g0183a0002c0002t0001g0086others(10): Show | 13 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-1787G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589597 | ||||||
chr11:589619
|
T | C | 1 | a0001c0006t0002g0013 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.421-1765T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589619 | ||||||
chr11:589639
|
C | T | 13 | a0001c0006t0002g0008a0001c0006t0002g0009a0003c0004t0003g0190others(10): Show | 13 | HG01346.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-1745C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589639 | ||||||
chr11:589641
|
G | C | 13 | a0001c0006t0002g0008a0001c0006t0002g0009a0003c0004t0003g0190others(10): Show | 13 | HG01346.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-1743G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589641 | ||||||
chr11:589643
|
C | T | 13 | a0001c0006t0002g0008a0001c0006t0002g0009a0003c0004t0003g0190others(10): Show | 13 | HG01346.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-1741C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589643 | ||||||
chr11:589647
|
G | T | 13 | a0001c0006t0002g0008a0001c0006t0002g0009a0003c0004t0003g0190others(10): Show | 13 | HG01346.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-1737G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589647 | ||||||
chr11:589659
|
G | A | 13 | a0001c0006t0002g0008a0001c0006t0002g0009a0003c0004t0003g0190others(10): Show | 13 | HG01346.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-1725G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589659 | ||||||
chr11:589661
|
C | T | 13 | a0001c0006t0002g0008a0001c0006t0002g0009a0003c0004t0003g0190others(10): Show | 13 | HG01346.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-1723C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589661 | ||||||
chr11:589662
|
T | C | 13 | a0001c0006t0002g0008a0001c0006t0002g0009a0003c0004t0003g0190others(10): Show | 13 | HG01346.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-1722T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589662 | ||||||
chr11:589673
|
G | A | 13 | a0001c0006t0002g0008a0001c0006t0002g0009a0003c0004t0003g0190others(10): Show | 13 | HG01346.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-1711G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589673 | ||||||
chr11:589747
|
A | G | 1 | a0004c0005t0002g0033 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.421-1637A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589747 | ||||||
chr11:589748
|
G | T | 9 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(6): Show | 9 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.421-1636G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589748 | ||||||
chr11:589752
|
C | T | 9 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(6): Show | 9 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.421-1632C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589752 | ||||||
chr11:589792
|
G | A | 8 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(5): Show | 8 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-1592G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589792 | ||||||
chr11:589794
|
T | A | 8 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(5): Show | 8 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-1590T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589794 | ||||||
chr11:589804
|
C | T | 8 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(5): Show | 8 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-1580C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589804 | ||||||
chr11:589810
|
C | T | 8 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(5): Show | 8 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-1574C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589810 | ||||||
chr11:589811
|
A | AGAGCGTG others(126): Show |
1 | a0001c0009t0002g0183 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.421-1566_421-1565i others(135): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589811 | |||||
chr11:589811
|
A | G | 11 | a0001c0003t0002g0015a0003c0004t0003g0177a0006c0008t0004g0080others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.421-1573A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589811 | ||||||
chr11:589816
|
G | A | 1 | a0016c0020t0009g0249 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.421-1568G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589816 | ||||||
chr11:589819
|
C | T | 53 | a0001c0001t0001g0202a0001c0003t0002g0017a0001c0003t0002g0020others(50): Show | 54 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.421-1565C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589819 | ||||||
chr11:589820
|
G | C | 1 | a0016c0020t0009g0249 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.421-1564G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589820 | ||||||
chr11:589821
|
G | A | 1 | a0016c0020t0009g0249 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.421-1563G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589821 | ||||||
chr11:589831
|
TGAGA | T | 11 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.421-1547_421-1544d others(6): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589831 | |||||
chr11:589838
|
G | A | 2 | a0001c0001t0001g0210a0001c0003t0002g0015 | 2 | HG01069.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.421-1546G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589838 | ||||||
chr11:589839
|
A | AGTCTGCA others(81): Show |
4 | a0001c0014t0001g0262a0001c0014t0001g0263a0001c0031t0001g0261others(1): Show | 4 | HG01943.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.421-1503_421-1416d others(90): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589839 | |||||
chr11:589839
|
A | AGTCTGCA others(167): Show |
2 | a0001c0009t0002g0131a0002c0011t0001g0065 | 2 | HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.421-1539_421-1366d others(176): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589839 | |||||
chr11:589839
|
A | T | 2 | a0001c0001t0001g0210a0001c0003t0002g0015 | 2 | HG01069.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.421-1545A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589839 | ||||||
chr11:589849
|
C | T | 1 | a0016c0020t0009g0249 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.421-1535C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589849 | ||||||
chr11:589855
|
C | CAGAGCGT others(167): Show |
1 | a0001c0001t0001g0233 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.421-1529_421-1528i others(176): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589855 | ||||||
chr11:589855
|
C | CGGAGCGT others(167): Show |
2 | a0001c0001t0001g0235a0001c0001t0001g0265 | 2 | HG01167.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.421-1481_421-1480i others(176): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589855 | |||||
chr11:589855
|
C | CGGAGCGT others(167): Show |
93 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0060others(90): Show | 93 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.421-1366_421-1365i others(176): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589855 | |||||
chr11:589855
|
C | CGGAGCGT others(166): Show |
1 | a0001c0001t0001g0119 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.421-1459_421-1458i others(175): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589855 | |||||
chr11:589855
|
C | T | 3 | a0001c0001t0001g0210a0001c0003t0002g0015a0016c0020t0009g0249 | 3 | HG01069.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.421-1529C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589855 | ||||||
chr11:589865
|
G | A | 1 | a0001c0003t0002g0015 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.421-1519G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589865 | ||||||
chr11:589869
|
C | T | 1 | a0001c0003t0002g0015 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.421-1515C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589869 | ||||||
chr11:589876
|
T | TGA | 11 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.421-1505_421-1504d others(4): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589876 | |||||
chr11:589881
|
A | G | 12 | a0001c0003t0002g0015a0006c0008t0004g0080a0006c0008t0004g0081others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.421-1503A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589881 | ||||||
chr11:589881
|
ATGTCTGC others(38): Show |
A | 1 | a0003c0004t0003g0084 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.421-1486_421-1442d others(47): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589881 | |||||
chr11:589882
|
T | A | 11 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.421-1502T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589882 | ||||||
chr11:589898
|
T | C | 2 | a0001c0003t0002g0015a0016c0020t0009g0249 | 2 | HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.421-1486T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589898 | ||||||
chr11:589898
|
T | TGGAGCGT others(210): Show |
1 | a0014c0019t0001g0090 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.421-1366_421-1365i others(219): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589898 | |||||
chr11:589907
|
C | T | 12 | a0001c0006t0002g0016a0006c0008t0004g0080a0006c0008t0004g0081others(9): Show | 12 | HG01192.hp1 HG02145.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.421-1477C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589907 | ||||||
chr11:589908
|
A | G | 14 | a0001c0003t0002g0015a0001c0006t0002g0016a0006c0008t0004g0080others(11): Show | 14 | HG01192.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.421-1476A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589908 | ||||||
chr11:589912
|
T | C | 14 | a0001c0003t0002g0015a0001c0006t0002g0016a0006c0008t0004g0080others(11): Show | 14 | HG01192.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.421-1472T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589912 | ||||||
chr11:589923
|
AGG | A | 12 | a0001c0006t0002g0016a0006c0008t0004g0080a0006c0008t0004g0081others(9): Show | 12 | HG01192.hp1 HG02145.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.421-1459_421-1458d others(4): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589923 | |||||
chr11:589925
|
G | A | 1 | a0016c0020t0009g0249 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.421-1459G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589925 | ||||||
chr11:589926
|
G | A | 12 | a0001c0006t0002g0016a0006c0008t0004g0080a0006c0008t0004g0081others(9): Show | 12 | HG01192.hp1 HG02145.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.421-1458G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589926 | ||||||
chr11:589927
|
T | A | 1 | a0016c0020t0009g0249 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.421-1457T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589927 | ||||||
chr11:589943
|
C | T | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.421-1441C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589943 | ||||||
chr11:589952
|
C | T | 2 | a0001c0003t0002g0015a0016c0020t0009g0249 | 2 | HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.421-1432C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589952 | ||||||
chr11:589953
|
G | A | 11 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.421-1431G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589953 | ||||||
chr11:589957
|
C | T | 11 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.421-1427C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589957 | ||||||
chr11:589968
|
A | AATGTCTG others(40): Show |
1 | a0016c0020t0009g0249 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.421-1416_421-1415i others(49): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589968 | ||||||
chr11:589968
|
A | AGGGT | 11 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.421-1415_421-1414i others(6): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 589968 | |||||
chr11:589968
|
A | T | 1 | a0001c0003t0002g0015 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.421-1416A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589968 | ||||||
chr11:589984
|
C | T | 1 | a0001c0003t0002g0015 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.421-1400C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589984 | ||||||
chr11:589993
|
T | C | 1 | a0001c0003t0002g0015 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.421-1391T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 589993 | ||||||
chr11:590012
|
G | A | 1 | a0001c0003t0002g0015 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.421-1372G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590012 | ||||||
chr11:590012
|
GTGTCTGT others(36): Show |
G | 4 | a0003c0004t0003g0177a0009c0012t0003g0067a0009c0012t0003g0082others(1): Show | 4 | HG02622.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.421-1365_421-1323d others(45): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 590012 | |||||
chr11:590019
|
T | C | 267 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0060others(264): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.421-1365T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590019 | ||||||
chr11:590029
|
T | C | 1 | a0001c0003t0002g0015 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.421-1355T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590029 | ||||||
chr11:590029
|
T | TGGAGCGT others(36): Show |
38 | a0001c0003t0002g0017a0001c0003t0002g0020a0001c0003t0002g0022others(35): Show | 39 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.421-1313_421-1312i others(45): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 590029 | |||||
chr11:590029
|
T | TGGAGCGT others(298): Show |
1 | a0001c0003t0002g0038 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.421-1313_421-1312i others(307): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 590029 | |||||
chr11:590072
|
T | C | 88 | a0001c0001t0001g0088a0001c0003t0002g0015a0001c0003t0002g0017others(85): Show | 90 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.421-1312T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590072 | ||||||
chr11:590072
|
T | TGGAGCGT others(167): Show |
9 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0141others(6): Show | 10 | HG00741.hp1 HG01099.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.421-1303_421-1302i others(176): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr11 | 590072 | |||||
chr11:590102
|
G | C | 37 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0077others(34): Show | 37 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.421-1282G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590102 | ||||||
chr11:590107
|
A | C | 2 | a0013c0021t0008g0251a0013c0022t0008g0123 | 2 | HG02896.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.421-1277A>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590107 | ||||||
chr11:590116
|
G | A | 1 | a0002c0002t0001g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.421-1268G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590116 | ||||||
chr11:590201
|
C | T | 36 | a0001c0001t0001g0202a0001c0001t0001g0257a0001c0027t0001g0254others(33): Show | 38 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.421-1183C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590201 | ||||||
chr11:590425
|
C | T | 2 | a0002c0002t0001g0225a0002c0002t0001g0226 | 2 | NA18941.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.421-959C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590425 | ||||||
chr11:590517
|
A | T | 1 | a0001c0014t0001g0144 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.421-867A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590517 | ||||||
chr11:590534
|
A | G | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.421-850A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590534 | ||||||
chr11:590605
|
C | G | 33 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0060others(30): Show | 33 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.421-779C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590605 | ||||||
chr11:590648
|
A | G | 73 | a0001c0003t0002g0015a0001c0003t0002g0017a0001c0003t0002g0020others(70): Show | 75 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.421-736A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590648 | ||||||
chr11:590660
|
A | C | 1 | a0002c0002t0001g0193 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.421-724A>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590660 | ||||||
chr11:590665
|
T | A | 1 | a0002c0002t0001g0193 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.421-719T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590665 | ||||||
chr11:590666
|
A | T | 1 | a0002c0002t0001g0193 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.421-718A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590666 | ||||||
chr11:590728
|
A | G | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.421-656A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590728 | ||||||
chr11:590775
|
C | G | 5 | a0001c0006t0002g0019a0001c0006t0002g0021a0001c0006t0002g0036others(2): Show | 5 | HG02486.hp2 HG02723.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.421-609C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590775 | ||||||
chr11:590945
|
T | G | 3 | a0001c0001t0001g0088a0002c0002t0001g0132a0002c0002t0001g0133 | 3 | HG01243.hp1 HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.421-439T>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590945 | ||||||
chr11:590999
|
G | A | 61 | a0001c0003t0002g0015a0001c0003t0002g0017a0001c0003t0002g0020others(58): Show | 63 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.421-385G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 590999 | ||||||
chr11:591083
|
G | A | 210 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0060others(207): Show | 213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.421-301G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 591083 | ||||||
chr11:591180
|
G | T | 3 | a0003c0004t0003g0190a0003c0004t0003g0222a0003c0004t0003g0269 | 3 | HG01346.hp1 HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.421-204G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 4/17 | chr11 | 591180 | ||||||
chr11:591480
|
G | A | 1 | a0001c0001t0007g0196 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.504+13G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 591480 | ||||||
chr11:591601
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.504+134G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 591601 | ||||||
chr11:591907
|
C | G | 1 | a0002c0002t0001g0193 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.504+440C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 591907 | ||||||
chr11:591908
|
G | C | 1 | a0002c0002t0001g0193 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.504+441G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 591908 | ||||||
chr11:591912
|
G | GT | 39 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(36): Show | 39 | HG00438.hp1 HG00438.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.504+462dupT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr11 | 591912 | |||||
chr11:591912
|
GT | G | 17 | a0001c0001t0001g0203a0001c0009t0002g0131a0001c0009t0002g0183others(14): Show | 18 | HG00280.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.504+462delT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr11 | 591912 | |||||
chr11:591932
|
C | T | 2 | a0013c0021t0008g0251a0013c0022t0008g0123 | 2 | HG02896.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.504+465C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 591932 | ||||||
chr11:591980
|
A | G | 2 | a0013c0021t0008g0251a0013c0022t0008g0123 | 2 | HG02896.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.504+513A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 591980 | ||||||
chr11:592023
|
G | C | 60 | a0001c0003t0002g0015a0001c0003t0002g0017a0001c0003t0002g0020others(57): Show | 62 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.505-536G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592023 | ||||||
chr11:592080
|
T | A | 1 | a0013c0022t0008g0123 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.505-479T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592080 | ||||||
chr11:592106
|
G | A | 2 | a0001c0001t0007g0196a0001c0001t0007g0201 | 2 | HG00597.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.505-453G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592106 | ||||||
chr11:592136
|
C | T | 3 | a0001c0006t0002g0019a0001c0006t0002g0021a0001c0006t0002g0036 | 3 | HG02486.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.505-423C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592136 | ||||||
chr11:592140
|
C | T | 1 | a0024c0037t0001g0125 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.505-419C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592140 | ||||||
chr11:592214
|
C | CT | 15 | a0001c0001t0001g0100a0001c0003t0005g0044a0003c0004t0003g0025others(12): Show | 15 | HG00639.hp2 HG00741.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.505-327dupT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr11 | 592214 | |||||
chr11:592222
|
T | A | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.505-337T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592222 | ||||||
chr11:592250
|
C | T | 1 | a0003c0004t0003g0084 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.505-309C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592250 | ||||||
chr11:592254
|
C | T | 2 | a0018c0029t0001g0217a0025c0038t0001g0181 | 2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.505-305C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592254 | ||||||
chr11:592306
|
G | A | 1 | a0001c0001t0001g0238 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.505-253G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592306 | ||||||
chr11:592329
|
G | A | 1 | a0002c0011t0001g0165 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.505-230G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592329 | ||||||
chr11:592377
|
C | T | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.505-182C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592377 | ||||||
chr11:592388
|
T | C | 1 | a0001c0001t0001g0257 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.505-171T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592388 | ||||||
chr11:592406
|
C | T | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.505-153C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592406 | ||||||
chr11:592415
|
C | T | 1 | a0001c0009t0002g0093 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.505-144C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592415 | ||||||
chr11:592510
|
T | C | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.505-49T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 5/17 | chr11 | 592510 | ||||||
chr11:592700
|
C | T | 1 | a0013c0021t0008g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.620+26C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 592700 | ||||||
chr11:592825
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.620+151G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 592825 | ||||||
chr11:592873
|
A | G | 1 | a0013c0022t0008g0123 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.620+199A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 592873 | ||||||
chr11:592902
|
A | T | 3 | a0001c0001t0001g0077a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | NA18943.hp2 NA19002.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.620+228A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 592902 | ||||||
chr11:593008
|
A | G | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.620+334A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 593008 | ||||||
chr11:593042
|
C | G | 4 | a0007c0010t0002g0010a0007c0010t0002g0011a0007c0010t0002g0012others(1): Show | 4 | HG01891.hp1 HG02922.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.620+368C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 593042 | ||||||
chr11:593098
|
C | T | 12 | a0003c0004t0003g0025a0003c0004t0003g0083a0003c0004t0003g0084others(9): Show | 12 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.620+424C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 593098 | ||||||
chr11:593219
|
G | A | 2 | a0018c0029t0001g0217a0025c0038t0001g0181 | 2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.620+545G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 593219 | ||||||
chr11:593453
|
T | C | 126 | a0001c0001t0001g0202a0001c0001t0001g0257a0001c0003t0002g0015others(123): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.620+779T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 593453 | ||||||
chr11:593572
|
C | G | 1 | a0002c0002t0001g0086 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.620+898C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 593572 | ||||||
chr11:593827
|
A | G | 1 | a0002c0002t0001g0255 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.620+1153A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 593827 | ||||||
chr11:593962
|
C | T | 6 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(3): Show | 6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.620+1288C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 593962 | ||||||
chr11:594005
|
T | C | 1 | a0013c0021t0008g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.620+1331T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594005 | ||||||
chr11:594069
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.620+1395G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594069 | ||||||
chr11:594072
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.620+1398T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594072 | ||||||
chr11:594196
|
G | A | 2 | a0013c0021t0008g0251a0013c0022t0008g0123 | 2 | HG02896.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.620+1522G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594196 | ||||||
chr11:594264
|
A | G | 4 | a0002c0011t0001g0058a0002c0011t0001g0065a0002c0011t0001g0165others(1): Show | 4 | HG02572.hp2 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.620+1590A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594264 | ||||||
chr11:594273
|
T | TAGAG | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.620+1602_620+1603i others(6): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr11 | 594273 | |||||
chr11:594329
|
C | T | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.620+1655C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594329 | ||||||
chr11:594414
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.620+1740T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594414 | ||||||
chr11:594422
|
T | A | 1 | a0001c0003t0012g0049 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.620+1748T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594422 | ||||||
chr11:594481
|
G | A | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.620+1807G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594481 | ||||||
chr11:594535
|
G | A | 6 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(3): Show | 6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.620+1861G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594535 | ||||||
chr11:594609
|
A | G | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.620+1935A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594609 | ||||||
chr11:594650
|
C | T | 2 | a0013c0021t0008g0251a0013c0022t0008g0123 | 2 | HG02896.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.620+1976C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594650 | ||||||
chr11:594698
|
T | G | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.620+2024T>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594698 | ||||||
chr11:594894
|
TAAAAC | T | 105 | a0001c0001t0001g0202a0001c0001t0001g0257a0001c0003t0002g0015others(102): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.621-2026_621-2022d others(7): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr11 | 594894 | |||||
chr11:594909
|
A | C | 2 | a0001c0001t0001g0107a0001c0001t0001g0238 | 2 | NA19000.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.621-2014A>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 594909 | ||||||
chr11:595093
|
C | T | 1 | a0009c0012t0003g0082 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.621-1830C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 595093 | ||||||
chr11:595168
|
A | T | 252 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0060others(249): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.621-1755A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 595168 | ||||||
chr11:595184
|
G | C | 2 | a0002c0002t0001g0085a0002c0002t0001g0086 | 2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.621-1739G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 595184 | ||||||
chr11:595209
|
G | A | 14 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(11): Show | 14 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.621-1714G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 595209 | ||||||
chr11:595305
|
A | G | 10 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(7): Show | 10 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.621-1618A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 595305 | ||||||
chr11:595314
|
CA | C | 3 | a0011c0016t0001g0069a0011c0016t0001g0087a0024c0037t0001g0125 | 3 | HG02257.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.621-1602delA | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr11 | 595314 | |||||
chr11:595362
|
CA | C | 6 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(3): Show | 6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.621-1560delA | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 595362 | ||||||
chr11:595683
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.621-1240C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 595683 | ||||||
chr11:595810
|
A | G | 60 | a0001c0003t0002g0015a0001c0003t0002g0017a0001c0003t0002g0020others(57): Show | 62 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.621-1113A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 595810 | ||||||
chr11:595890
|
G | A | 60 | a0001c0003t0002g0015a0001c0003t0002g0017a0001c0003t0002g0020others(57): Show | 62 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.621-1033G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 595890 | ||||||
chr11:595894
|
C | T | 1 | a0014c0019t0001g0090 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.621-1029C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 595894 | ||||||
chr11:595940
|
C | T | 3 | a0011c0016t0001g0069a0011c0016t0001g0087a0024c0037t0001g0125 | 3 | HG02257.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.621-983C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 595940 | ||||||
chr11:595992
|
A | G | 1 | a0013c0021t0008g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.621-931A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 595992 | ||||||
chr11:596002
|
A | G | 1 | a0002c0011t0001g0065 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.621-921A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596002 | ||||||
chr11:596005
|
A | G | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.621-918A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596005 | ||||||
chr11:596035
|
G | A | 7 | a0005c0007t0001g0127a0005c0007t0001g0252a0005c0007t0001g0253others(4): Show | 7 | HG02004.hp2 HG02040.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.621-888G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596035 | ||||||
chr11:596091
|
C | T | 1 | a0001c0001t0006g0241 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.621-832C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596091 | ||||||
chr11:596102
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.621-821G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596102 | ||||||
chr11:596118
|
G | T | 1 | a0021c0026t0001g0096 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.621-805G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596118 | ||||||
chr11:596248
|
G | A | 3 | a0011c0016t0001g0069a0011c0016t0001g0087a0024c0037t0001g0125 | 3 | HG02257.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.621-675G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596248 | ||||||
chr11:596299
|
C | G | 6 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(3): Show | 6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.621-624C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596299 | ||||||
chr11:596303
|
C | T | 1 | a0020c0032t0001g0167 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.621-620C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596303 | ||||||
chr11:596309
|
A | G | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.621-614A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596309 | ||||||
chr11:596480
|
T | C | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.621-443T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596480 | ||||||
chr11:596499
|
G | C | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.621-424G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596499 | ||||||
chr11:596518
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.621-405C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596518 | ||||||
chr11:596672
|
G | T | 37 | a0001c0001t0001g0202a0001c0001t0001g0257a0001c0027t0001g0254others(34): Show | 39 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.621-251G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596672 | ||||||
chr11:596842
|
G | A | 10 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(7): Show | 10 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.621-81G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596842 | ||||||
chr11:596866
|
A | C | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.621-57A>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 6/17 | chr11 | 596866 | ||||||
chr11:597064
|
A | G | 1 | a0023c0036t0001g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.718+44A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 7/17 | chr11 | 597064 | ||||||
chr11:597074
|
C | T | 5 | a0002c0002t0001g0085a0002c0002t0001g0086a0011c0016t0001g0069others(2): Show | 5 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.718+54C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 7/17 | chr11 | 597074 | ||||||
chr11:597153
|
G | A | 1 | a0001c0001t0007g0196 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.718+133G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 7/17 | chr11 | 597153 | ||||||
chr11:597318
|
G | A | 2 | a0001c0001t0001g0007a0001c0033t0014g0105 | 2 | NA18982.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.719-77G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 7/17 | chr11 | 597318 | ||||||
chr11:597348
|
C | T | 1 | a0002c0002t0001g0248 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.719-47C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 7/17 | chr11 | 597348 | ||||||
chr11:597349
|
G | A | 2 | a0002c0002t0001g0085a0002c0002t0001g0086 | 2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.719-46G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 7/17 | chr11 | 597349 | ||||||
chr11:597597
|
C | T | 1 | a0002c0002t0001g0086 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.894+27C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 8/17 | chr11 | 597597 | ||||||
chr11:597815
|
C | T | 1 | a0002c0002t0001g0189 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.894+245C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 8/17 | chr11 | 597815 | ||||||
chr11:597868
|
C | T | 11 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.894+298C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 8/17 | chr11 | 597868 | ||||||
chr11:598033
|
C | T | 60 | a0001c0003t0002g0015a0001c0003t0002g0017a0001c0003t0002g0020others(57): Show | 62 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.895-340C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 8/17 | chr11 | 598033 | ||||||
chr11:598148
|
C | T | 3 | a0003c0004t0003g0025a0003c0004t0003g0216a0003c0004t0003g0250 | 3 | HG01884.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.895-225C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 8/17 | chr11 | 598148 | ||||||
chr11:598205
|
C | G | 60 | a0001c0003t0002g0015a0001c0003t0002g0017a0001c0003t0002g0020others(57): Show | 62 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.895-168C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 8/17 | chr11 | 598205 | ||||||
chr11:598288
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.895-85G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 8/17 | chr11 | 598288 | ||||||
chr11:598288
|
G | C | 2 | a0002c0002t0001g0085a0002c0002t0001g0086 | 2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.895-85G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 8/17 | chr11 | 598288 | ||||||
chr11:598595
|
C | G | 3 | a0009c0012t0003g0067a0009c0012t0003g0082a0009c0012t0003g0176 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1024+93C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 598595 | ||||||
chr11:598723
|
A | C | 60 | a0001c0003t0002g0015a0001c0003t0002g0017a0001c0003t0002g0020others(57): Show | 62 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.1024+221A>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 598723 | ||||||
chr11:598793
|
C | T | 3 | a0009c0012t0003g0067a0009c0012t0003g0082a0009c0012t0003g0176 | 3 | HG02630.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1024+291C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 598793 | ||||||
chr11:598852
|
C | G | 1 | a0002c0002t0001g0215 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1024+350C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 598852 | ||||||
chr11:598874
|
A | C | 1 | a0001c0001t0001g0208 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1024+372A>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 598874 | ||||||
chr11:598879
|
A | G | 2 | a0018c0029t0001g0217a0025c0038t0001g0181 | 2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1024+377A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 598879 | ||||||
chr11:599132
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1024+630G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599132 | ||||||
chr11:599253
|
C | CT | 29 | a0001c0001t0001g0101a0001c0001t0001g0142a0001c0001t0001g0149others(26): Show | 29 | HG00597.hp2 HG00639.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1024+770dupT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 599253 | |||||
chr11:599253
|
CT | C | 72 | a0001c0001t0001g0088a0001c0001t0001g0153a0001c0001t0001g0214others(69): Show | 74 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.1024+770delT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 599253 | |||||
chr11:599280
|
A | T | 1 | a0005c0007t0001g0180 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1024+778A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599280 | ||||||
chr11:599287
|
C | T | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1024+785C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599287 | ||||||
chr11:599313
|
T | C | 84 | a0001c0003t0002g0015a0001c0003t0002g0017a0001c0003t0002g0020others(81): Show | 86 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.1024+811T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599313 | ||||||
chr11:599471
|
G | A | 12 | a0003c0004t0003g0025a0003c0004t0003g0083a0003c0004t0003g0084others(9): Show | 12 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.1024+969G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599471 | ||||||
chr11:599481
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1024+979C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599481 | ||||||
chr11:599542
|
T | C | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1024+1040T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599542 | ||||||
chr11:599588
|
C | T | 4 | a0005c0007t0001g0089a0005c0007t0001g0128a0005c0007t0001g0179others(1): Show | 4 | HG01168.hp2 HG02056.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024+1086C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599588 | ||||||
chr11:599654
|
T | C | 4 | a0009c0012t0003g0067a0009c0012t0003g0082a0009c0012t0003g0176others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024+1152T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599654 | ||||||
chr11:599668
|
A | G | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1024+1166A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599668 | ||||||
chr11:599700
|
C | T | 2 | a0002c0002t0001g0085a0002c0002t0001g0086 | 2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1024+1198C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599700 | ||||||
chr11:599711
|
G | A | 1 | a0001c0023t0001g0231 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1024+1209G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599711 | ||||||
chr11:599779
|
A | G | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1024+1277A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 599779 | ||||||
chr11:600097
|
T | C | 1 | a0002c0002t0001g0225 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1025-1477T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 600097 | ||||||
chr11:600098
|
C | T | 1 | a0002c0002t0001g0225 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1025-1476C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 600098 | ||||||
chr11:600222
|
C | G | 11 | a0005c0007t0001g0089a0005c0007t0001g0127a0005c0007t0001g0128others(8): Show | 11 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.1025-1352C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 600222 | ||||||
chr11:600254
|
C | CT | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1025-1306dupT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 600254 | |||||
chr11:600379
|
C | T | 1 | a0002c0002t0001g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1025-1195C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 600379 | ||||||
chr11:600474
|
G | A | 11 | a0002c0002t0001g0002a0002c0002t0001g0066a0002c0002t0001g0122others(8): Show | 13 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.1025-1100G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 600474 | ||||||
chr11:600493
|
A | AAT | 48 | a0001c0001t0001g0202a0001c0001t0001g0257a0001c0003t0002g0017others(45): Show | 53 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1025-1056_1025-105 others(6): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 600493 | |||||
chr11:600493
|
A | AATAAATA others(27): Show |
4 | a0009c0012t0003g0067a0009c0012t0003g0082a0009c0012t0003g0176others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025-1078_1025-107 others(38): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 600493 | |||||
chr11:600493
|
A | AATAAATA others(31): Show |
1 | a0006c0008t0004g0178 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1025-1078_1025-107 others(42): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 600493 | |||||
chr11:600493
|
A | AATAAATA others(35): Show |
5 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(2): Show | 5 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1025-1078_1025-107 others(46): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 600493 | |||||
chr11:600493
|
A | AATAAATA others(9): Show |
1 | a0013c0021t0008g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1025-1078_1025-107 others(20): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 600493 | |||||
chr11:600493
|
A | AATAAATA others(15): Show |
1 | a0013c0022t0008g0123 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1025-1078_1025-107 others(26): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 600493 | |||||
chr11:600493
|
A | AATAT | 13 | a0002c0002t0001g0059a0002c0002t0001g0066a0002c0002t0001g0122others(10): Show | 13 | HG00597.hp1 HG00609.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1025-1058_1025-105 others(8): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 600493 | |||||
chr11:600493
|
A | AATATATA others(1): Show |
5 | a0001c0009t0002g0131a0003c0004t0003g0190a0003c0004t0003g0222others(2): Show | 5 | HG01346.hp1 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1025-1062_1025-105 others(12): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 600493 | |||||
chr11:600493
|
A | AATATATA others(3): Show |
1 | a0001c0009t0002g0183 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1025-1064_1025-105 others(14): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 600493 | |||||
chr11:600493
|
AAT | A | 102 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0060others(99): Show | 102 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.1025-1056_1025-105 others(6): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 600493 | |||||
chr11:600493
|
AATAT | A | 7 | a0001c0001t0001g0236a0001c0001t0001g0271a0002c0002t0001g0085others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1025-1058_1025-105 others(8): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 600493 | |||||
chr11:600512
|
A | G | 11 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1025-1062A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 600512 | ||||||
chr11:600647
|
T | C | 1 | a0001c0006t0002g0124 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1025-927T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 600647 | ||||||
chr11:600693
|
A | G | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1025-881A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 600693 | ||||||
chr11:600790
|
C | G | 2 | a0013c0021t0008g0251a0013c0022t0008g0123 | 2 | HG02896.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1025-784C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 600790 | ||||||
chr11:600846
|
G | A | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1025-728G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 600846 | ||||||
chr11:600906
|
C | T | 1 | a0013c0021t0008g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1025-668C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 600906 | ||||||
chr11:601145
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1025-429C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 601145 | ||||||
chr11:601428
|
C | CA | 32 | a0001c0001t0001g0063a0001c0001t0001g0107a0001c0001t0001g0142others(29): Show | 32 | HG00639.hp2 HG01106.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.1025-128dupA | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 601428 | |||||
chr11:601470
|
C | T | 3 | a0001c0001t0001g0088a0002c0002t0001g0132a0002c0002t0001g0133 | 3 | HG01243.hp1 HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1025-104C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 601470 | ||||||
chr11:601479
|
G | A | 2 | a0013c0021t0008g0251a0013c0022t0008g0123 | 2 | HG02896.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1025-95G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 9/17 | chr11 | 601479 | ||||||
chr11:601785
|
T | C | 72 | a0001c0003t0002g0015a0001c0003t0002g0017a0001c0003t0002g0020others(69): Show | 74 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.1152+84T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 601785 | ||||||
chr11:601803
|
G | A | 3 | a0001c0006t0002g0019a0001c0006t0002g0021a0001c0006t0002g0036 | 3 | HG02486.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1152+102G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 601803 | ||||||
chr11:601804
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1152+103C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 601804 | ||||||
chr11:601953
|
A | G | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1152+252A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 601953 | ||||||
chr11:601985
|
A | G | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+284A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 601985 | ||||||
chr11:601986
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+285G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 601986 | ||||||
chr11:601987
|
C | A | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+286C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 601987 | ||||||
chr11:601988
|
T | G | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+287T>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 601988 | ||||||
chr11:601990
|
G | T | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+289G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 601990 | ||||||
chr11:601997
|
A | C | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+296A>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 601997 | ||||||
chr11:601998
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+297G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 601998 | ||||||
chr11:602006
|
T | A | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+305T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602006 | ||||||
chr11:602007
|
G | C | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+306G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602007 | ||||||
chr11:602009
|
G | C | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+308G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602009 | ||||||
chr11:602013
|
G | C | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+312G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602013 | ||||||
chr11:602014
|
G | C | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+313G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602014 | ||||||
chr11:602030
|
T | A | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+329T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602030 | ||||||
chr11:602036
|
A | T | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+335A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602036 | ||||||
chr11:602045
|
G | T | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+344G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602045 | ||||||
chr11:602046
|
G | C | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+345G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602046 | ||||||
chr11:602048
|
G | T | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+347G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602048 | ||||||
chr11:602054
|
G | C | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+353G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602054 | ||||||
chr11:602057
|
G | T | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+356G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602057 | ||||||
chr11:602059
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+358T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602059 | ||||||
chr11:602061
|
T | A | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+360T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602061 | ||||||
chr11:602065
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+364G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602065 | ||||||
chr11:602066
|
C | A | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+365C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602066 | ||||||
chr11:602068
|
G | T | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+367G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602068 | ||||||
chr11:602071
|
C | A | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+370C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602071 | ||||||
chr11:602073
|
G | T | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+372G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602073 | ||||||
chr11:602074
|
G | T | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+373G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602074 | ||||||
chr11:602080
|
C | A | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+379C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602080 | ||||||
chr11:602081
|
T | A | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+380T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602081 | ||||||
chr11:602082
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+381G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602082 | ||||||
chr11:602083
|
G | T | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+382G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602083 | ||||||
chr11:602085
|
T | A | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+384T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602085 | ||||||
chr11:602091
|
G | T | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+390G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602091 | ||||||
chr11:602093
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+392G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602093 | ||||||
chr11:602094
|
T | A | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+393T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602094 | ||||||
chr11:602095
|
G | T | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+394G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602095 | ||||||
chr11:602099
|
C | G | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+398C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602099 | ||||||
chr11:602102
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+401G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602102 | ||||||
chr11:602103
|
C | G | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+402C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602103 | ||||||
chr11:602105
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+404G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602105 | ||||||
chr11:602106
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+405T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602106 | ||||||
chr11:602108
|
T | A | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+407T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602108 | ||||||
chr11:602114
|
A | T | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+413A>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602114 | ||||||
chr11:602116
|
G | T | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+415G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602116 | ||||||
chr11:602130
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+429T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602130 | ||||||
chr11:602131
|
T | A | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+430T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602131 | ||||||
chr11:602134
|
G | C | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+433G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602134 | ||||||
chr11:602136
|
C | A | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+435C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602136 | ||||||
chr11:602150
|
G | C | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+449G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602150 | ||||||
chr11:602151
|
C | G | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+450C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602151 | ||||||
chr11:602154
|
T | A | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+453T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602154 | ||||||
chr11:602166
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1152+465C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602166 | ||||||
chr11:602238
|
T | G | 1 | a0001c0001t0001g0153 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1152+537T>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602238 | ||||||
chr11:602300
|
G | A | 2 | a0003c0004t0003g0174a0003c0004t0003g0175 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1152+599G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602300 | ||||||
chr11:602321
|
A | C | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1152+620A>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602321 | ||||||
chr11:602322
|
A | G | 37 | a0001c0001t0001g0202a0001c0001t0001g0257a0001c0027t0001g0254others(34): Show | 39 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.1152+621A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602322 | ||||||
chr11:602406
|
C | T | 1 | a0001c0014t0001g0263 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1152+705C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602406 | ||||||
chr11:602594
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1152+893C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602594 | ||||||
chr11:602749
|
GGTTTTGT others(4): Show |
G | 4 | a0009c0012t0003g0067a0009c0012t0003g0082a0009c0012t0003g0176others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1152+1054_1152+106 others(15): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr11 | 602749 | |||||
chr11:602749
|
GGTTTTGT others(6): Show |
G | 2 | a0013c0021t0008g0251a0013c0022t0008g0123 | 2 | HG02896.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1152+1049_1152+106 others(17): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602749 | ||||||
chr11:602751
|
TTTTGTTT others(3): Show |
T | 6 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(3): Show | 6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1152+1054_1152+106 others(14): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr11 | 602751 | |||||
chr11:602770
|
G | GT | 12 | a0001c0001t0001g0063a0001c0001t0001g0162a0001c0001t0001g0233others(9): Show | 12 | HG00735.hp1 HG01074.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1152+1080dupT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr11 | 602770 | |||||
chr11:602770
|
G | T | 21 | a0001c0001t0001g0161a0005c0007t0001g0089a0005c0007t0001g0127others(18): Show | 21 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(18): Show |
intron_variant | MODIFIER | c.1152+1069G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602770 | ||||||
chr11:602920
|
G | A | 2 | a0002c0002t0001g0136a0002c0002t0001g0188 | 2 | HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1152+1219G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602920 | ||||||
chr11:602963
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1152+1262A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 602963 | ||||||
chr11:603119
|
A | G | 3 | a0001c0001t0001g0088a0002c0002t0001g0132a0002c0002t0001g0133 | 3 | HG01243.hp1 HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1152+1418A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 603119 | ||||||
chr11:603167
|
C | A | 1 | a0002c0002t0001g0225 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1152+1466C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 603167 | ||||||
chr11:603168
|
A | C | 1 | a0002c0002t0001g0225 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1152+1467A>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 603168 | ||||||
chr11:603339
|
T | A | 1 | a0002c0002t0001g0225 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1152+1638T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 603339 | ||||||
chr11:603340
|
A | G | 1 | a0002c0002t0001g0225 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1152+1639A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 603340 | ||||||
chr11:603369
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0078 | 2 | HG03831.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1152+1668G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 603369 | ||||||
chr11:603413
|
C | A | 271 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0060others(268): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.1153-1706C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 603413 | ||||||
chr11:603476
|
C | G | 1 | a0001c0001t0001g0161 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1153-1643C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 603476 | ||||||
chr11:603724
|
AGTTT | A | 7 | a0006c0008t0004g0081a0006c0008t0004g0121a0006c0008t0004g0178others(4): Show | 7 | HG02145.hp2 HG02630.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1153-1390_1153-138 others(8): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr11 | 603724 | |||||
chr11:603728
|
TG | T | 8 | a0003c0004t0003g0083a0003c0004t0003g0084a0003c0004t0003g0164others(5): Show | 8 | HG00639.hp2 HG01169.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.1153-1390delG | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 603728 | ||||||
chr11:603729
|
G | GT | 58 | a0001c0001t0001g0071a0001c0001t0001g0162a0001c0001t0001g0202others(55): Show | 61 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.1153-1368dupT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr11 | 603729 | |||||
chr11:603729
|
GT | G | 103 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0060others(100): Show | 103 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1153-1368delT | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr11 | 603729 | |||||
chr11:603729
|
GTT | G | 6 | a0001c0001t0001g0156a0001c0001t0001g0197a0001c0001t0001g0244others(3): Show | 6 | HG01891.hp2 HG02083.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1153-1369_1153-136 others(6): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr11 | 603729 | |||||
chr11:603776
|
T | C | 64 | a0001c0003t0002g0015a0001c0003t0002g0017a0001c0003t0002g0020others(61): Show | 66 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.1153-1343T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 603776 | ||||||
chr11:603819
|
C | T | 1 | a0001c0003t0002g0029 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1153-1300C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 603819 | ||||||
chr11:603822
|
C | T | 4 | a0001c0014t0001g0144a0001c0014t0001g0262a0001c0014t0001g0263others(1): Show | 4 | HG01943.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153-1297C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 603822 | ||||||
chr11:604029
|
T | G | 43 | a0001c0001t0001g0162a0001c0001t0001g0202a0001c0001t0001g0213others(40): Show | 46 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.1153-1090T>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 604029 | ||||||
chr11:604040
|
G | A | 13 | a0001c0001t0001g0230a0002c0002t0001g0002a0002c0002t0001g0066others(10): Show | 15 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.1153-1079G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 604040 | ||||||
chr11:604257
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1153-862G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 604257 | ||||||
chr11:604344
|
A | G | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1153-775A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 604344 | ||||||
chr11:604438
|
G | T | 1 | a0001c0001t0001g0159 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1153-681G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 604438 | ||||||
chr11:604663
|
C | T | 6 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(3): Show | 6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1153-456C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 604663 | ||||||
chr11:604900
|
C | T | 2 | a0001c0001t0001g0091a0001c0001t0001g0130 | 2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1153-219C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 604900 | ||||||
chr11:604941
|
G | A | 11 | a0001c0003t0002g0017a0001c0003t0002g0022a0001c0003t0002g0027others(8): Show | 11 | HG01074.hp2 HG01123.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.1153-178G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 604941 | ||||||
chr11:604978
|
A | C | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1153-141A>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 604978 | ||||||
chr11:605108
|
A | G | 2 | a0002c0002t0001g0085a0002c0002t0001g0086 | 2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1153-11A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 10/17 | chr11 | 605108 | ||||||
chr11:605393
|
G | A | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1334+93G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 11/17 | chr11 | 605393 | ||||||
chr11:605767
|
T | C | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1454+43T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | chr11 | 605767 | ||||||
chr11:605856
|
T | C | 208 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0060others(205): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1454+132T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | chr11 | 605856 | ||||||
chr11:605857
|
G | A | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1454+133G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | chr11 | 605857 | ||||||
chr11:605915
|
A | G | 1 | a0013c0022t0008g0123 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1454+191A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | chr11 | 605915 | ||||||
chr11:605999
|
C | T | 13 | a0005c0007t0001g0089a0005c0007t0001g0127a0005c0007t0001g0128others(10): Show | 13 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.1454+275C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | chr11 | 605999 | ||||||
chr11:606089
|
G | A | 1 | a0002c0002t0001g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1455-353G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | chr11 | 606089 | ||||||
chr11:606156
|
C | T | 12 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1455-286C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | chr11 | 606156 | ||||||
chr11:606224
|
G | C | 26 | a0001c0001t0001g0142a0001c0001t0001g0229a0003c0004t0003g0025others(23): Show | 26 | HG00639.hp2 HG01106.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.1455-218G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | chr11 | 606224 | ||||||
chr11:606245
|
GCTCC | G | 26 | a0001c0001t0001g0142a0001c0001t0001g0229a0003c0004t0003g0025others(23): Show | 26 | HG00639.hp2 HG01106.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.1455-181_1455-178d others(6): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr11 | 606245 | |||||
chr11:606294
|
C | T | 20 | a0001c0001t0001g0142a0001c0001t0001g0229a0003c0004t0003g0025others(17): Show | 20 | HG00639.hp2 HG01106.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.1455-148C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | chr11 | 606294 | ||||||
chr11:606359
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0143 | 2 | HG00741.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1455-83C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | chr11 | 606359 | ||||||
chr11:606360
|
G | A | 1 | a0016c0020t0009g0249 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1455-82G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | chr11 | 606360 | ||||||
chr11:606399
|
C | T | 24 | a0003c0004t0003g0025a0003c0004t0003g0083a0003c0004t0003g0084others(21): Show | 24 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1455-43C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 12/17 | chr11 | 606399 | ||||||
chr11:606607
|
T | C | 24 | a0003c0004t0003g0025a0003c0004t0003g0083a0003c0004t0003g0084others(21): Show | 24 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1609+11T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 13/17 | chr11 | 606607 | ||||||
chr11:606629
|
T | A | 1 | a0002c0002t0001g0255 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1609+33T>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 13/17 | chr11 | 606629 | ||||||
chr11:606656
|
G | C | 208 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0060others(205): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1609+60G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 13/17 | chr11 | 606656 | ||||||
chr11:606749
|
G | A | 59 | a0001c0003t0002g0015a0001c0003t0002g0017a0001c0003t0002g0020others(56): Show | 61 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.1609+153G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 13/17 | chr11 | 606749 | ||||||
chr11:606770
|
C | T | 11 | a0001c0003t0002g0017a0001c0003t0002g0022a0001c0003t0002g0027others(8): Show | 11 | HG01074.hp2 HG01123.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.1609+174C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 13/17 | chr11 | 606770 | ||||||
chr11:606850
|
C | T | 1 | a0001c0003t0005g0044 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1610-216C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 13/17 | chr11 | 606850 | ||||||
chr11:606974
|
C | G | 3 | a0004c0005t0002g0031a0004c0005t0002g0034a0004c0005t0002g0041 | 3 | HG01346.hp2 HG01928.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.1610-92C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 13/17 | chr11 | 606974 | ||||||
chr11:607050
|
C | A | 3 | a0004c0005t0002g0031a0004c0005t0002g0034a0004c0005t0002g0041 | 3 | HG01346.hp2 HG01928.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.1610-16C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 13/17 | chr11 | 607050 | ||||||
chr11:609728
|
G | C | 3 | a0001c0006t0002g0019a0001c0006t0002g0021a0001c0006t0002g0036 | 3 | HG02486.hp2 HG02723.hp2 HG03139.hp1 |
splice_region_variant&intron_variant | LOW | c.4264+8G>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | chr11 | 609728 | ||||||
chr11:609729
|
T | TGCCCCGG others(73): Show |
1 | a0001c0001t0001g0210 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.4264+19_4264+98dup others(80): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr11 | 609729 | |||||
chr11:609739
|
C | CCCACCGA others(73): Show |
5 | a0001c0001t0001g0147a0001c0001t0001g0197a0001c0001t0001g0198others(2): Show | 5 | NA18948.hp2 NA18963.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.4264+40_4264+119du others(81): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr11 | 609739 | |||||
chr11:609760
|
A | AGTGAGTA others(113): Show |
2 | a0018c0029t0001g0217a0025c0038t0001g0181 | 2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.4264+128_4264+129i others(122): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr11 | 609760 | |||||
chr11:609760
|
A | C | 1 | a0013c0022t0008g0123 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.4264+40A>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | chr11 | 609760 | ||||||
chr11:609760
|
AGTGAGTA others(73): Show |
A | 1 | a0009c0012t0003g0067 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4264+48_4264+127de others(81): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr11 | 609760 | |||||
chr11:609768
|
A | G | 1 | a0013c0022t0008g0123 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.4264+48A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | chr11 | 609768 | ||||||
chr11:609769
|
G | T | 1 | a0013c0022t0008g0123 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.4264+49G>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | chr11 | 609769 | ||||||
chr11:609774
|
T | C | 1 | a0013c0022t0008g0123 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.4264+54T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | chr11 | 609774 | ||||||
chr11:609782
|
G | A | 1 | a0013c0022t0008g0123 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.4264+62G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | chr11 | 609782 | ||||||
chr11:609782
|
GCCGAGGA others(33): Show |
G | 22 | a0002c0002t0001g0059a0002c0002t0001g0194a0002c0002t0001g0246others(19): Show | 22 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.4264+88_4264+127de others(41): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr11 | 609782 | |||||
chr11:609800
|
C | A | 1 | a0013c0022t0008g0123 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.4264+80C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | chr11 | 609800 | ||||||
chr11:609808
|
A | G | 3 | a0003c0004t0003g0190a0003c0004t0003g0222a0003c0004t0003g0269 | 3 | HG01346.hp1 HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.4264+88A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | chr11 | 609808 | ||||||
chr11:609822
|
A | ACCGAGGA others(33): Show |
3 | a0011c0016t0001g0069a0011c0016t0001g0087a0024c0037t0001g0125 | 3 | HG02257.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4264+138_4264+139i others(42): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr11 | 609822 | |||||
chr11:609888
|
T | C | 99 | a0001c0001t0001g0149a0001c0001t0001g0207a0001c0001t0001g0259others(96): Show | 101 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.4264+168T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | chr11 | 609888 | ||||||
chr11:609930
|
G | A | 1 | a0023c0036t0001g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4264+210G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | chr11 | 609930 | ||||||
chr11:610124
|
T | C | 1 | a0005c0007t0001g0252 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4265-72T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 14/17 | chr11 | 610124 | ||||||
chr11:610448
|
G | A | 1 | a0004c0005t0002g0031 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.4417-53G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 15/17 | chr11 | 610448 | ||||||
chr11:610450
|
A | G | 2 | a0005c0007t0001g0127a0017c0028t0001g0129 | 2 | HG03710.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.4417-51A>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 15/17 | chr11 | 610450 | ||||||
chr11:610840
|
C | T | 3 | a0011c0016t0001g0069a0011c0016t0001g0087a0024c0037t0001g0125 | 3 | HG02257.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4677+79C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 16/17 | chr11 | 610840 | ||||||
chr11:611132
|
G | A | 2 | a0018c0029t0001g0217a0025c0038t0001g0181 | 2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.4806+50G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 17/17 | chr11 | 611132 | ||||||
chr11:611138
|
G | A | 3 | a0011c0016t0001g0069a0011c0016t0001g0087a0024c0037t0001g0125 | 3 | HG02257.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4806+56G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 17/17 | chr11 | 611138 | ||||||
chr11:611184
|
G | A | 3 | a0001c0006t0002g0019a0001c0006t0002g0021a0001c0006t0002g0036 | 3 | HG02486.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4806+102G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 17/17 | chr11 | 611184 | ||||||
chr11:611256
|
C | A | 1 | a0002c0002t0001g0086 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4806+174C>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 17/17 | chr11 | 611256 | ||||||
chr11:611419
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4807-215G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 17/17 | chr11 | 611419 | ||||||
chr11:611499
|
C | T | 1 | a0003c0004t0003g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4807-135C>T | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 17/17 | chr11 | 611499 | ||||||
chr11:611503
|
G | A | 84 | a0001c0003t0002g0015a0001c0003t0002g0017a0001c0003t0002g0020others(81): Show | 86 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.4807-131G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 17/17 | chr11 | 611503 | ||||||
chr11:611513
|
G | A | 2 | a0003c0004t0003g0174a0003c0004t0003g0175 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.4807-121G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 17/17 | chr11 | 611513 | ||||||
chr11:611531
|
G | A | 60 | a0001c0003t0002g0015a0001c0003t0002g0017a0001c0003t0002g0020others(57): Show | 62 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.4807-103G>A | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 17/17 | chr11 | 611531 | ||||||
chr11:611558
|
C | G | 1 | a0001c0001t0001g0211 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.4807-76C>G | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 17/17 | chr11 | 611558 | ||||||
chr11:611617
|
T | C | 6 | a0006c0008t0004g0080a0006c0008t0004g0081a0006c0008t0004g0121others(3): Show | 6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.4807-17T>C | PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 17/17 | chr11 | 611617 |