geneid | 57649 |
---|---|
ensemblid | ENSG00000109118.14 |
hgncid | 20816 |
symbol | PHF12 |
name | PHD finger protein 12 |
refseq_nuc | NM_001033561.2 |
refseq_prot | NP_001028733.1 |
ensembl_nuc | ENST00000332830.9 |
ensembl_prot | ENSP00000329933.4 |
mane_status | MANE Select |
chr | chr17 |
start | 28905250 |
end | 28951518 |
strand | - |
ver | v1.2 |
region | chr17:28905250-28951518 |
region5000 | chr17:28900250-28956518 |
regionname0 | PHF12_chr17_28905250_28951518 |
regionname5000 | PHF12_chr17_28900250_28956518 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1004 | 226 | 75 | 43 | 70 | 8 | 28 | 54 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0002 | 0/0 | 1004 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0003 | 0/0 | 1004 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0004 | 0/0 | 1004 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0005 | 0/0 | 1004 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 3015 | 218 | 73 | 42 | 69 | 8 | 24 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
c0002 | 0/0 | 3015 | 4 | 0 | 0 | 0 | 0 | 4 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
c0003 | 0/0 | 3015 | 2 | 0 | 2 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
c0004 | 0/0 | 3015 | 2 | 2 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
c0005 | 0/0 | 3015 | 2 | 2 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
c0006 | 0/0 | 3015 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
c0007 | 0/0 | 3015 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
c0008 | 0/0 | 3015 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
c0009 | 0/0 | 3015 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1492 | 224 | 74 | 46 | 68 | 8 | 26 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
t0002 | 0/0 | 1492 | 2 | 2 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
t0003 | 0/0 | 1492 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
t0004 | 0/0 | 1492 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
t0005 | 0/0 | 1492 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
t0006 | 0/0 | 1492 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
t0007 | 0/0 | 1492 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
t0008 | 0/0 | 1492 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 9 | 0 | 1 | 6 | 0 | 2 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0002 | 0/0 | 5 | 1 | 1 | 1 | 1 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0005 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0006 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0118 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 3015 | 218 | 73 | 42 | 69 | 8 | 24 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0001c0002 | 0/0 | 3015 | 4 | 0 | 0 | 0 | 0 | 4 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0001c0005 | 0/0 | 3015 | 2 | 2 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0001c0007 | 0/0 | 3015 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0001c0009 | 0/0 | 3015 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0002c0003 | 0/0 | 3015 | 2 | 0 | 2 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0003c0004 | 0/0 | 3015 | 2 | 2 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0004c0006 | 0/0 | 3015 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0005c0008 | 0/0 | 3015 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4506 | 211 | 69 | 42 | 67 | 8 | 23 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0001c0001t0002 | 0/0 | 4506 | 2 | 2 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0001c0001t0004 | 0/0 | 4506 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0001c0001t0005 | 0/0 | 4506 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0001c0001t0006 | 0/0 | 4506 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0001c0001t0007 | 0/0 | 4506 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0001c0001t0008 | 0/0 | 4506 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0001c0002t0001 | 0/0 | 4506 | 3 | 0 | 0 | 0 | 0 | 3 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0001c0002t0003 | 0/0 | 4506 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0001c0005t0001 | 0/0 | 4506 | 2 | 2 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0001c0007t0001 | 0/0 | 4506 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0001c0009t0001 | 0/0 | 4506 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0002c0003t0001 | 0/0 | 4506 | 2 | 0 | 2 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0003c0004t0001 | 0/0 | 4506 | 2 | 2 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0004c0006t0001 | 0/0 | 4506 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
a0005c0008t0001 | 0/0 | 4506 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | copy fasta | chr17 | 28900250 | 28956518 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 9 | 0 | 1 | 6 | 0 | 2 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0002 | 0/0 | 5 | 1 | 1 | 1 | 1 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0006 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0118 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0005g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0006g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0007g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0001t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0005t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0005t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0007t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0001c0009t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0002c0003t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0002c0003t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0003c0004t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0003c0004t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0004c0006t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
a0005c0008t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0168 | EUR | GBR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | GBR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG00639 | hp2 | a0002 | c0003 | t0001 | g0167 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG00673 | hp1 | a0001 | c0009 | t0001 | g0190 | EAS | CHS | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01192 | hp2 | a0001 | c0007 | t0001 | g0042 | AMR | PUR | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01261 | hp1 | a0002 | c0003 | t0001 | g0104 | AMR | CLM | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | IBS | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | IBS | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01891 | hp1 | a0001 | c0005 | t0001 | g0082 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CDX | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CDX | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02273 | hp2 | a0004 | c0006 | t0001 | g0164 | AMR | PEL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02451 | hp1 | a0001 | c0001 | t0008 | g0196 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02615 | hp1 | a0001 | c0001 | t0007 | g0195 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0144 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02738 | hp2 | a0001 | c0002 | t0003 | g0023 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02976 | hp2 | a0005 | c0008 | t0001 | g0033 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0062 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03130 | hp1 | a0003 | c0004 | t0001 | g0074 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03209 | hp1 | a0001 | c0005 | t0001 | g0081 | AFR | MSL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03239 | hp1 | a0001 | c0001 | t0005 | g0025 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | STU | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0145 | SAS | BEB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | STU | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | STU | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | YRI | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | YRI | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | YRI | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18974 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18974 | hp2 | a0001 | c0001 | t0006 | g0140 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA19240 | hp2 | a0003 | c0004 | t0001 | g0073 | AFR | YRI | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | TSI | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0051 | EUR | TSI | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | TSI | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | GIH | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | USA | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | USA | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | USA | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | LWK | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0058 | REF | REF | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0118 | REF | REF | PHF12_chr17_28900250_28956518 | PHF12 | chr17 | 28900250 | 28956518 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:28906897
|
G | A | 1 | a0004 | 1 | HG02273.hp2 | missense_variant | MODERATE | c.2639C>T | p.Thr880Ile | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 14/15 | 3197/4506 | 2639/3015 | 880/1004 | chr17 | 28906897 | ||
chr17:28911117
|
T | C | 1 | a0002 | 2 | HG00639.hp2 HG01261.hp1 |
missense_variant | MODERATE | c.2210A>G | p.Asn737Ser | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 10/15 | 2768/4506 | 2210/3015 | 737/1004 | chr17 | 28911117 | ||
chr17:28913986
|
G | A | 1 | a0003 | 2 | HG03130.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.1186C>T | p.Pro396Ser | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 8/15 | 1744/4506 | 1186/3015 | 396/1004 | chr17 | 28913986 | ||
chr17:28923938
|
T | C | 1 | a0005 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.686A>G | p.Asn229Ser | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/15 | 1244/4506 | 686/3015 | 229/1004 | chr17 | 28923938 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:28912612
|
C | T | 1 | a0001c0002 | 4 | HG02698.hp2 HG02738.hp2 HG03017.hp1 others(1): Show |
synonymous_variant | LOW | c.1959G>A | p.Pro653Pro | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 9/15 | 2517/4506 | 1959/3015 | 653/1004 | chr17 | 28912612 | ||
chr17:28921696
|
C | A | 1 | a0001c0007 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.828G>T | p.Thr276Thr | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/15 | 1386/4506 | 828/3015 | 276/1004 | chr17 | 28921696 | ||
chr17:28924114
|
G | A | 1 | a0001c0005 | 2 | HG01891.hp1 HG03209.hp1 |
synonymous_variant | LOW | c.510C>T | p.Ser170Ser | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/15 | 1068/4506 | 510/3015 | 170/1004 | chr17 | 28924114 | ||
chr17:28950223
|
G | A | 1 | a0001c0009 | 1 | HG00673.hp1 | synonymous_variant | LOW | c.90C>T | p.Pro30Pro | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/15 | 648/4506 | 90/3015 | 30/1004 | chr17 | 28950223 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:28905441
|
T | C | 1 | a0001c0001t0006 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*742A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 15/15 | 742 | chr17 | 28905441 | |||||
chr17:28951029
|
G | A | 1 | a0001c0001t0007 | 1 | HG02615.hp1 | 5_prime_UTR_variant | MODIFIER | c.-69C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 1/15 | 69 | chr17 | 28951029 | |||||
chr17:28951039
|
C | G | 1 | a0001c0001t0002 | 2 | HG02630.hp1 HG02896.hp1 |
5_prime_UTR_variant | MODIFIER | c.-79G>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 1/15 | 79 | chr17 | 28951039 | |||||
chr17:28951244
|
C | T | 1 | a0001c0001t0005 | 1 | HG03239.hp1 | 5_prime_UTR_variant | MODIFIER | c.-284G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 1/15 | 284 | chr17 | 28951244 | |||||
chr17:28951267
|
G | A | 1 | a0001c0001t0008 | 1 | HG02451.hp1 | 5_prime_UTR_variant | MODIFIER | c.-307C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 1/15 | 307 | chr17 | 28951267 | |||||
chr17:28951395
|
G | T | 1 | a0001c0001t0004 | 1 | NA18974.hp1 | 5_prime_UTR_variant | MODIFIER | c.-435C>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 1/15 | 435 | chr17 | 28951395 | |||||
chr17:28951474
|
G | T | 1 | a0001c0002t0003 | 1 | HG02738.hp2 | 5_prime_UTR_variant | MODIFIER | c.-514C>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 1/15 | 514 | chr17 | 28951474 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:28907285
|
C | A | 1 | a0001c0001t0001g0044 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2542-291G>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 13/14 | chr17 | 28907285 | ||||||
chr17:28907489
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2541+101G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 13/14 | chr17 | 28907489 | ||||||
chr17:28907813
|
C | T | 3 | a0001c0001t0001g0137a0001c0001t0001g0141a0001c0001t0001g0166 | 3 | NA19056.hp1 NA19087.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2459-141G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 12/14 | chr17 | 28907813 | ||||||
chr17:28907972
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2459-300C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 12/14 | chr17 | 28907972 | ||||||
chr17:28907974
|
G | T | 1 | a0001c0001t0001g0119 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2459-302C>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 12/14 | chr17 | 28907974 | ||||||
chr17:28908123
|
C | G | 1 | a0001c0001t0001g0037 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2459-451G>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 12/14 | chr17 | 28908123 | ||||||
chr17:28908181
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2459-509T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 12/14 | chr17 | 28908181 | ||||||
chr17:28908232
|
T | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0064 | 3 | HG02559.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2458+551A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 12/14 | chr17 | 28908232 | ||||||
chr17:28908962
|
T | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0064 | 3 | HG02559.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2360-81A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 11/14 | chr17 | 28908962 | ||||||
chr17:28909358
|
A | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.2360-477T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 11/14 | chr17 | 28909358 | ||||||
chr17:28909417
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2360-536C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 11/14 | chr17 | 28909417 | ||||||
chr17:28910119
|
G | A | 2 | a0001c0001t0001g0075a0001c0001t0001g0087 | 2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2359+107C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 11/14 | chr17 | 28910119 | ||||||
chr17:28910567
|
A | G | 1 | a0001c0002t0001g0145 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2216-198T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 10/14 | chr17 | 28910567 | ||||||
chr17:28910633
|
G | A | 2 | a0003c0004t0001g0073a0003c0004t0001g0074 | 2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2216-264C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 10/14 | chr17 | 28910633 | ||||||
chr17:28910660
|
CTGTGGGG others(11): Show |
C | 6 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(3): Show | 6 | HG02280.hp1 HG02818.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2216-309_2216-292d others(20): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 10/14 | chr17 | 28910660 | ||||||
chr17:28911057
|
G | A | 31 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0071others(28): Show | 31 | HG00408.hp2 HG01069.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.2215+55C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 10/14 | chr17 | 28911057 | ||||||
chr17:28911082
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2215+30G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 10/14 | chr17 | 28911082 | ||||||
chr17:28911813
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2090-576C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 9/14 | chr17 | 28911813 | ||||||
chr17:28911838
|
C | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2090-601G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 9/14 | chr17 | 28911838 | ||||||
chr17:28912358
|
G | C | 40 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(37): Show | 55 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.2089+124C>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 9/14 | chr17 | 28912358 | ||||||
chr17:28913325
|
G | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1294-48C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 8/14 | chr17 | 28913325 | ||||||
chr17:28913363
|
T | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1294-86A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 8/14 | chr17 | 28913363 | ||||||
chr17:28913390
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0174 | 4 | HG01069.hp2 HG01071.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1294-113A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 8/14 | chr17 | 28913390 | ||||||
chr17:28913556
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1294-279A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 8/14 | chr17 | 28913556 | ||||||
chr17:28913563
|
G | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1294-286C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 8/14 | chr17 | 28913563 | ||||||
chr17:28913573
|
G | C | 1 | a0001c0001t0001g0105 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1294-296C>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 8/14 | chr17 | 28913573 | ||||||
chr17:28914064
|
G | T | 1 | a0001c0001t0001g0032 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1135-27C>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914064 | ||||||
chr17:28914438
|
C | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1135-401G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914438 | ||||||
chr17:28914589
|
A | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1135-552T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914589 | ||||||
chr17:28914671
|
C | CA | 54 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0019others(51): Show | 59 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.1135-635dupT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914671 | ||||||
chr17:28914671
|
C | CAA | 19 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0030others(16): Show | 22 | HG00408.hp2 HG01069.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1135-636_1135-635d others(4): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914671 | ||||||
chr17:28914671
|
C | CAAA | 12 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0001g0038others(9): Show | 13 | HG02055.hp1 HG02293.hp2 HG02735.hp2 others(10): Show |
intron_variant | MODIFIER | c.1135-637_1135-635d others(5): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914671 | ||||||
chr17:28914671
|
C | CAAAA | 17 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0028others(14): Show | 26 | HG00544.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.1135-638_1135-635d others(6): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914671 | ||||||
chr17:28914671
|
C | CAAAAA | 12 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0050others(9): Show | 15 | HG00408.hp1 HG01106.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.1135-639_1135-635d others(7): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914671 | ||||||
chr17:28914671
|
C | CAAAAAA | 11 | a0001c0001t0001g0011a0001c0001t0001g0045a0001c0001t0001g0047others(8): Show | 12 | HG00673.hp1 HG02257.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1135-640_1135-635d others(8): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914671 | ||||||
chr17:28914671
|
C | CAAAAAAA others(1): Show |
6 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0068others(3): Show | 9 | HG01109.hp1 HG01891.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.1135-642_1135-635d others(10): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914671 | ||||||
chr17:28914671
|
C | CAAAAAAA others(2): Show |
5 | a0001c0001t0001g0013a0001c0001t0001g0048a0001c0001t0001g0054others(2): Show | 6 | HG01346.hp1 HG02293.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1135-643_1135-635d others(11): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914671 | ||||||
chr17:28914671
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0138 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1135-644_1135-635d others(12): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914671 | ||||||
chr17:28914671
|
CAAA | C | 5 | a0001c0001t0001g0037a0001c0001t0001g0109a0001c0001t0001g0111others(2): Show | 5 | HG02280.hp1 HG03225.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1135-637_1135-635d others(5): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914671 | ||||||
chr17:28914703
|
T | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0125 | 3 | HG00140.hp2 HG01175.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1135-666A>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914703 | ||||||
chr17:28914841
|
A | C | 1 | a0001c0001t0001g0079 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1135-804T>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28914841 | ||||||
chr17:28915071
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1135-1034A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28915071 | ||||||
chr17:28915071
|
T | G | 1 | a0001c0001t0001g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1135-1034A>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28915071 | ||||||
chr17:28915224
|
T | C | 1 | a0001c0001t0001g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1135-1187A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28915224 | ||||||
chr17:28915302
|
G | GA | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1135-1266dupT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28915302 | ||||||
chr17:28915343
|
G | A | 1 | a0004c0006t0001g0164 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1135-1306C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28915343 | ||||||
chr17:28915411
|
G | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG00673.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1135-1374C>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28915411 | ||||||
chr17:28915425
|
TGGA | T | 85 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 104 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.1135-1391_1135-138 others(7): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28915425 | ||||||
chr17:28915497
|
T | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1135-1460A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28915497 | ||||||
chr17:28915682
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1134+1603G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28915682 | ||||||
chr17:28915687
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1134+1598G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28915687 | ||||||
chr17:28915721
|
A | G | 3 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173 | 3 | HG02055.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1134+1564T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28915721 | ||||||
chr17:28915987
|
C | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0138 | 2 | HG01496.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1134+1298G>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28915987 | ||||||
chr17:28916175
|
G | T | 1 | a0001c0001t0001g0114 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1134+1110C>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28916175 | ||||||
chr17:28916398
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1134+887C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28916398 | ||||||
chr17:28916462
|
C | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(38): Show | 56 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(53): Show |
intron_variant | MODIFIER | c.1134+823G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28916462 | ||||||
chr17:28916637
|
G | C | 5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(2): Show | 5 | HG02486.hp1 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1134+648C>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28916637 | ||||||
chr17:28916719
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0135 | 2 | HG01361.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1134+566G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28916719 | ||||||
chr17:28916770
|
C | T | 3 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173 | 3 | HG02055.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1134+515G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28916770 | ||||||
chr17:28916803
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1134+482C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 7/14 | chr17 | 28916803 | ||||||
chr17:28917455
|
G | A | 40 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(37): Show | 55 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(52): Show |
splice_region_variant&intron_variant | LOW | c.970-6C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 6/14 | chr17 | 28917455 | ||||||
chr17:28917732
|
G | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.970-283C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 6/14 | chr17 | 28917732 | ||||||
chr17:28917934
|
G | A | 1 | a0001c0001t0001g0014 | 2 | HG01109.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.970-485C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 6/14 | chr17 | 28917934 | ||||||
chr17:28918300
|
T | C | 1 | a0001c0001t0001g0036 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.969+843A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 6/14 | chr17 | 28918300 | ||||||
chr17:28918301
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.969+842G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 6/14 | chr17 | 28918301 | ||||||
chr17:28918391
|
A | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG01433.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.969+752T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 6/14 | chr17 | 28918391 | ||||||
chr17:28918604
|
A | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.969+539T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 6/14 | chr17 | 28918604 | ||||||
chr17:28918721
|
T | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0163 | 2 | HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.969+422A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 6/14 | chr17 | 28918721 | ||||||
chr17:28919350
|
CCTCCCCT others(16): Show |
C | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 226 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.837-98_837-76delAA others(21): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28919350 | ||||||
chr17:28919445
|
T | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.837-170A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28919445 | ||||||
chr17:28919524
|
GGAGACT | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.837-255_837-250del others(6): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28919524 | ||||||
chr17:28919624
|
C | T | 9 | a0001c0001t0001g0006a0001c0001t0001g0103a0001c0001t0001g0171others(6): Show | 11 | HG01069.hp2 HG01071.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.837-349G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28919624 | ||||||
chr17:28919653
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.837-378A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28919653 | ||||||
chr17:28919664
|
T | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 167 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(164): Show |
intron_variant | MODIFIER | c.837-389A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28919664 | ||||||
chr17:28919847
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.837-572G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28919847 | ||||||
chr17:28919917
|
C | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | NA18960.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.837-642G>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28919917 | ||||||
chr17:28920216
|
A | G | 1 | a0001c0001t0001g0021 | 2 | HG00639.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.837-941T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28920216 | ||||||
chr17:28920665
|
T | G | 1 | a0001c0001t0001g0036 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.836+1023A>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28920665 | ||||||
chr17:28920674
|
T | G | 1 | a0001c0001t0001g0036 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.836+1014A>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28920674 | ||||||
chr17:28920936
|
C | T | 1 | a0001c0001t0001g0004 | 3 | HG02886.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.836+752G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28920936 | ||||||
chr17:28921050
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.836+638C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28921050 | ||||||
chr17:28921175
|
C | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.836+513G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28921175 | ||||||
chr17:28921462
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0163 | 2 | HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.836+226G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28921462 | ||||||
chr17:28921665
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.836+23G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 5/14 | chr17 | 28921665 | ||||||
chr17:28921842
|
T | A | 7 | a0001c0001t0001g0037a0001c0001t0001g0109a0001c0001t0001g0110others(4): Show | 7 | HG02280.hp1 HG02818.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.716-34A>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28921842 | ||||||
chr17:28922118
|
AATGTCCA others(4): Show |
A | 17 | a0001c0001t0001g0113a0001c0001t0001g0136a0001c0001t0001g0137others(14): Show | 17 | HG00408.hp1 HG00673.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.716-321_716-311del others(11): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28922118 | ||||||
chr17:28922214
|
T | G | 1 | a0001c0001t0001g0070 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.716-406A>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28922214 | ||||||
chr17:28922420
|
T | C | 7 | a0001c0001t0001g0037a0001c0001t0001g0109a0001c0001t0001g0110others(4): Show | 7 | HG02280.hp1 HG02818.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.716-612A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28922420 | ||||||
chr17:28922688
|
C | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0161a0001c0001t0001g0162 | 3 | HG01071.hp1 NA20752.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.716-880G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28922688 | ||||||
chr17:28922807
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.716-999C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28922807 | ||||||
chr17:28922854
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0127 | 2 | HG02559.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.716-1046C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28922854 | ||||||
chr17:28922937
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.715+972C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28922937 | ||||||
chr17:28922954
|
A | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(84): Show | 106 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.715+955T>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28922954 | ||||||
chr17:28923046
|
C | CA | 30 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0071others(27): Show | 30 | HG00408.hp2 HG01069.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.715+862dupT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923046 | ||||||
chr17:28923046
|
CA | C | 7 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(4): Show | 11 | HG01074.hp1 HG01109.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.715+862delT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923046 | ||||||
chr17:28923206
|
GAGA | G | 37 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(34): Show | 52 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.715+700_715+702del others(3): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923206 | ||||||
chr17:28923280
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.715+629C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923280 | ||||||
chr17:28923349
|
C | CT | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(188): Show | 227 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.715+559dupA | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923349 | ||||||
chr17:28923361
|
A | T | 1 | a0001c0001t0001g0121 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.715+548T>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923361 | ||||||
chr17:28923476
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.715+433C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923476 | ||||||
chr17:28923651
|
C | CAAAAAAA others(5): Show |
1 | a0003c0004t0001g0074 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.715+257_715+258ins others(12): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923651 | ||||||
chr17:28923651
|
C | CAAAAAAA others(8): Show |
2 | a0001c0005t0001g0081a0001c0005t0001g0082 | 2 | HG01891.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.715+257_715+258ins others(15): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923651 | ||||||
chr17:28923651
|
C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0034a0001c0001t0001g0078 | 2 | HG02615.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.715+257_715+258ins others(16): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923651 | ||||||
chr17:28923651
|
C | CAAAAAAA others(10): Show |
10 | a0001c0001t0001g0035a0001c0001t0001g0075a0001c0001t0001g0080others(7): Show | 10 | HG00408.hp2 HG02615.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.715+257_715+258ins others(17): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923651 | ||||||
chr17:28923651
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0098 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.715+257_715+258ins others(18): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923651 | ||||||
chr17:28923651
|
C | CAAAAAAA others(12): Show |
3 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0181 | 3 | HG01515.hp2 HG02572.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.715+257_715+258ins others(19): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923651 | ||||||
chr17:28923651
|
C | CAAAAAAA others(13): Show |
4 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0084others(1): Show | 4 | HG01069.hp1 HG01109.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.715+257_715+258ins others(20): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923651 | ||||||
chr17:28923651
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0099 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.715+257_715+258ins others(21): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923651 | ||||||
chr17:28923651
|
C | CAAAAAAA others(17): Show |
2 | a0001c0001t0001g0092a0001c0001t0001g0100 | 2 | HG02622.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.715+257_715+258ins others(24): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923651 | ||||||
chr17:28923651
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0085 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.715+257_715+258ins others(25): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923651 | ||||||
chr17:28923651
|
C | CAAAAAAA others(19): Show |
1 | a0001c0001t0001g0079 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.715+257_715+258ins others(26): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923651 | ||||||
chr17:28923653
|
C | A | 31 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0071others(28): Show | 31 | HG00408.hp2 HG01069.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.715+256G>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CA | 13 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0105others(10): Show | 14 | HG00621.hp1 HG01258.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.715+255dupT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAA | 19 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(16): Show | 30 | HG00544.hp2 HG00642.hp2 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.715+254_715+255dup others(2): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAA | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0061others(3): Show | 8 | HG01106.hp1 HG01952.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.715+253_715+255dup others(3): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAAAA | 10 | a0001c0001t0001g0006a0001c0001t0001g0040a0001c0001t0001g0113others(7): Show | 12 | HG00673.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.715+251_715+255dup others(5): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAAAAAA others(3): Show |
4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0178others(1): Show | 4 | HG01884.hp2 HG02922.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.715+246_715+255dup others(10): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0176a0001c0002t0001g0144a0001c0002t0001g0145 | 3 | HG02698.hp2 HG03139.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.715+245_715+255dup others(11): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAAAAAA others(5): Show |
1 | a0001c0002t0003g0023 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.715+244_715+255dup others(12): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0188 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.715+243_715+255dup others(13): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAAAAAA others(7): Show |
4 | a0001c0001t0001g0146a0001c0001t0001g0160a0001c0001t0001g0187others(1): Show | 4 | HG00621.hp2 HG01175.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.715+242_715+255dup others(14): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAAAAAA others(9): Show |
3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0147 | 3 | HG01258.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.715+240_715+255dup others(16): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAAAAAA others(10): Show |
4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0112others(1): Show | 4 | HG00733.hp1 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.715+239_715+255dup others(17): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0111 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.715+238_715+255dup others(18): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAAAAAA others(12): Show |
4 | a0001c0001t0001g0012a0001c0001t0001g0039a0001c0001t0001g0139others(1): Show | 5 | HG02451.hp2 HG03225.hp2 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.715+237_715+255dup others(19): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0064 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.715+236_715+255dup others(20): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAAAAAA others(14): Show |
4 | a0001c0001t0001g0008a0001c0001t0001g0041a0001c0001t0001g0048others(1): Show | 5 | HG01074.hp2 HG01168.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.715+235_715+255dup others(21): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.715+234_715+255dup others(22): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.715+255_715+256ins others(23): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAAAAAA others(17): Show |
1 | a0001c0001t0001g0149 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.715+255_715+256ins others(24): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAAAAAA others(19): Show |
5 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0106others(2): Show | 5 | HG01261.hp2 HG01433.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.715+255_715+256ins others(26): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAAAAAA others(20): Show |
2 | a0001c0001t0001g0163a0001c0001t0001g0172 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.715+255_715+256ins others(27): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAAAAAA others(21): Show |
2 | a0001c0001t0001g0077a0001c0001t0001g0173 | 2 | HG01515.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.715+255_715+256ins others(28): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAAAAAA others(24): Show |
3 | a0001c0001t0001g0134a0001c0001t0001g0136a0001c0001t0001g0152 | 3 | HG02630.hp2 NA18955.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.715+255_715+256ins others(31): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAAAAAA others(25): Show |
2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG00408.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.715+255_715+256ins others(32): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAAAAAA others(26): Show |
1 | a0001c0001t0002g0026 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.715+255_715+256ins others(33): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAAAAAA others(27): Show |
1 | a0001c0001t0001g0155 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.715+255_715+256ins others(34): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAAAAAA others(33): Show |
1 | a0001c0001t0002g0027 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.715+255_715+256ins others(40): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAAAAAA others(34): Show |
1 | a0001c0001t0001g0156 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.715+255_715+256ins others(41): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
C | CAAAAAAA others(35): Show |
1 | a0001c0001t0001g0157 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.715+255_715+256ins others(42): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28923653
|
CAAAAA | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.715+251_715+255del others(5): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 4/14 | chr17 | 28923653 | ||||||
chr17:28924452
|
G | T | 1 | a0001c0001t0001g0139 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.322-150C>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28924452 | ||||||
chr17:28924950
|
C | CA | 5 | a0001c0001t0001g0036a0001c0001t0001g0130a0001c0001t0001g0131others(2): Show | 5 | HG03195.hp1 NA19001.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.322-649dupT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28924950 | ||||||
chr17:28924950
|
C | CAAA | 4 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 8 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.322-651_322-649dup others(3): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28924950 | ||||||
chr17:28924950
|
CA | C | 68 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0045others(65): Show | 68 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.322-649delT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28924950 | ||||||
chr17:28925399
|
C | T | 7 | a0001c0001t0001g0076a0001c0001t0001g0079a0001c0001t0001g0083others(4): Show | 7 | HG01069.hp1 HG01109.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.322-1097G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28925399 | ||||||
chr17:28925694
|
G | A | 2 | a0001c0001t0001g0040a0001c0007t0001g0042 | 2 | HG01192.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.321+1297C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28925694 | ||||||
chr17:28925759
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.321+1232C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28925759 | ||||||
chr17:28925941
|
C | T | 1 | a0001c0001t0001g0021 | 2 | HG00639.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.321+1050G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28925941 | ||||||
chr17:28925971
|
C | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(39): Show | 57 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.321+1020G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28925971 | ||||||
chr17:28926343
|
C | CA | 3 | a0001c0001t0001g0019a0001c0001t0001g0116a0001c0001t0001g0132 | 4 | HG00544.hp1 NA18952.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.321+647dupT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28926343 | ||||||
chr17:28926460
|
C | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.321+531G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28926460 | ||||||
chr17:28926502
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.321+489T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28926502 | ||||||
chr17:28926719
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.321+272G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28926719 | ||||||
chr17:28926952
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.321+39G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 3/14 | chr17 | 28926952 | ||||||
chr17:28927161
|
C | T | 40 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(37): Show | 55 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.249-98G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28927161 | ||||||
chr17:28927323
|
G | C | 28 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0075others(25): Show | 28 | HG00408.hp2 HG01069.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.249-260C>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28927323 | ||||||
chr17:28927649
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.249-586G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28927649 | ||||||
chr17:28927734
|
T | A | 1 | a0001c0001t0001g0060 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.249-671A>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28927734 | ||||||
chr17:28927938
|
C | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(1): Show | 4 | HG03041.hp2 HG03225.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.249-875G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28927938 | ||||||
chr17:28928009
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.249-946C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28928009 | ||||||
chr17:28928173
|
T | C | 43 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(40): Show | 58 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.249-1110A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28928173 | ||||||
chr17:28928599
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.249-1536G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28928599 | ||||||
chr17:28928714
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.249-1651C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28928714 | ||||||
chr17:28928777
|
A | AAAAC | 5 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(2): Show | 9 | HG01109.hp1 HG01891.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.249-1718_249-1715d others(6): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28928777 | ||||||
chr17:28928845
|
C | G | 1 | a0001c0001t0001g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.249-1782G>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28928845 | ||||||
chr17:28929075
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.249-2012C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28929075 | ||||||
chr17:28929103
|
AAAC | A | 40 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(37): Show | 55 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.249-2043_249-2041d others(5): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28929103 | ||||||
chr17:28929176
|
C | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0132 | 2 | HG00544.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.249-2113G>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28929176 | ||||||
chr17:28929189
|
G | T | 1 | a0001c0001t0001g0180 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.249-2126C>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28929189 | ||||||
chr17:28929228
|
T | TA | 13 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(10): Show | 17 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.249-2166dupT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28929228 | ||||||
chr17:28930048
|
T | A | 1 | a0001c0001t0001g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.249-2985A>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28930048 | ||||||
chr17:28930345
|
C | CA | 2 | a0001c0001t0001g0088a0001c0001t0001g0093 | 2 | NA18986.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.249-3283dupT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28930345 | ||||||
chr17:28930460
|
G | C | 31 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0071others(28): Show | 31 | HG00408.hp2 HG01069.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.249-3397C>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28930460 | ||||||
chr17:28930667
|
A | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-3604T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28930667 | ||||||
chr17:28930699
|
T | TA | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-3637dupT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28930699 | ||||||
chr17:28930768
|
C | G | 2 | a0001c0001t0001g0047a0001c0001t0001g0063 | 2 | HG02257.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.249-3705G>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28930768 | ||||||
chr17:28930792
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.249-3729G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28930792 | ||||||
chr17:28930822
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.249-3759C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28930822 | ||||||
chr17:28930937
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0174 | 4 | HG01069.hp2 HG01071.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.249-3874G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28930937 | ||||||
chr17:28930943
|
GAGCCTAT | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | NA18960.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.249-3887_249-3881d others(9): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28930943 | ||||||
chr17:28931104
|
C | T | 80 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(77): Show | 99 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.249-4041G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28931104 | ||||||
chr17:28931128
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.249-4065G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28931128 | ||||||
chr17:28931214
|
C | T | 3 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173 | 3 | HG02055.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.249-4151G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28931214 | ||||||
chr17:28931256
|
C | CT | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01891.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-4194dupA | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28931256 | ||||||
chr17:28931256
|
CT | C | 107 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 125 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.249-4194delA | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28931256 | ||||||
chr17:28931288
|
C | T | 3 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173 | 3 | HG02055.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.249-4225G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28931288 | ||||||
chr17:28931501
|
C | T | 1 | a0001c0001t0001g0016 | 2 | HG00642.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.249-4438G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28931501 | ||||||
chr17:28931536
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.249-4473G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28931536 | ||||||
chr17:28931818
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.249-4755C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28931818 | ||||||
chr17:28931834
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.249-4771C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28931834 | ||||||
chr17:28932161
|
T | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-5098A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28932161 | ||||||
chr17:28932596
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.249-5533G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28932596 | ||||||
chr17:28932763
|
T | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-5700A>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28932763 | ||||||
chr17:28932927
|
C | CAGA | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(44): Show | 66 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(63): Show |
intron_variant | MODIFIER | c.249-5865_249-5864i others(5): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28932927 | ||||||
chr17:28932964
|
T | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(129): Show | 153 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.249-5901A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28932964 | ||||||
chr17:28932999
|
C | T | 46 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(43): Show | 65 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(62): Show |
intron_variant | MODIFIER | c.249-5936G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28932999 | ||||||
chr17:28933127
|
C | T | 37 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(34): Show | 52 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.249-6064G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28933127 | ||||||
chr17:28933638
|
C | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(76): Show | 98 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.249-6575G>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28933638 | ||||||
chr17:28933842
|
G | A | 1 | a0001c0001t0008g0196 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.249-6779C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28933842 | ||||||
chr17:28933917
|
T | G | 1 | a0001c0001t0001g0159 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.249-6854A>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28933917 | ||||||
chr17:28934005
|
C | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-6942G>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28934005 | ||||||
chr17:28934089
|
T | C | 1 | a0001c0001t0001g0058 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.249-7026A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28934089 | ||||||
chr17:28934092
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.249-7029T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28934092 | ||||||
chr17:28934458
|
T | C | 2 | a0001c0001t0002g0026a0001c0001t0002g0027 | 2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.249-7395A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28934458 | ||||||
chr17:28934609
|
TA | T | 2 | a0001c0005t0001g0081a0001c0005t0001g0082 | 2 | HG01891.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.249-7547delT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28934609 | ||||||
chr17:28934610
|
AT | A | 12 | a0001c0001t0001g0012a0001c0001t0001g0049a0001c0001t0001g0050others(9): Show | 13 | HG02559.hp1 HG02735.hp2 HG03041.hp1 others(10): Show |
intron_variant | MODIFIER | c.249-7548delA | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28934610 | ||||||
chr17:28934610
|
ATT | A | 41 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(38): Show | 59 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.249-7549_249-7548d others(4): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28934610 | ||||||
chr17:28934773
|
G | C | 1 | a0001c0001t0001g0160 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.249-7710C>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28934773 | ||||||
chr17:28934951
|
T | C | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0007g0195 | 3 | HG02615.hp1 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.249-7888A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28934951 | ||||||
chr17:28934978
|
C | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0193 | 3 | NA19003.hp2 NA19056.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.249-7915G>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28934978 | ||||||
chr17:28935122
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.249-8059T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28935122 | ||||||
chr17:28935134
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249-8071G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28935134 | ||||||
chr17:28935256
|
CTATTT | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-8198_249-8194d others(7): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28935256 | ||||||
chr17:28935335
|
G | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(22): Show | 38 | HG00544.hp2 HG00642.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.249-8272C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28935335 | ||||||
chr17:28935364
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.249-8301G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28935364 | ||||||
chr17:28935365
|
G | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0161a0001c0001t0001g0162 | 3 | HG01071.hp1 NA20752.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.249-8302C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28935365 | ||||||
chr17:28935428
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.249-8365G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28935428 | ||||||
chr17:28935455
|
A | G | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02155.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.249-8392T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28935455 | ||||||
chr17:28935583
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG01433.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.249-8520A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28935583 | ||||||
chr17:28935891
|
A | G | 2 | a0003c0004t0001g0073a0003c0004t0001g0074 | 2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.249-8828T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28935891 | ||||||
chr17:28936044
|
T | C | 2 | a0001c0001t0002g0026a0001c0001t0002g0027 | 2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.249-8981A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28936044 | ||||||
chr17:28936085
|
T | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-9022A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28936085 | ||||||
chr17:28936101
|
C | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-9038G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28936101 | ||||||
chr17:28936147
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.249-9084C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28936147 | ||||||
chr17:28936877
|
TA | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-9815delT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28936877 | ||||||
chr17:28936923
|
C | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-9860G>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28936923 | ||||||
chr17:28937075
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.249-10012G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28937075 | ||||||
chr17:28937453
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.249-10390A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28937453 | ||||||
chr17:28937609
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.249-10546T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28937609 | ||||||
chr17:28937844
|
T | C | 4 | a0001c0001t0001g0094a0001c0001t0001g0165a0001c0001t0001g0169others(1): Show | 4 | HG02273.hp2 HG02300.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.249-10781A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28937844 | ||||||
chr17:28938048
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.249-10985A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28938048 | ||||||
chr17:28938400
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.249-11337A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28938400 | ||||||
chr17:28938952
|
G | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.248+11113C>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28938952 | ||||||
chr17:28939125
|
G | A | 40 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(37): Show | 55 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.248+10940C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28939125 | ||||||
chr17:28939314
|
C | G | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.248+10751G>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28939314 | ||||||
chr17:28939422
|
C | T | 46 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(43): Show | 65 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(62): Show |
intron_variant | MODIFIER | c.248+10643G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28939422 | ||||||
chr17:28939716
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.248+10349C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28939716 | ||||||
chr17:28940067
|
T | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.248+9998A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28940067 | ||||||
chr17:28940157
|
A | C | 1 | a0001c0001t0008g0196 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.248+9908T>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28940157 | ||||||
chr17:28940314
|
C | A | 1 | a0001c0001t0001g0112 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.248+9751G>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28940314 | ||||||
chr17:28940490
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.248+9575T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28940490 | ||||||
chr17:28940855
|
C | T | 3 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173 | 3 | HG02055.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.248+9210G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28940855 | ||||||
chr17:28941039
|
C | CT | 45 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(42): Show | 49 | HG00408.hp2 HG01069.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.248+9025dupA | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28941039 | ||||||
chr17:28941039
|
CT | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(35): Show | 53 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.248+9025delA | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28941039 | ||||||
chr17:28941319
|
T | G | 1 | a0002c0003t0001g0167 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.248+8746A>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28941319 | ||||||
chr17:28941495
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0168 | 3 | HG00140.hp1 HG01175.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.248+8570C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28941495 | ||||||
chr17:28941580
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.248+8485A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28941580 | ||||||
chr17:28941779
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.248+8286C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28941779 | ||||||
chr17:28941859
|
G | A | 1 | a0001c0001t0001g0021 | 2 | HG00639.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.248+8206C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28941859 | ||||||
chr17:28941919
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.248+8146G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28941919 | ||||||
chr17:28942546
|
G | A | 1 | a0001c0002t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.248+7519C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28942546 | ||||||
chr17:28942577
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.248+7488G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28942577 | ||||||
chr17:28942703
|
C | A | 1 | a0001c0001t0001g0170 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.248+7362G>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28942703 | ||||||
chr17:28942752
|
G | A | 3 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173 | 3 | HG02055.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.248+7313C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28942752 | ||||||
chr17:28942864
|
G | A | 1 | a0001c0001t0001g0004 | 3 | HG02886.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.248+7201C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28942864 | ||||||
chr17:28943122
|
G | A | 1 | a0005c0008t0001g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.248+6943C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28943122 | ||||||
chr17:28943278
|
C | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.248+6787G>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28943278 | ||||||
chr17:28943503
|
A | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.248+6562T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28943503 | ||||||
chr17:28943612
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.248+6453C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28943612 | ||||||
chr17:28943636
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.248+6429A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28943636 | ||||||
chr17:28943636
|
T | TAAAC | 46 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(43): Show | 65 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(62): Show |
intron_variant | MODIFIER | c.248+6425_248+6428d others(6): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28943636 | ||||||
chr17:28943636
|
TAAAC | T | 5 | a0001c0001t0001g0075a0001c0001t0001g0105a0001c0001t0001g0106others(2): Show | 5 | HG03130.hp1 HG03130.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.248+6425_248+6428d others(6): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28943636 | ||||||
chr17:28943699
|
CACA | C | 3 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0007t0001g0042 | 3 | HG01192.hp2 HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.248+6363_248+6365d others(5): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28943699 | ||||||
chr17:28943774
|
T | TA | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(44): Show | 66 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(63): Show |
intron_variant | MODIFIER | c.248+6290_248+6291i others(3): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28943774 | ||||||
chr17:28944203
|
C | T | 1 | a0002c0003t0001g0104 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.248+5862G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28944203 | ||||||
chr17:28944438
|
C | G | 1 | a0001c0001t0001g0043 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.248+5627G>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28944438 | ||||||
chr17:28944787
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0174 | 4 | HG01069.hp2 HG01071.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.248+5278C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28944787 | ||||||
chr17:28944830
|
T | G | 1 | a0001c0001t0001g0175 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.248+5235A>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28944830 | ||||||
chr17:28945088
|
A | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.248+4977T>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28945088 | ||||||
chr17:28945190
|
T | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0064 | 3 | HG02559.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.248+4875A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28945190 | ||||||
chr17:28945314
|
G | C | 1 | a0001c0001t0001g0070 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.248+4751C>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28945314 | ||||||
chr17:28945680
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.248+4385G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28945680 | ||||||
chr17:28945780
|
G | T | 1 | a0001c0001t0001g0029 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.248+4285C>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28945780 | ||||||
chr17:28945857
|
C | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(38): Show | 56 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(53): Show |
intron_variant | MODIFIER | c.248+4208G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28945857 | ||||||
chr17:28946094
|
T | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.248+3971A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28946094 | ||||||
chr17:28946106
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.248+3959A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28946106 | ||||||
chr17:28946107
|
C | T | 2 | a0001c0001t0001g0040a0001c0007t0001g0042 | 2 | HG01192.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.248+3958G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28946107 | ||||||
chr17:28946322
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.248+3743G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28946322 | ||||||
chr17:28946923
|
AG | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0007g0195 | 3 | HG02615.hp1 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.248+3141delC | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28946923 | ||||||
chr17:28947210
|
T | G | 1 | a0001c0001t0001g0177 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.248+2855A>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28947210 | ||||||
chr17:28947294
|
G | T | 1 | a0001c0001t0001g0041 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.248+2771C>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28947294 | ||||||
chr17:28947475
|
G | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | HG00642.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.248+2590C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28947475 | ||||||
chr17:28947492
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.248+2573G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28947492 | ||||||
chr17:28947611
|
A | C | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.248+2454T>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28947611 | ||||||
chr17:28947887
|
C | CA | 25 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0067others(22): Show | 25 | HG00408.hp2 HG01069.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.248+2177dupT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28947887 | ||||||
chr17:28947887
|
C | CAA | 6 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.248+2176_248+2177d others(4): Show |
PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28947887 | ||||||
chr17:28947887
|
CA | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(8): Show | 16 | HG01071.hp1 HG01109.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.248+2177delT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28947887 | ||||||
chr17:28947967
|
T | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.248+2098A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28947967 | ||||||
chr17:28948102
|
T | C | 1 | a0001c0001t0001g0036 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.248+1963A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28948102 | ||||||
chr17:28948213
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.248+1852A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28948213 | ||||||
chr17:28948291
|
T | TA | 6 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 10 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.248+1773dupT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28948291 | ||||||
chr17:28948378
|
G | A | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01258.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.248+1687C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28948378 | ||||||
chr17:28948580
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.248+1485C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28948580 | ||||||
chr17:28948603
|
T | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(44): Show | 66 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(63): Show |
intron_variant | MODIFIER | c.248+1462A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28948603 | ||||||
chr17:28948847
|
CA | C | 33 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0071others(30): Show | 33 | HG00408.hp2 HG01069.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.248+1217delT | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28948847 | ||||||
chr17:28949105
|
G | A | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.248+960C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28949105 | ||||||
chr17:28949216
|
A | G | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.248+849T>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28949216 | ||||||
chr17:28949286
|
G | A | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.248+779C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28949286 | ||||||
chr17:28949356
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(4): Show | 11 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.248+709C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28949356 | ||||||
chr17:28949403
|
G | T | 46 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(43): Show | 65 | HG00544.hp2 HG00642.hp2 HG01074.hp2 others(62): Show |
intron_variant | MODIFIER | c.248+662C>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28949403 | ||||||
chr17:28949593
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.248+472A>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28949593 | ||||||
chr17:28949700
|
A | C | 1 | a0001c0001t0001g0037 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.248+365T>G | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28949700 | ||||||
chr17:28949707
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.248+358G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28949707 | ||||||
chr17:28950060
|
C | G | 1 | a0001c0001t0001g0036 | 1 | NA19001.hp2 | splice_region_variant&intron_variant | LOW | c.248+5G>C | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 2/14 | chr17 | 28950060 | ||||||
chr17:28950265
|
G | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0191a0001c0001t0001g0192others(1): Show | 5 | NA18975.hp1 NA19003.hp2 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-19C>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 1/14 | chr17 | 28950265 | ||||||
chr17:28950330
|
C | T | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0007g0195 | 3 | HG02615.hp1 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.67-84G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 1/14 | chr17 | 28950330 | ||||||
chr17:28950732
|
C | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0030others(4): Show | 8 | HG01934.hp2 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.66+163G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 1/14 | chr17 | 28950732 | ||||||
chr17:28950857
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.66+38G>A | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 1/14 | chr17 | 28950857 | ||||||
chr17:28950886
|
C | A | 1 | a0001c0001t0001g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.66+9G>T | PHF12 | ENSG00000109118.14 | transcript | ENST00000332830.9 | protein_coding | 1/14 | chr17 | 28950886 |