geneid | 23469 |
---|---|
ensemblid | ENSG00000118482.12 |
hgncid | 8921 |
symbol | PHF3 |
name | PHD finger protein 3 |
refseq_nuc | NM_001370348.2 |
refseq_prot | NP_001357277.1 |
ensembl_nuc | ENST00000262043.8 |
ensembl_prot | ENSP00000262043.4 |
mane_status | MANE Select |
chr | chr6 |
start | 63635802 |
end | 63726011 |
strand | + |
ver | v1.2 |
region | chr6:63635802-63726011 |
region5000 | chr6:63630802-63731011 |
regionname0 | PHF3_chr6_63635802_63726011 |
regionname5000 | PHF3_chr6_63630802_63731011 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 2039 | 291 | 61 | 60 | 123 | 13 | 33 | 88 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0002 | 0/0 | 2039 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0003 | 0/0 | 2039 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0004 | 0/0 | 2039 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0005 | 0/0 | 2039 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0006 | 0/0 | 2039 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0007 | 0/0 | 2039 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0008 | 0/0 | 2039 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0009 | 0/0 | 2039 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0010 | 0/1 | 2039 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0011 | 0/0 | 2039 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0012 | 0/0 | 2039 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0013 | 0/0 | 2039 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0014 | 0/0 | 2039 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0015 | 0/0 | 2039 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0016 | 0/0 | 2039 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0017 | 0/0 | 2039 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 6120 | 286 | 60 | 59 | 120 | 13 | 33 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
c0002 | 0/0 | 6120 | 8 | 8 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
c0003 | 0/0 | 6120 | 3 | 0 | 0 | 3 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
c0004 | 0/0 | 6120 | 3 | 3 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
c0005 | 0/0 | 6120 | 2 | 2 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
c0006 | 0/0 | 6120 | 2 | 2 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
c0007 | 0/0 | 6120 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
c0008 | 0/0 | 6120 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
c0009 | 0/0 | 6120 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
c0010 | 0/0 | 6120 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
c0011 | 0/1 | 6120 | 1 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
c0012 | 0/0 | 6120 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
c0013 | 0/0 | 6120 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
c0014 | 0/0 | 6120 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
c0015 | 0/0 | 6120 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
c0016 | 0/0 | 6120 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
c0017 | 0/0 | 6120 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
c0018 | 0/0 | 6120 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
c0019 | 0/0 | 6120 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
c0020 | 0/0 | 6120 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
c0021 | 0/0 | 6120 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
c0022 | 0/0 | 6120 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 12675 | 47 | 0 | 11 | 28 | 3 | 5 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0002 | 0/0 | 12670 | 43 | 3 | 9 | 26 | 2 | 3 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0003 | 0/1 | 12669 | 37 | 6 | 8 | 13 | 1 | 8 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0004 | 0/0 | 12678 | 24 | 5 | 7 | 10 | 1 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0005 | 0/0 | 12672 | 8 | 0 | 5 | 3 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0006 | 0/0 | 12669 | 8 | 0 | 0 | 8 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0007 | 0/0 | 12672 | 8 | 1 | 2 | 2 | 2 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0008 | 0/0 | 12676 | 8 | 0 | 4 | 1 | 0 | 3 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0009 | 0/0 | 12681 | 7 | 1 | 0 | 4 | 0 | 2 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0010 | 0/0 | 12673 | 5 | 0 | 0 | 4 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0011 | 0/0 | 12681 | 5 | 4 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0012 | 0/0 | 12675 | 5 | 2 | 0 | 2 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0013 | 0/0 | 12673 | 5 | 3 | 2 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0014 | 0/0 | 12670 | 4 | 4 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0015 | 0/0 | 12652 | 4 | 4 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0016 | 0/0 | 12678 | 4 | 2 | 0 | 1 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0017 | 0/0 | 12673 | 4 | 4 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0018 | 0/0 | 12684 | 3 | 2 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0019 | 0/0 | 12678 | 3 | 0 | 0 | 0 | 0 | 3 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0020 | 0/0 | 12675 | 3 | 0 | 0 | 3 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0021 | 0/0 | 12675 | 3 | 0 | 3 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0022 | 0/0 | 12669 | 3 | 0 | 0 | 3 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0023 | 0/0 | 12666 | 3 | 0 | 1 | 0 | 0 | 2 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0024 | 0/0 | 12679 | 3 | 3 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0025 | 0/0 | 12676 | 3 | 1 | 0 | 2 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0026 | 0/0 | 12678 | 3 | 0 | 1 | 0 | 2 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0027 | 0/0 | 12669 | 2 | 0 | 1 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0028 | 0/0 | 12663 | 2 | 0 | 1 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0029 | 0/0 | 12671 | 2 | 2 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0030 | 0/0 | 12669 | 2 | 2 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0031 | 0/0 | 12676 | 2 | 2 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0032 | 0/0 | 12679 | 2 | 0 | 0 | 0 | 0 | 2 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0033 | 0/0 | 12673 | 2 | 2 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0034 | 0/0 | 12676 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0035 | 0/0 | 12670 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0036 | 0/0 | 12671 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0037 | 0/0 | 12670 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0038 | 0/0 | 12667 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0039 | 0/0 | 12670 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0040 | 0/0 | 12682 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0041 | 0/0 | 12676 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0042 | 0/0 | 12673 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0043 | 0/0 | 12670 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0044 | 0/0 | 12670 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0045 | 0/0 | 12670 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0046 | 0/0 | 12670 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0047 | 0/0 | 12670 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0048 | 0/0 | 12669 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0049 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0050 | 0/0 | 12670 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0051 | 0/0 | 12679 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0052 | 0/0 | 12678 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0053 | 1/0 | 12678 | 1 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0054 | 0/0 | 12672 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0055 | 0/0 | 12678 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0056 | 0/0 | 12678 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0057 | 0/0 | 12678 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0058 | 0/0 | 12675 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0059 | 0/0 | 12675 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0060 | 0/0 | 12678 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0061 | 0/0 | 12672 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0062 | 0/0 | 12678 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0063 | 0/0 | 12670 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0064 | 0/0 | 12666 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0065 | 0/0 | 12669 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0066 | 0/0 | 12669 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0067 | 0/0 | 12684 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0068 | 0/0 | 12681 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0069 | 0/0 | 12668 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0070 | 0/0 | 12669 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0071 | 0/0 | 12663 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0072 | 0/0 | 12669 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0073 | 0/0 | 12679 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0074 | 0/0 | 12676 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0075 | 0/0 | 12679 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0076 | 0/0 | 12676 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0077 | 0/0 | 12668 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0078 | 0/0 | 12679 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0079 | 0/0 | 12673 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0080 | 0/0 | 12682 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0081 | 0/0 | 12679 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0082 | 0/0 | 12673 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0083 | 0/0 | 12682 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0084 | 0/0 | 12685 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0085 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
t0086 | 0/0 | 12678 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0292 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 6120 | 286 | 60 | 59 | 120 | 13 | 33 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0010 | 0/0 | 6120 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0012 | 0/0 | 6120 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0013 | 0/0 | 6120 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0015 | 0/0 | 6120 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0016 | 0/0 | 6120 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0002c0002 | 0/0 | 6120 | 8 | 8 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0003c0004 | 0/0 | 6120 | 3 | 3 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0004c0003 | 0/0 | 6120 | 3 | 0 | 0 | 3 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0005c0005 | 0/0 | 6120 | 2 | 2 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0006c0006 | 0/0 | 6120 | 2 | 2 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0007c0007 | 0/0 | 6120 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0008c0008 | 0/0 | 6120 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0009c0017 | 0/0 | 6120 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0010c0011 | 0/1 | 6120 | 1 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0011c0014 | 0/0 | 6120 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0012c0009 | 0/0 | 6120 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0013c0018 | 0/0 | 6120 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0014c0019 | 0/0 | 6120 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0015c0020 | 0/0 | 6120 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0016c0021 | 0/0 | 6120 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0017c0022 | 0/0 | 6120 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 18794 | 44 | 0 | 11 | 27 | 2 | 4 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0002 | 0/0 | 18789 | 38 | 0 | 8 | 25 | 2 | 3 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0003 | 0/0 | 18788 | 36 | 6 | 8 | 13 | 1 | 8 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0004 | 0/0 | 18797 | 22 | 4 | 7 | 9 | 1 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0005 | 0/0 | 18791 | 8 | 0 | 5 | 3 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0006 | 0/0 | 18788 | 7 | 0 | 0 | 7 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0007 | 0/0 | 18791 | 8 | 1 | 2 | 2 | 2 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0008 | 0/0 | 18795 | 6 | 0 | 3 | 0 | 0 | 3 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0009 | 0/0 | 18800 | 7 | 1 | 0 | 4 | 0 | 2 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0010 | 0/0 | 18792 | 5 | 0 | 0 | 4 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0011 | 0/0 | 18800 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0012 | 0/0 | 18794 | 5 | 2 | 0 | 2 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0013 | 0/0 | 18792 | 5 | 3 | 2 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0014 | 0/0 | 18789 | 4 | 4 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0015 | 0/0 | 18771 | 4 | 4 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0016 | 0/0 | 18797 | 2 | 0 | 0 | 1 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0017 | 0/0 | 18792 | 4 | 4 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0018 | 0/0 | 18803 | 3 | 2 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0019 | 0/0 | 18797 | 3 | 0 | 0 | 0 | 0 | 3 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0020 | 0/0 | 18794 | 3 | 0 | 0 | 3 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0021 | 0/0 | 18794 | 3 | 0 | 3 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0023 | 0/0 | 18785 | 3 | 0 | 1 | 0 | 0 | 2 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0024 | 0/0 | 18798 | 3 | 3 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0025 | 0/0 | 18795 | 3 | 1 | 0 | 2 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0026 | 0/0 | 18797 | 3 | 0 | 1 | 0 | 2 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0027 | 0/0 | 18788 | 2 | 0 | 1 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0028 | 0/0 | 18782 | 2 | 0 | 1 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0030 | 0/0 | 18788 | 2 | 2 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0031 | 0/0 | 18795 | 2 | 2 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0032 | 0/0 | 18798 | 2 | 0 | 0 | 0 | 0 | 2 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0033 | 0/0 | 18792 | 2 | 2 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0034 | 0/0 | 18795 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0035 | 0/0 | 18789 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0037 | 0/0 | 18789 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0038 | 0/0 | 18786 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0039 | 0/0 | 18789 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0040 | 0/0 | 18801 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0041 | 0/0 | 18795 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0042 | 0/0 | 18792 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0044 | 0/0 | 18789 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0045 | 0/0 | 18789 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0046 | 0/0 | 18789 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0047 | 0/0 | 18789 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0048 | 0/0 | 18788 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0049 | 0/0 | 18794 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0050 | 0/0 | 18789 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0052 | 0/0 | 18797 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0053 | 1/0 | 18797 | 1 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0054 | 0/0 | 18791 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0056 | 0/0 | 18797 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0057 | 0/0 | 18797 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0058 | 0/0 | 18794 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0059 | 0/0 | 18794 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0060 | 0/0 | 18797 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0061 | 0/0 | 18791 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0062 | 0/0 | 18797 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0064 | 0/0 | 18785 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0065 | 0/0 | 18788 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0066 | 0/0 | 18788 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0067 | 0/0 | 18803 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0069 | 0/0 | 18787 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0070 | 0/0 | 18788 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0071 | 0/0 | 18782 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0072 | 0/0 | 18788 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0073 | 0/0 | 18798 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0074 | 0/0 | 18795 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0075 | 0/0 | 18798 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0076 | 0/0 | 18795 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0077 | 0/0 | 18787 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0078 | 0/0 | 18798 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0079 | 0/0 | 18792 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0081 | 0/0 | 18798 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0082 | 0/0 | 18792 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0083 | 0/0 | 18801 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0001t0086 | 0/0 | 18797 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0010t0002 | 0/0 | 18789 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0012t0002 | 0/0 | 18789 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0013t0006 | 0/0 | 18788 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0015t0080 | 0/0 | 18801 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0001c0016t0008 | 0/0 | 18795 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0002c0002t0011 | 0/0 | 18800 | 4 | 4 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0002c0002t0016 | 0/0 | 18797 | 2 | 2 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0002c0002t0063 | 0/0 | 18789 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0002c0002t0068 | 0/0 | 18800 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0003c0004t0029 | 0/0 | 18790 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0003c0004t0036 | 0/0 | 18790 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0003c0004t0051 | 0/0 | 18798 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0004c0003t0022 | 0/0 | 18788 | 3 | 0 | 0 | 3 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0005c0005t0002 | 0/0 | 18789 | 2 | 2 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0006c0006t0002 | 0/0 | 18789 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0006c0006t0043 | 0/0 | 18789 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0007c0007t0001 | 0/0 | 18794 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0008c0008t0001 | 0/0 | 18794 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0009c0017t0085 | 0/0 | 18794 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0010c0011t0003 | 0/1 | 18788 | 1 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0011c0014t0001 | 0/0 | 18794 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0012c0009t0008 | 0/0 | 18795 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0013c0018t0004 | 0/0 | 18797 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0014c0019t0084 | 0/0 | 18804 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0015c0020t0055 | 0/0 | 18797 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0016c0021t0029 | 0/0 | 18790 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
a0017c0022t0004 | 0/0 | 18797 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | copy fasta | chr6 | 63630802 | 63731011 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0005g0001 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0005g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0005g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0006g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0006g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0007g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0007g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0007g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0007g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0007g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0007g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0007g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0008g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0008g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0008g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0008g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0008g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0008g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0009g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0009g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0009g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0009g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0009g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0009g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0009g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0010g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0010g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0010g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0010g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0010g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0011g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0012g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0012g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0012g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0012g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0012g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0013g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0013g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0013g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0013g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0013g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0014g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0014g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0014g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0014g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0015g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0015g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0015g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0015g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0016g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0016g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0017g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0017g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0017g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0017g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0018g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0018g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0018g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0019g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0019g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0019g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0020g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0020g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0020g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0021g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0021g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0023g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0023g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0023g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0024g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0024g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0025g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0025g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0025g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0026g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0026g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0026g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0027g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0027g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0028g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0028g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0030g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0030g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0031g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0031g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0032g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0032g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0033g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0033g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0034g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0035g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0037g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0038g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0039g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0040g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0041g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0042g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0044g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0045g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0046g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0047g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0048g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0049g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0050g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0052g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0053g0292 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0054g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0056g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0057g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0058g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0059g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0060g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0061g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0062g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0064g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0065g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0066g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0067g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0069g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0070g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0071g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0072g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0073g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0074g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0075g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0076g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0077g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0078g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0079g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0081g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0082g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0083g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0086g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0010t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0012t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0013t0006g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0015t0080g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0016t0008g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0002c0002t0011g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0002c0002t0011g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0002c0002t0016g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0002c0002t0016g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0002c0002t0063g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0002c0002t0068g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0003c0004t0029g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0003c0004t0036g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0003c0004t0051g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0004c0003t0022g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0004c0003t0022g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0004c0003t0022g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0005c0005t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0005c0005t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0006c0006t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0006c0006t0043g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0007c0007t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0008c0008t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0009c0017t0085g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0010c0011t0003g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0011c0014t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0012c0009t0008g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0013c0018t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0014c0019t0084g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0015c0020t0055g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0016c0021t0029g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0017c0022t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0058 | g0131 | EUR | GBR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0010 | EUR | GBR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00280 | hp1 | a0008 | c0008 | t0001 | g0133 | EUR | FIN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0247 | EUR | FIN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0053 | EUR | FIN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | FIN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00408 | hp1 | a0001 | c0001 | t0006 | g0103 | EAS | CHS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | CHS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00423 | hp2 | a0004 | c0003 | t0022 | g0086 | EAS | CHS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00544 | hp2 | a0001 | c0001 | t0040 | g0224 | EAS | CHS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | CHS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00558 | hp2 | a0001 | c0001 | t0025 | g0283 | EAS | CHS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00597 | hp1 | a0001 | c0001 | t0072 | g0079 | EAS | CHS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | CHS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00609 | hp1 | a0001 | c0001 | t0062 | g0007 | EAS | CHS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00609 | hp2 | a0001 | c0001 | t0046 | g0280 | EAS | CHS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00639 | hp1 | a0001 | c0001 | t0008 | g0252 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0163 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00735 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0182 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0071 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0181 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00741 | hp2 | a0001 | c0001 | t0013 | g0105 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01069 | hp1 | a0001 | c0001 | t0021 | g0172 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01069 | hp2 | a0001 | c0001 | t0028 | g0045 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0096 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01071 | hp1 | a0001 | c0001 | t0021 | g0001 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01074 | hp2 | a0001 | c0001 | t0007 | g0063 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0100 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0127 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01099 | hp2 | a0001 | c0001 | t0008 | g0256 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0085 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01109 | hp1 | a0001 | c0001 | t0037 | g0020 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01109 | hp2 | a0001 | c0001 | t0057 | g0035 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0061 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01169 | hp2 | a0001 | c0001 | t0013 | g0003 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01192 | hp1 | a0001 | c0001 | t0021 | g0001 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01192 | hp2 | a0001 | c0001 | t0026 | g0204 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01243 | hp2 | a0001 | c0001 | t0023 | g0124 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0068 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01346 | hp1 | a0001 | c0001 | t0086 | g0162 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01346 | hp2 | a0001 | c0001 | t0070 | g0083 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01358 | hp2 | a0015 | c0020 | t0055 | g0029 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01361 | hp2 | a0001 | c0001 | t0008 | g0257 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01433 | hp2 | a0001 | c0001 | t0027 | g0120 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01496 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01515 | hp1 | a0001 | c0001 | t0026 | g0202 | EUR | IBS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01515 | hp2 | a0001 | c0001 | t0007 | g0070 | EUR | IBS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01517 | hp1 | a0001 | c0001 | t0028 | g0166 | EUR | IBS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01517 | hp2 | a0001 | c0001 | t0026 | g0203 | EUR | IBS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01884 | hp1 | a0001 | c0001 | t0012 | g0058 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01884 | hp2 | a0002 | c0002 | t0016 | g0025 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01934 | hp2 | a0001 | c0010 | t0002 | g0250 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01943 | hp1 | a0001 | c0001 | t0005 | g0050 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01952 | hp1 | a0001 | c0001 | t0048 | g0084 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01952 | hp2 | a0001 | c0001 | t0045 | g0273 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0185 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0215 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02040 | hp1 | a0001 | c0001 | t0005 | g0081 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02056 | hp2 | a0001 | c0001 | t0006 | g0102 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02080 | hp1 | a0001 | c0001 | t0035 | g0271 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02080 | hp2 | a0001 | c0001 | t0050 | g0223 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0299 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02132 | hp1 | a0001 | c0016 | t0008 | g0261 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02135 | hp1 | a0001 | c0001 | t0004 | g0158 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02145 | hp1 | a0001 | c0001 | t0012 | g0082 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02145 | hp2 | a0001 | c0001 | t0015 | g0121 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | CDX | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02155 | hp2 | a0001 | c0001 | t0052 | g0143 | EAS | CDX | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02258 | hp1 | a0001 | c0001 | t0015 | g0178 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02258 | hp2 | a0002 | c0002 | t0011 | g0002 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02273 | hp1 | a0001 | c0001 | t0005 | g0074 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0197 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02280 | hp2 | a0001 | c0001 | t0034 | g0287 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02300 | hp1 | a0001 | c0001 | t0007 | g0051 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02300 | hp2 | a0012 | c0009 | t0008 | g0258 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02451 | hp2 | a0005 | c0005 | t0002 | g0288 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02572 | hp1 | a0001 | c0001 | t0017 | g0107 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02572 | hp2 | a0002 | c0002 | t0063 | g0026 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02615 | hp1 | a0001 | c0001 | t0015 | g0179 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02622 | hp1 | a0001 | c0001 | t0018 | g0214 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02622 | hp2 | a0001 | c0001 | t0013 | g0108 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0060 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02630 | hp2 | a0001 | c0001 | t0024 | g0285 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02647 | hp1 | a0001 | c0001 | t0079 | g0253 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0101 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02683 | hp1 | a0001 | c0001 | t0010 | g0233 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02683 | hp2 | a0001 | c0001 | t0023 | g0180 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02698 | hp1 | a0001 | c0001 | t0008 | g0264 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0142 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02717 | hp1 | a0003 | c0004 | t0029 | g0295 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02717 | hp2 | a0001 | c0001 | t0018 | g0196 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02723 | hp1 | a0001 | c0001 | t0064 | g0111 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02735 | hp1 | a0001 | c0001 | t0059 | g0030 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02735 | hp2 | a0001 | c0001 | t0008 | g0263 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02738 | hp1 | a0001 | c0001 | t0019 | g0032 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02738 | hp2 | a0001 | c0001 | t0023 | g0123 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02809 | hp1 | a0001 | c0001 | t0013 | g0112 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02818 | hp1 | a0001 | c0015 | t0080 | g0293 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02818 | hp2 | a0001 | c0001 | t0077 | g0094 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02886 | hp1 | a0001 | c0001 | t0014 | g0015 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02886 | hp2 | a0001 | c0001 | t0015 | g0122 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02896 | hp1 | a0001 | c0001 | t0024 | g0012 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02896 | hp2 | a0001 | c0001 | t0030 | g0057 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02897 | hp1 | a0001 | c0001 | t0014 | g0016 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02897 | hp2 | a0001 | c0001 | t0024 | g0012 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02922 | hp1 | a0002 | c0002 | t0011 | g0022 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02922 | hp2 | a0001 | c0001 | t0074 | g0003 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02965 | hp1 | a0002 | c0002 | t0011 | g0002 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02965 | hp2 | a0001 | c0001 | t0075 | g0006 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02970 | hp1 | a0001 | c0001 | t0025 | g0284 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02970 | hp2 | a0002 | c0002 | t0016 | g0023 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02976 | hp1 | a0002 | c0002 | t0068 | g0024 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02976 | hp2 | a0001 | c0001 | t0017 | g0003 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03041 | hp1 | a0001 | c0001 | t0038 | g0014 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03041 | hp2 | a0001 | c0001 | t0083 | g0301 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03098 | hp1 | a0001 | c0001 | t0066 | g0013 | AFR | MSL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03098 | hp2 | a0001 | c0001 | t0061 | g0164 | AFR | MSL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03139 | hp1 | a0014 | c0019 | t0084 | g0300 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03139 | hp2 | a0001 | c0001 | t0076 | g0109 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03195 | hp1 | a0006 | c0006 | t0002 | g0217 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0028 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03209 | hp1 | a0001 | c0001 | t0031 | g0254 | AFR | MSL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03209 | hp2 | a0001 | c0001 | t0069 | g0017 | AFR | MSL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0054 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03453 | hp1 | a0001 | c0001 | t0013 | g0043 | AFR | MSL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0200 | AFR | MSL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03486 | hp1 | a0001 | c0001 | t0017 | g0106 | AFR | MSL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03486 | hp2 | a0001 | c0001 | t0030 | g0052 | AFR | MSL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0236 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0042 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0237 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03516 | hp1 | a0001 | c0001 | t0033 | g0265 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0216 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03540 | hp1 | a0005 | c0005 | t0002 | g0289 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03540 | hp2 | a0009 | c0017 | t0085 | g0114 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03579 | hp1 | a0001 | c0001 | t0033 | g0251 | AFR | MSL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03579 | hp2 | a0001 | c0001 | t0067 | g0064 | AFR | MSL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03669 | hp1 | a0001 | c0001 | t0019 | g0021 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03669 | hp2 | a0001 | c0001 | t0071 | g0072 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03688 | hp1 | a0001 | c0001 | t0009 | g0153 | SAS | STU | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0290 | SAS | STU | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03704 | hp1 | a0001 | c0001 | t0016 | g0091 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0249 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0090 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03831 | hp1 | a0001 | c0001 | t0019 | g0031 | SAS | BEB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0036 | SAS | BEB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03927 | hp1 | a0001 | c0001 | t0032 | g0259 | SAS | BEB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03942 | hp1 | a0001 | c0001 | t0008 | g0262 | SAS | BEB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0093 | SAS | BEB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0206 | SAS | STU | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG04199 | hp2 | a0007 | c0007 | t0001 | g0118 | SAS | STU | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0095 | SAS | STU | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG04228 | hp2 | a0001 | c0001 | t0032 | g0260 | SAS | STU | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18522 | hp1 | a0002 | c0002 | t0011 | g0002 | AFR | YRI | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18522 | hp2 | a0001 | c0001 | t0031 | g0255 | AFR | YRI | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18612 | hp1 | a0001 | c0001 | t0041 | g0225 | EAS | CHB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18747 | hp1 | a0001 | c0001 | t0027 | g0150 | EAS | CHB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18747 | hp2 | a0001 | c0013 | t0006 | g0046 | EAS | CHB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18941 | hp2 | a0001 | c0001 | t0065 | g0039 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18942 | hp1 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18943 | hp2 | a0001 | c0001 | t0010 | g0232 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18945 | hp1 | a0001 | c0001 | t0044 | g0005 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0210 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18951 | hp2 | a0001 | c0001 | t0011 | g0075 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18952 | hp1 | a0001 | c0001 | t0018 | g0194 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18954 | hp1 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18960 | hp1 | a0001 | c0001 | t0039 | g0238 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18964 | hp2 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18969 | hp1 | a0001 | c0001 | t0006 | g0047 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18969 | hp2 | a0001 | c0001 | t0010 | g0219 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18970 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18971 | hp1 | a0001 | c0001 | t0020 | g0193 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18973 | hp2 | a0001 | c0001 | t0049 | g0298 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18975 | hp1 | a0004 | c0003 | t0022 | g0088 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18978 | hp2 | a0001 | c0001 | t0007 | g0037 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18980 | hp1 | a0001 | c0001 | t0020 | g0007 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18980 | hp2 | a0001 | c0001 | t0042 | g0220 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18981 | hp1 | a0001 | c0001 | t0007 | g0076 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18983 | hp1 | a0011 | c0014 | t0001 | g0205 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18986 | hp2 | a0001 | c0012 | t0002 | g0275 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18988 | hp1 | a0001 | c0001 | t0009 | g0132 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18989 | hp1 | a0001 | c0001 | t0016 | g0041 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18990 | hp2 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18995 | hp1 | a0001 | c0001 | t0009 | g0175 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19000 | hp1 | a0001 | c0001 | t0006 | g0066 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19000 | hp2 | a0001 | c0001 | t0009 | g0173 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19002 | hp1 | a0001 | c0001 | t0012 | g0167 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19003 | hp1 | a0001 | c0001 | t0010 | g0246 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19003 | hp2 | a0001 | c0001 | t0004 | g0154 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19030 | hp1 | a0003 | c0004 | t0036 | g0294 | AFR | LWK | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19030 | hp2 | a0001 | c0001 | t0054 | g0170 | AFR | LWK | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19043 | hp1 | a0001 | c0001 | t0081 | g0291 | AFR | LWK | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19043 | hp2 | a0001 | c0001 | t0017 | g0104 | AFR | LWK | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19062 | hp1 | a0001 | c0001 | t0025 | g0286 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19062 | hp2 | a0013 | c0018 | t0004 | g0008 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19064 | hp1 | a0001 | c0001 | t0012 | g0168 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19064 | hp2 | a0001 | c0001 | t0006 | g0065 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19065 | hp1 | a0001 | c0001 | t0004 | g0144 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19068 | hp1 | a0001 | c0001 | t0047 | g0240 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19068 | hp2 | a0001 | c0001 | t0006 | g0087 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19074 | hp1 | a0001 | c0001 | t0020 | g0192 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19074 | hp2 | a0001 | c0001 | t0010 | g0243 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19077 | hp1 | a0001 | c0001 | t0006 | g0038 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19080 | hp2 | a0001 | c0001 | t0060 | g0161 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19082 | hp2 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19085 | hp1 | a0004 | c0003 | t0022 | g0048 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19091 | hp2 | a0001 | c0001 | t0009 | g0009 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19240 | hp1 | a0006 | c0006 | t0043 | g0218 | AFR | YRI | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0209 | AFR | YRI | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA20129 | hp1 | a0001 | c0001 | t0056 | g0119 | AFR | ASW | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA20129 | hp2 | a0001 | c0001 | t0082 | g0006 | AFR | ASW | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA20752 | hp1 | a0001 | c0001 | t0012 | g0078 | EUR | TSI | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | TSI | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0128 | EUR | TSI | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA20805 | hp2 | a0001 | c0001 | t0007 | g0055 | EUR | TSI | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA20905 | hp1 | a0001 | c0001 | t0007 | g0067 | SAS | GIH | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA20905 | hp2 | a0001 | c0001 | t0009 | g0212 | SAS | GIH | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02109 | hp1 | a0001 | c0001 | t0014 | g0019 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02109 | hp2 | a0001 | c0001 | t0073 | g0110 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02486 | hp1 | a0017 | c0022 | t0004 | g0135 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02486 | hp2 | a0003 | c0004 | t0051 | g0296 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG06807 | hp1 | a0016 | c0021 | t0029 | g0297 | AFR | USA | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG06807 | hp2 | a0001 | c0001 | t0078 | g0266 | AFR | USA | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA21309 | hp1 | a0001 | c0001 | t0009 | g0191 | AFR | LWK | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA21309 | hp2 | a0001 | c0001 | t0014 | g0018 | AFR | LWK | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
homoSapiens_chm13v2 | hp1 | a0010 | c0011 | t0003 | g0098 | REF | REF | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0053 | g0292 | REF | REF | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:63684165
|
A | G | 1 | a0017 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.443A>G | p.Lys148Arg | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/16 | 817/18797 | 443/6120 | 148/2039 | chr6 | 63684165 | ||
chr6:63684176
|
G | T | 1 | a0016 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.454G>T | p.Ala152Ser | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/16 | 828/18797 | 454/6120 | 152/2039 | chr6 | 63684176 | ||
chr6:63684350
|
G | C | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.628G>C | p.Val210Leu | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/16 | 1002/18797 | 628/6120 | 210/2039 | chr6 | 63684350 | ||
chr6:63684419
|
G | A | 1 | a0015 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.697G>A | p.Gly233Arg | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/16 | 1071/18797 | 697/6120 | 233/2039 | chr6 | 63684419 | ||
chr6:63684549
|
G | A | 1 | a0004 | 3 | HG00423.hp2 NA18975.hp1 NA19085.hp1 |
missense_variant | MODERATE | c.827G>A | p.Cys276Tyr | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/16 | 1201/18797 | 827/6120 | 276/2039 | chr6 | 63684549 | ||
chr6:63685016
|
G | A | 1 | a0002 | 8 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(5): Show |
missense_variant | MODERATE | c.1294G>A | p.Glu432Lys | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/16 | 1668/18797 | 1294/6120 | 432/2039 | chr6 | 63685016 | ||
chr6:63685295
|
G | A | 1 | a0008 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.1573G>A | p.Val525Ile | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/16 | 1947/18797 | 1573/6120 | 525/2039 | chr6 | 63685295 | ||
chr6:63685649
|
G | A | 1 | a0005 | 2 | HG02451.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.1927G>A | p.Val643Met | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/16 | 2301/18797 | 1927/6120 | 643/2039 | chr6 | 63685649 | ||
chr6:63694644
|
G | A | 1 | a0006 | 2 | HG03195.hp1 NA19240.hp1 |
missense_variant | MODERATE | c.2560G>A | p.Ala854Thr | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 6/16 | 2934/18797 | 2560/6120 | 854/2039 | chr6 | 63694644 | ||
chr6:63698223
|
G | T | 1 | a0014 | 1 | HG03139.hp1 | missense_variant&splice_region_variant | MODERATE | c.2681G>T | p.Gly894Val | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 7/16 | 3055/18797 | 2681/6120 | 894/2039 | chr6 | 63698223 | ||
chr6:63703543
|
C | T | 1 | a0013 | 1 | NA19062.hp2 | missense_variant | MODERATE | c.3239C>T | p.Ala1080Val | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 11/16 | 3613/18797 | 3239/6120 | 1080/2039 | chr6 | 63703543 | ||
chr6:63703580
|
A | C | 1 | a0009 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.3276A>C | p.Glu1092Asp | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 11/16 | 3650/18797 | 3276/6120 | 1092/2039 | chr6 | 63703580 | ||
chr6:63711679
|
T | C | 1 | a0012 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.4091T>C | p.Ile1364Thr | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 4465/18797 | 4091/6120 | 1364/2039 | chr6 | 63711679 | ||
chr6:63712609
|
G | A | 1 | a0010 | 1 | homoSapiens_chm13v2.hp1 | missense_variant | MODERATE | c.5021G>A | p.Arg1674Gln | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 5395/18797 | 5021/6120 | 1674/2039 | chr6 | 63712609 | ||
chr6:63712963
|
G | C | 2 | a0003a0016 | 4 | HG02486.hp2 HG02717.hp1 HG06807.hp1 others(1): Show |
missense_variant | MODERATE | c.5375G>C | p.Ser1792Thr | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 5749/18797 | 5375/6120 | 1792/2039 | chr6 | 63712963 | ||
chr6:63713088
|
C | T | 1 | a0011 | 1 | NA18983.hp1 | missense_variant | MODERATE | c.5500C>T | p.His1834Tyr | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 5874/18797 | 5500/6120 | 1834/2039 | chr6 | 63713088 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:63684220
|
A | G | 1 | a0015c0020 | 1 | HG01358.hp2 | synonymous_variant | LOW | c.498A>G | p.Val166Val | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/16 | 872/18797 | 498/6120 | 166/2039 | chr6 | 63684220 | ||
chr6:63706849
|
A | G | 1 | a0001c0016 | 1 | HG02132.hp1 | synonymous_variant | LOW | c.3684A>G | p.Val1228Val | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 13/16 | 4058/18797 | 3684/6120 | 1228/2039 | chr6 | 63706849 | ||
chr6:63711791
|
T | A | 1 | a0001c0010 | 1 | HG01934.hp2 | synonymous_variant | LOW | c.4203T>A | p.Ser1401Ser | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 4577/18797 | 4203/6120 | 1401/2039 | chr6 | 63711791 | ||
chr6:63712118
|
A | G | 1 | a0001c0015 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.4530A>G | p.Thr1510Thr | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 4904/18797 | 4530/6120 | 1510/2039 | chr6 | 63712118 | ||
chr6:63712712
|
G | A | 1 | a0001c0012 | 1 | NA18986.hp2 | synonymous_variant | LOW | c.5124G>A | p.Ser1708Ser | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 5498/18797 | 5124/6120 | 1708/2039 | chr6 | 63712712 | ||
chr6:63713333
|
G | A | 1 | a0015c0020 | 1 | HG01358.hp2 | synonymous_variant | LOW | c.5745G>A | p.Arg1915Arg | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 6119/18797 | 5745/6120 | 1915/2039 | chr6 | 63713333 | ||
chr6:63713360
|
T | C | 1 | a0001c0013 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.5772T>C | p.Tyr1924Tyr | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 6146/18797 | 5772/6120 | 1924/2039 | chr6 | 63713360 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:63635926
|
C | T | 1 | a0001c0001t0026 | 3 | HG01192.hp2 HG01515.hp1 HG01517.hp2 |
5_prime_UTR_variant | MODIFIER | c.-250C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/16 | 10626 | chr6 | 63635926 | |||||
chr6:63636014
|
G | T | 1 | a0001c0001t0086 | 1 | HG01346.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-162G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/16 | chr6 | 63636014 | ||||||
chr6:63713786
|
G | A | 1 | a0001c0001t0034 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*78G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 78 | chr6 | 63713786 | |||||
chr6:63714001
|
G | A | 1 | a0001c0001t0035 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*293G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 293 | chr6 | 63714001 | |||||
chr6:63714113
|
T | C | 1 | a0003c0004t0036 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*405T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 405 | chr6 | 63714113 | |||||
chr6:63714175
|
A | G | 1 | a0009c0017t0085 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*467A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 467 | chr6 | 63714175 | |||||
chr6:63714452
|
CT | C | 3 | a0001c0001t0014a0001c0001t0037a0001c0001t0038 | 6 | HG01109.hp1 HG02109.hp1 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*745delT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 745 | chr6 | 63714452 | |||||
chr6:63714629
|
G | A | 16 | a0001c0001t0002a0001c0001t0010a0001c0001t0035others(13): Show | 58 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*921G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 921 | chr6 | 63714629 | |||||
chr6:63714738
|
A | G | 3 | a0001c0001t0082a0001c0001t0083a0014c0019t0084 | 3 | HG03041.hp2 HG03139.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1030A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 1030 | chr6 | 63714738 | |||||
chr6:63714779
|
C | G | 2 | a0001c0001t0083a0014c0019t0084 | 2 | HG03041.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1071C>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 1071 | chr6 | 63714779 | |||||
chr6:63714799
|
G | A | 1 | a0001c0001t0048 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1091G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 1091 | chr6 | 63714799 | |||||
chr6:63714800
|
T | G | 1 | a0001c0001t0049 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1092T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 1092 | chr6 | 63714800 | |||||
chr6:63714886
|
A | T | 31 | a0001c0001t0002a0001c0001t0008a0001c0001t0010others(28): Show | 85 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1178A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 1178 | chr6 | 63714886 | |||||
chr6:63714903
|
TAATTC | T | 1 | a0001c0001t0015 | 4 | HG02145.hp2 HG02258.hp1 HG02615.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1198_*1202delTTCA others(1): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 1198 | INFO_REALIGN_3_PRIME | chr6 | 63714903 | ||||
chr6:63715663
|
A | C | 1 | a0001c0001t0047 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1955A>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 1955 | chr6 | 63715663 | |||||
chr6:63715810
|
A | G | 2 | a0001c0001t0083a0014c0019t0084 | 2 | HG03041.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2102A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 2102 | chr6 | 63715810 | |||||
chr6:63716137
|
A | G | 1 | a0001c0001t0081 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2429A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 2429 | chr6 | 63716137 | |||||
chr6:63716246
|
A | T | 1 | a0001c0001t0077 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2538A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 2538 | chr6 | 63716246 | |||||
chr6:63716491
|
A | G | 1 | a0001c0001t0033 | 2 | HG03516.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2783A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 2783 | chr6 | 63716491 | |||||
chr6:63716580
|
C | T | 1 | a0001c0015t0080 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2872C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 2872 | chr6 | 63716580 | |||||
chr6:63716774
|
GTCT | G | 2 | a0001c0001t0023a0009c0017t0085 | 4 | HG01243.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3068_*3070delCTT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 3068 | INFO_REALIGN_3_PRIME | chr6 | 63716774 | ||||
chr6:63716998
|
A | G | 72 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(69): Show | 207 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*3290A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 3290 | chr6 | 63716998 | |||||
chr6:63717199
|
C | T | 72 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(69): Show | 207 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*3491C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 3491 | chr6 | 63717199 | |||||
chr6:63717289
|
C | T | 1 | a0001c0001t0046 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3581C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 3581 | chr6 | 63717289 | |||||
chr6:63717521
|
C | CAAAG | 37 | a0001c0001t0002a0001c0001t0008a0001c0001t0010others(34): Show | 91 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*3815_*3816insAGAA | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 3816 | INFO_REALIGN_3_PRIME | chr6 | 63717521 | ||||
chr6:63717527
|
T | C | 1 | a0001c0001t0052 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3819T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 3819 | chr6 | 63717527 | |||||
chr6:63717731
|
T | C | 1 | a0001c0015t0080 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4023T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 4023 | chr6 | 63717731 | |||||
chr6:63717897
|
A | T | 1 | a0009c0017t0085 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4189A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 4189 | chr6 | 63717897 | |||||
chr6:63717940
|
C | T | 4 | a0003c0004t0029a0003c0004t0036a0003c0004t0051others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG06807.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4232C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 4232 | chr6 | 63717940 | |||||
chr6:63717961
|
G | A | 2 | a0001c0001t0083a0014c0019t0084 | 2 | HG03041.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4253G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 4253 | chr6 | 63717961 | |||||
chr6:63718032
|
T | C | 21 | a0001c0001t0002a0001c0001t0010a0001c0001t0035others(18): Show | 63 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*4324T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 4324 | chr6 | 63718032 | |||||
chr6:63718091
|
C | G | 101 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(98): Show | 319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
3_prime_UTR_variant | MODIFIER | c.*4383C>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 4383 | chr6 | 63718091 | |||||
chr6:63718177
|
T | G | 2 | a0001c0001t0083a0014c0019t0084 | 2 | HG03041.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4469T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 4469 | chr6 | 63718177 | |||||
chr6:63718330
|
T | G | 4 | a0001c0001t0005a0001c0001t0006a0001c0001t0021others(1): Show | 19 | HG00408.hp1 HG00735.hp2 HG01069.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4622T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 4622 | chr6 | 63718330 | |||||
chr6:63718423
|
C | G | 2 | a0001c0001t0020a0001c0001t0062 | 4 | HG00609.hp1 NA18971.hp1 NA18980.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4715C>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 4715 | chr6 | 63718423 | |||||
chr6:63718637
|
T | C | 4 | a0003c0004t0029a0003c0004t0036a0003c0004t0051others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG06807.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4929T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 4929 | chr6 | 63718637 | |||||
chr6:63718905
|
C | T | 19 | a0001c0001t0002a0001c0001t0010a0001c0001t0035others(16): Show | 61 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*5197C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 5197 | chr6 | 63718905 | |||||
chr6:63719203
|
T | G | 1 | a0001c0001t0039 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5495T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 5495 | chr6 | 63719203 | |||||
chr6:63719421
|
GA | G | 7 | a0001c0001t0013a0001c0001t0017a0001c0001t0073others(4): Show | 14 | HG00741.hp2 HG01169.hp2 HG02109.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*5714delA | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 5714 | chr6 | 63719421 | |||||
chr6:63719467
|
C | T | 2 | a0001c0001t0083a0014c0019t0084 | 2 | HG03041.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5759C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 5759 | chr6 | 63719467 | |||||
chr6:63719495
|
A | G | 1 | a0002c0002t0063 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5787A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 5787 | chr6 | 63719495 | |||||
chr6:63719544
|
A | G | 4 | a0001c0001t0008a0001c0001t0032a0001c0016t0008others(1): Show | 10 | HG00639.hp1 HG01099.hp2 HG01361.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5836A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 5836 | chr6 | 63719544 | |||||
chr6:63719567
|
G | A | 1 | a0001c0001t0054 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5859G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 5859 | chr6 | 63719567 | |||||
chr6:63719956
|
T | G | 9 | a0001c0001t0013a0001c0001t0017a0001c0001t0064others(6): Show | 16 | HG00741.hp2 HG01169.hp2 HG01358.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*6248T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 6248 | chr6 | 63719956 | |||||
chr6:63720067
|
T | G | 1 | a0001c0001t0065 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6359T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 6359 | chr6 | 63720067 | |||||
chr6:63720082
|
T | C | 1 | a0001c0001t0037 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6374T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 6374 | chr6 | 63720082 | |||||
chr6:63720794
|
T | C | 1 | a0004c0003t0022 | 3 | HG00423.hp2 NA18975.hp1 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7086T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 7086 | chr6 | 63720794 | |||||
chr6:63720822
|
A | G | 1 | a0001c0001t0072 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7114A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 7114 | chr6 | 63720822 | |||||
chr6:63721001
|
T | C | 2 | a0001c0001t0083a0014c0019t0084 | 2 | HG03041.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7293T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 7293 | chr6 | 63721001 | |||||
chr6:63721602
|
G | A | 2 | a0001c0001t0054a0001c0001t0056 | 2 | NA19030.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7894G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 7894 | chr6 | 63721602 | |||||
chr6:63721609
|
C | T | 2 | a0001c0001t0024a0001c0001t0025 | 6 | HG00558.hp2 HG02630.hp2 HG02896.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7901C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 7901 | chr6 | 63721609 | |||||
chr6:63722388
|
C | T | 2 | a0001c0001t0083a0014c0019t0084 | 2 | HG03041.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8680C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 8680 | chr6 | 63722388 | |||||
chr6:63722449
|
T | C | 1 | a0001c0001t0034 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8741T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 8741 | chr6 | 63722449 | |||||
chr6:63722523
|
G | A | 3 | a0001c0001t0017a0001c0001t0073a0001c0001t0074 | 6 | HG02109.hp2 HG02572.hp1 HG02922.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8815G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 8815 | chr6 | 63722523 | |||||
chr6:63722569
|
C | A | 2 | a0001c0001t0083a0014c0019t0084 | 2 | HG03041.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8861C>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 8861 | chr6 | 63722569 | |||||
chr6:63722682
|
T | C | 1 | a0001c0015t0080 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8974T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 8974 | chr6 | 63722682 | |||||
chr6:63722738
|
C | T | 1 | a0014c0019t0084 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9030C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 9030 | chr6 | 63722738 | |||||
chr6:63722740
|
A | T | 1 | a0014c0019t0084 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9032A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 9032 | chr6 | 63722740 | |||||
chr6:63722864
|
T | A | 1 | a0001c0001t0064 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9156T>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 9156 | chr6 | 63722864 | |||||
chr6:63722915
|
A | G | 18 | a0001c0001t0002a0001c0001t0010a0001c0001t0035others(15): Show | 60 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*9207A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 9207 | chr6 | 63722915 | |||||
chr6:63722920
|
A | C | 1 | a0001c0001t0045 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9212A>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 9212 | chr6 | 63722920 | |||||
chr6:63722925
|
G | A | 1 | a0002c0002t0063 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9217G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 9217 | chr6 | 63722925 | |||||
chr6:63722968
|
G | A | 1 | a0001c0001t0066 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9260G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 9260 | chr6 | 63722968 | |||||
chr6:63722990
|
G | A | 1 | a0001c0001t0056 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9282G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 9282 | chr6 | 63722990 | |||||
chr6:63723002
|
G | C | 1 | a0001c0001t0057 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9294G>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 9294 | chr6 | 63723002 | |||||
chr6:63723240
|
T | C | 2 | a0001c0001t0083a0014c0019t0084 | 2 | HG03041.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9532T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 9532 | chr6 | 63723240 | |||||
chr6:63723309
|
A | G | 1 | a0001c0001t0034 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9601A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 9601 | chr6 | 63723309 | |||||
chr6:63723332
|
G | A | 33 | a0001c0001t0002a0001c0001t0008a0001c0001t0010others(30): Show | 87 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*9624G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 9624 | chr6 | 63723332 | |||||
chr6:63723522
|
A | G | 18 | a0001c0001t0002a0001c0001t0010a0001c0001t0035others(15): Show | 60 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*9814A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 9814 | chr6 | 63723522 | |||||
chr6:63723788
|
C | CATT | 7 | a0001c0001t0009a0001c0001t0011a0001c0001t0074others(4): Show | 16 | HG02258.hp2 HG02922.hp1 HG02922.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*10126_*10128dupAT others(1): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 10129 | INFO_REALIGN_3_PRIME | chr6 | 63723788 | ||||
chr6:63723788
|
C | CATTATT | 4 | a0001c0001t0018a0001c0001t0067a0001c0001t0073others(1): Show | 6 | HG02109.hp2 HG02622.hp1 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*10123_*10128dupAT others(4): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 10129 | INFO_REALIGN_3_PRIME | chr6 | 63723788 | ||||
chr6:63723788
|
CATT | C | 15 | a0001c0001t0001a0001c0001t0012a0001c0001t0020others(12): Show | 69 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*10126_*10128delAT others(1): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 10126 | INFO_REALIGN_3_PRIME | chr6 | 63723788 | ||||
chr6:63723788
|
CATTATT | C | 14 | a0001c0001t0005a0001c0001t0007a0001c0001t0008others(11): Show | 41 | HG00558.hp2 HG00639.hp1 HG00735.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*10123_*10128delAT others(4): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 10123 | INFO_REALIGN_3_PRIME | chr6 | 63723788 | ||||
chr6:63723788
|
CATTATTA others(2): Show |
C | 22 | a0001c0001t0003a0001c0001t0006a0001c0001t0010others(19): Show | 72 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*10120_*10128delAT others(7): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 10120 | INFO_REALIGN_3_PRIME | chr6 | 63723788 | ||||
chr6:63723788
|
CATTATTA others(5): Show |
C | 15 | a0001c0001t0002a0001c0001t0035a0001c0001t0039others(12): Show | 53 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*10117_*10128delAT others(10): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 10117 | INFO_REALIGN_3_PRIME | chr6 | 63723788 | ||||
chr6:63723788
|
CATTATTA others(8): Show |
C | 2 | a0001c0001t0028a0001c0001t0071 | 3 | HG01069.hp2 HG01517.hp1 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10114_*10128delAT others(13): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 10114 | INFO_REALIGN_3_PRIME | chr6 | 63723788 | ||||
chr6:63723788
|
CATTATTA others(14): Show |
C | 1 | a0001c0001t0015 | 4 | HG02145.hp2 HG02258.hp1 HG02615.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*10108_*10128delAT others(19): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 10108 | INFO_REALIGN_3_PRIME | chr6 | 63723788 | ||||
chr6:63723831
|
A | C | 1 | a0001c0001t0060 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10123A>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 10123 | chr6 | 63723831 | |||||
chr6:63723866
|
A | G | 12 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(9): Show | 24 | HG00558.hp2 HG00639.hp1 HG01099.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*10158A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 10158 | chr6 | 63723866 | |||||
chr6:63723964
|
C | T | 2 | a0001c0001t0019a0001c0001t0059 | 4 | HG02735.hp1 HG02738.hp1 HG03669.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*10256C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 10256 | chr6 | 63723964 | |||||
chr6:63724090
|
T | A | 2 | a0001c0001t0083a0014c0019t0084 | 2 | HG03041.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10382T>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 10382 | chr6 | 63724090 | |||||
chr6:63724115
|
G | A | 1 | a0001c0001t0069 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10407G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 10407 | chr6 | 63724115 | |||||
chr6:63724230
|
G | A | 2 | a0001c0001t0083a0014c0019t0084 | 2 | HG03041.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10522G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 10522 | chr6 | 63724230 | |||||
chr6:63724412
|
CTTAT | C | 7 | a0001c0001t0013a0001c0001t0017a0001c0001t0073others(4): Show | 14 | HG00741.hp2 HG01169.hp2 HG02109.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*10709_*10712delTT others(2): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 10709 | INFO_REALIGN_3_PRIME | chr6 | 63724412 | ||||
chr6:63724416
|
T | C | 1 | a0001c0001t0070 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10708T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 10708 | chr6 | 63724416 | |||||
chr6:63724436
|
T | A | 1 | a0001c0015t0080 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10728T>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 10728 | chr6 | 63724436 | |||||
chr6:63724546
|
C | T | 1 | a0001c0001t0030 | 2 | HG02896.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10838C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 10838 | chr6 | 63724546 | |||||
chr6:63724791
|
T | A | 1 | a0002c0002t0068 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11083T>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 11083 | chr6 | 63724791 | |||||
chr6:63724799
|
G | A | 2 | a0001c0001t0024a0001c0001t0025 | 6 | HG00558.hp2 HG02630.hp2 HG02896.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*11091G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 11091 | chr6 | 63724799 | |||||
chr6:63724873
|
A | T | 1 | a0001c0001t0042 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11165A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 11165 | chr6 | 63724873 | |||||
chr6:63724885
|
TAGC | T | 1 | a0001c0001t0023 | 3 | HG01243.hp2 HG02683.hp2 HG02738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11180_*11182delCA others(1): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 11180 | INFO_REALIGN_3_PRIME | chr6 | 63724885 | ||||
chr6:63725148
|
G | A | 1 | a0006c0006t0043 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11440G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 11440 | chr6 | 63725148 | |||||
chr6:63725213
|
A | G | 1 | a0001c0001t0058 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11505A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 11505 | chr6 | 63725213 | |||||
chr6:63725328
|
CAA | C | 3 | a0003c0004t0029a0003c0004t0036a0016c0021t0029 | 3 | HG02717.hp1 HG06807.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*11622_*11623delAA | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 11622 | INFO_REALIGN_3_PRIME | chr6 | 63725328 | ||||
chr6:63725349
|
AT | A | 5 | a0001c0001t0014a0001c0001t0037a0001c0001t0038others(2): Show | 8 | HG01109.hp1 HG02109.hp1 HG02818.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*11643delT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 11643 | INFO_REALIGN_3_PRIME | chr6 | 63725349 | ||||
chr6:63725425
|
G | A | 1 | a0001c0001t0044 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11717G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 11717 | chr6 | 63725425 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:63636214
|
A | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-26+64A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63636214 | ||||||
chr6:63636290
|
A | C | 1 | a0001c0001t0003g0299 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-26+140A>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63636290 | ||||||
chr6:63636349
|
G | T | 1 | a0001c0001t0049g0298 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-26+199G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63636349 | ||||||
chr6:63636451
|
A | C | 4 | a0003c0004t0029g0295a0003c0004t0036g0294a0003c0004t0051g0296others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26+301A>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63636451 | ||||||
chr6:63636461
|
T | C | 308 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0033others(305): Show | 318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.-26+311T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63636461 | ||||||
chr6:63636497
|
G | C | 226 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0033others(223): Show | 232 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.-26+347G>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63636497 | ||||||
chr6:63636673
|
T | C | 1 | a0001c0001t0066g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-26+523T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63636673 | ||||||
chr6:63636874
|
C | T | 1 | a0001c0001t0004g0216 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-26+724C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63636874 | ||||||
chr6:63637046
|
C | T | 1 | a0001c0001t0003g0215 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-26+896C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63637046 | ||||||
chr6:63637057
|
T | C | 7 | a0001c0001t0014g0015a0001c0001t0014g0016a0001c0001t0014g0018others(4): Show | 7 | HG01109.hp1 HG02109.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-26+907T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63637057 | ||||||
chr6:63637095
|
T | C | 1 | a0001c0001t0038g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-26+945T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63637095 | ||||||
chr6:63637235
|
G | A | 2 | a0006c0006t0002g0217a0006c0006t0043g0218 | 2 | HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-26+1085G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63637235 | ||||||
chr6:63637412
|
T | A | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-26+1262T>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63637412 | ||||||
chr6:63637467
|
T | C | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-26+1317T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63637467 | ||||||
chr6:63637484
|
C | G | 1 | a0001c0001t0018g0214 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-26+1334C>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63637484 | ||||||
chr6:63637535
|
A | G | 1 | a0001c0001t0003g0213 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-26+1385A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63637535 | ||||||
chr6:63637557
|
A | G | 4 | a0003c0004t0029g0295a0003c0004t0036g0294a0003c0004t0051g0296others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26+1407A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63637557 | ||||||
chr6:63637637
|
T | TTCA | 306 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0033others(303): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.-26+1493_-26+1495d others(5): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 63637637 | |||||
chr6:63637699
|
A | T | 4 | a0003c0004t0029g0295a0003c0004t0036g0294a0003c0004t0051g0296others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26+1549A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63637699 | ||||||
chr6:63637711
|
T | C | 1 | a0001c0001t0019g0021 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-26+1561T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63637711 | ||||||
chr6:63637766
|
C | T | 308 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0033others(305): Show | 318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.-26+1616C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63637766 | ||||||
chr6:63638005
|
CTT | C | 6 | a0002c0002t0011g0002a0002c0002t0011g0022a0002c0002t0016g0023others(3): Show | 8 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-26+1857_-26+1858d others(4): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 63638005 | |||||
chr6:63638157
|
T | G | 1 | a0014c0019t0084g0300 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-26+2007T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63638157 | ||||||
chr6:63638192
|
G | A | 2 | a0001c0001t0010g0219a0001c0001t0042g0220 | 2 | NA18969.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.-26+2042G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63638192 | ||||||
chr6:63638248
|
T | C | 1 | a0001c0001t0003g0027 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-26+2098T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63638248 | ||||||
chr6:63638298
|
G | A | 1 | a0001c0001t0007g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-26+2148G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63638298 | ||||||
chr6:63638489
|
A | G | 1 | a0001c0001t0009g0212 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-26+2339A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63638489 | ||||||
chr6:63638506
|
A | G | 1 | a0001c0001t0081g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-26+2356A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63638506 | ||||||
chr6:63638536
|
A | G | 227 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0033others(224): Show | 233 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.-26+2386A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63638536 | ||||||
chr6:63638681
|
T | A | 1 | a0015c0020t0055g0029 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-26+2531T>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63638681 | ||||||
chr6:63638716
|
T | C | 33 | a0001c0001t0002g0010a0001c0001t0002g0221a0001c0001t0002g0222others(30): Show | 34 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.-26+2566T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63638716 | ||||||
chr6:63638748
|
ACT | A | 4 | a0001c0001t0019g0021a0001c0001t0019g0031a0001c0001t0019g0032others(1): Show | 4 | HG02735.hp1 HG02738.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26+2604_-26+2605d others(4): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 63638748 | |||||
chr6:63638893
|
A | C | 2 | a0001c0001t0004g0210a0001c0001t0004g0211 | 2 | NA18945.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-26+2743A>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63638893 | ||||||
chr6:63638948
|
T | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG02074.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.-26+2798T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63638948 | ||||||
chr6:63639071
|
A | G | 1 | a0001c0001t0003g0209 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-26+2921A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63639071 | ||||||
chr6:63639180
|
G | T | 1 | a0001c0001t0001g0208 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-26+3030G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63639180 | ||||||
chr6:63639208
|
T | C | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-26+3058T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63639208 | ||||||
chr6:63639345
|
A | G | 1 | a0001c0001t0003g0207 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-26+3195A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63639345 | ||||||
chr6:63639445
|
T | A | 1 | a0001c0001t0033g0251 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-26+3295T>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63639445 | ||||||
chr6:63639605
|
G | A | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-26+3455G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63639605 | ||||||
chr6:63639990
|
A | G | 2 | a0005c0005t0002g0288a0005c0005t0002g0289 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-26+3840A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63639990 | ||||||
chr6:63640081
|
T | C | 17 | a0001c0001t0008g0252a0001c0001t0008g0256a0001c0001t0008g0257others(14): Show | 17 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.-26+3931T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63640081 | ||||||
chr6:63640087
|
T | A | 17 | a0001c0001t0008g0252a0001c0001t0008g0256a0001c0001t0008g0257others(14): Show | 17 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.-26+3937T>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63640087 | ||||||
chr6:63640618
|
G | T | 1 | a0001c0001t0019g0032 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-26+4468G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63640618 | ||||||
chr6:63640621
|
C | G | 17 | a0001c0001t0008g0252a0001c0001t0008g0256a0001c0001t0008g0257others(14): Show | 17 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.-26+4471C>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63640621 | ||||||
chr6:63640735
|
A | G | 4 | a0003c0004t0029g0295a0003c0004t0036g0294a0003c0004t0051g0296others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26+4585A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63640735 | ||||||
chr6:63640855
|
T | G | 3 | a0001c0001t0002g0221a0001c0001t0010g0219a0001c0001t0042g0220 | 3 | NA18969.hp2 NA18980.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.-26+4705T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63640855 | ||||||
chr6:63641011
|
A | T | 1 | a0001c0010t0002g0250 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-26+4861A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63641011 | ||||||
chr6:63641152
|
C | A | 1 | a0001c0001t0019g0021 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-26+5002C>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63641152 | ||||||
chr6:63641236
|
G | A | 56 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(53): Show | 59 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.-26+5086G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63641236 | ||||||
chr6:63641248
|
T | C | 1 | a0001c0001t0008g0252 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-26+5098T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63641248 | ||||||
chr6:63641320
|
C | T | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-26+5170C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63641320 | ||||||
chr6:63641363
|
T | A | 3 | a0001c0001t0003g0036a0001c0001t0003g0299a0001c0001t0007g0037 | 3 | HG02129.hp1 HG03831.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.-25-5164T>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63641363 | ||||||
chr6:63641385
|
C | T | 1 | a0001c0001t0003g0206 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-25-5142C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63641385 | ||||||
chr6:63641412
|
C | G | 1 | a0011c0014t0001g0205 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-25-5115C>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63641412 | ||||||
chr6:63641454
|
G | C | 103 | a0001c0001t0003g0027a0001c0001t0003g0036a0001c0001t0003g0040others(100): Show | 106 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-25-5073G>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63641454 | ||||||
chr6:63641517
|
G | T | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-25-5010G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63641517 | ||||||
chr6:63641521
|
GGTGTGTA others(3): Show |
G | 1 | a0014c0019t0084g0300 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-25-4999_-25-4990d others(12): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 63641521 | |||||
chr6:63641521
|
GGTGTGTA others(5): Show |
G | 1 | a0001c0001t0083g0301 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-25-4999_-25-4988d others(14): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 63641521 | |||||
chr6:63641524
|
GTGTA | G | 3 | a0001c0001t0026g0202a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG01192.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-25-4999_-25-4996d others(6): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 63641524 | |||||
chr6:63641528
|
A | ATG | 20 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(17): Show | 23 | HG01074.hp1 HG01243.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.-25-4959_-25-4958d others(4): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 63641528 | |||||
chr6:63641528
|
A | G | 2 | a0001c0001t0001g0201a0001c0001t0018g0214 | 2 | HG02622.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.-25-4999A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63641528 | ||||||
chr6:63641528
|
ATG | A | 64 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0186others(61): Show | 67 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.-25-4959_-25-4958d others(4): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 63641528 | |||||
chr6:63641528
|
ATGTG | A | 29 | a0001c0001t0001g0198a0001c0001t0002g0249a0001c0001t0003g0040others(26): Show | 29 | HG00558.hp1 HG01099.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.-25-4961_-25-4958d others(6): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 63641528 | |||||
chr6:63641528
|
ATGTGTG | A | 92 | a0001c0001t0002g0282a0001c0001t0003g0027a0001c0001t0003g0036others(89): Show | 95 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.-25-4963_-25-4958d others(8): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 63641528 | |||||
chr6:63641528
|
ATGTGTGT others(1): Show |
A | 6 | a0001c0001t0001g0199a0001c0001t0004g0200a0001c0001t0014g0018others(3): Show | 6 | HG01109.hp1 HG02056.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25-4965_-25-4958d others(10): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 63641528 | |||||
chr6:63641528
|
ATGTGTGT others(3): Show |
A | 5 | a0001c0001t0003g0215a0001c0001t0033g0251a0001c0001t0033g0265others(2): Show | 5 | HG01358.hp2 HG01978.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25-4967_-25-4958d others(12): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 63641528 | |||||
chr6:63641528
|
ATGTGTGT others(5): Show |
A | 4 | a0003c0004t0029g0295a0003c0004t0036g0294a0003c0004t0051g0296others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-4969_-25-4958d others(14): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 63641528 | |||||
chr6:63641528
|
ATGTGTGT others(7): Show |
A | 1 | a0001c0001t0078g0266 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-25-4971_-25-4958d others(16): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 63641528 | |||||
chr6:63641701
|
G | A | 2 | a0001c0001t0004g0125a0001c0001t0004g0126 | 2 | NA18990.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-25-4826G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63641701 | ||||||
chr6:63641749
|
C | T | 3 | a0001c0001t0023g0123a0001c0001t0023g0124a0001c0001t0023g0180 | 3 | HG01243.hp2 HG02683.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-25-4778C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63641749 | ||||||
chr6:63641856
|
A | G | 1 | a0001c0001t0002g0281 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-25-4671A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63641856 | ||||||
chr6:63641991
|
A | G | 1 | a0001c0001t0005g0113 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-25-4536A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63641991 | ||||||
chr6:63642105
|
C | A | 10 | a0001c0001t0023g0123a0001c0001t0023g0124a0001c0001t0023g0180others(7): Show | 12 | HG01243.hp2 HG01884.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-25-4422C>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63642105 | ||||||
chr6:63642197
|
A | T | 1 | a0002c0002t0063g0026 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-25-4330A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63642197 | ||||||
chr6:63642244
|
C | T | 2 | a0001c0001t0031g0254a0001c0001t0031g0255 | 2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-25-4283C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63642244 | ||||||
chr6:63642272
|
C | T | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-25-4255C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63642272 | ||||||
chr6:63642301
|
A | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-25-4226A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63642301 | ||||||
chr6:63642491
|
A | G | 5 | a0001c0001t0031g0254a0001c0001t0031g0255a0001c0001t0033g0251others(2): Show | 5 | HG02647.hp1 HG03209.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25-4036A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63642491 | ||||||
chr6:63642529
|
A | C | 5 | a0001c0001t0024g0012a0001c0001t0024g0285a0001c0001t0025g0283others(2): Show | 6 | HG00558.hp2 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25-3998A>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63642529 | ||||||
chr6:63642638
|
A | G | 4 | a0001c0001t0015g0121a0001c0001t0015g0122a0001c0001t0015g0178others(1): Show | 4 | HG02145.hp2 HG02258.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-3889A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63642638 | ||||||
chr6:63642643
|
C | T | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-25-3884C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63642643 | ||||||
chr6:63642695
|
A | G | 15 | a0001c0001t0013g0003a0001c0001t0013g0043a0001c0001t0013g0105others(12): Show | 15 | HG00741.hp2 HG01169.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-25-3832A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63642695 | ||||||
chr6:63642700
|
A | G | 1 | a0001c0015t0080g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-25-3827A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63642700 | ||||||
chr6:63642728
|
A | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-25-3799A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63642728 | ||||||
chr6:63642782
|
A | G | 12 | a0001c0001t0008g0252a0001c0001t0008g0256a0001c0001t0008g0257others(9): Show | 12 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-25-3745A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63642782 | ||||||
chr6:63642850
|
C | G | 1 | a0001c0001t0008g0264 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-25-3677C>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63642850 | ||||||
chr6:63642854
|
A | G | 1 | a0001c0001t0020g0193 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-25-3673A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63642854 | ||||||
chr6:63643115
|
G | A | 82 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(79): Show | 86 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-25-3412G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63643115 | ||||||
chr6:63643116
|
G | GT | 15 | a0001c0001t0001g0174a0001c0001t0001g0176a0001c0001t0001g0177others(12): Show | 15 | HG00408.hp1 HG01081.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.-25-3402dupT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 63643116 | |||||
chr6:63643201
|
A | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-25-3326A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63643201 | ||||||
chr6:63643364
|
G | A | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-25-3163G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63643364 | ||||||
chr6:63643454
|
T | C | 1 | a0001c0001t0002g0229 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-25-3073T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63643454 | ||||||
chr6:63643538
|
C | T | 7 | a0001c0001t0014g0015a0001c0001t0014g0016a0001c0001t0014g0018others(4): Show | 7 | HG01109.hp1 HG02109.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-25-2989C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63643538 | ||||||
chr6:63643589
|
C | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-25-2938C>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63643589 | ||||||
chr6:63643703
|
G | T | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-25-2824G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63643703 | ||||||
chr6:63643742
|
A | G | 56 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(53): Show | 59 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.-25-2785A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63643742 | ||||||
chr6:63644168
|
A | G | 1 | a0001c0001t0009g0212 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-25-2359A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63644168 | ||||||
chr6:63644242
|
ACT | A | 5 | a0001c0001t0024g0012a0001c0001t0024g0285a0001c0001t0025g0283others(2): Show | 6 | HG00558.hp2 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25-2280_-25-2279d others(4): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 63644242 | |||||
chr6:63644319
|
C | G | 1 | a0001c0001t0021g0172 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-25-2208C>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63644319 | ||||||
chr6:63644440
|
A | G | 1 | a0001c0001t0001g0198 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-25-2087A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63644440 | ||||||
chr6:63644717
|
T | A | 1 | a0001c0015t0080g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-25-1810T>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63644717 | ||||||
chr6:63644718
|
T | A | 14 | a0001c0001t0001g0115a0001c0001t0023g0123a0001c0001t0023g0124others(11): Show | 16 | HG01243.hp2 HG01884.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-25-1809T>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63644718 | ||||||
chr6:63644719
|
A | T | 11 | a0001c0001t0004g0171a0001c0001t0008g0263a0001c0001t0024g0012others(8): Show | 12 | HG00558.hp2 HG02486.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.-25-1808A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63644719 | ||||||
chr6:63644720
|
A | T | 3 | a0003c0004t0029g0295a0003c0004t0051g0296a0016c0021t0029g0297 | 3 | HG02486.hp2 HG02717.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-25-1807A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63644720 | ||||||
chr6:63644757
|
T | C | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-25-1770T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63644757 | ||||||
chr6:63644786
|
C | T | 1 | a0014c0019t0084g0300 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-25-1741C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63644786 | ||||||
chr6:63644822
|
G | C | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-25-1705G>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63644822 | ||||||
chr6:63644887
|
A | AT | 8 | a0001c0001t0003g0097a0001c0001t0013g0112a0001c0001t0015g0179others(5): Show | 8 | HG01109.hp1 HG02071.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-25-1624dupT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 63644887 | |||||
chr6:63644887
|
AT | A | 53 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(50): Show | 56 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.-25-1624delT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 63644887 | |||||
chr6:63644898
|
T | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-25-1629T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63644898 | ||||||
chr6:63644954
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-25-1573C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63644954 | ||||||
chr6:63644974
|
G | A | 56 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(53): Show | 59 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.-25-1553G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63644974 | ||||||
chr6:63645020
|
A | G | 6 | a0002c0002t0011g0002a0002c0002t0011g0022a0002c0002t0016g0023others(3): Show | 8 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-25-1507A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63645020 | ||||||
chr6:63645055
|
A | AT | 93 | a0001c0001t0003g0027a0001c0001t0003g0036a0001c0001t0003g0040others(90): Show | 96 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.-25-1463dupT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 63645055 | |||||
chr6:63645254
|
C | T | 197 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(194): Show | 204 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.-25-1273C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63645254 | ||||||
chr6:63645327
|
A | C | 1 | a0001c0001t0020g0193 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-25-1200A>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63645327 | ||||||
chr6:63645370
|
T | A | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-25-1157T>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63645370 | ||||||
chr6:63645380
|
C | T | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-25-1147C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63645380 | ||||||
chr6:63645405
|
T | A | 1 | a0001c0001t0023g0180 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-25-1122T>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63645405 | ||||||
chr6:63645500
|
G | A | 1 | a0001c0001t0003g0044 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-25-1027G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63645500 | ||||||
chr6:63645682
|
A | G | 267 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0033others(264): Show | 277 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.-25-845A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63645682 | ||||||
chr6:63645891
|
G | T | 2 | a0001c0001t0001g0169a0001c0001t0001g0208 | 2 | HG01358.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.-25-636G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63645891 | ||||||
chr6:63646806
|
CT | C | 187 | a0001c0001t0001g0141a0001c0001t0002g0005a0001c0001t0002g0010others(184): Show | 196 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.244+33delT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63646806 | |||||
chr6:63646806
|
CTT | C | 11 | a0001c0001t0002g0230a0001c0001t0002g0279a0001c0001t0003g0049others(8): Show | 11 | HG00639.hp2 HG01069.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.244+32_244+33delTT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63646806 | |||||
chr6:63646888
|
T | C | 1 | a0001c0001t0005g0050 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.244+93T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63646888 | ||||||
chr6:63646891
|
T | C | 1 | a0001c0001t0057g0035 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.244+96T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63646891 | ||||||
chr6:63647062
|
A | G | 1 | a0001c0001t0002g0247 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.244+267A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63647062 | ||||||
chr6:63647131
|
C | T | 1 | a0001c0001t0004g0140 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.244+336C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63647131 | ||||||
chr6:63647160
|
A | G | 11 | a0001c0001t0008g0252a0001c0001t0008g0256a0001c0001t0008g0257others(8): Show | 11 | HG00639.hp1 HG01099.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.244+365A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63647160 | ||||||
chr6:63647208
|
A | C | 10 | a0001c0001t0023g0123a0001c0001t0023g0124a0001c0001t0023g0180others(7): Show | 12 | HG01243.hp2 HG01884.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.244+413A>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63647208 | ||||||
chr6:63647287
|
G | A | 1 | a0001c0001t0081g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.244+492G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63647287 | ||||||
chr6:63647424
|
A | G | 1 | a0001c0001t0015g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.244+629A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63647424 | ||||||
chr6:63647524
|
G | T | 4 | a0003c0004t0029g0295a0003c0004t0036g0294a0003c0004t0051g0296others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+729G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63647524 | ||||||
chr6:63647549
|
T | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.244+754T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63647549 | ||||||
chr6:63647598
|
T | C | 1 | a0001c0001t0004g0211 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.244+803T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63647598 | ||||||
chr6:63647865
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.244+1070C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63647865 | ||||||
chr6:63647867
|
T | G | 57 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(54): Show | 60 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.244+1072T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63647867 | ||||||
chr6:63647884
|
A | C | 1 | a0006c0006t0043g0218 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.244+1089A>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63647884 | ||||||
chr6:63648025
|
G | T | 1 | a0001c0001t0003g0042 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.244+1230G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63648025 | ||||||
chr6:63648026
|
G | T | 1 | a0001c0001t0034g0287 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.244+1231G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63648026 | ||||||
chr6:63648082
|
G | A | 1 | a0001c0001t0002g0231 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.244+1287G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63648082 | ||||||
chr6:63648168
|
T | C | 9 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0004g0009others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.244+1373T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63648168 | ||||||
chr6:63648420
|
G | A | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.244+1625G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63648420 | ||||||
chr6:63648481
|
A | G | 2 | a0001c0001t0003g0040a0001c0001t0016g0041 | 2 | HG00558.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.244+1686A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63648481 | ||||||
chr6:63648533
|
G | A | 1 | a0001c0001t0010g0232 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.244+1738G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63648533 | ||||||
chr6:63648599
|
G | A | 4 | a0003c0004t0029g0295a0003c0004t0036g0294a0003c0004t0051g0296others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+1804G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63648599 | ||||||
chr6:63648691
|
G | C | 56 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(53): Show | 59 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.244+1896G>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63648691 | ||||||
chr6:63648782
|
A | G | 4 | a0001c0001t0015g0121a0001c0001t0015g0122a0001c0001t0015g0178others(1): Show | 4 | HG02145.hp2 HG02258.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+1987A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63648782 | ||||||
chr6:63649035
|
T | A | 56 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(53): Show | 59 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.244+2240T>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63649035 | ||||||
chr6:63649079
|
C | CTTAT | 96 | a0001c0001t0003g0027a0001c0001t0003g0036a0001c0001t0003g0040others(93): Show | 99 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.244+2314_244+2317d others(6): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63649079 | |||||
chr6:63649079
|
C | CTTATTTA others(1): Show |
8 | a0001c0001t0003g0095a0001c0001t0003g0096a0001c0001t0003g0299others(5): Show | 8 | HG00639.hp1 HG01070.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.244+2310_244+2317d others(10): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63649079 | |||||
chr6:63649079
|
C | CTTATTTA others(5): Show |
1 | a0001c0001t0078g0266 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.244+2306_244+2317d others(14): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63649079 | |||||
chr6:63649079
|
CTTATTTA others(1): Show |
C | 56 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(53): Show | 59 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.244+2310_244+2317d others(10): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63649079 | |||||
chr6:63649079
|
CTTATTTA others(5): Show |
C | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.244+2306_244+2317d others(14): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63649079 | |||||
chr6:63649109
|
T | TATTTATT others(5): Show |
1 | a0001c0001t0032g0260 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.244+2317_244+2318i others(14): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63649109 | |||||
chr6:63649242
|
C | T | 1 | a0001c0001t0003g0096 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.244+2447C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63649242 | ||||||
chr6:63649460
|
G | A | 3 | a0001c0001t0003g0100a0001c0001t0003g0215a0001c0001t0007g0055 | 3 | HG01081.hp1 HG01978.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.244+2665G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63649460 | ||||||
chr6:63649488
|
T | A | 1 | a0001c0001t0003g0290 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.244+2693T>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63649488 | ||||||
chr6:63649643
|
A | G | 1 | a0001c0001t0081g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.244+2848A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63649643 | ||||||
chr6:63649667
|
G | C | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.244+2872G>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63649667 | ||||||
chr6:63649808
|
T | C | 60 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(57): Show | 63 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.244+3013T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63649808 | ||||||
chr6:63649904
|
T | C | 1 | a0001c0001t0003g0042 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.244+3109T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63649904 | ||||||
chr6:63649951
|
T | C | 21 | a0001c0001t0008g0252a0001c0001t0008g0256a0001c0001t0008g0257others(18): Show | 22 | HG00558.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.244+3156T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63649951 | ||||||
chr6:63650095
|
G | A | 1 | a0009c0017t0085g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.244+3300G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63650095 | ||||||
chr6:63650116
|
T | C | 2 | a0001c0001t0003g0056a0001c0001t0003g0101 | 2 | HG02615.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.244+3321T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63650116 | ||||||
chr6:63650123
|
T | G | 57 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(54): Show | 60 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.244+3328T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63650123 | ||||||
chr6:63650168
|
C | T | 1 | a0002c0002t0068g0024 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.244+3373C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63650168 | ||||||
chr6:63650194
|
G | A | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.244+3399G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63650194 | ||||||
chr6:63650389
|
T | C | 22 | a0001c0001t0008g0252a0001c0001t0008g0256a0001c0001t0008g0257others(19): Show | 23 | HG00558.hp2 HG00639.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.244+3594T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63650389 | ||||||
chr6:63650539
|
T | G | 2 | a0001c0001t0004g0127a0001c0001t0004g0181 | 2 | HG00741.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.244+3744T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63650539 | ||||||
chr6:63650726
|
T | G | 1 | a0001c0001t0064g0111 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.244+3931T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63650726 | ||||||
chr6:63650905
|
AT | A | 15 | a0001c0001t0013g0003a0001c0001t0013g0043a0001c0001t0013g0105others(12): Show | 15 | HG00741.hp2 HG01169.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.244+4113delT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63650905 | |||||
chr6:63651190
|
G | A | 1 | a0001c0001t0002g0270 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.244+4395G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63651190 | ||||||
chr6:63651233
|
T | C | 1 | a0001c0001t0004g0142 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.244+4438T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63651233 | ||||||
chr6:63651297
|
G | A | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.244+4502G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63651297 | ||||||
chr6:63651454
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.244+4659C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63651454 | ||||||
chr6:63651535
|
T | C | 3 | a0001c0001t0001g0145a0001c0001t0004g0144a0001c0001t0052g0143 | 3 | HG02155.hp2 NA18994.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.244+4740T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63651535 | ||||||
chr6:63651543
|
G | T | 3 | a0001c0001t0001g0145a0001c0001t0004g0144a0001c0001t0052g0143 | 3 | HG02155.hp2 NA18994.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.244+4748G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63651543 | ||||||
chr6:63651795
|
A | C | 1 | a0001c0001t0076g0109 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.244+5000A>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63651795 | ||||||
chr6:63651967
|
C | T | 57 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(54): Show | 60 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.244+5172C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63651967 | ||||||
chr6:63651973
|
C | T | 1 | a0001c0015t0080g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.244+5178C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63651973 | ||||||
chr6:63652295
|
A | T | 213 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(210): Show | 222 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.244+5500A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63652295 | ||||||
chr6:63652482
|
T | A | 13 | a0001c0001t0004g0197a0001c0001t0004g0200a0001c0001t0004g0216others(10): Show | 13 | HG01069.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.244+5687T>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63652482 | ||||||
chr6:63652703
|
T | A | 1 | a0001c0001t0001g0146 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.244+5908T>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63652703 | ||||||
chr6:63652992
|
A | T | 1 | a0001c0001t0083g0301 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.244+6197A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63652992 | ||||||
chr6:63653019
|
G | GT | 17 | a0001c0001t0001g0139a0001c0001t0002g0278a0001c0001t0010g0246others(14): Show | 18 | HG00558.hp2 HG02155.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.244+6238dupT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63653019 | |||||
chr6:63653019
|
G | GTT | 10 | a0001c0001t0023g0124a0001c0001t0023g0180a0002c0002t0011g0002others(7): Show | 12 | HG01243.hp2 HG01358.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.244+6237_244+6238d others(4): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63653019 | |||||
chr6:63653054
|
T | G | 3 | a0001c0001t0024g0012a0001c0001t0081g0291a0006c0006t0043g0218 | 4 | HG02896.hp1 HG02897.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+6259T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63653054 | ||||||
chr6:63653154
|
GT | G | 18 | a0001c0001t0004g0197a0001c0001t0004g0200a0001c0001t0004g0216others(15): Show | 18 | HG01069.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.244+6371delT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63653154 | |||||
chr6:63653196
|
G | A | 1 | a0001c0001t0010g0233 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.244+6401G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63653196 | ||||||
chr6:63653205
|
AT | A | 8 | a0001c0001t0003g0059a0001c0001t0003g0060a0001c0001t0003g0209others(5): Show | 8 | HG01884.hp1 HG02630.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.244+6419delT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63653205 | |||||
chr6:63653267
|
A | G | 1 | a0001c0001t0003g0093 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.244+6472A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63653267 | ||||||
chr6:63653395
|
C | T | 1 | a0015c0020t0055g0029 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.244+6600C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63653395 | ||||||
chr6:63653451
|
C | T | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.244+6656C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63653451 | ||||||
chr6:63653452
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.244+6657G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63653452 | ||||||
chr6:63653497
|
T | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.244+6702T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63653497 | ||||||
chr6:63653622
|
C | G | 4 | a0001c0001t0003g0049a0001c0001t0003g0092a0001c0001t0003g0207others(1): Show | 4 | NA18952.hp2 NA18974.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.244+6827C>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63653622 | ||||||
chr6:63653843
|
A | G | 1 | a0001c0001t0004g0163 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.244+7048A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63653843 | ||||||
chr6:63653863
|
C | G | 1 | a0001c0001t0008g0252 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.244+7068C>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63653863 | ||||||
chr6:63654045
|
A | G | 1 | a0001c0001t0003g0290 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.244+7250A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63654045 | ||||||
chr6:63654068
|
G | C | 57 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(54): Show | 60 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.244+7273G>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63654068 | ||||||
chr6:63654110
|
G | C | 1 | a0001c0001t0083g0301 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.244+7315G>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63654110 | ||||||
chr6:63654115
|
A | C | 1 | a0005c0005t0002g0289 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.244+7320A>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63654115 | ||||||
chr6:63654177
|
G | T | 1 | a0001c0015t0080g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.244+7382G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63654177 | ||||||
chr6:63654212
|
G | C | 57 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(54): Show | 60 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.244+7417G>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63654212 | ||||||
chr6:63654213
|
A | G | 3 | a0001c0001t0003g0042a0001c0001t0003g0090a0001c0001t0016g0091 | 3 | HG03492.hp1 HG03704.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.244+7418A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63654213 | ||||||
chr6:63654430
|
G | A | 56 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(53): Show | 59 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.244+7635G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63654430 | ||||||
chr6:63654707
|
A | T | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.244+7912A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63654707 | ||||||
chr6:63654750
|
G | A | 1 | a0001c0001t0023g0180 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.244+7955G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63654750 | ||||||
chr6:63654809
|
C | T | 82 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(79): Show | 86 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.244+8014C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63654809 | ||||||
chr6:63654830
|
G | T | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.244+8035G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63654830 | ||||||
chr6:63654889
|
C | CT | 111 | a0001c0001t0001g0190a0001c0001t0002g0235a0001c0001t0003g0027others(108): Show | 114 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.244+8114dupT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63654889 | |||||
chr6:63654889
|
C | CTT | 64 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(61): Show | 69 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.244+8113_244+8114d others(4): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63654889 | |||||
chr6:63655038
|
T | A | 1 | a0001c0001t0078g0266 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.244+8243T>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63655038 | ||||||
chr6:63655040
|
T | C | 1 | a0001c0015t0080g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.244+8245T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63655040 | ||||||
chr6:63655226
|
C | T | 1 | a0001c0001t0064g0111 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.244+8431C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63655226 | ||||||
chr6:63655239
|
C | T | 1 | a0001c0001t0046g0280 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.244+8444C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63655239 | ||||||
chr6:63655266
|
A | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.244+8471A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63655266 | ||||||
chr6:63655372
|
C | T | 1 | a0001c0001t0081g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.244+8577C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63655372 | ||||||
chr6:63655381
|
T | G | 1 | a0001c0001t0009g0212 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.244+8586T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63655381 | ||||||
chr6:63655574
|
A | G | 1 | a0001c0001t0081g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.244+8779A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63655574 | ||||||
chr6:63655660
|
T | A | 1 | a0001c0001t0001g0174 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.244+8865T>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63655660 | ||||||
chr6:63655704
|
T | C | 1 | a0001c0001t0019g0021 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.244+8909T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63655704 | ||||||
chr6:63655882
|
A | G | 1 | a0015c0020t0055g0029 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.244+9087A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63655882 | ||||||
chr6:63656145
|
C | T | 1 | a0002c0002t0068g0024 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.244+9350C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63656145 | ||||||
chr6:63656403
|
T | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.244+9608T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63656403 | ||||||
chr6:63656442
|
T | A | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.244+9647T>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63656442 | ||||||
chr6:63656566
|
A | AT | 10 | a0001c0001t0023g0123a0001c0001t0023g0124a0001c0001t0023g0180others(7): Show | 12 | HG01243.hp2 HG01884.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.244+9776dupT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63656566 | |||||
chr6:63656673
|
G | A | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.244+9878G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63656673 | ||||||
chr6:63656674
|
T | C | 1 | a0002c0002t0011g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.244+9879T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63656674 | ||||||
chr6:63656813
|
C | T | 57 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(54): Show | 60 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.244+10018C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63656813 | ||||||
chr6:63657167
|
T | C | 1 | a0001c0001t0003g0062 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.244+10372T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63657167 | ||||||
chr6:63657190
|
G | A | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.244+10395G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63657190 | ||||||
chr6:63657296
|
G | A | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.244+10501G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63657296 | ||||||
chr6:63657364
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.244+10569C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63657364 | ||||||
chr6:63657468
|
C | T | 200 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(197): Show | 209 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.244+10673C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63657468 | ||||||
chr6:63657982
|
A | G | 5 | a0001c0001t0024g0012a0001c0001t0024g0285a0001c0001t0025g0283others(2): Show | 6 | HG00558.hp2 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.244+11187A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63657982 | ||||||
chr6:63658112
|
T | TA | 10 | a0001c0001t0023g0123a0001c0001t0023g0124a0001c0001t0023g0180others(7): Show | 12 | HG01243.hp2 HG01884.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.244+11320dupA | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63658112 | |||||
chr6:63658192
|
T | C | 4 | a0003c0004t0029g0295a0003c0004t0036g0294a0003c0004t0051g0296others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+11397T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63658192 | ||||||
chr6:63658517
|
T | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.244+11722T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63658517 | ||||||
chr6:63658544
|
C | T | 102 | a0001c0001t0003g0027a0001c0001t0003g0036a0001c0001t0003g0040others(99): Show | 105 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.244+11749C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63658544 | ||||||
chr6:63658558
|
T | C | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.244+11763T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63658558 | ||||||
chr6:63658707
|
TTTGTGTG others(4): Show |
T | 1 | a0001c0001t0002g0272 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.244+11914_244+1192 others(15): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63658707 | |||||
chr6:63658708
|
T | G | 1 | a0001c0001t0035g0271 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.244+11913T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63658708 | ||||||
chr6:63658708
|
T | TTG | 8 | a0001c0001t0004g0128a0001c0001t0015g0121a0001c0001t0015g0122others(5): Show | 8 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.244+11961_244+1196 others(6): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63658708 | |||||
chr6:63658708
|
T | TTGTG | 6 | a0001c0001t0001g0116a0001c0001t0002g0221a0001c0001t0002g0222others(3): Show | 6 | HG01496.hp1 HG02717.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.244+11959_244+1196 others(8): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63658708 | |||||
chr6:63658708
|
TTG | T | 19 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0129others(16): Show | 19 | HG00323.hp2 HG00738.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.244+11961_244+1196 others(6): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63658708 | |||||
chr6:63658708
|
TTGTG | T | 76 | a0001c0001t0001g0008a0001c0001t0001g0115a0001c0001t0001g0134others(73): Show | 76 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.244+11959_244+1196 others(8): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63658708 | |||||
chr6:63658708
|
TTGTGTG | T | 15 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0199others(12): Show | 16 | HG02056.hp1 HG02132.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.244+11957_244+1196 others(10): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63658708 | |||||
chr6:63658708
|
TTGTGTGT others(1): Show |
T | 10 | a0001c0001t0008g0252a0001c0001t0008g0256a0001c0001t0008g0257others(7): Show | 10 | HG00639.hp1 HG01099.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.244+11955_244+1196 others(12): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63658708 | |||||
chr6:63658708
|
TTGTGTGT others(3): Show |
T | 7 | a0001c0001t0002g0011a0001c0001t0002g0279a0001c0001t0032g0260others(4): Show | 8 | HG00544.hp2 HG00639.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.244+11953_244+1196 others(14): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63658708 | |||||
chr6:63658708
|
TTGTGTGT others(5): Show |
T | 40 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0226others(37): Show | 42 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.244+11951_244+1196 others(16): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63658708 | |||||
chr6:63658708
|
TTGTGTGT others(11): Show |
T | 15 | a0001c0001t0003g0059a0001c0001t0003g0060a0001c0001t0003g0090others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.244+11945_244+1196 others(22): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63658708 | |||||
chr6:63658708
|
TTGTGTGT others(13): Show |
T | 98 | a0001c0001t0003g0027a0001c0001t0003g0036a0001c0001t0003g0040others(95): Show | 103 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.244+11943_244+1196 others(24): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63658708 | |||||
chr6:63658708
|
TTGTGTGT others(15): Show |
T | 2 | a0004c0003t0022g0048a0004c0003t0022g0088 | 2 | NA18975.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.244+11941_244+1196 others(26): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63658708 | |||||
chr6:63658983
|
T | C | 22 | a0001c0001t0008g0252a0001c0001t0008g0256a0001c0001t0008g0257others(19): Show | 23 | HG00558.hp2 HG00639.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.244+12188T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63658983 | ||||||
chr6:63658986
|
T | C | 1 | a0001c0001t0003g0042 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.244+12191T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63658986 | ||||||
chr6:63659209
|
A | G | 1 | a0001c0001t0006g0087 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.244+12414A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63659209 | ||||||
chr6:63659241
|
A | G | 1 | a0014c0019t0084g0300 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.244+12446A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63659241 | ||||||
chr6:63659323
|
A | G | 1 | a0001c0001t0003g0056 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.244+12528A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63659323 | ||||||
chr6:63659465
|
G | T | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.244+12670G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63659465 | ||||||
chr6:63659608
|
A | G | 1 | a0004c0003t0022g0086 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.244+12813A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63659608 | ||||||
chr6:63659615
|
A | T | 1 | a0001c0001t0001g0160 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.244+12820A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63659615 | ||||||
chr6:63659637
|
A | G | 1 | a0001c0001t0006g0087 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.244+12842A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63659637 | ||||||
chr6:63660040
|
G | T | 1 | a0001c0001t0038g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.244+13245G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63660040 | ||||||
chr6:63660123
|
G | T | 1 | a0001c0001t0001g0199 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.244+13328G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63660123 | ||||||
chr6:63660157
|
C | T | 1 | a0001c0001t0034g0287 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.244+13362C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63660157 | ||||||
chr6:63660344
|
T | A | 4 | a0001c0001t0023g0123a0001c0001t0023g0124a0001c0001t0023g0180others(1): Show | 4 | HG01243.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.244+13549T>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63660344 | ||||||
chr6:63660400
|
G | T | 4 | a0001c0001t0003g0049a0001c0001t0003g0092a0001c0001t0003g0207others(1): Show | 4 | NA18952.hp2 NA18974.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.244+13605G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63660400 | ||||||
chr6:63660640
|
T | A | 1 | a0004c0003t0022g0086 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.244+13845T>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63660640 | ||||||
chr6:63660704
|
A | T | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.244+13909A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63660704 | ||||||
chr6:63660753
|
T | G | 2 | a0001c0001t0006g0038a0001c0001t0006g0065 | 2 | NA19064.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.244+13958T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63660753 | ||||||
chr6:63660840
|
C | A | 1 | a0001c0001t0017g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.244+14045C>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63660840 | ||||||
chr6:63660845
|
T | C | 90 | a0001c0001t0003g0027a0001c0001t0003g0036a0001c0001t0003g0040others(87): Show | 93 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.244+14050T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63660845 | ||||||
chr6:63661248
|
C | T | 22 | a0001c0001t0008g0252a0001c0001t0008g0256a0001c0001t0008g0257others(19): Show | 23 | HG00558.hp2 HG00639.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.244+14453C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63661248 | ||||||
chr6:63661344
|
A | T | 3 | a0001c0001t0026g0202a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG01192.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.244+14549A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63661344 | ||||||
chr6:63661349
|
T | C | 1 | a0001c0001t0003g0209 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.244+14554T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63661349 | ||||||
chr6:63661349
|
T | G | 1 | a0001c0015t0080g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.244+14554T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63661349 | ||||||
chr6:63661548
|
A | G | 1 | a0001c0001t0003g0061 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.244+14753A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63661548 | ||||||
chr6:63661722
|
A | G | 16 | a0001c0001t0008g0252a0001c0001t0008g0256a0001c0001t0008g0257others(13): Show | 16 | HG00639.hp1 HG01099.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.244+14927A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63661722 | ||||||
chr6:63661759
|
G | T | 1 | a0001c0001t0086g0162 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.244+14964G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63661759 | ||||||
chr6:63662085
|
G | A | 1 | a0001c0001t0046g0280 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.244+15290G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63662085 | ||||||
chr6:63662138
|
A | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.244+15343A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63662138 | ||||||
chr6:63662324
|
C | T | 3 | a0001c0001t0001g0145a0001c0001t0004g0144a0001c0001t0052g0143 | 3 | HG02155.hp2 NA18994.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.244+15529C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63662324 | ||||||
chr6:63662417
|
G | T | 1 | a0001c0001t0001g0138 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.244+15622G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63662417 | ||||||
chr6:63662758
|
C | T | 85 | a0001c0001t0003g0027a0001c0001t0003g0036a0001c0001t0003g0040others(82): Show | 88 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.244+15963C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63662758 | ||||||
chr6:63663094
|
C | T | 2 | a0001c0001t0003g0085a0001c0001t0048g0084 | 2 | HG01106.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.244+16299C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63663094 | ||||||
chr6:63663468
|
C | G | 1 | a0001c0001t0050g0223 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.245-16532C>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63663468 | ||||||
chr6:63663561
|
T | C | 10 | a0001c0001t0008g0252a0001c0001t0008g0256a0001c0001t0008g0257others(7): Show | 10 | HG00639.hp1 HG01099.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.245-16439T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63663561 | ||||||
chr6:63663755
|
A | T | 1 | a0001c0001t0010g0246 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.245-16245A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63663755 | ||||||
chr6:63663766
|
G | A | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-16234G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63663766 | ||||||
chr6:63663827
|
A | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-16173A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63663827 | ||||||
chr6:63663962
|
A | G | 1 | a0001c0001t0070g0083 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.245-16038A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63663962 | ||||||
chr6:63663992
|
C | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-16008C>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63663992 | ||||||
chr6:63664078
|
G | A | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-15922G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63664078 | ||||||
chr6:63664314
|
C | T | 5 | a0001c0001t0024g0012a0001c0001t0024g0285a0001c0001t0025g0283others(2): Show | 6 | HG00558.hp2 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-15686C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63664314 | ||||||
chr6:63664740
|
T | A | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-15260T>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63664740 | ||||||
chr6:63664941
|
A | G | 1 | a0001c0001t0003g0101 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.245-15059A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63664941 | ||||||
chr6:63665154
|
A | G | 1 | a0001c0001t0081g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.245-14846A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63665154 | ||||||
chr6:63665476
|
G | T | 3 | a0001c0001t0003g0100a0001c0001t0003g0215a0001c0001t0007g0055 | 3 | HG01081.hp1 HG01978.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.245-14524G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63665476 | ||||||
chr6:63665477
|
T | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-14523T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63665477 | ||||||
chr6:63665486
|
G | GT | 34 | a0001c0001t0001g0033a0001c0001t0001g0130a0001c0001t0001g0137others(31): Show | 34 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.245-14496dupT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63665486 | |||||
chr6:63665486
|
G | GTT | 90 | a0001c0001t0001g0034a0001c0001t0002g0279a0001c0001t0003g0027others(87): Show | 95 | HG00423.hp2 HG00597.hp1 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.245-14497_245-1449 others(6): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63665486 | |||||
chr6:63665486
|
G | GTTT | 9 | a0001c0001t0003g0080a0001c0001t0003g0100a0001c0001t0003g0206others(6): Show | 9 | HG00408.hp1 HG01081.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.245-14498_245-1449 others(7): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63665486 | |||||
chr6:63665486
|
G | T | 2 | a0001c0001t0034g0287a0001c0001t0069g0017 | 2 | HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.245-14514G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63665486 | ||||||
chr6:63665590
|
A | G | 1 | a0001c0001t0034g0287 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.245-14410A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63665590 | ||||||
chr6:63665655
|
T | C | 3 | a0004c0003t0022g0048a0004c0003t0022g0086a0004c0003t0022g0088 | 3 | HG00423.hp2 NA18975.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.245-14345T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63665655 | ||||||
chr6:63665747
|
C | T | 1 | a0001c0015t0080g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.245-14253C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63665747 | ||||||
chr6:63665930
|
T | G | 1 | a0001c0015t0080g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.245-14070T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63665930 | ||||||
chr6:63666048
|
A | G | 2 | a0001c0001t0004g0142a0001c0001t0009g0212 | 2 | HG02698.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.245-13952A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63666048 | ||||||
chr6:63666118
|
C | G | 7 | a0001c0001t0014g0015a0001c0001t0014g0016a0001c0001t0014g0018others(4): Show | 7 | HG01109.hp1 HG02109.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.245-13882C>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63666118 | ||||||
chr6:63666294
|
A | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-13706A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63666294 | ||||||
chr6:63666755
|
C | CT | 6 | a0001c0001t0003g0059a0001c0001t0003g0060a0001c0001t0003g0209others(3): Show | 6 | HG02630.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-13231dupT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63666755 | |||||
chr6:63666823
|
C | T | 1 | a0001c0015t0080g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.245-13177C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63666823 | ||||||
chr6:63666844
|
C | T | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-13156C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63666844 | ||||||
chr6:63666845
|
G | A | 1 | a0001c0001t0007g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.245-13155G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63666845 | ||||||
chr6:63666920
|
T | C | 1 | a0001c0001t0056g0119 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.245-13080T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63666920 | ||||||
chr6:63666941
|
A | G | 1 | a0001c0001t0081g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.245-13059A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63666941 | ||||||
chr6:63667126
|
T | G | 2 | a0006c0006t0002g0217a0006c0006t0043g0218 | 2 | HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.245-12874T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63667126 | ||||||
chr6:63667196
|
T | C | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-12804T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63667196 | ||||||
chr6:63667278
|
A | G | 1 | a0001c0001t0064g0111 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.245-12722A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63667278 | ||||||
chr6:63667340
|
T | C | 1 | a0001c0001t0001g0146 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.245-12660T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63667340 | ||||||
chr6:63667361
|
T | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-12639T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63667361 | ||||||
chr6:63667522
|
A | G | 1 | a0001c0001t0001g0188 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.245-12478A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63667522 | ||||||
chr6:63667633
|
T | C | 87 | a0001c0001t0003g0027a0001c0001t0003g0036a0001c0001t0003g0040others(84): Show | 90 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.245-12367T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63667633 | ||||||
chr6:63667638
|
C | T | 87 | a0001c0001t0003g0027a0001c0001t0003g0036a0001c0001t0003g0040others(84): Show | 90 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.245-12362C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63667638 | ||||||
chr6:63667671
|
T | C | 1 | a0001c0001t0014g0018 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.245-12329T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63667671 | ||||||
chr6:63667681
|
T | C | 1 | a0001c0001t0003g0093 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.245-12319T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63667681 | ||||||
chr6:63667695
|
C | T | 1 | a0001c0001t0003g0062 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.245-12305C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63667695 | ||||||
chr6:63667903
|
C | T | 1 | a0001c0001t0041g0225 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.245-12097C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63667903 | ||||||
chr6:63668277
|
G | A | 10 | a0001c0001t0008g0252a0001c0001t0008g0256a0001c0001t0008g0257others(7): Show | 10 | HG00639.hp1 HG01099.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.245-11723G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63668277 | ||||||
chr6:63668363
|
G | A | 4 | a0003c0004t0029g0295a0003c0004t0036g0294a0003c0004t0051g0296others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-11637G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63668363 | ||||||
chr6:63668400
|
C | T | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-11600C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63668400 | ||||||
chr6:63668418
|
C | T | 1 | a0001c0001t0004g0126 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.245-11582C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63668418 | ||||||
chr6:63668460
|
A | G | 1 | a0001c0001t0006g0066 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.245-11540A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63668460 | ||||||
chr6:63668553
|
G | T | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-11447G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63668553 | ||||||
chr6:63668858
|
C | A | 1 | a0001c0001t0067g0064 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.245-11142C>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63668858 | ||||||
chr6:63668914
|
A | G | 1 | a0001c0001t0078g0266 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.245-11086A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63668914 | ||||||
chr6:63668960
|
T | C | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-11040T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63668960 | ||||||
chr6:63669160
|
C | T | 2 | a0001c0001t0001g0145a0001c0001t0004g0144 | 2 | NA18994.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.245-10840C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63669160 | ||||||
chr6:63669178
|
A | G | 21 | a0001c0001t0008g0252a0001c0001t0008g0256a0001c0001t0008g0257others(18): Show | 22 | HG00558.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.245-10822A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63669178 | ||||||
chr6:63669330
|
G | A | 56 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(53): Show | 59 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.245-10670G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63669330 | ||||||
chr6:63669454
|
C | T | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-10546C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63669454 | ||||||
chr6:63669475
|
A | C | 1 | a0001c0001t0002g0245 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.245-10525A>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63669475 | ||||||
chr6:63669493
|
A | G | 70 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(67): Show | 75 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.245-10507A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63669493 | ||||||
chr6:63669632
|
G | A | 1 | a0001c0001t0032g0260 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.245-10368G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63669632 | ||||||
chr6:63669745
|
A | T | 1 | a0001c0015t0080g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.245-10255A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63669745 | ||||||
chr6:63669789
|
C | A | 1 | a0014c0019t0084g0300 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.245-10211C>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63669789 | ||||||
chr6:63669884
|
T | G | 2 | a0006c0006t0002g0217a0006c0006t0043g0218 | 2 | HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.245-10116T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63669884 | ||||||
chr6:63669968
|
A | G | 1 | a0001c0016t0008g0261 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.245-10032A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63669968 | ||||||
chr6:63669975
|
A | T | 11 | a0001c0001t0008g0252a0001c0001t0008g0256a0001c0001t0008g0257others(8): Show | 11 | HG00639.hp1 HG01099.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.245-10025A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63669975 | ||||||
chr6:63670045
|
C | T | 2 | a0001c0001t0003g0056a0001c0001t0003g0101 | 2 | HG02615.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.245-9955C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63670045 | ||||||
chr6:63670046
|
C | T | 2 | a0001c0001t0031g0254a0001c0001t0031g0255 | 2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.245-9954C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63670046 | ||||||
chr6:63670299
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.245-9701G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63670299 | ||||||
chr6:63670307
|
C | T | 1 | a0003c0004t0051g0296 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.245-9693C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63670307 | ||||||
chr6:63670583
|
G | A | 1 | a0001c0001t0003g0299 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.245-9417G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63670583 | ||||||
chr6:63670734
|
T | A | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-9266T>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63670734 | ||||||
chr6:63670987
|
A | G | 106 | a0001c0001t0003g0027a0001c0001t0003g0036a0001c0001t0003g0040others(103): Show | 109 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.245-9013A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63670987 | ||||||
chr6:63671106
|
C | CT | 7 | a0001c0001t0003g0085a0001c0001t0032g0259a0001c0001t0048g0084others(4): Show | 7 | HG01106.hp2 HG01952.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.245-8882dupT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63671106 | |||||
chr6:63671414
|
G | A | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-8586G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63671414 | ||||||
chr6:63671468
|
C | T | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-8532C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63671468 | ||||||
chr6:63671490
|
G | T | 1 | a0001c0001t0081g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.245-8510G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63671490 | ||||||
chr6:63671560
|
C | T | 198 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(195): Show | 207 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.245-8440C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63671560 | ||||||
chr6:63671747
|
T | C | 2 | a0001c0001t0001g0176a0001c0001t0027g0150 | 2 | HG02071.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.245-8253T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63671747 | ||||||
chr6:63671813
|
C | A | 4 | a0001c0001t0015g0121a0001c0001t0015g0122a0001c0001t0015g0178others(1): Show | 4 | HG02145.hp2 HG02258.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-8187C>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63671813 | ||||||
chr6:63671815
|
C | T | 1 | a0004c0003t0022g0086 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.245-8185C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63671815 | ||||||
chr6:63672076
|
T | C | 309 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0033others(306): Show | 319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.245-7924T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63672076 | ||||||
chr6:63672096
|
C | T | 1 | a0001c0001t0034g0287 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.245-7904C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63672096 | ||||||
chr6:63672438
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.245-7562G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63672438 | ||||||
chr6:63672578
|
A | G | 1 | a0001c0001t0072g0079 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.245-7422A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63672578 | ||||||
chr6:63672630
|
G | A | 2 | a0001c0001t0006g0038a0001c0001t0006g0065 | 2 | NA19064.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.245-7370G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63672630 | ||||||
chr6:63672706
|
C | T | 4 | a0001c0001t0002g0010a0001c0001t0002g0235a0001c0001t0002g0244others(1): Show | 5 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.245-7294C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63672706 | ||||||
chr6:63672723
|
A | T | 54 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(51): Show | 57 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.245-7277A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63672723 | ||||||
chr6:63672948
|
A | C | 1 | a0001c0001t0057g0035 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.245-7052A>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63672948 | ||||||
chr6:63673079
|
C | T | 198 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(195): Show | 207 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.245-6921C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63673079 | ||||||
chr6:63673122
|
T | C | 1 | a0001c0001t0003g0093 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.245-6878T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63673122 | ||||||
chr6:63673501
|
T | C | 1 | a0001c0015t0080g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.245-6499T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63673501 | ||||||
chr6:63674039
|
A | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-5961A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63674039 | ||||||
chr6:63674273
|
TA | T | 85 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(82): Show | 89 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.245-5722delA | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63674273 | |||||
chr6:63674283
|
T | TATATATG others(118): Show |
2 | a0001c0001t0012g0167a0001c0001t0012g0168 | 2 | NA19002.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.245-5696_245-5695i others(127): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63674283 | |||||
chr6:63674283
|
T | TATATATG others(73): Show |
1 | a0001c0001t0021g0172 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.245-5696_245-5695i others(82): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63674283 | |||||
chr6:63674283
|
T | TATATATG others(77): Show |
103 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0033others(100): Show | 104 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.245-5696_245-5695i others(86): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63674283 | |||||
chr6:63674283
|
T | TATATATG others(79): Show |
1 | a0001c0001t0056g0119 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.245-5696_245-5695i others(88): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63674283 | |||||
chr6:63674283
|
T | TATATATG others(75): Show |
1 | a0001c0001t0001g0157 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.245-5696_245-5695i others(84): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63674283 | |||||
chr6:63674283
|
T | TATATATG others(79): Show |
1 | a0001c0001t0001g0148 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.245-5703_245-5702i others(88): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63674283 | |||||
chr6:63674285
|
T | TATATGTG others(77): Show |
1 | a0001c0001t0004g0126 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.245-5696_245-5695i others(86): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63674285 | |||||
chr6:63674286
|
A | ATATGTGT others(124): Show |
84 | a0001c0001t0003g0027a0001c0001t0003g0036a0001c0001t0003g0040others(81): Show | 87 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.245-5696_245-5695i others(133): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63674286 | |||||
chr6:63674286
|
A | ATATGTGT others(122): Show |
1 | a0001c0001t0003g0093 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.245-5696_245-5695i others(131): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63674286 | |||||
chr6:63674286
|
A | ATATGTGT others(79): Show |
22 | a0001c0001t0008g0252a0001c0001t0008g0256a0001c0001t0008g0257others(19): Show | 23 | HG00558.hp2 HG00639.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.245-5696_245-5695i others(88): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63674286 | |||||
chr6:63674286
|
A | ATATGTGT others(83): Show |
27 | a0001c0001t0013g0003a0001c0001t0013g0043a0001c0001t0013g0105others(24): Show | 29 | HG00741.hp2 HG01169.hp2 HG01358.hp2 others(26): Show |
intron_variant | MODIFIER | c.245-5696_245-5695i others(92): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63674286 | |||||
chr6:63674286
|
A | ATATGTGT others(81): Show |
1 | a0002c0002t0016g0025 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.245-5696_245-5695i others(90): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63674286 | |||||
chr6:63674286
|
A | ATATGTGT others(79): Show |
4 | a0001c0001t0023g0123a0001c0001t0023g0124a0001c0001t0023g0180others(1): Show | 4 | HG01243.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.245-5696_245-5695i others(88): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63674286 | |||||
chr6:63674286
|
A | ATATGTGT others(126): Show |
1 | a0001c0001t0016g0041 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.245-5696_245-5695i others(135): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63674286 | |||||
chr6:63674286
|
A | ATATGTGT others(83): Show |
1 | a0001c0015t0080g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.245-5696_245-5695i others(92): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63674286 | |||||
chr6:63674286
|
A | ATATGTGT others(115): Show |
2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-5696_245-5695i others(124): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63674286 | |||||
chr6:63674290
|
G | GTGTGTGT others(27): Show |
56 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(53): Show | 59 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.245-5696_245-5695i others(36): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63674290 | |||||
chr6:63674437
|
A | C | 4 | a0003c0004t0029g0295a0003c0004t0036g0294a0003c0004t0051g0296others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-5563A>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63674437 | ||||||
chr6:63674619
|
G | A | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-5381G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63674619 | ||||||
chr6:63674846
|
G | C | 1 | a0015c0020t0055g0029 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.245-5154G>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63674846 | ||||||
chr6:63674947
|
A | G | 1 | a0001c0001t0056g0119 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.245-5053A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63674947 | ||||||
chr6:63675088
|
A | G | 7 | a0001c0001t0002g0226a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG00544.hp2 NA18612.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.245-4912A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63675088 | ||||||
chr6:63675174
|
A | G | 1 | a0003c0004t0036g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.245-4826A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63675174 | ||||||
chr6:63675255
|
T | C | 1 | a0001c0001t0003g0093 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.245-4745T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63675255 | ||||||
chr6:63675335
|
G | A | 3 | a0001c0001t0002g0236a0001c0001t0002g0237a0001c0001t0002g0249 | 3 | HG03491.hp2 HG03492.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.245-4665G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63675335 | ||||||
chr6:63675481
|
T | C | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-4519T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63675481 | ||||||
chr6:63675602
|
T | C | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-4398T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63675602 | ||||||
chr6:63675763
|
C | G | 5 | a0001c0001t0024g0012a0001c0001t0024g0285a0001c0001t0025g0283others(2): Show | 6 | HG00558.hp2 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-4237C>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63675763 | ||||||
chr6:63675902
|
C | T | 4 | a0001c0001t0015g0121a0001c0001t0015g0122a0001c0001t0015g0178others(1): Show | 4 | HG02145.hp2 HG02258.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-4098C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63675902 | ||||||
chr6:63675977
|
T | G | 1 | a0001c0001t0081g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.245-4023T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63675977 | ||||||
chr6:63676159
|
C | T | 202 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(199): Show | 211 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.245-3841C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63676159 | ||||||
chr6:63676433
|
T | C | 55 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(52): Show | 58 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.245-3567T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63676433 | ||||||
chr6:63676453
|
G | C | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-3547G>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63676453 | ||||||
chr6:63676459
|
A | T | 1 | a0001c0001t0001g0141 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.245-3541A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63676459 | ||||||
chr6:63676610
|
G | C | 7 | a0001c0001t0014g0015a0001c0001t0014g0016a0001c0001t0014g0018others(4): Show | 7 | HG01109.hp1 HG02109.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.245-3390G>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63676610 | ||||||
chr6:63676610
|
G | T | 1 | a0001c0001t0001g0157 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.245-3390G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63676610 | ||||||
chr6:63676739
|
A | G | 1 | a0015c0020t0055g0029 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.245-3261A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63676739 | ||||||
chr6:63676825
|
G | A | 1 | a0009c0017t0085g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.245-3175G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63676825 | ||||||
chr6:63676878
|
A | T | 1 | a0001c0001t0008g0256 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.245-3122A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63676878 | ||||||
chr6:63676909
|
T | C | 1 | a0001c0015t0080g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.245-3091T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63676909 | ||||||
chr6:63676946
|
C | T | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-3054C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63676946 | ||||||
chr6:63677125
|
A | C | 3 | a0001c0001t0023g0123a0001c0001t0023g0124a0009c0017t0085g0114 | 3 | HG01243.hp2 HG02738.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.245-2875A>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63677125 | ||||||
chr6:63677303
|
A | G | 1 | a0001c0015t0080g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.245-2697A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63677303 | ||||||
chr6:63677545
|
C | G | 1 | a0001c0001t0081g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.245-2455C>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63677545 | ||||||
chr6:63677724
|
TGAA | T | 3 | a0003c0004t0029g0295a0003c0004t0051g0296a0016c0021t0029g0297 | 3 | HG02486.hp2 HG02717.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.245-2274_245-2272d others(5): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63677724 | |||||
chr6:63677740
|
A | G | 1 | a0001c0001t0031g0255 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.245-2260A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63677740 | ||||||
chr6:63677818
|
CA | C | 55 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(52): Show | 58 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.245-2181delA | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63677818 | ||||||
chr6:63677834
|
A | G | 1 | a0002c0002t0063g0026 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.245-2166A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63677834 | ||||||
chr6:63677977
|
C | T | 1 | a0001c0001t0081g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.245-2023C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63677977 | ||||||
chr6:63678162
|
G | A | 1 | a0001c0001t0002g0274 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.245-1838G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63678162 | ||||||
chr6:63678178
|
G | A | 1 | a0002c0002t0068g0024 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.245-1822G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63678178 | ||||||
chr6:63678220
|
C | CA | 19 | a0001c0001t0003g0049a0001c0001t0003g0092a0001c0001t0003g0207others(16): Show | 19 | HG00741.hp2 HG01169.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.245-1769dupA | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63678220 | |||||
chr6:63678220
|
CA | C | 56 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(53): Show | 59 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.245-1769delA | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63678220 | |||||
chr6:63678231
|
A | G | 1 | a0001c0001t0010g0233 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.245-1769A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63678231 | ||||||
chr6:63678232
|
G | A | 1 | a0001c0001t0010g0233 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.245-1768G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63678232 | ||||||
chr6:63678270
|
A | G | 1 | a0010c0011t0003g0098 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.245-1730A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63678270 | ||||||
chr6:63678355
|
A | G | 1 | a0001c0001t0002g0242 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.245-1645A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63678355 | ||||||
chr6:63678583
|
C | CT | 10 | a0001c0001t0003g0059a0001c0001t0003g0060a0001c0001t0003g0209others(7): Show | 10 | HG01884.hp1 HG02135.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.245-1405dupT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63678583 | |||||
chr6:63678722
|
G | A | 1 | a0014c0019t0084g0300 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.245-1278G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63678722 | ||||||
chr6:63678724
|
A | G | 1 | a0001c0001t0003g0093 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.245-1276A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63678724 | ||||||
chr6:63679098
|
G | GT | 15 | a0001c0001t0001g0034a0001c0001t0001g0136a0001c0001t0001g0156others(12): Show | 16 | HG00558.hp2 HG01255.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.245-887dupT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63679098 | |||||
chr6:63679228
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.245-772G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63679228 | ||||||
chr6:63679246
|
A | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-754A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63679246 | ||||||
chr6:63679460
|
CCT | C | 51 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(48): Show | 54 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.245-533_245-532del others(2): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 63679460 | |||||
chr6:63679483
|
C | T | 5 | a0001c0001t0031g0254a0001c0001t0031g0255a0001c0001t0033g0251others(2): Show | 5 | HG02647.hp1 HG03209.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-517C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63679483 | ||||||
chr6:63679738
|
T | C | 5 | a0001c0001t0003g0059a0001c0001t0003g0060a0001c0001t0003g0209others(2): Show | 5 | HG01884.hp1 HG02630.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.245-262T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63679738 | ||||||
chr6:63679828
|
G | C | 1 | a0001c0001t0001g0159 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.245-172G>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63679828 | ||||||
chr6:63679958
|
C | A | 1 | a0001c0001t0004g0216 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.245-42C>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63679958 | ||||||
chr6:63680247
|
A | G | 5 | a0001c0001t0031g0254a0001c0001t0031g0255a0001c0001t0033g0251others(2): Show | 5 | HG02647.hp1 HG03209.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.406+86A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | chr6 | 63680247 | ||||||
chr6:63680295
|
T | C | 3 | a0002c0002t0011g0002a0002c0002t0011g0022a0002c0002t0016g0023 | 5 | HG02258.hp2 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.406+134T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | chr6 | 63680295 | ||||||
chr6:63680382
|
ACT | A | 16 | a0001c0001t0008g0252a0001c0001t0008g0256a0001c0001t0008g0257others(13): Show | 16 | HG00639.hp1 HG01099.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.406+224_406+225del others(2): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 63680382 | |||||
chr6:63680398
|
A | AT | 26 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0136others(23): Show | 26 | HG00423.hp1 HG01109.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.406+260dupT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 63680398 | |||||
chr6:63680398
|
AT | A | 26 | a0001c0001t0001g0160a0001c0001t0002g0236a0001c0001t0002g0237others(23): Show | 26 | HG00738.hp1 HG01099.hp2 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.406+260delT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 63680398 | |||||
chr6:63680398
|
ATT | A | 8 | a0001c0001t0008g0252a0001c0001t0024g0012a0001c0001t0024g0285others(5): Show | 9 | HG00558.hp2 HG00639.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.406+259_406+260del others(2): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 63680398 | |||||
chr6:63680438
|
G | T | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.406+277G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | chr6 | 63680438 | ||||||
chr6:63680547
|
C | CACGAAAA others(25): Show |
2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.406+387_406+388ins others(32): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 63680547 | |||||
chr6:63680852
|
A | G | 1 | a0001c0001t0067g0064 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.406+691A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | chr6 | 63680852 | ||||||
chr6:63680992
|
T | G | 1 | a0001c0001t0001g0117 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.406+831T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | chr6 | 63680992 | ||||||
chr6:63681003
|
A | G | 56 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(53): Show | 59 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.406+842A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | chr6 | 63681003 | ||||||
chr6:63681057
|
A | G | 1 | a0001c0001t0081g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.406+896A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | chr6 | 63681057 | ||||||
chr6:63681296
|
A | G | 11 | a0001c0001t0001g0008a0001c0001t0001g0146a0001c0001t0001g0147others(8): Show | 11 | HG00408.hp2 HG00544.hp1 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.406+1135A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | chr6 | 63681296 | ||||||
chr6:63681340
|
T | C | 14 | a0001c0001t0013g0003a0001c0001t0013g0043a0001c0001t0013g0105others(11): Show | 14 | HG00741.hp2 HG01169.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.406+1179T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | chr6 | 63681340 | ||||||
chr6:63681733
|
G | A | 5 | a0001c0001t0024g0012a0001c0001t0024g0285a0001c0001t0025g0283others(2): Show | 6 | HG00558.hp2 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.406+1572G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | chr6 | 63681733 | ||||||
chr6:63681765
|
G | A | 2 | a0006c0006t0002g0217a0006c0006t0043g0218 | 2 | HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.406+1604G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | chr6 | 63681765 | ||||||
chr6:63681965
|
C | T | 1 | a0001c0015t0080g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.406+1804C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | chr6 | 63681965 | ||||||
chr6:63682233
|
A | G | 207 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(204): Show | 216 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.407-1896A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | chr6 | 63682233 | ||||||
chr6:63682327
|
A | G | 4 | a0001c0001t0023g0123a0001c0001t0023g0124a0001c0001t0023g0180others(1): Show | 4 | HG01243.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.407-1802A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | chr6 | 63682327 | ||||||
chr6:63682462
|
C | T | 1 | a0001c0001t0065g0039 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.407-1667C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | chr6 | 63682462 | ||||||
chr6:63682507
|
A | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.407-1622A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | chr6 | 63682507 | ||||||
chr6:63682580
|
A | G | 4 | a0001c0001t0015g0121a0001c0001t0015g0122a0001c0001t0015g0178others(1): Show | 4 | HG02145.hp2 HG02258.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.407-1549A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | chr6 | 63682580 | ||||||
chr6:63683289
|
T | C | 1 | a0001c0001t0081g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.407-840T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | chr6 | 63683289 | ||||||
chr6:63683372
|
A | G | 1 | a0001c0010t0002g0250 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.407-757A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | chr6 | 63683372 | ||||||
chr6:63683597
|
G | A | 1 | a0001c0001t0020g0192 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.407-532G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | chr6 | 63683597 | ||||||
chr6:63683680
|
T | C | 8 | a0001c0001t0003g0069a0001c0001t0003g0080a0001c0001t0003g0099others(5): Show | 8 | HG00423.hp2 HG00597.hp1 NA18955.hp2 others(5): Show |
intron_variant | MODIFIER | c.407-449T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | chr6 | 63683680 | ||||||
chr6:63683721
|
T | C | 1 | a0001c0001t0004g0125 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.407-408T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 3/15 | chr6 | 63683721 | ||||||
chr6:63686177
|
CAG | C | 11 | a0001c0001t0008g0252a0001c0001t0008g0256a0001c0001t0008g0257others(8): Show | 11 | HG00639.hp1 HG01099.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.2189+267_2189+268d others(4): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63686177 | ||||||
chr6:63686242
|
T | C | 3 | a0001c0001t0024g0012a0001c0001t0024g0285a0001c0001t0025g0284 | 4 | HG02630.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2189+331T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63686242 | ||||||
chr6:63686343
|
GT | G | 7 | a0001c0001t0001g0148a0001c0001t0003g0101a0001c0001t0031g0254others(4): Show | 7 | HG02647.hp1 HG02647.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2189+443delT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63686343 | |||||
chr6:63686395
|
T | C | 1 | a0001c0001t0007g0070 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2189+484T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63686395 | ||||||
chr6:63686880
|
A | C | 1 | a0006c0006t0043g0218 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2189+969A>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63686880 | ||||||
chr6:63686992
|
C | T | 1 | a0001c0001t0067g0064 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2189+1081C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63686992 | ||||||
chr6:63687009
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2189+1098G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63687009 | ||||||
chr6:63687037
|
C | T | 10 | a0001c0001t0008g0252a0001c0001t0008g0256a0001c0001t0008g0257others(7): Show | 10 | HG00639.hp1 HG01099.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.2189+1126C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63687037 | ||||||
chr6:63687120
|
T | C | 1 | a0007c0007t0001g0118 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2189+1209T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63687120 | ||||||
chr6:63687228
|
A | G | 5 | a0001c0001t0024g0012a0001c0001t0024g0285a0001c0001t0025g0283others(2): Show | 6 | HG00558.hp2 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2189+1317A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63687228 | ||||||
chr6:63687351
|
G | A | 3 | a0001c0001t0002g0231a0001c0001t0040g0224a0001c0001t0041g0225 | 3 | HG00544.hp2 NA18612.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2189+1440G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63687351 | ||||||
chr6:63687445
|
A | G | 1 | a0016c0021t0029g0297 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2189+1534A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63687445 | ||||||
chr6:63687532
|
T | C | 4 | a0003c0004t0029g0295a0003c0004t0036g0294a0003c0004t0051g0296others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2189+1621T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63687532 | ||||||
chr6:63687572
|
G | C | 1 | a0001c0001t0001g0115 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2189+1661G>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63687572 | ||||||
chr6:63687644
|
T | TAGTAAGT others(10): Show |
1 | a0001c0012t0002g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2189+1734_2189+175 others(21): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63687644 | |||||
chr6:63687645
|
A | C | 1 | a0001c0001t0081g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2189+1734A>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63687645 | ||||||
chr6:63687828
|
A | G | 4 | a0001c0001t0001g0157a0001c0001t0004g0158a0001c0001t0012g0167others(1): Show | 4 | HG02135.hp1 NA19002.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.2189+1917A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63687828 | ||||||
chr6:63687887
|
G | C | 1 | a0001c0001t0001g0186 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2189+1976G>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63687887 | ||||||
chr6:63687930
|
T | C | 4 | a0001c0001t0015g0121a0001c0001t0015g0122a0001c0001t0015g0178others(1): Show | 4 | HG02145.hp2 HG02258.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2189+2019T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63687930 | ||||||
chr6:63687952
|
A | C | 201 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(198): Show | 210 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.2189+2041A>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63687952 | ||||||
chr6:63687958
|
C | T | 2 | a0001c0001t0010g0219a0001c0001t0042g0220 | 2 | NA18969.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.2189+2047C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63687958 | ||||||
chr6:63688057
|
G | A | 3 | a0001c0001t0002g0010a0001c0001t0002g0235a0001c0001t0002g0244 | 4 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.2189+2146G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63688057 | ||||||
chr6:63688110
|
C | T | 5 | a0001c0001t0001g0145a0001c0001t0001g0189a0001c0001t0004g0144others(2): Show | 5 | HG02155.hp2 NA18943.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.2189+2199C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63688110 | ||||||
chr6:63688185
|
C | CA | 75 | a0001c0001t0001g0115a0001c0001t0001g0138a0001c0001t0001g0141others(72): Show | 76 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.2189+2289dupA | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688185 | |||||
chr6:63688185
|
C | CAA | 9 | a0001c0001t0002g0227a0001c0001t0002g0230a0001c0001t0003g0071others(6): Show | 9 | HG00597.hp2 HG00639.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.2189+2288_2189+228 others(6): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688185 | |||||
chr6:63688205
|
A | G | 1 | a0001c0001t0003g0093 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2189+2294A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63688205 | ||||||
chr6:63688213
|
G | GT | 19 | a0001c0001t0001g0034a0001c0001t0001g0134a0001c0001t0001g0145others(16): Show | 19 | HG00735.hp1 HG02071.hp2 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.2189+2309dupT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688213 | |||||
chr6:63688220
|
T | TC | 5 | a0001c0001t0001g0169a0001c0001t0002g0241a0001c0001t0014g0019others(2): Show | 5 | HG01358.hp1 HG02109.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2189+2313dupC | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688220 | |||||
chr6:63688224
|
C | CCCCCTCC others(46): Show |
1 | a0001c0001t0034g0287 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2189+2313_2189+231 others(57): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63688224 | ||||||
chr6:63688225
|
T | C | 1 | a0001c0001t0034g0287 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2189+2314T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63688225 | ||||||
chr6:63688225
|
T | TCCCCCTC others(153): Show |
1 | a0001c0001t0077g0094 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2189+2318_2189+231 others(164): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688225 | |||||
chr6:63688225
|
T | TCCCCTCC others(132): Show |
1 | a0001c0001t0023g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(143): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688225 | |||||
chr6:63688225
|
T | TCCCCTCC others(135): Show |
1 | a0009c0017t0085g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(146): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688225 | |||||
chr6:63688225
|
T | TCCCCTCC others(133): Show |
1 | a0001c0001t0038g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(144): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688225 | |||||
chr6:63688225
|
T | TCCCCTCC others(152): Show |
1 | a0001c0001t0003g0101 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(163): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688225 | |||||
chr6:63688225
|
T | TCCCCTCC others(151): Show |
1 | a0001c0001t0003g0056 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(162): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688225 | |||||
chr6:63688225
|
T | TCCCCTCC others(131): Show |
2 | a0001c0001t0023g0123a0001c0001t0023g0180 | 2 | HG02683.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.2189+2324_2189+232 others(142): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688225 | |||||
chr6:63688225
|
T | TCCCCTCC others(132): Show |
5 | a0002c0002t0011g0002a0002c0002t0011g0022a0002c0002t0016g0023others(2): Show | 7 | HG02258.hp2 HG02572.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2189+2324_2189+232 others(143): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688225 | |||||
chr6:63688225
|
T | TCCCCTCC others(132): Show |
1 | a0002c0002t0016g0025 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(143): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688225 | |||||
chr6:63688225
|
T | TCCCCTCC others(134): Show |
1 | a0001c0015t0080g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(145): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688225 | |||||
chr6:63688231
|
C | CCCCCCCC others(191): Show |
1 | a0001c0001t0002g0229 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(202): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCCC others(171): Show |
1 | a0001c0001t0002g0282 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(182): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCCC others(164): Show |
1 | a0004c0003t0022g0088 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(175): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCCT others(153): Show |
1 | a0001c0001t0001g0165 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(164): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCCT others(152): Show |
1 | a0001c0001t0001g0146 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(163): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCCT others(152): Show |
1 | a0003c0004t0036g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(163): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCCT others(153): Show |
1 | a0015c0020t0055g0029 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(164): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCCT others(154): Show |
1 | a0001c0001t0003g0089 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(165): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCCT others(152): Show |
2 | a0001c0001t0003g0073a0001c0001t0064g0111 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2189+2324_2189+232 others(163): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCCT others(150): Show |
1 | a0001c0001t0004g0154 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(161): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCCT others(187): Show |
2 | a0001c0001t0002g0236a0001c0001t0045g0273 | 2 | HG01952.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.2189+2324_2189+232 others(198): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCCT others(151): Show |
12 | a0001c0001t0001g0137a0001c0001t0001g0141a0001c0001t0001g0156others(9): Show | 12 | HG01243.hp1 HG02071.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.2189+2324_2189+232 others(162): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCCT others(150): Show |
1 | a0001c0001t0078g0266 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(161): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCCT others(151): Show |
5 | a0001c0001t0003g0290a0001c0001t0005g0074a0001c0001t0007g0037others(2): Show | 5 | HG02145.hp1 HG02273.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.2189+2324_2189+232 others(162): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCCT others(173): Show |
1 | a0001c0001t0002g0227 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(184): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(151): Show |
3 | a0001c0001t0001g0145a0001c0001t0004g0142a0001c0001t0026g0203 | 3 | HG01517.hp2 HG02698.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.2189+2324_2189+232 others(162): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(191): Show |
1 | a0001c0001t0002g0278 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(202): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(153): Show |
1 | a0001c0001t0001g0199 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(164): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(152): Show |
1 | a0001c0001t0057g0035 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(163): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(205): Show |
1 | a0001c0001t0002g0244 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(216): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(151): Show |
1 | a0001c0001t0004g0182 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(162): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(150): Show |
1 | a0012c0009t0008g0258 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(161): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(151): Show |
1 | a0001c0001t0032g0259 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(162): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(151): Show |
1 | a0001c0001t0001g0152 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(162): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(151): Show |
1 | a0001c0001t0007g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(162): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(152): Show |
1 | a0001c0001t0014g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(163): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(152): Show |
1 | a0001c0001t0003g0077 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(163): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(151): Show |
33 | a0001c0001t0003g0059a0001c0001t0003g0060a0001c0001t0003g0062others(30): Show | 33 | HG01069.hp1 HG01069.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.2189+2324_2189+232 others(162): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(150): Show |
1 | a0001c0001t0001g0159 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(161): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(151): Show |
1 | a0001c0001t0001g0169 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(162): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(199): Show |
1 | a0001c0001t0081g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(210): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(151): Show |
1 | a0001c0001t0031g0254 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(162): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(151): Show |
1 | a0001c0001t0009g0175 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(162): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(188): Show |
1 | a0001c0001t0002g0222 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(199): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(151): Show |
2 | a0001c0001t0015g0179a0001c0001t0026g0204 | 2 | HG01192.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2189+2324_2189+232 others(162): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(169): Show |
1 | a0001c0001t0002g0231 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(180): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(150): Show |
1 | a0001c0001t0008g0257 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(161): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(151): Show |
2 | a0001c0001t0001g0129a0001c0001t0015g0178 | 2 | HG02258.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.2189+2324_2189+232 others(162): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(151): Show |
1 | a0001c0001t0061g0164 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(162): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(187): Show |
1 | a0001c0010t0002g0250 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(198): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(186): Show |
1 | a0001c0001t0010g0232 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(197): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(204): Show |
2 | a0001c0001t0002g0010a0001c0001t0002g0235 | 3 | HG00140.hp2 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2189+2324_2189+232 others(215): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(168): Show |
4 | a0001c0001t0002g0242a0001c0001t0002g0281a0001c0001t0004g0171others(1): Show | 4 | HG02273.hp2 HG02723.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.2189+2324_2189+232 others(179): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(186): Show |
31 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0221others(28): Show | 34 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.2189+2324_2189+232 others(197): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(150): Show |
76 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0034others(73): Show | 77 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.2189+2324_2189+232 others(161): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(168): Show |
9 | a0001c0001t0002g0226a0001c0001t0002g0234a0001c0001t0010g0243others(6): Show | 9 | HG00544.hp2 HG02451.hp2 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.2189+2324_2189+232 others(179): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(186): Show |
1 | a0001c0001t0002g0245 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(197): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(161): Show |
1 | a0003c0004t0051g0296 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(172): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(149): Show |
6 | a0001c0001t0008g0252a0001c0001t0008g0256a0001c0001t0008g0262others(3): Show | 6 | HG00639.hp1 HG01099.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.2189+2324_2189+232 others(160): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(149): Show |
1 | a0001c0001t0032g0260 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(160): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(185): Show |
1 | a0001c0001t0002g0247 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(196): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(150): Show |
2 | a0001c0001t0004g0140a0001c0001t0009g0132 | 2 | NA18954.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.2189+2324_2189+232 others(161): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(149): Show |
1 | a0001c0001t0001g0033 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(160): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(150): Show |
1 | a0008c0008t0001g0133 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(161): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(186): Show |
1 | a0001c0001t0035g0271 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(197): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(150): Show |
1 | a0001c0001t0003g0080 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(161): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(149): Show |
1 | a0001c0001t0072g0079 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(160): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(151): Show |
1 | a0001c0001t0006g0047 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(162): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(151): Show |
1 | a0004c0003t0022g0086 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(162): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(151): Show |
1 | a0001c0001t0003g0100 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(162): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(168): Show |
2 | a0001c0001t0006g0038a0001c0001t0006g0065 | 2 | NA19064.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2189+2324_2189+232 others(179): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(150): Show |
41 | a0001c0001t0003g0027a0001c0001t0003g0036a0001c0001t0003g0040others(38): Show | 44 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.2189+2324_2189+232 others(161): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(145): Show |
1 | a0001c0001t0003g0044 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(156): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(122): Show |
1 | a0001c0001t0016g0091 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(133): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(120): Show |
2 | a0001c0001t0003g0042a0001c0001t0003g0090 | 2 | HG03492.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.2189+2324_2189+232 others(131): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(202): Show |
1 | a0001c0012t0002g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(213): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(169): Show |
1 | a0001c0001t0002g0230 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(180): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | CCCCCCTC others(157): Show |
1 | a0001c0001t0013g0105 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(168): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688231 | |||||
chr6:63688231
|
C | T | 1 | a0001c0001t0077g0094 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2189+2320C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63688231 | ||||||
chr6:63688233
|
C | CCCCTCCC others(135): Show |
1 | a0001c0001t0083g0301 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(146): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688233 | |||||
chr6:63688234
|
C | CCCTCCCC others(168): Show |
1 | a0014c0019t0084g0300 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(179): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688234 | |||||
chr6:63688235
|
C | CCTCCCCT others(153): Show |
1 | a0001c0001t0014g0016 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.2189+2324_2189+232 others(164): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63688235 | ||||||
chr6:63688236
|
T | C | 2 | a0001c0001t0014g0016a0014c0019t0084g0300 | 2 | HG02897.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2189+2325T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63688236 | ||||||
chr6:63688238
|
C | T | 16 | a0001c0001t0008g0252a0001c0001t0008g0256a0001c0001t0008g0257others(13): Show | 16 | HG00639.hp1 HG01099.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.2189+2327C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63688238 | ||||||
chr6:63688242
|
C | CCCCATCC others(148): Show |
1 | a0001c0001t0020g0192 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2189+2334_2189+233 others(159): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688242 | |||||
chr6:63688245
|
C | CATCCCCT others(183): Show |
3 | a0001c0001t0001g0116a0001c0001t0001g0136a0001c0001t0004g0128 | 3 | HG01255.hp1 HG01496.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2189+2334_2189+233 others(194): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63688245 | ||||||
chr6:63688249
|
T | C | 1 | a0014c0019t0084g0300 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2189+2338T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63688249 | ||||||
chr6:63688254
|
T | TCCCCTCC others(17): Show |
1 | a0001c0001t0083g0301 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2189+2345_2189+234 others(28): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688254 | |||||
chr6:63688257
|
T | C | 1 | a0001c0001t0004g0154 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2189+2346T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63688257 | ||||||
chr6:63688257
|
T | TC | 13 | a0001c0001t0001g0159a0001c0001t0001g0183a0001c0001t0001g0184others(10): Show | 13 | HG00558.hp2 HG01070.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.2189+2352dupC | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688257 | |||||
chr6:63688263
|
C | CT | 56 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(53): Show | 59 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.2189+2353dupT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688263 | |||||
chr6:63688264
|
T | C | 1 | a0001c0001t0083g0301 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2189+2353T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63688264 | ||||||
chr6:63688265
|
C | T | 2 | a0001c0001t0083g0301a0001c0012t0002g0275 | 2 | HG03041.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.2189+2354C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63688265 | ||||||
chr6:63688269
|
T | C | 1 | a0001c0001t0083g0301 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2189+2358T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63688269 | ||||||
chr6:63688272
|
T | TC | 14 | a0001c0001t0001g0151a0001c0001t0002g0226a0001c0001t0002g0278others(11): Show | 14 | HG00558.hp2 HG01192.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.2189+2367dupC | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688272 | |||||
chr6:63688290
|
T | C | 307 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0033others(304): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.2189+2379T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63688290 | ||||||
chr6:63688303
|
CTCCCCCT others(5): Show |
C | 1 | a0001c0001t0031g0254 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2189+2403_2189+241 others(16): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688303 | |||||
chr6:63688378
|
AG | A | 306 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0033others(303): Show | 316 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(313): Show |
intron_variant | MODIFIER | c.2189+2471delG | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 63688378 | |||||
chr6:63688468
|
T | C | 1 | a0001c0001t0064g0111 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2189+2557T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63688468 | ||||||
chr6:63688493
|
G | A | 1 | a0001c0001t0083g0301 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2189+2582G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63688493 | ||||||
chr6:63688535
|
G | A | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2189+2624G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63688535 | ||||||
chr6:63688579
|
C | G | 56 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(53): Show | 59 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.2189+2668C>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63688579 | ||||||
chr6:63688637
|
T | C | 1 | a0001c0001t0010g0233 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2189+2726T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63688637 | ||||||
chr6:63688676
|
T | C | 1 | a0001c0001t0023g0180 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2189+2765T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63688676 | ||||||
chr6:63688704
|
T | G | 1 | a0001c0015t0080g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2189+2793T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63688704 | ||||||
chr6:63688926
|
C | T | 1 | a0001c0001t0067g0064 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2190-2811C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63688926 | ||||||
chr6:63689009
|
G | A | 85 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(82): Show | 89 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.2190-2728G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63689009 | ||||||
chr6:63689219
|
C | T | 5 | a0001c0001t0002g0228a0001c0001t0002g0245a0001c0001t0010g0233others(2): Show | 5 | HG02683.hp1 NA18960.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.2190-2518C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63689219 | ||||||
chr6:63689220
|
G | C | 1 | a0001c0001t0031g0254 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2190-2517G>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63689220 | ||||||
chr6:63689223
|
A | G | 1 | a0001c0001t0008g0257 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2190-2514A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63689223 | ||||||
chr6:63689277
|
T | C | 1 | a0001c0001t0003g0095 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2190-2460T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63689277 | ||||||
chr6:63689393
|
G | T | 1 | a0001c0001t0083g0301 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2190-2344G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63689393 | ||||||
chr6:63689469
|
A | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0117a0001c0001t0001g0169others(4): Show | 8 | HG01074.hp1 HG01106.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2190-2268A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63689469 | ||||||
chr6:63689520
|
G | A | 3 | a0001c0001t0001g0134a0001c0001t0001g0138a0001c0001t0058g0131 | 3 | HG00140.hp1 HG00735.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.2190-2217G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63689520 | ||||||
chr6:63689955
|
C | T | 1 | a0001c0001t0038g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2190-1782C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63689955 | ||||||
chr6:63690006
|
G | A | 1 | a0001c0001t0057g0035 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2190-1731G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63690006 | ||||||
chr6:63690106
|
A | G | 3 | a0001c0001t0001g0151a0001c0001t0001g0155a0001c0001t0004g0163 | 3 | HG00733.hp1 HG01934.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.2190-1631A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63690106 | ||||||
chr6:63690235
|
A | G | 5 | a0001c0001t0024g0012a0001c0001t0024g0285a0001c0001t0025g0283others(2): Show | 6 | HG00558.hp2 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2190-1502A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63690235 | ||||||
chr6:63690707
|
T | C | 1 | a0001c0001t0007g0063 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2190-1030T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63690707 | ||||||
chr6:63690811
|
A | G | 16 | a0001c0001t0013g0003a0001c0001t0013g0043a0001c0001t0013g0105others(13): Show | 16 | HG00741.hp2 HG01169.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.2190-926A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63690811 | ||||||
chr6:63690861
|
A | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2190-876A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63690861 | ||||||
chr6:63691175
|
A | G | 1 | a0001c0001t0010g0243 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2190-562A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63691175 | ||||||
chr6:63691225
|
C | T | 1 | a0005c0005t0002g0288 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2190-512C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63691225 | ||||||
chr6:63691241
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2190-496T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63691241 | ||||||
chr6:63691312
|
C | A | 3 | a0001c0001t0004g0197a0001c0001t0004g0200a0001c0001t0018g0196 | 3 | HG02280.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2190-425C>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63691312 | ||||||
chr6:63691384
|
C | A | 1 | a0001c0001t0001g0116 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2190-353C>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63691384 | ||||||
chr6:63691491
|
C | T | 1 | a0002c0002t0063g0026 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2190-246C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | 63691491 | ||||||
chr6:63692169
|
A | G | 1 | a0011c0014t0001g0205 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2496+126A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 5/15 | chr6 | 63692169 | ||||||
chr6:63692205
|
C | T | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2496+162C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 5/15 | chr6 | 63692205 | ||||||
chr6:63692486
|
A | T | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2496+443A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 5/15 | chr6 | 63692486 | ||||||
chr6:63692605
|
T | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2496+562T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 5/15 | chr6 | 63692605 | ||||||
chr6:63692610
|
A | C | 1 | a0001c0001t0064g0111 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2496+567A>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 5/15 | chr6 | 63692610 | ||||||
chr6:63692818
|
T | G | 5 | a0001c0001t0031g0254a0001c0001t0031g0255a0001c0001t0033g0251others(2): Show | 5 | HG02647.hp1 HG03209.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.2496+775T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 5/15 | chr6 | 63692818 | ||||||
chr6:63692820
|
G | T | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2496+777G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 5/15 | chr6 | 63692820 | ||||||
chr6:63692963
|
A | T | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2496+920A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 5/15 | chr6 | 63692963 | ||||||
chr6:63692995
|
C | T | 1 | a0001c0001t0003g0096 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2496+952C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 5/15 | chr6 | 63692995 | ||||||
chr6:63693078
|
A | T | 1 | a0001c0001t0032g0259 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2496+1035A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 5/15 | chr6 | 63693078 | ||||||
chr6:63693145
|
C | T | 1 | a0001c0001t0034g0287 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2496+1102C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 5/15 | chr6 | 63693145 | ||||||
chr6:63693147
|
G | C | 1 | a0001c0001t0033g0265 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2496+1104G>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 5/15 | chr6 | 63693147 | ||||||
chr6:63693157
|
A | G | 1 | a0001c0001t0003g0061 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2496+1114A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 5/15 | chr6 | 63693157 | ||||||
chr6:63693194
|
A | G | 1 | a0001c0001t0067g0064 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2496+1151A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 5/15 | chr6 | 63693194 | ||||||
chr6:63693291
|
C | A | 55 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(52): Show | 58 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.2496+1248C>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 5/15 | chr6 | 63693291 | ||||||
chr6:63693318
|
A | G | 2 | a0001c0001t0003g0056a0001c0001t0003g0101 | 2 | HG02615.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2497-1263A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 5/15 | chr6 | 63693318 | ||||||
chr6:63693541
|
A | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2497-1040A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 5/15 | chr6 | 63693541 | ||||||
chr6:63693594
|
G | A | 1 | a0001c0001t0002g0269 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2497-987G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 5/15 | chr6 | 63693594 | ||||||
chr6:63693932
|
A | G | 1 | a0001c0001t0005g0113 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2497-649A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 5/15 | chr6 | 63693932 | ||||||
chr6:63694049
|
G | A | 1 | a0001c0001t0003g0100 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2497-532G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 5/15 | chr6 | 63694049 | ||||||
chr6:63694211
|
A | G | 1 | a0015c0020t0055g0029 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2497-370A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 5/15 | chr6 | 63694211 | ||||||
chr6:63694572
|
A | G | 3 | a0001c0001t0002g0221a0001c0001t0010g0219a0001c0001t0042g0220 | 3 | NA18969.hp2 NA18980.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.2497-9A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 5/15 | chr6 | 63694572 | ||||||
chr6:63695260
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2680+496G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 6/15 | chr6 | 63695260 | ||||||
chr6:63695386
|
G | A | 5 | a0001c0001t0031g0254a0001c0001t0031g0255a0001c0001t0033g0251others(2): Show | 5 | HG02647.hp1 HG03209.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.2680+622G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 6/15 | chr6 | 63695386 | ||||||
chr6:63695912
|
C | T | 1 | a0001c0001t0083g0301 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2680+1148C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 6/15 | chr6 | 63695912 | ||||||
chr6:63696452
|
T | TG | 59 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(56): Show | 62 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.2680+1690dupG | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr6 | 63696452 | |||||
chr6:63696598
|
G | T | 57 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(54): Show | 60 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.2681-1625G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 6/15 | chr6 | 63696598 | ||||||
chr6:63696723
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2681-1500G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 6/15 | chr6 | 63696723 | ||||||
chr6:63697063
|
G | A | 86 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(83): Show | 90 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.2681-1160G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 6/15 | chr6 | 63697063 | ||||||
chr6:63697385
|
T | C | 2 | a0001c0001t0004g0210a0001c0001t0004g0211 | 2 | NA18945.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2681-838T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 6/15 | chr6 | 63697385 | ||||||
chr6:63697509
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2681-714G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 6/15 | chr6 | 63697509 | ||||||
chr6:63697785
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2681-438C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 6/15 | chr6 | 63697785 | ||||||
chr6:63697943
|
A | C | 4 | a0003c0004t0029g0295a0003c0004t0036g0294a0003c0004t0051g0296others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2681-280A>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 6/15 | chr6 | 63697943 | ||||||
chr6:63698816
|
G | A | 56 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(53): Show | 59 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.2982+211G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 8/15 | chr6 | 63698816 | ||||||
chr6:63698994
|
T | C | 1 | a0001c0016t0008g0261 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2982+389T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 8/15 | chr6 | 63698994 | ||||||
chr6:63699082
|
T | C | 1 | a0014c0019t0084g0300 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2982+477T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 8/15 | chr6 | 63699082 | ||||||
chr6:63699264
|
C | G | 1 | a0001c0001t0001g0129 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2982+659C>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 8/15 | chr6 | 63699264 | ||||||
chr6:63699480
|
G | T | 1 | a0001c0001t0023g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2983-870G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 8/15 | chr6 | 63699480 | ||||||
chr6:63699514
|
G | A | 4 | a0001c0001t0002g0226a0001c0001t0002g0230a0001c0001t0002g0234others(1): Show | 4 | NA18942.hp2 NA18948.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.2983-836G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 8/15 | chr6 | 63699514 | ||||||
chr6:63699630
|
C | T | 56 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(53): Show | 59 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.2983-720C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 8/15 | chr6 | 63699630 | ||||||
chr6:63699684
|
G | A | 2 | a0001c0001t0004g0125a0001c0001t0004g0126 | 2 | NA18990.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.2983-666G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 8/15 | chr6 | 63699684 | ||||||
chr6:63699738
|
A | G | 57 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(54): Show | 60 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.2983-612A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 8/15 | chr6 | 63699738 | ||||||
chr6:63699748
|
G | A | 1 | a0014c0019t0084g0300 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2983-602G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 8/15 | chr6 | 63699748 | ||||||
chr6:63699780
|
G | A | 5 | a0001c0001t0002g0228a0001c0001t0002g0245a0001c0001t0010g0233others(2): Show | 5 | HG02683.hp1 NA18960.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.2983-570G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 8/15 | chr6 | 63699780 | ||||||
chr6:63699784
|
T | A | 57 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(54): Show | 60 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.2983-566T>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 8/15 | chr6 | 63699784 | ||||||
chr6:63699918
|
T | G | 4 | a0003c0004t0029g0295a0003c0004t0036g0294a0003c0004t0051g0296others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2983-432T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 8/15 | chr6 | 63699918 | ||||||
chr6:63700094
|
T | C | 8 | a0001c0001t0003g0059a0001c0001t0003g0060a0001c0001t0003g0209others(5): Show | 8 | HG01884.hp1 HG02630.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.2983-256T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 8/15 | chr6 | 63700094 | ||||||
chr6:63700138
|
T | TATATGTT others(1): Show |
15 | a0001c0001t0013g0003a0001c0001t0013g0043a0001c0001t0013g0105others(12): Show | 15 | HG00741.hp2 HG01169.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2983-209_2983-202d others(10): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 63700138 | |||||
chr6:63700238
|
TTAAG | T | 16 | a0001c0001t0013g0003a0001c0001t0013g0043a0001c0001t0013g0105others(13): Show | 16 | HG00741.hp2 HG01169.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.2983-109_2983-106d others(6): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 63700238 | |||||
chr6:63700509
|
G | A | 1 | a0001c0001t0034g0287 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3099+43G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 9/15 | chr6 | 63700509 | ||||||
chr6:63700589
|
C | G | 1 | a0001c0010t0002g0250 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3099+123C>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 9/15 | chr6 | 63700589 | ||||||
chr6:63700591
|
T | G | 15 | a0001c0001t0013g0003a0001c0001t0013g0043a0001c0001t0013g0105others(12): Show | 15 | HG00741.hp2 HG01169.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.3099+125T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 9/15 | chr6 | 63700591 | ||||||
chr6:63700834
|
A | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3099+368A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 9/15 | chr6 | 63700834 | ||||||
chr6:63700875
|
A | G | 1 | a0001c0001t0004g0125 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3099+409A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 9/15 | chr6 | 63700875 | ||||||
chr6:63701153
|
C | G | 4 | a0001c0001t0023g0123a0001c0001t0023g0124a0001c0001t0023g0180others(1): Show | 4 | HG01243.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.3099+687C>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 9/15 | chr6 | 63701153 | ||||||
chr6:63701160
|
C | T | 1 | a0001c0001t0003g0089 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3099+694C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 9/15 | chr6 | 63701160 | ||||||
chr6:63701258
|
A | G | 1 | a0001c0001t0003g0299 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3099+792A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 9/15 | chr6 | 63701258 | ||||||
chr6:63701493
|
G | A | 5 | a0001c0001t0024g0012a0001c0001t0024g0285a0001c0001t0025g0283others(2): Show | 6 | HG00558.hp2 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.3100-1015G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 9/15 | chr6 | 63701493 | ||||||
chr6:63701513
|
T | G | 1 | a0001c0001t0050g0223 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3100-995T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 9/15 | chr6 | 63701513 | ||||||
chr6:63701651
|
A | C | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3100-857A>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 9/15 | chr6 | 63701651 | ||||||
chr6:63701682
|
A | T | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3100-826A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 9/15 | chr6 | 63701682 | ||||||
chr6:63701779
|
T | C | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3100-729T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 9/15 | chr6 | 63701779 | ||||||
chr6:63701847
|
A | G | 5 | a0001c0001t0024g0012a0001c0001t0024g0285a0001c0001t0025g0283others(2): Show | 6 | HG00558.hp2 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.3100-661A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 9/15 | chr6 | 63701847 | ||||||
chr6:63701924
|
A | G | 91 | a0001c0001t0003g0027a0001c0001t0003g0036a0001c0001t0003g0040others(88): Show | 94 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.3100-584A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 9/15 | chr6 | 63701924 | ||||||
chr6:63701979
|
T | G | 1 | a0002c0002t0063g0026 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3100-529T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 9/15 | chr6 | 63701979 | ||||||
chr6:63702011
|
G | A | 4 | a0001c0001t0002g0270a0001c0001t0002g0272a0001c0001t0002g0276others(1): Show | 4 | HG02523.hp1 NA18970.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.3100-497G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 9/15 | chr6 | 63702011 | ||||||
chr6:63702016
|
A | G | 1 | a0001c0001t0081g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3100-492A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 9/15 | chr6 | 63702016 | ||||||
chr6:63702295
|
G | A | 87 | a0001c0001t0003g0027a0001c0001t0003g0036a0001c0001t0003g0040others(84): Show | 90 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.3100-213G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 9/15 | chr6 | 63702295 | ||||||
chr6:63702299
|
C | T | 201 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(198): Show | 210 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.3100-209C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 9/15 | chr6 | 63702299 | ||||||
chr6:63702311
|
C | T | 1 | a0001c0001t0009g0132 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.3100-197C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 9/15 | chr6 | 63702311 | ||||||
chr6:63702683
|
T | C | 5 | a0001c0001t0003g0085a0001c0001t0003g0093a0001c0001t0007g0067others(2): Show | 5 | HG01106.hp2 HG01346.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.3231+44T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 10/15 | chr6 | 63702683 | ||||||
chr6:63702688
|
A | T | 1 | a0001c0001t0054g0170 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3231+49A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 10/15 | chr6 | 63702688 | ||||||
chr6:63702743
|
A | G | 1 | a0001c0001t0083g0301 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3231+104A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 10/15 | chr6 | 63702743 | ||||||
chr6:63702815
|
T | C | 1 | a0001c0001t0009g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3231+176T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 10/15 | chr6 | 63702815 | ||||||
chr6:63702933
|
A | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3231+294A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 10/15 | chr6 | 63702933 | ||||||
chr6:63702946
|
C | T | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3231+307C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 10/15 | chr6 | 63702946 | ||||||
chr6:63702980
|
C | T | 1 | a0001c0001t0050g0223 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3231+341C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 10/15 | chr6 | 63702980 | ||||||
chr6:63702989
|
C | A | 56 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(53): Show | 59 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.3231+350C>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 10/15 | chr6 | 63702989 | ||||||
chr6:63703078
|
A | T | 1 | a0003c0004t0036g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3231+439A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 10/15 | chr6 | 63703078 | ||||||
chr6:63703220
|
T | C | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3232-316T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 10/15 | chr6 | 63703220 | ||||||
chr6:63703241
|
T | C | 3 | a0001c0001t0003g0042a0001c0001t0003g0090a0001c0001t0016g0091 | 3 | HG03492.hp1 HG03704.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.3232-295T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 10/15 | chr6 | 63703241 | ||||||
chr6:63703309
|
G | C | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3232-227G>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 10/15 | chr6 | 63703309 | ||||||
chr6:63703319
|
T | C | 1 | a0001c0001t0054g0170 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3232-217T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 10/15 | chr6 | 63703319 | ||||||
chr6:63703389
|
T | TA | 5 | a0001c0001t0001g0034a0001c0001t0006g0102a0003c0004t0029g0295others(2): Show | 5 | HG02056.hp2 HG02074.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3232-138dupA | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr6 | 63703389 | |||||
chr6:63703530
|
C | T | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
splice_region_variant&intron_variant | LOW | c.3232-6C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 10/15 | chr6 | 63703530 | ||||||
chr6:63703682
|
G | T | 1 | a0006c0006t0002g0217 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3367+11G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 11/15 | chr6 | 63703682 | ||||||
chr6:63703720
|
G | T | 1 | a0001c0001t0005g0074 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.3367+49G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 11/15 | chr6 | 63703720 | ||||||
chr6:63703798
|
C | A | 11 | a0001c0001t0008g0252a0001c0001t0008g0256a0001c0001t0008g0257others(8): Show | 11 | HG00639.hp1 HG01099.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.3367+127C>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 11/15 | chr6 | 63703798 | ||||||
chr6:63704088
|
T | G | 3 | a0003c0004t0029g0295a0003c0004t0036g0294a0016c0021t0029g0297 | 3 | HG02717.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3367+417T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 11/15 | chr6 | 63704088 | ||||||
chr6:63704115
|
A | C | 1 | a0015c0020t0055g0029 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3367+444A>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 11/15 | chr6 | 63704115 | ||||||
chr6:63704146
|
C | T | 3 | a0003c0004t0029g0295a0003c0004t0036g0294a0016c0021t0029g0297 | 3 | HG02717.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3367+475C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 11/15 | chr6 | 63704146 | ||||||
chr6:63704165
|
C | T | 56 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(53): Show | 59 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.3367+494C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 11/15 | chr6 | 63704165 | ||||||
chr6:63704435
|
A | G | 2 | a0001c0001t0033g0251a0001c0001t0033g0265 | 2 | HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3367+764A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 11/15 | chr6 | 63704435 | ||||||
chr6:63704438
|
G | A | 1 | a0001c0001t0034g0287 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3367+767G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 11/15 | chr6 | 63704438 | ||||||
chr6:63704466
|
T | C | 56 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(53): Show | 59 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.3367+795T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 11/15 | chr6 | 63704466 | ||||||
chr6:63704680
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.3367+1009A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 11/15 | chr6 | 63704680 | ||||||
chr6:63704838
|
A | T | 82 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(79): Show | 86 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.3367+1167A>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 11/15 | chr6 | 63704838 | ||||||
chr6:63704872
|
G | A | 1 | a0001c0001t0056g0119 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3368-1157G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 11/15 | chr6 | 63704872 | ||||||
chr6:63704916
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3368-1113C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 11/15 | chr6 | 63704916 | ||||||
chr6:63705022
|
G | A | 111 | a0001c0001t0003g0027a0001c0001t0003g0036a0001c0001t0003g0040others(108): Show | 116 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.3368-1007G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 11/15 | chr6 | 63705022 | ||||||
chr6:63705098
|
A | G | 1 | a0001c0001t0008g0263 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3368-931A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 11/15 | chr6 | 63705098 | ||||||
chr6:63705103
|
C | T | 3 | a0001c0001t0026g0202a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG01192.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.3368-926C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 11/15 | chr6 | 63705103 | ||||||
chr6:63705119
|
A | G | 2 | a0001c0001t0083g0301a0014c0019t0084g0300 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3368-910A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 11/15 | chr6 | 63705119 | ||||||
chr6:63705334
|
C | G | 1 | a0001c0015t0080g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3368-695C>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 11/15 | chr6 | 63705334 | ||||||
chr6:63705342
|
G | A | 2 | a0001c0001t0014g0018a0001c0001t0037g0020 | 2 | HG01109.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3368-687G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 11/15 | chr6 | 63705342 | ||||||
chr6:63705600
|
G | A | 1 | a0001c0001t0003g0071 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3368-429G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 11/15 | chr6 | 63705600 | ||||||
chr6:63705802
|
G | A | 1 | a0001c0001t0004g0211 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.3368-227G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 11/15 | chr6 | 63705802 | ||||||
chr6:63706253
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3563+29T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 12/15 | chr6 | 63706253 | ||||||
chr6:63707101
|
T | G | 53 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(50): Show | 56 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.3711+225T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 13/15 | chr6 | 63707101 | ||||||
chr6:63707112
|
A | G | 2 | a0001c0001t0004g0210a0001c0001t0004g0211 | 2 | NA18945.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.3711+236A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 13/15 | chr6 | 63707112 | ||||||
chr6:63707291
|
A | G | 5 | a0001c0001t0031g0254a0001c0001t0031g0255a0001c0001t0033g0251others(2): Show | 5 | HG02647.hp1 HG03209.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3711+415A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 13/15 | chr6 | 63707291 | ||||||
chr6:63707611
|
A | G | 1 | a0001c0001t0083g0301 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3711+735A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 13/15 | chr6 | 63707611 | ||||||
chr6:63707619
|
C | T | 1 | a0001c0001t0081g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3711+743C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 13/15 | chr6 | 63707619 | ||||||
chr6:63707649
|
C | T | 10 | a0001c0001t0008g0252a0001c0001t0008g0256a0001c0001t0008g0257others(7): Show | 10 | HG00639.hp1 HG01099.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.3711+773C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 13/15 | chr6 | 63707649 | ||||||
chr6:63707725
|
C | CT | 16 | a0001c0001t0001g0208a0001c0001t0003g0056a0001c0001t0013g0003others(13): Show | 16 | HG00741.hp2 HG01169.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.3711+863dupT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr6 | 63707725 | |||||
chr6:63707725
|
CT | C | 59 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(56): Show | 62 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.3711+863delT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr6 | 63707725 | |||||
chr6:63707739
|
T | G | 1 | a0001c0001t0008g0257 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3711+863T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 13/15 | chr6 | 63707739 | ||||||
chr6:63707773
|
AG | A | 3 | a0001c0001t0026g0202a0001c0001t0026g0203a0001c0001t0026g0204 | 3 | HG01192.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.3711+899delG | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr6 | 63707773 | |||||
chr6:63707847
|
G | GTTTGTT | 237 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0033others(234): Show | 244 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.3711+1004_3711+100 others(10): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr6 | 63707847 | |||||
chr6:63707847
|
G | GTTTGTTT others(5): Show |
8 | a0001c0001t0001g0199a0001c0001t0002g0230a0001c0001t0002g0274others(5): Show | 8 | HG00423.hp1 HG02056.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.3711+998_3711+1009 others(15): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr6 | 63707847 | |||||
chr6:63707847
|
G | GTTTGTTT others(11): Show |
54 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(51): Show | 57 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.3711+992_3711+1009 others(21): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr6 | 63707847 | |||||
chr6:63707905
|
C | T | 16 | a0001c0001t0005g0001a0001c0001t0005g0050a0001c0001t0005g0068others(13): Show | 19 | HG00408.hp1 HG00735.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.3711+1029C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 13/15 | chr6 | 63707905 | ||||||
chr6:63707959
|
C | T | 1 | a0001c0001t0004g0142 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3711+1083C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 13/15 | chr6 | 63707959 | ||||||
chr6:63708345
|
G | A | 14 | a0001c0001t0013g0003a0001c0001t0013g0043a0001c0001t0013g0105others(11): Show | 14 | HG00741.hp2 HG01169.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.3712-806G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 13/15 | chr6 | 63708345 | ||||||
chr6:63708797
|
G | T | 1 | a0001c0001t0008g0262 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3712-354G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 13/15 | chr6 | 63708797 | ||||||
chr6:63708881
|
C | G | 23 | a0001c0001t0003g0095a0001c0001t0008g0252a0001c0001t0008g0256others(20): Show | 24 | HG00558.hp2 HG00639.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.3712-270C>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 13/15 | chr6 | 63708881 | ||||||
chr6:63709095
|
G | A | 1 | a0001c0001t0078g0266 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3712-56G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 13/15 | chr6 | 63709095 | ||||||
chr6:63709130
|
T | C | 1 | a0001c0015t0080g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3712-21T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 13/15 | chr6 | 63709130 | ||||||
chr6:63709301
|
G | T | 4 | a0001c0001t0020g0007a0001c0001t0020g0192a0001c0001t0020g0193others(1): Show | 4 | HG00609.hp1 NA18971.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.3801+61G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 14/15 | chr6 | 63709301 | ||||||
chr6:63709405
|
G | T | 1 | a0001c0001t0017g0106 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3801+165G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 14/15 | chr6 | 63709405 | ||||||
chr6:63709422
|
AT | A | 59 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(56): Show | 62 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.3801+194delT | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 63709422 | |||||
chr6:63709470
|
A | G | 3 | a0003c0004t0029g0295a0003c0004t0036g0294a0016c0021t0029g0297 | 3 | HG02717.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3801+230A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 14/15 | chr6 | 63709470 | ||||||
chr6:63709750
|
C | T | 14 | a0001c0001t0013g0003a0001c0001t0013g0043a0001c0001t0013g0105others(11): Show | 14 | HG00741.hp2 HG01169.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.3801+510C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 14/15 | chr6 | 63709750 | ||||||
chr6:63709863
|
C | T | 84 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(81): Show | 88 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.3801+623C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 14/15 | chr6 | 63709863 | ||||||
chr6:63709972
|
A | G | 1 | a0001c0001t0008g0263 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3801+732A>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 14/15 | chr6 | 63709972 | ||||||
chr6:63710404
|
G | T | 1 | a0001c0001t0081g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3802-763G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 14/15 | chr6 | 63710404 | ||||||
chr6:63710516
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3802-651G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 14/15 | chr6 | 63710516 | ||||||
chr6:63710773
|
T | G | 59 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0011others(56): Show | 62 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.3802-394T>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 14/15 | chr6 | 63710773 | ||||||
chr6:63710792
|
C | G | 8 | a0001c0001t0014g0015a0001c0001t0014g0016a0001c0001t0014g0018others(5): Show | 8 | HG01109.hp1 HG02109.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.3802-375C>G | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 14/15 | chr6 | 63710792 | ||||||
chr6:63710940
|
G | A | 1 | a0001c0001t0007g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3802-227G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 14/15 | chr6 | 63710940 | ||||||
chr6:63710940
|
G | T | 5 | a0001c0001t0024g0012a0001c0001t0024g0285a0001c0001t0025g0283others(2): Show | 6 | HG00558.hp2 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.3802-227G>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 14/15 | chr6 | 63710940 |