Item | Value |
---|---|
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 | MDIVD others(2034): Show |
chr6 | 63630802 | 63731011 |
a0002 | 0/0 | 2039 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | MDIVD others(2034): Show |
chr6 | 63630802 | 63731011 |
a0003 | 0/0 | 2039 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | PHF3_chr6_63630802_63731011 | PHF3 | MDIVD others(2034): Show |
chr6 | 63630802 | 63731011 |
a0004 | 0/0 | 2039 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | MDIVD others(2034): Show |
chr6 | 63630802 | 63731011 |
a0005 | 0/0 | 2039 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | MDIVD others(2034): Show |
chr6 | 63630802 | 63731011 |
a0006 | 0/0 | 2039 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | MDIVD others(2034): Show |
chr6 | 63630802 | 63731011 |
a0007 | 0/0 | 2039 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | MDIVD others(2034): Show |
chr6 | 63630802 | 63731011 |
a0008 | 0/0 | 2039 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | MDIVD others(2034): Show |
chr6 | 63630802 | 63731011 |
a0009 | 0/0 | 2039 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | MDIVD others(2034): Show |
chr6 | 63630802 | 63731011 |
a0010 | 0/0 | 2039 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | MDIVD others(2034): Show |
chr6 | 63630802 | 63731011 |
a0011 | 0/0 | 2039 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | MDIVD others(2034): Show |
chr6 | 63630802 | 63731011 |
a0012 | 0/0 | 2039 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | MDIVD others(2034): Show |
chr6 | 63630802 | 63731011 |
a0013 | 0/0 | 2039 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | MDIVD others(2034): Show |
chr6 | 63630802 | 63731011 |
a0014 | 0/0 | 2039 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | MDIVD others(2034): Show |
chr6 | 63630802 | 63731011 |
a0015 | 0/0 | 2039 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | MDIVD others(2034): Show |
chr6 | 63630802 | 63731011 |
a0016 | 0/0 | 2039 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | MDIVD others(2034): Show |
chr6 | 63630802 | 63731011 |
a0017 | 0/1 | 2039 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | MDIVD others(2034): Show |
chr6 | 63630802 | 63731011 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 6117 | 286 | 60 | 59 | 120 | 13 | 33 | PHF3_chr6_63630802_63731011 | PHF3 | ATGGA others(6112): Show |
chr6 | 63630802 | 63731011 | ||
a0001c0010 | 0/0 | 6117 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | ATGGA others(6112): Show |
chr6 | 63630802 | 63731011 | ||
a0001c0012 | 0/0 | 6117 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | ATGGA others(6112): Show |
chr6 | 63630802 | 63731011 | ||
a0001c0013 | 0/0 | 6117 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | ATGGA others(6112): Show |
chr6 | 63630802 | 63731011 | ||
a0001c0015 | 0/0 | 6117 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | ATGGA others(6112): Show |
chr6 | 63630802 | 63731011 | ||
a0001c0016 | 0/0 | 6117 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | ATGGA others(6112): Show |
chr6 | 63630802 | 63731011 | ||
a0002c0002 | 0/0 | 6117 | 8 | 8 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | ATGGA others(6112): Show |
chr6 | 63630802 | 63731011 | ||
a0003c0003 | 0/0 | 6117 | 3 | 0 | 0 | 3 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | ATGGA others(6112): Show |
chr6 | 63630802 | 63731011 | ||
a0004c0004 | 0/0 | 6117 | 3 | 3 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | ATGGA others(6112): Show |
chr6 | 63630802 | 63731011 | ||
a0005c0005 | 0/0 | 6117 | 2 | 2 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | ATGGA others(6112): Show |
chr6 | 63630802 | 63731011 | ||
a0006c0006 | 0/0 | 6117 | 2 | 2 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | ATGGA others(6112): Show |
chr6 | 63630802 | 63731011 | ||
a0007c0008 | 0/0 | 6117 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | ATGGA others(6112): Show |
chr6 | 63630802 | 63731011 | ||
a0008c0020 | 0/0 | 6117 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | ATGGA others(6112): Show |
chr6 | 63630802 | 63731011 | ||
a0009c0009 | 0/0 | 6117 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | ATGGA others(6112): Show |
chr6 | 63630802 | 63731011 | ||
a0010c0022 | 0/0 | 6117 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | ATGGA others(6112): Show |
chr6 | 63630802 | 63731011 | ||
a0011c0019 | 0/0 | 6117 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | ATGGA others(6112): Show |
chr6 | 63630802 | 63731011 | ||
a0012c0017 | 0/0 | 6117 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | ATGGA others(6112): Show |
chr6 | 63630802 | 63731011 | ||
a0013c0007 | 0/0 | 6117 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | ATGGA others(6112): Show |
chr6 | 63630802 | 63731011 | ||
a0014c0021 | 0/0 | 6117 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | ATGGA others(6112): Show |
chr6 | 63630802 | 63731011 | ||
a0015c0014 | 0/0 | 6117 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | ATGGA others(6112): Show |
chr6 | 63630802 | 63731011 | ||
a0016c0018 | 0/0 | 6117 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | ATGGA others(6112): Show |
chr6 | 63630802 | 63731011 | ||
a0017c0011 | 0/1 | 6117 | 1 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | ATGGA others(6112): Show |
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 | AGTGG others(18789): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0002 | 0/0 | 18788 | 44 | 6 | 9 | 20 | 1 | 8 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18783): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0003 | 0/0 | 18789 | 38 | 0 | 8 | 25 | 2 | 3 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18784): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0004 | 1/0 | 18797 | 23 | 4 | 7 | 9 | 1 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18792): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0005 | 0/0 | 18791 | 16 | 1 | 7 | 5 | 2 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18786): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0006 | 0/0 | 18794 | 8 | 2 | 3 | 2 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18789): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0007 | 0/0 | 18795 | 6 | 0 | 3 | 0 | 0 | 3 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18790): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0008 | 0/0 | 18800 | 7 | 1 | 0 | 4 | 0 | 2 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18795): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0009 | 0/0 | 18792 | 5 | 0 | 0 | 4 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18787): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0010 | 0/0 | 18800 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18795): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0011 | 0/0 | 18792 | 5 | 3 | 2 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18787): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0012 | 0/0 | 18789 | 4 | 4 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18784): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0013 | 0/0 | 18771 | 4 | 4 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18766): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0014 | 0/0 | 18797 | 2 | 0 | 0 | 1 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18792): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0015 | 0/0 | 18792 | 4 | 4 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18787): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0016 | 0/0 | 18803 | 3 | 2 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18798): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0017 | 0/0 | 18797 | 3 | 0 | 0 | 0 | 0 | 3 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18792): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0018 | 0/0 | 18794 | 3 | 0 | 0 | 3 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18789): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0020 | 0/0 | 18785 | 3 | 0 | 1 | 0 | 0 | 2 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18780): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0021 | 0/0 | 18798 | 3 | 3 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18793): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0022 | 0/0 | 18795 | 3 | 1 | 0 | 2 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18790): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0023 | 0/0 | 18797 | 3 | 0 | 1 | 0 | 2 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18792): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0024 | 0/0 | 18788 | 2 | 0 | 1 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18783): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0025 | 0/0 | 18782 | 2 | 0 | 1 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18777): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0027 | 0/0 | 18788 | 2 | 2 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18783): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0028 | 0/0 | 18795 | 2 | 2 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18790): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0029 | 0/0 | 18798 | 2 | 0 | 0 | 0 | 0 | 2 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18793): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0030 | 0/0 | 18792 | 2 | 2 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18787): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0031 | 0/0 | 18795 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18790): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0032 | 0/0 | 18789 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18784): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0034 | 0/0 | 18789 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18784): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0035 | 0/0 | 18786 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18781): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0036 | 0/0 | 18789 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18784): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0037 | 0/0 | 18801 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18796): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0038 | 0/0 | 18795 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18790): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0039 | 0/0 | 18792 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18787): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0041 | 0/0 | 18789 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18784): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0042 | 0/0 | 18789 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18784): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0043 | 0/0 | 18789 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18784): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0044 | 0/0 | 18789 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18784): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0045 | 0/0 | 18788 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18783): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0046 | 0/0 | 18794 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18789): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0047 | 0/0 | 18789 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18784): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0049 | 0/0 | 18797 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18792): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0050 | 0/0 | 18791 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18786): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0052 | 0/0 | 18797 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18792): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0053 | 0/0 | 18797 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18792): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0054 | 0/0 | 18794 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18789): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0055 | 0/0 | 18794 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18789): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0056 | 0/0 | 18797 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18792): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0057 | 0/0 | 18791 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18786): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0058 | 0/0 | 18797 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18792): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0060 | 0/0 | 18785 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18780): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0061 | 0/0 | 18788 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18783): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0062 | 0/0 | 18788 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18783): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0063 | 0/0 | 18803 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18798): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0065 | 0/0 | 18787 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18782): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0066 | 0/0 | 18782 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18777): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0067 | 0/0 | 18788 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18783): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0068 | 0/0 | 18798 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18793): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0069 | 0/0 | 18795 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18790): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0070 | 0/0 | 18798 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18793): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0071 | 0/0 | 18795 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18790): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0073 | 0/0 | 18787 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18782): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0074 | 0/0 | 18798 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18793): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0075 | 0/0 | 18792 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18787): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0077 | 0/0 | 18798 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18793): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0078 | 0/0 | 18792 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18787): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0079 | 0/0 | 18801 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18796): Show |
chr6 | 63630802 | 63731011 |
a0001c0001t0082 | 0/0 | 18797 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18792): Show |
chr6 | 63630802 | 63731011 |
a0001c0010t0003 | 0/0 | 18789 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18784): Show |
chr6 | 63630802 | 63731011 |
a0001c0012t0003 | 0/0 | 18789 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18784): Show |
chr6 | 63630802 | 63731011 |
a0001c0013t0002 | 0/0 | 18788 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18783): Show |
chr6 | 63630802 | 63731011 |
a0001c0015t0076 | 0/0 | 18801 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18796): Show |
chr6 | 63630802 | 63731011 |
a0001c0016t0007 | 0/0 | 18795 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18790): Show |
chr6 | 63630802 | 63731011 |
a0002c0002t0010 | 0/0 | 18800 | 4 | 4 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18795): Show |
chr6 | 63630802 | 63731011 |
a0002c0002t0014 | 0/0 | 18797 | 2 | 2 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18792): Show |
chr6 | 63630802 | 63731011 |
a0002c0002t0059 | 0/0 | 18789 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18784): Show |
chr6 | 63630802 | 63731011 |
a0002c0002t0064 | 0/0 | 18800 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18795): Show |
chr6 | 63630802 | 63731011 |
a0003c0003t0019 | 0/0 | 18788 | 3 | 0 | 0 | 3 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18783): Show |
chr6 | 63630802 | 63731011 |
a0004c0004t0026 | 0/0 | 18790 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18785): Show |
chr6 | 63630802 | 63731011 |
a0004c0004t0033 | 0/0 | 18790 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18785): Show |
chr6 | 63630802 | 63731011 |
a0004c0004t0048 | 0/0 | 18798 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18793): Show |
chr6 | 63630802 | 63731011 |
a0005c0005t0003 | 0/0 | 18789 | 2 | 2 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18784): Show |
chr6 | 63630802 | 63731011 |
a0006c0006t0003 | 0/0 | 18789 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18784): Show |
chr6 | 63630802 | 63731011 |
a0006c0006t0040 | 0/0 | 18789 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18784): Show |
chr6 | 63630802 | 63731011 |
a0007c0008t0001 | 0/0 | 18794 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18789): Show |
chr6 | 63630802 | 63731011 |
a0008c0020t0051 | 0/0 | 18797 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18792): Show |
chr6 | 63630802 | 63731011 |
a0009c0009t0007 | 0/0 | 18795 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18790): Show |
chr6 | 63630802 | 63731011 |
a0010c0022t0004 | 0/0 | 18797 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18792): Show |
chr6 | 63630802 | 63731011 |
a0011c0019t0080 | 0/0 | 18804 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18799): Show |
chr6 | 63630802 | 63731011 |
a0012c0017t0081 | 0/0 | 18794 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18789): Show |
chr6 | 63630802 | 63731011 |
a0013c0007t0001 | 0/0 | 18794 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18789): Show |
chr6 | 63630802 | 63731011 |
a0014c0021t0026 | 0/0 | 18790 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18785): Show |
chr6 | 63630802 | 63731011 |
a0015c0014t0001 | 0/0 | 18794 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18789): Show |
chr6 | 63630802 | 63731011 |
a0016c0018t0004 | 0/0 | 18797 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18792): Show |
chr6 | 63630802 | 63731011 |
a0017c0011t0072 | 0/1 | 18788 | 1 | 0 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | AGTGG others(18783): Show |
chr6 | 63630802 | 63731011 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0001c0001t0001g0164 | 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 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0001g0185 | 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 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 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 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0117 | 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 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0155 | 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 |
a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0004g0284 | 1/0 | 1 | 0 | 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 |
a0001c0001t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0005g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0005g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0005g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0005g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0005g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0005g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0006g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0006g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0006g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0006g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0006g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0007g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0007g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0007g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0007g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0007g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0007g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0008g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0008g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0008g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0008g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0008g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0008g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0008g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0009g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0009g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0009g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0009g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0009g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0010g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0011g0002 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0011g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0011g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0012g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0012g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0012g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0012g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0013g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0013g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0013g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0013g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0014g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0014g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0015g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0015g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0015g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0015g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0016g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0016g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0016g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0017g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0017g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0017g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0018g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0018g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0018g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0020g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0020g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0020g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0021g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0021g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0022g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0022g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0022g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0023g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0023g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0023g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0024g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0024g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0025g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0025g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0027g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0027g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0028g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0028g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0029g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0029g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0030g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0030g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0031g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0032g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0034g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0035g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0036g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0037g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0038g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0039g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0041g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0042g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0043g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0044g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0045g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0046g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0047g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0049g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0050g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0052g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0053g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0054g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0055g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0056g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0057g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0058g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0060g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0061g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0062g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0063g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0065g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0066g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0067g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0068g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0069g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0070g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0071g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0073g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0074g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0075g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0077g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0078g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0079g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0001t0082g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0010t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0012t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0013t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0015t0076g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0001c0016t0007g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0002c0002t0010g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0002c0002t0010g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0002c0002t0014g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0002c0002t0014g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0002c0002t0059g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0002c0002t0064g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0003c0003t0019g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0003c0003t0019g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0003c0003t0019g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0004c0004t0026g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0004c0004t0033g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0004c0004t0048g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0005c0005t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0005c0005t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0006c0006t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0006c0006t0040g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0007c0008t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0008c0020t0051g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0009c0009t0007g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0010c0022t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0011c0019t0080g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0012c0017t0081g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0013c0007t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0014c0021t0026g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0015c0014t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0016c0018t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
a0017c0011t0072g0109 | 0/1 | 1 | 0 | 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 | t0054 | g0122 | EUR | GBR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0015 | EUR | GBR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00280 | hp1 | a0007 | c0008 | t0001 | g0126 | EUR | FIN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0239 | EUR | FIN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0006 | EUR | FIN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | FIN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | CHS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00423 | hp2 | a0003 | c0003 | t0019 | g0081 | EAS | CHS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00544 | hp2 | a0001 | c0001 | t0037 | g0231 | EAS | CHS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | CHS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00558 | hp2 | a0001 | c0001 | t0022 | g0278 | EAS | CHS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00597 | hp1 | a0001 | c0001 | t0067 | g0075 | EAS | CHS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | CHS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00609 | hp1 | a0001 | c0001 | t0058 | g0012 | EAS | CHS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00609 | hp2 | a0001 | c0001 | t0043 | g0273 | EAS | CHS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00639 | hp1 | a0001 | c0001 | t0007 | g0244 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0272 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0167 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0234 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0129 | 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 | g0115 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0010 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG00741 | hp2 | a0001 | c0001 | t0011 | g0102 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01069 | hp1 | a0001 | c0001 | t0006 | g0181 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01069 | hp2 | a0001 | c0001 | t0025 | g0045 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0220 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01071 | hp1 | a0001 | c0001 | t0006 | g0001 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01074 | hp2 | a0001 | c0001 | t0005 | g0071 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0010 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01099 | hp2 | a0001 | c0001 | t0007 | g0245 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01109 | hp1 | a0001 | c0001 | t0034 | g0024 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01109 | hp2 | a0001 | c0001 | t0053 | g0039 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01169 | hp2 | a0001 | c0001 | t0011 | g0002 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01192 | hp1 | a0001 | c0001 | t0006 | g0001 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01192 | hp2 | a0001 | c0001 | t0023 | g0135 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01243 | hp2 | a0001 | c0001 | t0020 | g0196 | AMR | PUR | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0061 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01346 | hp1 | a0001 | c0001 | t0082 | g0163 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01358 | hp2 | a0008 | c0020 | t0051 | g0033 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01361 | hp2 | a0001 | c0001 | t0007 | g0246 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01433 | hp2 | a0001 | c0001 | t0024 | g0187 | AMR | CLM | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0127 | 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 | t0023 | g0114 | EUR | IBS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01515 | hp2 | a0001 | c0001 | t0005 | g0064 | EUR | IBS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01517 | hp1 | a0001 | c0001 | t0025 | g0173 | EUR | IBS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01517 | hp2 | a0001 | c0001 | t0023 | g0134 | EUR | IBS | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0054 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01884 | hp2 | a0002 | c0002 | t0014 | g0026 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01934 | hp2 | a0001 | c0010 | t0003 | g0242 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01943 | hp1 | a0001 | c0001 | t0005 | g0048 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0214 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01952 | hp1 | a0001 | c0001 | t0045 | g0078 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01952 | hp2 | a0001 | c0001 | t0042 | g0264 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0117 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02040 | hp1 | a0001 | c0001 | t0005 | g0067 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02080 | hp1 | a0001 | c0001 | t0032 | g0267 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02080 | hp2 | a0001 | c0001 | t0047 | g0237 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02132 | hp1 | a0001 | c0016 | t0007 | g0250 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0200 | 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 | t0002 | g0074 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02145 | hp1 | a0001 | c0001 | t0006 | g0068 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02145 | hp2 | a0001 | c0001 | t0013 | g0191 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0271 | EAS | CDX | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02155 | hp2 | a0001 | c0001 | t0049 | g0140 | EAS | CDX | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02258 | hp1 | a0001 | c0001 | t0013 | g0190 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02258 | hp2 | a0002 | c0002 | t0010 | g0004 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02273 | hp1 | a0001 | c0001 | t0005 | g0070 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0230 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0170 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02280 | hp2 | a0001 | c0001 | t0031 | g0275 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02300 | hp1 | a0001 | c0001 | t0005 | g0049 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02300 | hp2 | a0009 | c0009 | t0007 | g0247 | AMR | PEL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02451 | hp2 | a0005 | c0005 | t0003 | g0280 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0265 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02572 | hp1 | a0001 | c0001 | t0015 | g0101 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02572 | hp2 | a0002 | c0002 | t0059 | g0030 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02615 | hp1 | a0001 | c0001 | t0013 | g0193 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02622 | hp1 | a0001 | c0001 | t0016 | g0206 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02622 | hp2 | a0001 | c0001 | t0011 | g0002 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02630 | hp2 | a0001 | c0001 | t0021 | g0277 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02647 | hp1 | a0001 | c0001 | t0075 | g0255 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02683 | hp1 | a0001 | c0001 | t0009 | g0218 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02683 | hp2 | a0001 | c0001 | t0020 | g0194 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02698 | hp1 | a0001 | c0001 | t0007 | g0254 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0139 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02717 | hp1 | a0004 | c0004 | t0026 | g0287 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02717 | hp2 | a0001 | c0001 | t0016 | g0014 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02723 | hp1 | a0001 | c0001 | t0060 | g0106 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0179 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02735 | hp1 | a0001 | c0001 | t0055 | g0034 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02735 | hp2 | a0001 | c0001 | t0007 | g0253 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02738 | hp1 | a0001 | c0001 | t0017 | g0036 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02738 | hp2 | a0001 | c0001 | t0020 | g0195 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02809 | hp1 | a0001 | c0001 | t0011 | g0107 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02818 | hp1 | a0001 | c0015 | t0076 | g0285 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02818 | hp2 | a0001 | c0001 | t0073 | g0088 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02886 | hp1 | a0001 | c0001 | t0012 | g0021 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02886 | hp2 | a0001 | c0001 | t0013 | g0192 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02896 | hp1 | a0001 | c0001 | t0021 | g0016 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02896 | hp2 | a0001 | c0001 | t0027 | g0053 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02897 | hp1 | a0001 | c0001 | t0012 | g0020 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02897 | hp2 | a0001 | c0001 | t0021 | g0016 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02922 | hp1 | a0002 | c0002 | t0010 | g0027 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02922 | hp2 | a0001 | c0001 | t0069 | g0002 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02965 | hp1 | a0002 | c0002 | t0010 | g0004 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02965 | hp2 | a0001 | c0001 | t0070 | g0009 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02970 | hp1 | a0001 | c0001 | t0022 | g0276 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02970 | hp2 | a0002 | c0002 | t0014 | g0028 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02976 | hp1 | a0002 | c0002 | t0064 | g0029 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02976 | hp2 | a0001 | c0001 | t0015 | g0002 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03041 | hp1 | a0001 | c0001 | t0035 | g0018 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03041 | hp2 | a0001 | c0001 | t0079 | g0293 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03098 | hp1 | a0001 | c0001 | t0062 | g0017 | AFR | MSL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03098 | hp2 | a0001 | c0001 | t0057 | g0169 | AFR | MSL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03139 | hp1 | a0011 | c0019 | t0080 | g0292 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03139 | hp2 | a0001 | c0001 | t0071 | g0104 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03195 | hp1 | a0006 | c0006 | t0003 | g0209 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0032 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03209 | hp1 | a0001 | c0001 | t0028 | g0257 | AFR | MSL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03209 | hp2 | a0001 | c0001 | t0065 | g0022 | AFR | MSL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03453 | hp1 | a0001 | c0001 | t0011 | g0002 | AFR | MSL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | MSL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03486 | hp1 | a0001 | c0001 | t0015 | g0103 | AFR | MSL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03486 | hp2 | a0001 | c0001 | t0027 | g0050 | AFR | MSL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0221 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0093 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0222 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03516 | hp1 | a0001 | c0001 | t0030 | g0256 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0208 | AFR | ESN | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03540 | hp1 | a0005 | c0005 | t0003 | g0281 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03540 | hp2 | a0012 | c0017 | t0081 | g0112 | AFR | GWD | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03579 | hp1 | a0001 | c0001 | t0030 | g0243 | AFR | MSL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03579 | hp2 | a0001 | c0001 | t0063 | g0080 | AFR | MSL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03669 | hp1 | a0001 | c0001 | t0017 | g0025 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03669 | hp2 | a0001 | c0001 | t0066 | g0066 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03688 | hp1 | a0001 | c0001 | t0008 | g0150 | SAS | STU | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0282 | SAS | STU | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03704 | hp1 | a0001 | c0001 | t0014 | g0084 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0223 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03831 | hp1 | a0001 | c0001 | t0017 | g0035 | SAS | BEB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | BEB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03927 | hp1 | a0001 | c0001 | t0029 | g0248 | SAS | BEB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03942 | hp1 | a0001 | c0001 | t0007 | g0251 | SAS | BEB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0087 | SAS | BEB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | STU | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG04199 | hp2 | a0013 | c0007 | t0001 | g0148 | SAS | STU | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | STU | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG04228 | hp2 | a0001 | c0001 | t0029 | g0249 | SAS | STU | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18522 | hp1 | a0002 | c0002 | t0010 | g0004 | AFR | YRI | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18522 | hp2 | a0001 | c0001 | t0028 | g0258 | AFR | YRI | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18612 | hp1 | a0001 | c0001 | t0038 | g0236 | EAS | CHB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18747 | hp1 | a0001 | c0001 | t0024 | g0145 | EAS | CHB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18747 | hp2 | a0001 | c0013 | t0002 | g0046 | EAS | CHB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18941 | hp2 | a0001 | c0001 | t0061 | g0072 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18942 | hp1 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18943 | hp2 | a0001 | c0001 | t0009 | g0217 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18945 | hp1 | a0001 | c0001 | t0041 | g0003 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0202 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18949 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18951 | hp2 | a0001 | c0001 | t0010 | g0008 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18952 | hp1 | a0001 | c0001 | t0016 | g0161 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18954 | hp1 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18960 | hp1 | a0001 | c0001 | t0036 | g0224 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18964 | hp2 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18969 | hp2 | a0001 | c0001 | t0009 | g0211 | 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 | t0003 | g0270 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18971 | hp1 | a0001 | c0001 | t0018 | g0189 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18973 | hp2 | a0001 | c0001 | t0046 | g0290 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18975 | hp1 | a0003 | c0003 | t0019 | g0059 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18978 | hp2 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18980 | hp1 | a0001 | c0001 | t0018 | g0012 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18980 | hp2 | a0001 | c0001 | t0039 | g0212 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18981 | hp1 | a0001 | c0001 | t0005 | g0073 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18983 | hp1 | a0015 | c0014 | t0001 | g0197 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18986 | hp2 | a0001 | c0012 | t0003 | g0262 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18988 | hp1 | a0001 | c0001 | t0008 | g0125 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18989 | hp1 | a0001 | c0001 | t0014 | g0092 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18990 | hp2 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18995 | hp1 | a0001 | c0001 | t0008 | g0186 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19000 | hp2 | a0001 | c0001 | t0008 | g0182 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19002 | hp1 | a0001 | c0001 | t0006 | g0174 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19003 | hp1 | a0001 | c0001 | t0009 | g0238 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19003 | hp2 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19030 | hp1 | a0004 | c0004 | t0033 | g0286 | AFR | LWK | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19030 | hp2 | a0001 | c0001 | t0050 | g0178 | AFR | LWK | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19043 | hp1 | a0001 | c0001 | t0077 | g0283 | AFR | LWK | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19043 | hp2 | a0001 | c0001 | t0015 | g0100 | AFR | LWK | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19062 | hp1 | a0001 | c0001 | t0022 | g0279 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19062 | hp2 | a0016 | c0018 | t0004 | g0013 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19064 | hp1 | a0001 | c0001 | t0006 | g0175 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19065 | hp1 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19068 | hp1 | a0001 | c0001 | t0044 | g0227 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19074 | hp1 | a0001 | c0001 | t0018 | g0177 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19074 | hp2 | a0001 | c0001 | t0009 | g0233 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19080 | hp2 | a0001 | c0001 | t0056 | g0152 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19082 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19085 | hp1 | a0003 | c0003 | t0019 | g0043 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19091 | hp2 | a0001 | c0001 | t0008 | g0011 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19240 | hp1 | a0006 | c0006 | t0040 | g0210 | AFR | YRI | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | YRI | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA20129 | hp1 | a0001 | c0001 | t0052 | g0168 | AFR | ASW | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA20129 | hp2 | a0001 | c0001 | t0078 | g0009 | AFR | ASW | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA20752 | hp1 | a0001 | c0001 | t0006 | g0008 | EUR | TSI | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0180 | 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 | t0005 | g0051 | EUR | TSI | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA20905 | hp1 | a0001 | c0001 | t0005 | g0060 | SAS | GIH | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA20905 | hp2 | a0001 | c0001 | t0008 | g0204 | SAS | GIH | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02109 | hp1 | a0001 | c0001 | t0012 | g0023 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02109 | hp2 | a0001 | c0001 | t0068 | g0105 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02486 | hp1 | a0010 | c0022 | t0004 | g0130 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG02486 | hp2 | a0004 | c0004 | t0048 | g0288 | AFR | ACB | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG06807 | hp1 | a0014 | c0021 | t0026 | g0289 | AFR | USA | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
HG06807 | hp2 | a0001 | c0001 | t0074 | g0252 | AFR | USA | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA21309 | hp1 | a0001 | c0001 | t0008 | g0171 | AFR | LWK | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
NA21309 | hp2 | a0001 | c0001 | t0012 | g0019 | AFR | LWK | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
homoSapiens | chm13v2 | a0017 | c0011 | t0072 | g0109 | REF | REF | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0284 | REF | REF | PHF3_chr6_63630802_63731011 | PHF3 | chr6 | 63630802 | 63731011 |
view | 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 | a0010 | 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 | a0014 | 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 | a0013 | 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 | a0008 | 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 | a0003 | 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 | a0007 | 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 | a0011 | 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 | a0016 | 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 | a0012 | 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 | a0009 | 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 | |||
chr6:63712963 | G | C | 2 | a0004 a0014 |
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 | a0015 | 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 |
view | 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 | a0008c0020 | 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 | a0008c0020 | 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 |
view | 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 | a0001c0001t0023 | 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 | a0001c0001t0082 | 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 | a0001c0001t0031 | 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 | a0001c0001t0032 | 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 | a0004c0004t0033 | 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 | a0012c0017t0081 | 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 | a0001c0001t0012 a0001c0001t0034 a0001c0001t0035 |
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 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0032 others(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 | a0001c0001t0078 a0001c0001t0079 a0011c0019t0080 |
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 | a0001c0001t0079 a0011c0019t0080 |
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 | a0001c0001t0045 | 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 | a0001c0001t0046 | 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 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0009 others(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 | a0001c0001t0013 | 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 | a0001c0001t0044 | 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 | a0001c0001t0079 a0011c0019t0080 |
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 | a0001c0001t0077 | 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 | a0001c0001t0073 | 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 | a0001c0001t0030 | 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 | a0001c0015t0076 | 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 | a0001c0001t0020 a0012c0017t0081 |
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 | 67 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(64): Show |
206 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(203): 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 | 67 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(64): Show |
206 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(203): 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 | a0001c0001t0043 | 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 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0009 others(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 | a0001c0001t0049 | 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 | a0001c0015t0076 | 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 | a0012c0017t0081 | 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 | a0004c0004t0026 a0004c0004t0033 a0004c0004t0048 others(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 | a0001c0001t0079 a0011c0019t0080 |
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 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0032 others(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 | ||||||
chr6:63718177 | T | G | 2 | a0001c0001t0079 a0011c0019t0080 |
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 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(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 | a0001c0001t0018 a0001c0001t0058 |
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 | a0004c0004t0026 a0004c0004t0033 a0004c0004t0048 others(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 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0032 others(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 | a0001c0001t0036 | 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 | a0001c0001t0011 a0001c0001t0015 a0001c0001t0068 others(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 | a0001c0001t0079 a0011c0019t0080 |
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 | a0002c0002t0059 | 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 | a0001c0001t0007 a0001c0001t0029 a0001c0016t0007 others(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 | a0001c0001t0050 | 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 | a0001c0001t0011 a0001c0001t0015 a0001c0001t0060 others(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 | a0001c0001t0061 | 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 | a0001c0001t0034 | 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 | a0003c0003t0019 | 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 | a0001c0001t0067 | 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 | a0001c0001t0079 a0011c0019t0080 |
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 | a0001c0001t0050 a0001c0001t0052 |
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 | a0001c0001t0021 a0001c0001t0022 |
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 | a0001c0001t0079 a0011c0019t0080 |
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 | a0001c0001t0031 | 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 | a0001c0001t0015 a0001c0001t0068 a0001c0001t0069 |
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 | a0001c0001t0079 a0011c0019t0080 |
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 | a0001c0015t0076 | 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 | a0011c0019t0080 | 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 | a0011c0019t0080 | 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 | a0001c0001t0060 | 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 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0032 others(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 | a0001c0001t0042 | 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 | a0002c0002t0059 | 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 | a0001c0001t0062 | 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 | a0001c0001t0052 | 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 | a0001c0001t0053 | 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 | a0001c0001t0079 a0011c0019t0080 |
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 | a0001c0001t0031 | 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 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0009 others(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 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0032 others(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 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0069 others(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 | a0001c0001t0016 a0001c0001t0063 a0001c0001t0068 others(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 | 14 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0018 others(11): 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 | 13 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0012 others(10): 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 | 19 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0024 others(16): Show |
71 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(68): 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 | a0001c0001t0003 a0001c0001t0032 a0001c0001t0036 others(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 | a0001c0001t0025 a0001c0001t0066 |
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 | a0001c0001t0013 | 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 | a0001c0001t0056 | 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 | a0001c0001t0007 a0001c0001t0021 a0001c0001t0022 others(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 | a0001c0001t0017 a0001c0001t0055 |
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 | a0001c0001t0079 a0011c0019t0080 |
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 | a0001c0001t0065 | 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 | a0001c0001t0079 a0011c0019t0080 |
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 | a0001c0001t0011 a0001c0001t0015 a0001c0001t0068 others(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 | a0001c0001t0002 | 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 | a0001c0015t0076 | 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 | a0001c0001t0027 | 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 | a0002c0002t0064 | 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 | a0001c0001t0021 a0001c0001t0022 |
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 | a0001c0001t0039 | 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 | a0001c0001t0020 | 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 | a0006c0006t0040 | 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 | a0001c0001t0054 | 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 | a0004c0004t0026 a0004c0004t0033 a0014c0021t0026 |
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 | a0001c0001t0012 a0001c0001t0034 a0001c0001t0035 others(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 | a0001c0001t0041 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11717G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 16/16 | 11717 | chr6 | 63725425 |
view | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0002g0291 | 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 | a0001c0001t0046g0290 | 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 | a0004c0004t0026g0287 a0004c0004t0033g0286 a0004c0004t0048g0288 others(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 | 301 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0037 others(298): Show |
317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.-26+311T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 1/15 | chr6 | 63636461 | |||||||
chr6:63636497 | G | C | 220 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0037 others(217): Show |
231 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(228): 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 | a0001c0001t0062g0017 | 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 | a0001c0001t0004g0208 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0012g0019 a0001c0001t0012g0020 a0001c0001t0012g0021 others(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 | a0001c0001t0035g0018 | 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 | a0006c0006t0003g0209 a0006c0006t0040g0210 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0016g0206 | 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 | a0001c0001t0002g0205 | 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 | a0004c0004t0026g0287 a0004c0004t0033g0286 a0004c0004t0048g0288 others(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 | 299 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0037 others(296): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): 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 | a0004c0004t0026g0287 a0004c0004t0033g0286 a0004c0004t0048g0288 others(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 | a0001c0001t0017g0025 | 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 | 301 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0037 others(298): Show |
317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): 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 | a0002c0002t0010g0004 a0002c0002t0010g0027 a0002c0002t0014g0026 others(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 | a0011c0019t0080g0292 | 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 | a0001c0001t0009g0211 a0001c0001t0039g0212 |
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 | a0001c0001t0002g0031 | 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 | a0001c0001t0005g0032 | 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 | a0001c0001t0008g0204 | 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 | a0001c0001t0077g0283 | 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 | 221 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0037 others(218): Show |
232 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(229): 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 | a0008c0020t0051g0033 | 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 | a0001c0001t0003g0015 a0001c0001t0003g0213 a0001c0001t0003g0214 others(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 | a0001c0001t0017g0025 a0001c0001t0017g0035 a0001c0001t0017g0036 others(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 | a0001c0001t0004g0202 a0001c0001t0004g0203 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
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 | a0001c0001t0002g0201 | 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 | a0001c0001t0001g0200 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0002g0199 | 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 | a0001c0001t0030g0243 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0005c0005t0003g0280 a0005c0005t0003g0281 |
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 | a0001c0001t0007g0244 a0001c0001t0007g0245 a0001c0001t0007g0246 others(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 | a0001c0001t0007g0244 a0001c0001t0007g0245 a0001c0001t0007g0246 others(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 | a0001c0001t0017g0036 | 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 | a0001c0001t0007g0244 a0001c0001t0007g0245 a0001c0001t0007g0246 others(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 | a0004c0004t0026g0287 a0004c0004t0033g0286 a0004c0004t0048g0288 others(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 | a0001c0001t0003g0213 a0001c0001t0009g0211 a0001c0001t0039g0212 |
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 | a0001c0010t0003g0242 | 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 | a0001c0001t0017g0025 | 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 | 55 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(52): 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 | a0001c0001t0007g0244 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0002g0040 a0001c0001t0002g0291 a0001c0001t0005g0041 |
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 | a0001c0001t0002g0198 | 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 | a0015c0014t0001g0197 | 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 | 98 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0031 others(95): Show |
105 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(102): 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0011c0019t0080g0292 | 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 | a0001c0001t0079g0293 | 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 | a0001c0001t0023g0114 a0001c0001t0023g0134 a0001c0001t0023g0135 |
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 | a0001c0001t0001g0113 a0001c0001t0001g0127 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0183 a0001c0001t0016g0206 |
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 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0120 others(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 | a0001c0001t0001g0180 a0001c0001t0002g0007 a0001c0001t0002g0091 others(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 | 89 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0031 others(86): Show |
94 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(91): 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 | a0001c0001t0001g0164 a0001c0001t0004g0014 a0001c0001t0012g0019 others(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 | a0001c0001t0002g0207 a0001c0001t0030g0243 a0001c0001t0030g0256 others(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 | a0004c0004t0026g0287 a0004c0004t0033g0286 a0004c0004t0048g0288 others(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 | a0001c0001t0074g0252 | 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 | a0001c0001t0004g0110 a0001c0001t0004g0111 |
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 | a0001c0001t0020g0194 a0001c0001t0020g0195 a0001c0001t0020g0196 |
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 | a0001c0001t0003g0274 | 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 | a0001c0001t0005g0108 | 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 | a0001c0001t0020g0194 a0001c0001t0020g0195 a0001c0001t0020g0196 others(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 | a0002c0002t0059g0030 | 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 | a0001c0001t0028g0257 a0001c0001t0028g0258 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0028g0257 a0001c0001t0028g0258 a0001c0001t0030g0243 others(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 | a0001c0001t0021g0016 a0001c0001t0021g0277 a0001c0001t0022g0276 others(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 | a0001c0001t0013g0190 a0001c0001t0013g0191 a0001c0001t0013g0192 others(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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | 13 | a0001c0001t0011g0002 a0001c0001t0011g0102 a0001c0001t0011g0107 others(10): 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 | a0001c0015t0076g0285 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0007g0244 a0001c0001t0007g0245 a0001c0001t0007g0246 others(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 | a0001c0001t0007g0254 | 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 | a0001c0001t0018g0189 | 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 | 81 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(78): 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 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0003g0214 | 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 | a0001c0001t0012g0019 a0001c0001t0012g0020 a0001c0001t0012g0021 others(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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | 55 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(52): 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 | a0001c0001t0008g0204 | 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 | a0001c0001t0021g0016 a0001c0001t0021g0277 a0001c0001t0022g0276 others(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 | a0001c0001t0006g0181 | 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 | a0001c0001t0001g0180 | 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 | a0001c0015t0076g0285 | 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 | a0001c0001t0001g0113 a0001c0001t0020g0194 a0001c0001t0020g0195 others(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 | a0001c0001t0004g0179 a0001c0001t0007g0253 a0001c0001t0021g0016 others(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 | a0004c0004t0026g0287 a0004c0004t0048g0288 a0014c0021t0026g0289 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0011c0019t0080g0292 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | 7 | a0001c0001t0002g0094 a0001c0001t0011g0107 a0001c0001t0013g0193 others(4): Show |
7 | HG01109.hp1 HG02071.hp1 HG02615.hp1 others(4): 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 | 52 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(49): 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0001g0176 | 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 | 55 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(52): 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 | a0002c0002t0010g0004 a0002c0002t0010g0027 a0002c0002t0014g0026 others(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 | 90 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0031 others(87): Show |
95 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(92): 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 | 191 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0031 others(188): Show |
203 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(200): 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 | a0001c0001t0018g0189 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0020g0194 | 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 | a0001c0001t0002g0042 | 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 | 261 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0037 others(258): Show |
276 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(273): 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 | a0001c0001t0001g0176 a0001c0001t0001g0200 |
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 | 181 | a0001c0001t0001g0138 a0001c0001t0002g0006 a0001c0001t0002g0007 others(178): Show |
195 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(192): 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 | a0001c0001t0002g0044 a0001c0001t0002g0047 a0001c0001t0003g0215 others(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 | a0001c0001t0005g0048 | 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 | a0001c0001t0053g0039 | 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 | a0001c0001t0003g0239 | 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 | a0001c0001t0004g0137 | 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 | a0001c0001t0007g0244 a0001c0001t0007g0245 a0001c0001t0007g0246 others(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 | a0001c0001t0020g0194 a0001c0001t0020g0195 a0001c0001t0020g0196 others(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 | a0001c0001t0077g0283 | 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 | a0001c0001t0013g0192 | 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 | a0004c0004t0026g0287 a0004c0004t0033g0286 a0004c0004t0048g0288 others(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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0004g0203 | 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 | a0001c0001t0001g0188 | 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 | 56 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(53): 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 | a0006c0006t0040g0210 | 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 | a0001c0001t0002g0093 | 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 | a0001c0001t0031g0275 | 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 | a0001c0001t0003g0216 | 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 | 8 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0004g0010 others(5): 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0002g0091 a0001c0001t0014g0092 |
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 | a0001c0001t0009g0217 | 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 | a0004c0004t0026g0287 a0004c0004t0033g0286 a0004c0004t0048g0288 others(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 | 55 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(52): 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 | a0001c0001t0013g0190 a0001c0001t0013g0191 a0001c0001t0013g0192 others(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 | 55 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(52): 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 | 94 | a0001c0001t0002g0007 a0001c0001t0002g0031 a0001c0001t0002g0040 others(91): Show |
98 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(95): 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 | a0001c0001t0002g0089 a0001c0001t0002g0090 a0001c0001t0002g0291 others(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 | a0001c0001t0074g0252 | 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 | 55 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(52): 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0029g0249 | 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 | a0001c0001t0002g0090 | 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 | a0001c0001t0002g0096 a0001c0001t0002g0207 a0001c0001t0005g0051 |
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 | a0001c0001t0002g0282 | 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 | a0001c0001t0077g0283 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | 59 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(56): 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 | a0001c0001t0002g0093 | 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 | a0001c0001t0007g0244 a0001c0001t0007g0245 a0001c0001t0007g0246 others(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 | a0012c0017t0081g0112 | 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 | a0001c0001t0002g0052 a0001c0001t0002g0097 |
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 | 56 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(53): 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 | a0002c0002t0064g0029 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0007g0244 a0001c0001t0007g0245 a0001c0001t0007g0246 others(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 | 1 | a0001c0001t0004g0010 | 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 | a0001c0001t0060g0106 | 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 | 13 | a0001c0001t0011g0002 a0001c0001t0011g0102 a0001c0001t0011g0107 others(10): 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 | a0001c0001t0003g0259 | 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 | a0001c0001t0004g0139 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0001g0172 | 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 | a0001c0001t0001g0142 a0001c0001t0004g0141 a0001c0001t0049g0140 |
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 | a0001c0001t0001g0142 a0001c0001t0004g0141 a0001c0001t0049g0140 |
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 | a0001c0001t0071g0104 | 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 | 56 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(53): 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 | a0001c0015t0076g0285 | 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 | 207 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0031 others(204): Show |
221 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(218): 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 | a0001c0001t0004g0014 a0001c0001t0004g0170 a0001c0001t0004g0208 others(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 | a0001c0001t0001g0143 | 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 | a0001c0001t0079g0293 | 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 | a0001c0001t0001g0136 a0001c0001t0003g0271 a0001c0001t0009g0238 others(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 | a0001c0001t0020g0194 a0001c0001t0020g0196 a0002c0002t0010g0004 others(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 | a0001c0001t0021g0016 a0001c0001t0077g0283 a0006c0006t0040g0210 |
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 | a0001c0001t0004g0014 a0001c0001t0004g0170 a0001c0001t0004g0208 others(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 | a0001c0001t0009g0218 | 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 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0201 others(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 | a0001c0001t0002g0087 | 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 | a0008c0020t0051g0033 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0001g0144 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0002g0047 a0001c0001t0002g0086 a0001c0001t0002g0199 others(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 | a0001c0001t0004g0167 | 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 | a0001c0001t0007g0244 | 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 | a0001c0001t0002g0282 | 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 | 56 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(53): 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 | a0001c0001t0079g0293 | 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 | a0005c0005t0003g0281 | 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 | a0001c0015t0076g0285 | 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 | 56 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(53): 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 | a0001c0001t0002g0085 a0001c0001t0002g0093 a0001c0001t0014g0084 |
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 | 55 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(52): 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0020g0194 | 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 | 81 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(78): 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | 106 | a0001c0001t0001g0166 a0001c0001t0002g0006 a0001c0001t0002g0007 others(103): Show |
113 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(110): 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 | 63 | a0001c0001t0002g0083 a0001c0001t0003g0003 a0001c0001t0003g0015 others(60): 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 | a0001c0001t0074g0252 | 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 | a0001c0015t0076g0285 | 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 | a0001c0001t0060g0106 | 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 | a0001c0001t0043g0273 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0077g0283 | 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 | a0001c0001t0008g0204 | 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 | a0001c0001t0077g0283 | 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0017g0025 | 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 | a0008c0020t0051g0033 | 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 | a0002c0002t0064g0029 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0020g0194 a0001c0001t0020g0195 a0001c0001t0020g0196 others(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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0002c0002t0010g0027 | 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 | 56 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(53): 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 | a0001c0001t0002g0058 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0001g0113 | 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 | 194 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0031 others(191): Show |
208 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(205): 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 | a0001c0001t0021g0016 a0001c0001t0021g0277 a0001c0001t0022g0276 others(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 | a0001c0001t0020g0194 a0001c0001t0020g0195 a0001c0001t0020g0196 others(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 | a0004c0004t0026g0287 a0004c0004t0033g0286 a0004c0004t0048g0288 others(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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | 97 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0031 others(94): Show |
104 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(101): 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0003g0260 | 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 | a0001c0001t0032g0267 | 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 | a0001c0001t0004g0128 a0001c0001t0013g0190 a0001c0001t0013g0191 others(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 | a0001c0001t0001g0127 a0001c0001t0003g0213 a0001c0001t0003g0228 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0113 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0147 a0001c0001t0001g0164 a0001c0001t0001g0165 others(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 | a0001c0001t0007g0244 a0001c0001t0007g0245 a0001c0001t0007g0246 others(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 | a0001c0001t0003g0003 a0001c0001t0003g0272 a0001c0001t0029g0249 others(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 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0214 others(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 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0085 others(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 | 93 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0031 others(90): Show |
102 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(99): 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 | a0003c0003t0019g0043 a0003c0003t0019g0059 |
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 | a0001c0001t0007g0244 a0001c0001t0007g0245 a0001c0001t0007g0246 others(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 | a0001c0001t0002g0093 | 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 | a0001c0001t0002g0082 | 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 | a0011c0019t0080g0292 | 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 | a0001c0001t0002g0052 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0003c0003t0019g0081 | 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0002g0082 | 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 | a0001c0001t0035g0018 | 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 | a0001c0001t0001g0164 | 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 | a0001c0001t0031g0275 | 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 | a0001c0001t0020g0194 a0001c0001t0020g0195 a0001c0001t0020g0196 others(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 | a0001c0001t0002g0047 a0001c0001t0002g0086 a0001c0001t0002g0199 others(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 | a0003c0003t0019g0081 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | 1 | a0001c0001t0002g0007 | 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 | a0001c0001t0015g0100 | 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 | 87 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0031 others(84): Show |
92 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(89): 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 | a0001c0001t0007g0244 a0001c0001t0007g0245 a0001c0001t0007g0246 others(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 | a0001c0001t0023g0114 a0001c0001t0023g0134 a0001c0001t0023g0135 |
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 | a0001c0001t0002g0201 | 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 | a0001c0015t0076g0285 | 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 | a0001c0001t0002g0057 | 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 | a0001c0001t0007g0244 a0001c0001t0007g0245 a0001c0001t0007g0246 others(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 | a0001c0001t0082g0163 | 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 | a0001c0001t0043g0273 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0001g0142 a0001c0001t0004g0141 a0001c0001t0049g0140 |
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 | a0001c0001t0001g0133 | 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 | 82 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0031 others(79): Show |
87 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(84): 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 | a0001c0001t0002g0079 a0001c0001t0045g0078 |
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 | a0001c0001t0047g0237 | 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 | a0001c0001t0007g0244 a0001c0001t0007g0245 a0001c0001t0007g0246 others(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 | a0001c0001t0009g0238 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0002g0077 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0021g0016 a0001c0001t0021g0277 a0001c0001t0022g0276 others(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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0002g0097 | 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 | a0001c0001t0077g0283 | 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 | a0001c0001t0002g0096 a0001c0001t0002g0207 a0001c0001t0005g0051 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | 33 | a0001c0001t0001g0037 a0001c0001t0001g0121 a0001c0001t0001g0123 others(30): 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 | 88 | a0001c0001t0001g0038 a0001c0001t0002g0006 a0001c0001t0002g0007 others(85): Show |
94 | HG00423.hp2 HG00597.hp1 HG00639.hp2 others(91): 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 | a0001c0001t0002g0044 a0001c0001t0002g0062 a0001c0001t0002g0082 others(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 | a0001c0001t0031g0275 a0001c0001t0065g0022 |
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 | a0001c0001t0031g0275 | 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 | a0003c0003t0019g0043 a0003c0003t0019g0059 a0003c0003t0019g0081 |
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 | a0001c0015t0076g0285 | 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 | a0001c0015t0076g0285 | 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 | a0001c0001t0004g0139 a0001c0001t0008g0204 |
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 | a0001c0001t0012g0019 a0001c0001t0012g0020 a0001c0001t0012g0021 others(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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0201 others(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 | a0001c0015t0076g0285 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0005g0060 | 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 | a0001c0001t0052g0168 | 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 | a0001c0001t0077g0283 | 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 | a0006c0006t0003g0209 a0006c0006t0040g0210 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0060g0106 | 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 | a0001c0001t0001g0143 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0001g0132 | 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 | 84 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0031 others(81): Show |
89 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.245-12367T>C | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63667633 | |||||||
chr6:63667638 | C | T | 84 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0031 others(81): Show |
89 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(86): 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 | a0001c0001t0012g0019 | 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 | a0001c0001t0002g0087 | 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 | a0001c0001t0002g0058 | 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 | a0001c0001t0038g0236 | 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 | a0001c0001t0007g0244 a0001c0001t0007g0245 a0001c0001t0007g0246 others(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 | a0004c0004t0026g0287 a0004c0004t0033g0286 a0004c0004t0048g0288 others(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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0004g0111 | 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 | a0001c0001t0002g0076 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0063g0080 | 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 | a0001c0001t0074g0252 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0001g0142 a0001c0001t0004g0141 |
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 | a0001c0001t0007g0244 a0001c0001t0007g0245 a0001c0001t0007g0246 others(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 | 55 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(52): 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0003g0235 | 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 | 69 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(66): 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 | a0001c0001t0029g0249 | 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 | a0001c0015t0076g0285 | 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 | a0011c0019t0080g0292 | 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 | a0006c0006t0003g0209 a0006c0006t0040g0210 |
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 | a0001c0016t0007g0250 | 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 | a0001c0001t0007g0244 a0001c0001t0007g0245 a0001c0001t0007g0246 others(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 | a0001c0001t0002g0052 a0001c0001t0002g0097 |
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 | a0001c0001t0028g0257 a0001c0001t0028g0258 |
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 | a0001c0001t0001g0113 | 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 | a0004c0004t0048g0288 | 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 | a0001c0001t0002g0291 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | 101 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0031 others(98): Show |
108 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(105): 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 | a0001c0001t0002g0079 a0001c0001t0029g0248 a0001c0001t0045g0078 others(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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0077g0283 | 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 | 192 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0031 others(189): Show |
206 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(203): 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 | a0001c0001t0001g0185 a0001c0001t0024g0145 |
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 | a0001c0001t0013g0190 a0001c0001t0013g0191 a0001c0001t0013g0192 others(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 | a0003c0003t0019g0081 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.245-8185C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63671815 | |||||||
chr6:63672096 | C | T | 1 | a0001c0001t0031g0275 | 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0067g0075 | 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 | 1 | a0001c0001t0002g0007 | 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 | a0001c0001t0003g0015 a0001c0001t0003g0220 a0001c0001t0003g0234 others(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 | 53 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(50): 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 | a0001c0001t0053g0039 | 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 | 192 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0031 others(189): Show |
206 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(203): 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 | a0001c0001t0002g0087 | 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 | a0001c0015t0076g0285 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | 84 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(81): 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 | a0001c0001t0006g0174 a0001c0001t0006g0175 |
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 | a0001c0001t0006g0181 | 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 |
102 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0037 others(99): 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 | a0001c0001t0052g0168 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0160 | 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 | a0001c0001t0004g0111 | 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 |
81 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0031 others(78): Show |
86 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(83): 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 | a0001c0001t0002g0087 | 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 | a0001c0001t0007g0244 a0001c0001t0007g0245 a0001c0001t0007g0246 others(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 |
25 | a0001c0001t0011g0002 a0001c0001t0011g0102 a0001c0001t0011g0107 others(22): 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 | a0002c0002t0014g0026 | 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 | a0001c0001t0020g0194 a0001c0001t0020g0195 a0001c0001t0020g0196 others(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 | a0001c0001t0014g0092 | 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 | a0001c0015t0076g0285 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 |
55 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(52): 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 | a0004c0004t0026g0287 a0004c0004t0033g0286 a0004c0004t0048g0288 others(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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0008c0020t0051g0033 | 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 | a0001c0001t0052g0168 | 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 | a0001c0001t0003g0215 a0001c0001t0003g0216 a0001c0001t0003g0219 others(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 | a0004c0004t0033g0286 | 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 | a0001c0001t0002g0087 | 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 | a0001c0001t0003g0221 a0001c0001t0003g0222 a0001c0001t0003g0223 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0021g0016 a0001c0001t0021g0277 a0001c0001t0022g0276 others(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 | a0001c0001t0013g0190 a0001c0001t0013g0191 a0001c0001t0013g0192 others(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 | a0001c0001t0077g0283 | 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 | 196 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0031 others(193): Show |
210 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.245-3841C>T | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63676159 | |||||||
chr6:63676433 | T | C | 54 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(51): 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0001g0138 | 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 | a0001c0001t0012g0019 a0001c0001t0012g0020 a0001c0001t0012g0021 others(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 | a0001c0001t0001g0159 | 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 | a0008c0020t0051g0033 | 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 | a0012c0017t0081g0112 | 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 | a0001c0001t0007g0245 | 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 | a0001c0015t0076g0285 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0020g0195 a0001c0001t0020g0196 a0012c0017t0081g0112 |
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 | a0001c0015t0076g0285 | 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 | a0001c0001t0077g0283 | 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 | a0004c0004t0026g0287 a0004c0004t0048g0288 a0014c0021t0026g0289 |
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 | a0001c0001t0028g0258 | 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 | 54 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(51): 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 | a0002c0002t0059g0030 | 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 | a0001c0001t0077g0283 | 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 | a0001c0001t0003g0261 | 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 | a0002c0002t0064g0029 | 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 | 17 | a0001c0001t0002g0047 a0001c0001t0002g0086 a0001c0001t0002g0199 others(14): 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 | 55 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(52): 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 | a0001c0001t0009g0218 | 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 | a0001c0001t0009g0218 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.245-1768G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 2/15 | chr6 | 63678232 | |||||||
chr6:63678355 | A | G | 1 | a0001c0001t0003g0230 | 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 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0201 others(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 | a0011c0019t0080g0292 | 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 | a0001c0001t0002g0087 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0131 a0001c0001t0001g0151 others(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 | a0001c0001t0001g0146 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | 50 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(47): 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 | a0001c0001t0028g0257 a0001c0001t0028g0258 a0001c0001t0030g0243 others(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 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0201 others(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 | a0001c0001t0001g0147 | 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 | a0001c0001t0004g0208 | 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 | a0001c0001t0028g0257 a0001c0001t0028g0258 a0001c0001t0030g0243 others(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 | a0002c0002t0010g0004 a0002c0002t0010g0027 a0002c0002t0014g0028 |
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 | a0001c0001t0007g0244 a0001c0001t0007g0245 a0001c0001t0007g0246 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0131 others(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 | a0001c0001t0001g0165 a0001c0001t0002g0055 a0001c0001t0003g0221 others(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 | a0001c0001t0007g0244 a0001c0001t0021g0016 a0001c0001t0021g0277 others(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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0063g0080 | 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 | a0001c0001t0001g0144 | 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 | 55 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(52): 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 | a0001c0001t0077g0283 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0143 a0001c0001t0001g0146 others(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 | 12 | a0001c0001t0011g0002 a0001c0001t0011g0102 a0001c0001t0011g0107 others(9): 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 | a0001c0001t0021g0016 a0001c0001t0021g0277 a0001c0001t0022g0276 others(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 | a0006c0006t0003g0209 a0006c0006t0040g0210 |
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 | a0001c0015t0076g0285 | 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 | 201 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0031 others(198): Show |
215 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(212): 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 | a0001c0001t0020g0194 a0001c0001t0020g0195 a0001c0001t0020g0196 others(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 | a0001c0001t0061g0072 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0013g0190 a0001c0001t0013g0191 a0001c0001t0013g0192 others(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 | a0001c0001t0077g0283 | 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 | a0001c0010t0003g0242 | 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 | a0001c0001t0018g0177 | 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 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0095 others(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 | a0001c0001t0004g0110 | 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 | a0001c0001t0007g0244 a0001c0001t0007g0245 a0001c0001t0007g0246 others(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 | a0001c0001t0021g0016 a0001c0001t0021g0277 a0001c0001t0022g0276 |
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 | a0001c0001t0001g0160 a0001c0001t0002g0097 a0001c0001t0028g0257 others(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 | a0001c0001t0005g0064 | 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 | a0006c0006t0040g0210 | 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 | a0001c0001t0063g0080 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0007g0244 a0001c0001t0007g0245 a0001c0001t0007g0246 others(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 | a0013c0007t0001g0148 | 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 | a0001c0001t0021g0016 a0001c0001t0021g0277 a0001c0001t0022g0276 others(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 | a0001c0001t0003g0216 a0001c0001t0037g0231 a0001c0001t0038g0236 |
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 | a0014c0021t0026g0289 | 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 | a0004c0004t0026g0287 a0004c0004t0033g0286 a0004c0004t0048g0288 others(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 | a0001c0001t0001g0113 | 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 | a0001c0012t0003g0262 | 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 | a0001c0001t0077g0283 | 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 | a0001c0001t0001g0159 a0001c0001t0004g0158 a0001c0001t0006g0174 others(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 | a0001c0001t0001g0120 | 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 | a0001c0001t0013g0190 a0001c0001t0013g0191 a0001c0001t0013g0192 others(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 | 195 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0031 others(192): Show |
209 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(206): 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 | a0001c0001t0009g0211 a0001c0001t0039g0212 |
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 | a0001c0001t0003g0015 a0001c0001t0003g0220 a0001c0001t0003g0234 |
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 | a0001c0001t0001g0142 a0001c0001t0001g0154 a0001c0001t0004g0141 others(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 | a0001c0001t0001g0113 a0001c0001t0001g0116 a0001c0001t0001g0133 others(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 | a0001c0001t0002g0065 a0001c0001t0003g0215 a0001c0001t0003g0225 others(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 | a0001c0001t0002g0087 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0118 a0001c0001t0001g0129 others(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 | a0001c0001t0001g0176 a0001c0001t0003g0229 a0001c0001t0012g0023 others(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 | a0001c0001t0031g0275 | 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 | a0001c0001t0031g0275 | 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 | a0001c0001t0073g0088 | 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 | a0001c0001t0020g0196 | 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 | a0012c0017t0081g0112 | 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 | a0001c0001t0035g0018 | 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 | a0001c0001t0002g0097 | 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 | a0001c0001t0002g0052 | 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 | a0001c0001t0020g0194 a0001c0001t0020g0195 |
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 | a0002c0002t0010g0004 a0002c0002t0010g0027 a0002c0002t0014g0028 others(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 | a0002c0002t0014g0026 | 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 | a0001c0015t0076g0285 | 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 | a0001c0001t0003g0214 | 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 | a0001c0001t0003g0268 | 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 | a0003c0003t0019g0059 | 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 | a0001c0001t0001g0172 | 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 | a0001c0001t0001g0143 | 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 | a0004c0004t0033g0286 | 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 | a0008c0020t0051g0033 | 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 | a0001c0001t0002g0083 | 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 | a0001c0001t0002g0069 a0001c0001t0060g0106 |
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 | a0001c0001t0004g0155 | 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 | a0001c0001t0003g0221 a0001c0001t0042g0264 |
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 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0001g0138 others(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 | a0001c0001t0074g0252 | 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 | a0001c0001t0002g0282 a0001c0001t0005g0041 a0001c0001t0005g0049 others(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 | a0001c0001t0003g0225 | 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 | a0001c0001t0001g0142 a0001c0001t0004g0139 a0001c0001t0023g0134 |
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 | a0001c0001t0003g0271 | 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 | a0001c0001t0001g0164 | 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 | a0001c0001t0053g0039 | 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 | a0001c0001t0003g0234 | 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 | a0001c0001t0004g0115 | 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 | a0009c0009t0007g0247 | 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 | a0001c0001t0029g0248 | 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 | a0001c0001t0001g0149 | 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 | a0001c0001t0005g0032 | 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 | a0001c0001t0012g0023 | 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 | a0001c0001t0002g0074 | 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 |
31 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0058 others(28): 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 | a0001c0001t0001g0147 | 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 | a0001c0001t0001g0176 | 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 | a0001c0001t0077g0283 | 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 | a0001c0001t0028g0257 | 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 | a0001c0001t0008g0186 | 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 | a0001c0001t0003g0228 | 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 | a0001c0001t0013g0193 a0001c0001t0023g0135 |
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 | a0001c0001t0003g0216 | 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 | a0001c0001t0007g0246 | 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 | a0001c0001t0001g0119 a0001c0001t0013g0190 |
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 | a0001c0001t0057g0169 | 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 | a0001c0010t0003g0242 | 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 | a0001c0001t0009g0217 | 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 | a0001c0001t0003g0015 a0001c0001t0003g0220 |
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 | a0001c0001t0003g0230 a0001c0001t0003g0274 a0001c0001t0004g0179 others(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 |
30 | a0001c0001t0003g0003 a0001c0001t0003g0213 a0001c0001t0003g0222 others(27): 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 |
75 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0038 others(72): 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 | a0001c0001t0003g0219 a0001c0001t0003g0232 a0001c0001t0009g0233 others(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 | a0001c0001t0003g0235 | 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 | a0004c0004t0048g0288 | 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 | a0001c0001t0007g0244 a0001c0001t0007g0245 a0001c0001t0007g0251 others(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 | a0001c0001t0029g0249 | 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 | a0001c0001t0003g0239 | 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 | a0001c0001t0004g0137 a0001c0001t0008g0125 |
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 | a0001c0001t0001g0037 | 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 | a0007c0008t0001g0126 | 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 | a0001c0001t0032g0267 | 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 | a0001c0001t0002g0062 | 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 | a0001c0001t0067g0075 | 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 | a0001c0001t0002g0044 | 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 | a0003c0003t0019g0081 | 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 | a0001c0001t0002g0096 | 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 |
1 | a0001c0001t0002g0007 | 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 |
39 | a0001c0001t0002g0006 a0001c0001t0002g0031 a0001c0001t0002g0040 others(36): Show |
43 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(40): 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 | a0001c0001t0002g0042 | 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 | a0001c0001t0014g0084 | 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 | a0001c0001t0002g0085 a0001c0001t0002g0093 |
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 | a0001c0012t0003g0262 | 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 | a0001c0001t0003g0215 | 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 | a0001c0001t0011g0102 | 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 | a0001c0001t0073g0088 | 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 | a0001c0001t0079g0293 | 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 | a0011c0019t0080g0292 | 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 | a0001c0001t0012g0020 | 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 | a0001c0001t0012g0020 a0011c0019t0080g0292 |
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 | a0001c0001t0007g0244 a0001c0001t0007g0245 a0001c0001t0007g0246 others(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 | a0001c0001t0018g0177 | 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 | a0001c0001t0001g0127 a0001c0001t0001g0131 a0001c0001t0004g0128 |
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 | a0011c0019t0080g0292 | 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 | a0001c0001t0079g0293 | 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 | a0001c0001t0004g0155 | 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 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0147 others(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 | 55 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(52): 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 | a0001c0001t0079g0293 | 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 | a0001c0001t0079g0293 a0001c0012t0003g0262 |
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 | a0001c0001t0079g0293 | 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 | a0001c0001t0001g0146 a0001c0001t0002g0098 a0001c0001t0003g0232 others(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 | 300 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0037 others(297): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): 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 | a0001c0001t0028g0257 | 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 | 299 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0037 others(296): Show |
315 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(312): 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 | a0001c0001t0060g0106 | 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 | a0001c0001t0079g0293 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | 55 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(52): 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 | a0001c0001t0009g0218 | 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 | a0001c0001t0020g0194 | 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 | a0001c0015t0076g0285 | 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 | a0001c0001t0063g0080 | 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 | 84 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(81): 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 | a0001c0001t0003g0235 a0001c0001t0003g0241 a0001c0001t0009g0218 others(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 | a0001c0001t0028g0257 | 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 | a0001c0001t0007g0246 | 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 | a0001c0001t0002g0089 | 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 | a0001c0001t0079g0293 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0144 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0129 a0001c0001t0001g0133 a0001c0001t0054g0122 |
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 | a0001c0001t0035g0018 | 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 | a0001c0001t0053g0039 | 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 | a0001c0001t0001g0146 a0001c0001t0001g0157 a0001c0001t0004g0167 |
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 | a0001c0001t0021g0016 a0001c0001t0021g0277 a0001c0001t0022g0276 others(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 | a0001c0001t0005g0071 | 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 | 14 | a0001c0001t0011g0002 a0001c0001t0011g0102 a0001c0001t0011g0107 others(11): 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0009g0233 | 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 | a0005c0005t0003g0280 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0004g0014 a0001c0001t0004g0170 a0001c0001t0016g0014 |
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 | a0001c0001t0001g0127 | 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 | a0002c0002t0059g0030 | 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 | a0015c0014t0001g0197 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0060g0106 | 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 | a0001c0001t0028g0257 a0001c0001t0028g0258 a0001c0001t0030g0243 others(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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0002g0090 | 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 | a0001c0001t0029g0248 | 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 | a0001c0001t0031g0275 | 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 | a0001c0001t0030g0256 | 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 | a0001c0001t0002g0057 | 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 | a0001c0001t0063g0080 | 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 | 54 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(51): 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 | a0001c0001t0002g0052 a0001c0001t0002g0097 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0003g0269 | 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 | a0001c0001t0005g0108 | 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 | a0001c0001t0002g0096 | 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 | a0008c0020t0051g0033 | 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 | a0001c0001t0003g0213 a0001c0001t0009g0211 a0001c0001t0039g0212 |
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 | a0001c0001t0001g0123 | 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 | a0001c0001t0028g0257 a0001c0001t0028g0258 a0001c0001t0030g0243 others(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 | a0001c0001t0079g0293 | 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 | 58 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(55): 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 | 56 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(53): 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 | a0001c0001t0001g0157 | 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 | 85 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(82): 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 | a0001c0001t0004g0202 a0001c0001t0004g0203 |
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 | a0001c0001t0001g0151 | 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 | a0001c0001t0001g0183 | 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 | a0004c0004t0026g0287 a0004c0004t0033g0286 a0004c0004t0048g0288 others(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 | 55 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(52): 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 | a0001c0016t0007g0250 | 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 | a0011c0019t0080g0292 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0020g0196 | 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 | a0001c0001t0003g0215 a0001c0001t0003g0219 a0001c0001t0003g0232 others(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 | 55 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(52): 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 | a0001c0001t0004g0110 a0001c0001t0004g0111 |
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 | 56 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(53): 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 | a0011c0019t0080g0292 | 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 | a0001c0001t0003g0235 a0001c0001t0003g0241 a0001c0001t0009g0218 others(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 | 56 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(53): 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 | a0004c0004t0026g0287 a0004c0004t0033g0286 a0004c0004t0048g0288 others(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 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0201 others(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 |
13 | a0001c0001t0011g0002 a0001c0001t0011g0102 a0001c0001t0011g0107 others(10): 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 | 14 | a0001c0001t0011g0002 a0001c0001t0011g0102 a0001c0001t0011g0107 others(11): 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 | a0001c0001t0031g0275 | 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 | a0001c0010t0003g0242 | 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 | 13 | a0001c0001t0011g0002 a0001c0001t0011g0102 a0001c0001t0011g0107 others(10): 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0004g0110 | 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 | a0001c0001t0020g0194 a0001c0001t0020g0195 a0001c0001t0020g0196 others(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 | a0001c0001t0002g0083 | 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 | a0001c0001t0002g0291 | 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 | a0001c0001t0021g0016 a0001c0001t0021g0277 a0001c0001t0022g0276 others(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 | a0001c0001t0047g0237 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0021g0016 a0001c0001t0021g0277 a0001c0001t0022g0276 others(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 | 88 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0031 others(85): Show |
93 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(90): 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 | a0002c0002t0059g0030 | 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 | a0001c0001t0003g0259 a0001c0001t0003g0260 a0001c0001t0003g0265 others(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 | a0001c0001t0077g0283 | 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 | 84 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0031 others(81): Show |
89 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.3100-213G>A | PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 9/15 | chr6 | 63702295 | |||||||
chr6:63702299 | C | T | 195 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0031 others(192): Show |
209 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(206): 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 | a0001c0001t0008g0125 | 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 | a0001c0001t0002g0077 a0001c0001t0002g0079 a0001c0001t0002g0087 others(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 | a0001c0001t0050g0178 | 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 | a0001c0001t0079g0293 | 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 | a0001c0001t0008g0150 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0047g0237 | 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 | 55 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(52): 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 | a0004c0004t0033g0286 | 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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0002g0085 a0001c0001t0002g0093 a0001c0001t0014g0084 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0001t0050g0178 | 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 | a0001c0001t0001g0038 a0001c0001t0002g0098 a0004c0004t0026g0287 others(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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0006c0006t0003g0209 | 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 | a0001c0001t0005g0070 | 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 | a0001c0001t0007g0244 a0001c0001t0007g0245 a0001c0001t0007g0246 others(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 | a0004c0004t0026g0287 a0004c0004t0033g0286 a0014c0021t0026g0289 |
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 | a0008c0020t0051g0033 | 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 | a0004c0004t0026g0287 a0004c0004t0033g0286 a0014c0021t0026g0289 |
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 | 55 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(52): 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 | a0001c0001t0030g0243 a0001c0001t0030g0256 |
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 | a0001c0001t0031g0275 | 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 | 55 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(52): 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 | a0001c0001t0001g0156 | 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 | 81 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(78): 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 | a0001c0001t0052g0168 | 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 | a0001c0001t0001g0184 | 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 | 106 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0031 others(103): Show |
115 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(112): 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 | a0001c0001t0007g0253 | 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 | a0001c0001t0023g0114 a0001c0001t0023g0134 a0001c0001t0023g0135 |
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 | a0001c0001t0079g0293 a0011c0019t0080g0292 |
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 | a0001c0015t0076g0285 | 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 | a0001c0001t0012g0019 a0001c0001t0034g0024 |
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 | a0001c0001t0002g0065 | 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 | a0001c0001t0004g0203 | 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 | a0001c0001t0001g0153 | 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 | 52 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(49): 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 | a0001c0001t0004g0202 a0001c0001t0004g0203 |
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 | a0001c0001t0028g0257 a0001c0001t0028g0258 a0001c0001t0030g0243 others(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 | a0001c0001t0079g0293 | 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 | a0001c0001t0077g0283 | 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 | a0001c0001t0007g0244 a0001c0001t0007g0245 a0001c0001t0007g0246 others(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 | 14 | a0001c0001t0001g0200 a0001c0001t0002g0052 a0001c0001t0011g0002 others(11): 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 | 58 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(55): 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 | a0001c0001t0007g0246 | 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 | a0001c0001t0023g0114 a0001c0001t0023g0134 a0001c0001t0023g0135 |
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 | 231 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0037 others(228): Show |
243 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(240): 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 | a0001c0001t0001g0164 a0001c0001t0002g0056 a0001c0001t0003g0215 others(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 |
53 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(50): 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 | 15 | a0001c0001t0002g0007 a0001c0001t0002g0044 a0001c0001t0002g0076 others(12): 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 | a0001c0001t0004g0139 | 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 | 12 | a0001c0001t0011g0002 a0001c0001t0011g0102 a0001c0001t0011g0107 others(9): 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 | a0001c0001t0007g0251 | 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 | a0001c0001t0002g0089 a0001c0001t0007g0244 a0001c0001t0007g0245 others(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 | a0001c0001t0074g0252 | 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 | a0001c0015t0076g0285 | 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 | a0001c0001t0018g0012 a0001c0001t0018g0177 a0001c0001t0018g0189 others(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 | a0001c0001t0015g0103 | 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 | 58 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(55): 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 | a0004c0004t0026g0287 a0004c0004t0033g0286 a0014c0021t0026g0289 |
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 | 12 | a0001c0001t0011g0002 a0001c0001t0011g0102 a0001c0001t0011g0107 others(9): 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 | 83 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(80): 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 | a0001c0001t0007g0253 | 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 | a0001c0001t0077g0283 | 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 | a0001c0001t0001g0166 | 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 | 58 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0213 others(55): 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 | a0001c0001t0012g0019 a0001c0001t0012g0020 a0001c0001t0012g0021 others(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 | a0001c0001t0005g0060 | 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 | a0001c0001t0021g0016 a0001c0001t0021g0277 a0001c0001t0022g0276 others(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 |